Publicações científicas
(103)
(Referências obtidas automaticamente do Web of Science e do SciELO, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores)
GUERRA, JOAO V. S.;
OLIVEIRA-SANTOS, JOSE;
OLIVEIRA, DANYLLO F.;
LEAL, GABRIELA F.;
OLIVEIRA, JOAO RICARDO M.;
COSTA, SILVIA S.;
KREPISCHI, V, ANA C.;
VIANNA-MORGANTE, ANGELA M.;
MASCHIETTO, MARIANA.
DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation.
EUROPEAN JOURNAL OF MEDICAL GENETICS,
v. 63,
n. 3
MAR 2020.
Citações Web of Science: 1.
DA SILVA MONTENEGRO, EDUARDA MORGANA;
COSTA, CLAUDIA SAMOGY;
CAMPOS, GABRIELE;
SCLIAR, MARILIA;
DE ALMEIDA, TATIANA FERREIRA;
ZACHI, ELAINE CRISTINA;
WAHYS SILVA, ISABELA MAYA;
CHAN, ADA J. S.;
ZARREI, MEHDI;
LOURENCO, V, NAILA C.;
YAMAMOTO, GUILHERME LOPES;
SCHERER, STEPHEN;
PASSOS-BUENO, MARIA RITA.
Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
Autism Research,
v. 13,
n. 2,
p. 199-206,
FEB 2020.
Citações Web of Science: 1.
FERNANDES, STEPHANIE A.;
ALMEIDA, CAMILA F.;
SOUZA, LUCAS S.;
LAZAR, MONIZE;
ONOFRE-OLIVEIRA, PAULA;
YAMAMOTO, GUILHERME L.;
NOGUEIRA, LETICIA;
TASAKI, LETICIA Y.;
CARDOSO, RAFAELA R.;
PAVANELLO, RITA C. M.;
SILVA, HELGA C. A.;
FERRARI, MERARI F. R.;
BIGOT, ANNE;
MOULY, VINCENT;
VAINZOF, MARIZ.
Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy.
Disease Models & Mechanisms,
v. 13,
n. 2, SI
FEB 2020.
Citações Web of Science: 2.
GRIESI-OLIVEIRA, K.;
FOGO, M. S.;
PINTO, B. G. G.;
ALVES, A. Y.;
SUZUKI, A. M.;
MORALES, A. G.;
EZQUINA, S.;
SOSA, O. J.;
SUTTON, G. J.;
SUNAGA-FRANZE, D. Y.;
BUENO, A. P.;
SEABRA, G.;
SARDINHA, L.;
COSTA, S. S.;
ROSENBERG, C.;
ZACHI, E. C.;
SERTIE, A. L.;
MARTINS-DE-SOUZA, D.;
REIS, E. M.;
VOINEAGU, I.;
PASSOS-BUENO, M. R.
Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder.
MOLECULAR PSYCHIATRY,
FEB 2020.
Citações Web of Science: 0.
GOULART, ERNESTO;
DE CAIRES-JUNIOR, LUIZ CARLOS;
TELLES-SILVA, KAYQUE ALVES;
SILVA ARAUJO, BRUNO HENRIQUE;
ROCCO, SILVANA APARECIDA;
SFORCA, MAURICIO;
DE SOUSA, IRENE LAYANE;
KOBAYASHI, GERSON S.;
MUSSO, CAMILA MANSO;
ASSONI, AMANDA FARIA;
OLIVEIRA, DANYLLO;
CALDINI, ELIA;
RAIA, SILVANO;
LELKES, PETER I.;
ZATZ, MAYANA.
3D bioprinting of liver spheroids derived from human induced pluripotent stem cells sustain liver function and viability in vitro.
BIOFABRICATION,
v. 12,
n. 1
JAN 2020.
Citações Web of Science: 0.
MOOSA, SHAHIDA;
YAMAMOTO, GUILHERME L.;
GARBES, LUTZ;
KEUPP, KATHARINA;
BELEZA-MEIRELES, ANA;
MORENO, CAROLINA ARAUJO;
VALADARES, EUGENIA RIBEIRO;
DE SOUSA, SERGIO B.;
MAIA, SOFIA;
SARAIVA, JORGE;
HONJO, RACHEL S.;
KIM, CHONG AE;
DE MENEZES, HAMILTON CABRAL;
LAUSCH, EKKEHART;
LORINI, PABLO VILLAVICENCIO;
LAMOUNIER, JR., ARSONVAL;
BEZERRA CARNIERO, TULIO CANELLA;
GIUNTA, CECILIA;
ROHRBACH, MARIANNE;
JANNER, MARCO;
SEMLER, OLIVER;
BELEGGIA, FILIPPO;
LI, YUN;
YIGIT, GOEKHAN;
REINTJES, NADINE;
ALTMUELLER, JANINE;
NUERNBERG, PETER;
CAVALCANTI, DENISE P.;
ZABEL, BERNHARD;
WARMAN, MATTHEW L.;
BERTOLA, DEBORA R.;
WOLLNIK, BERND;
NETZER, CHRISTIAN.
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.
American Journal of Human Genetics,
v. 105,
n. 4,
p. 836-843,
OCT 3 2019.
Citações Web of Science: 0.
LIMA, SHIRLEY O. A.;
FARIAS, ALLYSSON A.;
ALBINO, VICTOR A.;
MARQUES-ALVES, YANNA K.;
OLINDA, RICARDO;
SANTOS-SILVA, TAIS A.;
ALVES, LEANDRO U.;
ZATZ, MAYANA;
SANTOS, SILVANA.
A population-based study of inter-generational attitudes towards consanguineous marriages in north-eastern Brazil.
JOURNAL OF BIOSOCIAL SCIENCE,
v. 51,
n. 5,
p. 683-697,
SEP 2019.
Citações Web of Science: 0.
GOULART, ERNESTO;
DE CAIRES-JUNIOR, LUIZ CARLOS;
TELLES-SILVA, KAYQUE ALVES;
SILVA ARAUJO, BRUNO HENRIQUE;
KOBAYASHI, GERSON S.;
MUSSO, CAMILA MANSO;
ASSONI, AMANDA FARIA;
OLIVEIRA, DANYLLO;
CALDINI, ELIA;
GERSTENHABER, JONATHAN A.;
RAIA, SILVANO;
LELKES, PETER I.;
ZATZ, MAYANA.
Adult and iPS-derived non-parenchymal cells regulate liver organoid development through differential modulation of Wnt and TGF-beta.
STEM CELL RESEARCH & THERAPY,
v. 10,
n. 1
AUG 15 2019.
Citações Web of Science: 1.
ISHIBA, RENATA;
SANTOS, ANDRE LUIS F.;
ALMEIDA, CAMILA F.;
CAIRES, JR., LUIZ CARLOS;
RIBEIRO, JR., ANTONIO F.;
AYUB-GUERRIERI, DANIELLE;
FERNANDES, STEPHANIE A.;
SOUZA, LUCAS S.;
VAINZOF, MARIZ.
Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse.
Journal of Molecular Histology,
v. 50,
n. 4,
p. 375-387,
AUG 2019.
Citações Web of Science: 0.
SAMOGY-COSTA, CLAUDIA ISMANIA;
VARELLA-BRANCO, ELISA;
MONFARDINI, FREDERICO;
FERRAZ, HELEN;
FOCK, RODRIGO AMBROSIO;
ALMEIDA BARBOSA, RICARDO HENRIQUE;
SANTOS PESSOA, ANDRE LUIZ;
ALVAREZ PEREZ, ANA BEATRIZ;
LOURENCO, NAILA;
VIBRANOVSKI, MARIA;
KREPISCHI, ANA;
ROSENBERG, CARLA;
PASSOS-BUENO, MARIA RITA.
A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS,
v. 11,
JUL 18 2019.
Citações Web of Science: 1.
RIVAS, MARIA PRATES;
MARQUES AGUIAR, TALITA FERREIRA;
FERNANDES, GUSTAVO RIBEIRO;
CAIRES, LUIZ CARLOS;
GOULART, ERNESTO;
TELLES-SILVA, KAYQUE ALVES;
CYPRIANO, MONICA;
CAMINADA DE TOLEDO, SILVIA REGINA;
ROSENBERG, CARLA;
CARRARO, DIRCE MARIA;
LIMA DA COSTA, CECILIA MARIA;
DA CUNHA, ISABELA WERNECK;
VICTORINO KREPISCHI, ANA CRISTINA.
TET Upregulation Leads to 5-Hydroxymethylation Enrichment in Hepatoblastoma.
FRONTIERS IN GENETICS,
v. 10,
JUN 12 2019.
Citações Web of Science: 1.
GUO, LONG;
BERTOLA, DEBORA ROMEO;
TAKANOHASHI, ASAKO;
SAITO, ASUKA;
SEGAWA, YUKO;
YOKOTA, TAKANORI;
ISHIBASHI, SATORU;
NISHIDA, YOICHIRO;
YAMAMOTO, GUILHERME LOPES;
DA SILVA FRANCO, JOSE FRANCISCO;
HONJO, RACHEL SAYURI;
KIM, CHONG AE;
MUSSO, CAMILA MANSO;
TIMMONS, MARGARET;
PIZZINO, AMY;
TAFT, RYAN J.;
LAJOIE, BRYAN;
KNIGHT, MELANIE A.;
FISCHBECK, KENNETH H.;
SINGLETON, ANDREW B.;
FERREIRA, CARLOS R.;
WANG, ZHENG;
YAN, LI;
GARBERN, JAMES Y.;
SIMSEK-KIPER, PELIN O.;
OHASHI, HIROFUMI;
ROBEY, PAMELA G.;
BOYDE, ALAN;
MATSUMOTO, NAOMICHI;
MIYAKE, NORIKO;
SPRANGER, JUERGEN;
SCHIFFMANN, RAPHAEL;
VANDERVER, ADELINE;
NISHIMURA, GEN;
DOS SANTOS PASSOS-BUENO, MARIA RITA;
SIMONS, CAS;
ISHIKAWA, KINYA;
IKEGAWA, SHIRO.
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation.
American Journal of Human Genetics,
v. 104,
n. 5,
p. 925-935,
MAY 2 2019.
Citações Web of Science: 7.
BURRAGE, LINDSAY C.;
REYNOLDS, JOHN J.;
BARATANG, NISSAN VIDA;
PHILLIPS, JENNIFER B.;
WEGNER, JEREMY;
MCFARQUHAR, ASHLEY;
HIGGS, MARTIN R.;
CHRISTIANSEN, AUDREY E.;
LANZA, DENISE G.;
SEAVITT, JOHN R.;
JAIN, MAHIM;
LI, XIAOHUI;
PARRY, DAVID A.;
RAMAN, VANDANA;
CHITAYAT, DAVID;
CHINN, IVAN K.;
BERTUCH, ALISON A.;
KARAVITI, LEFKOTHEA;
SCHLESINGER, ALAN E.;
EARL, DAWN;
BAMSHAD, MICHAEL;
SAVARIRAYAN, RAVI;
DODDAPANENI, HARSHA;
MUZNY, DONNA;
JHANGIANI, SHALINI N.;
ENG, CHRISTINE M.;
GIBBS, RICHARD A.;
BI, WEIMIN;
EMRICK, LISA;
ROSENFELD, JILL A.;
POSTLETHWAIT, JOHN;
WESTERFIELD, MONTE;
DICKINSON, MARY E.;
BEAUDET, ARTHUR L.;
RANZA, EMMANUELLE;
HUBER, CELINE;
CORMIER-DAIRE, VALERIE;
SHEN, WEI;
MAO, RONG;
HEANEY, JASON D.;
ORANGE, I. JORDAN S.;
BERTOLA, DEBORA;
YAMAMOTO, GUILHERME L.;
BARATELA, WAGNER AR;
BUTLER, MERLIN G.;
ALI, ASIM;
ADELI, MEHDI;
COHN, DANIEL H.;
KRAKOW, DEBORAH;
JACKSON, ANDREW P.;
LEES, MELISSA;
OFFIAH, AMAKA C.;
CARLSTON, COLLEEN M.;
CAREY, JOHN C.;
STEWART, GRANT S.;
BACINO, CARLOS A.;
CAMPEAU, PHILIPPE M.;
LEE, BRENDAN;
MENDELIAN, UNIV WASHINGTON CTR;
NETWORK, UNDIAGNOSED DIS.
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
American Journal of Human Genetics,
v. 104,
n. 3,
p. 422-438,
MAR 7 2019.
Citações Web of Science: 0.
MELO, KARLA P.;
SILVA, CAROLLINY M.;
ALMEIDA, MICHAEL F.;
CHAVES, RODRIGO S.;
MARCOURAKIS, TANIA;
CARDOSO, SANDRA M.;
DEMASI, MARILENE;
NETTO, LUIS E. S.;
FERRARI, MERARI F. R.
Mild Exercise Differently Affects Proteostasis and Oxidative Stress on Motor Areas During Neurodegeneration: A Comparative Study of Three Treadmill Running Protocols.
NEUROTOXICITY RESEARCH,
v. 35,
n. 2,
p. 410-420,
FEB 2019.
Citações Web of Science: 1.
DE OLIVEIRA, JULIANA FERREIRA;
VITAL DO PRADO, PAULA FAVORETTI;
DA COSTA, SILVIA SOUZA;
SFORCA, MAURICIO LUIS;
CANATELI, CAMILA;
RANZANI, AMERICO TAVARES;
MASCHIETTO, MARIANA;
LOPES DE OLIVEIRA, PAULO SERGIO;
OTTO, PAULO A.;
KLEVIT, RACHEL E.;
VICTORINO KREPISCHI, ANA CRISTINA;
ROSENBERG, CARLA;
FRANCHINI, KLEBER GOMES.
Mechanistic insights revealed by a UBE2A mutation linked to intellectual disability.
Nature Chemical Biology,
v. 15,
n. 1,
p. 62+,
JAN 2019.
Citações Web of Science: 2.
PEREIRA, LARISSA VILELA;
BENTO, RICARDO FERREIRA;
CRUZ, DAYANE B.;
MARCHI, CLAUDIA;
SALOMONE, RAQUEL;
OITICICCA, JEANNE;
COSTA, MARCIO PAULINO;
HADDAD, LUCIANA A.;
MINGRONI-NETTO, REGINA CELIA;
ZABEU ROSSI COSTA, HELOISA JULIANA.
Stem Cells from Human Exfoliated Deciduous Teeth (SHED) Differentiate in vivo and Promote Facial Nerve Regeneration.
CELL TRANSPLANTATION,
v. 28,
n. 1,
p. 55-64,
JAN 2019.
Citações Web of Science: 3.
LUIZ GUSTAVO DUFNER-ALMEIDA;
DAYANE BERNARDINO DA CRUZ;
REGINA CÉLIA MINGRONI NETTO;
ANA CARLA BATISSOCO;
JEANNE OITICICA;
RODRIGO SALAZAR-SILVA.
Stem-cell therapy for hearing loss: are we there yet?.
Brazilian Journal of Otorhinolaryngology,
v. 85,
n. 4,
p. 520-529,
Ago. 2019.
ROMANELLI TAVARES, VANESSA L.;
KAGUE, ERIKA;
MUSSO, CAMILA M.;
ALEGRIA, THIAGO G. P.;
FREITAS, RENATO S.;
BERTOLA, DEBORA R.;
TWIGG, STEPHEN R. F.;
PASSOS-BUENO, MARIA R.
Craniofrontonasal Syndrome Caused by Introduction of a Novel uATG in the 5 ` UTR of EFNB1.
MOLECULAR SYNDROMOLOGY,
v. 10,
n. 1-2,
p. 40-47,
2019.
Citações Web of Science: 1.
DE FARIAS, ALLYSSON ALLAN;
NUNES, KELLY;
LEMES, RENAN BARBOSA;
MOURA, RONALD;
FERNANDES, GUSTAVO RIBEIRO;
MELO, UIRA SOUTO;
ZATZ, MAYANA;
KOK, FERNANDO;
SANTOS, SILVANA.
Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations.
SCIENTIFIC REPORTS,
v. 8,
NOV 8 2018.
Citações Web of Science: 0.
DOS SANTOS, ALEXSANDRO;
CAMPAGNARI, FRANCINE;
VICTORINO KREPISCHI, ANA CRISTINA;
RIBEIRO CAMARA, MARIA DE LOURDES;
DE ARRUDA BRASIL, RITA DE CASSIA E.;
VIEIRA, LIGIA;
VIANNA-MORGANTE, ANGELA M.;
OTTO, PAULO A.;
PEARSON, PETER L.;
ROSENBERG, CARLA.
Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion.
Chromosome Research,
v. 26,
n. 3,
p. 191-198,
SEP 2018.
Citações Web of Science: 1.
GOMES, JULIANA P.;
COATTI, GIULIANA C.;
VALADARES, MARCOS C.;
ASSONI, AMANDA F.;
PELATTI, MAYRA V.;
SECCO, MARIANE;
ZATZ, MAYANA.
Human Adipose-Derived CD146(+) Stem Cells Increase Life Span of a Muscular Dystrophy Mouse Model More Efficiently than Mesenchymal Stromal Cells.
DNA AND CELL BIOLOGY,
v. 37,
n. 9,
p. 798-804,
SEP 2018.
Citações Web of Science: 0.
GRIESI-OLIVEIRA, KARINA;
SUZUKI, ANGELA MAY;
ALVES, ALINE YASUDA;
CINTRA NUNES MAFRA, ANA CAROLINA;
YAMAMOTO, GUILHERME LOPES;
EZQUINA, SUZANA;
MAGALHAES, YULI THAMIRES;
FORTI, FABIO LUIS;
SERTIE, ANDREA LAURATO;
ZACHI, ELAINE CRISTINA;
VADASZ, ESTEVAO;
PASSOS-BUENO, MARIA RITA.
Actin cytoskeleton dynamics in stem cells from autistic individuals.
SCIENTIFIC REPORTS,
v. 8,
JUL 24 2018.
Citações Web of Science: 1.
ARAUJO, BRUNO H. S.;
KAID, CAROLINI;
DE SOUZA, JANAINA S.;
DA SILVA, SERGIO GOMES;
GOULART, ERNESTO;
CAIRES, LUIZ C. J.;
MUSSO, CAMILA M.;
TORRES, LAILA B.;
FERRASA, ADRIANO;
HERAI, ROBERTO;
ZATZ, MAYANA;
OKAMOTO, OSWALDO K.;
CAVALHEIRO, ESPER A.
Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro.
Molecular Neurobiology,
v. 55,
n. 7,
p. 5962-5975,
JUL 2018.
Citações Web of Science: 6.
MALCHER, CAROLINA;
YAMAMOTO, GUILHERME L.;
BURNHAM, PHILIP;
EZQUINA, SUZANA A. M.;
LOURENCO, V, NAILA C.;
BALKASSMI, SAHILLA;
MARCO ANTONIO, DAVID S.;
HSIA, GABRIELLA S. P.;
GOLLOP, THOMAZ;
PAVANELLO, RITA C.;
LOPES, MARCO ANTONIO;
BAKKER, EGBERT;
ZATZ, MAYANA;
BERTOLA, DEBORA;
DE VLAMINCK, IWIJN;
PASSOS-BUENO, MARIA RITA.
Development of a comprehensive noninvasive prenatal test.
GENETICS AND MOLECULAR BIOLOGY,
v. 41,
n. 3,
p. 545-554,
JUL-SEP 2018.
Citações Web of Science: 2.
KAID, CAROLINI;
GOULART, ERNESTO;
CAIRES-JUNIOR, LUIZ C.;
ARAUJO, BRUNO H. S.;
SOARES-SCHANOSKI, ALESSANDRA;
BUENO, HELOISA M. S.;
TELLES-SILVA, KAYQUE A.;
ASTRAY, RENATO M.;
ASSONI, AMANDA F.;
JUNIOR, ANTONIO F. R.;
VENTINI, DANIELLA C.;
PUGLIA, ANA L. P.;
GOMES, ROSELANE P.;
ZATZ, MAYANA;
OKAMOTO, OSWALDO K.
Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo.
Cancer Research,
v. 78,
n. 12,
p. 3363-3374,
JUN 15 2018.
Citações Web of Science: 6.
DANTAS, VITOR G. L.;
RAVAL, MANMEET H.;
BALLESTEROS, ANGELA;
CUI, RUNJIA;
GUNTHER, LAURA K.;
YAMAMOTO, GUILHERME L.;
ALVES, LEANDRO UCELA;
BUENO, ANDRE SILVA;
LEZIROVITZ, KARINA;
PIRANA, SULENE;
MENDES, BEATRIZ C. A.;
YENGO, CHRISTOPHER M.;
KACHAR, BECHARA;
MINGRONI-NETTO, REGINA C.
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss.
SCIENTIFIC REPORTS,
v. 8,
JUN 7 2018.
Citações Web of Science: 0.
HSIA, GABRIELLA S. P.;
MUSSO, CAMILA M.;
ALVIZI, LUCAS;
BRITO, LUCIANO A.;
KOBAYASHI, GERSON S.;
PAVANELLO, RITA C. M.;
ZATZ, MAYANA;
GARDHAM, ALICE;
WAKELING, EMMA;
ZECHI-CEIDE, ROSELI M.;
BERTOLA, DEBORA;
PASSOS-BUENO, MARIA RITA.
Complexity of the 5 ` Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development.
FRONTIERS IN GENETICS,
v. 9,
APR 25 2018.
Citações Web of Science: 0.
KAGUE, E.;
WITTEN, P. E.;
SOENENS, M.;
CAMPOS, C. L.;
LUBIANA, T.;
FISHER, S.;
HAMMOND, C.;
BROWN, K. ROBSON;
PASSOS-BUENO, M. R.;
HUYSSEUNE, A.
Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth.
Developmental Biology,
v. 435,
n. 2,
p. 176-184,
MAR 15 2018.
Citações Web of Science: 4.
DE CAIRES, JR., LUIZ CARLOS;
GOULART, ERNESTO;
MELO, UIRASOUTO;
HENRIQUE ARAUJO, BRUNO SILVA;
ALVIZI, LUCAS;
SCHANOSKI, ALESSANDRA SOARES;
DE OLIVEIRA, DANYLLO FELIPE;
KOBAYASHI, GERSON SHIGERU;
GRIESI-OLIVEIRA, KARINA;
MUSSO, CAMILA MANSO;
AMARAL, MURILOSENA;
DASILVA, LUCAS FERREIRA;
ASTRAY, RENATO MANCINI;
SUAREZ-PATINO, SANDRA FERNANDA;
VENTINI, DANIELLA CRISTINA;
DA SILVA, SERGIO GOMES;
YAMAMOTO, GUILHERME LOPES;
EZQUINA, SUZANA;
NASLAVSKY, MICHEL SATYA;
ALVES SILVA, KAYQUE TELLES;
WEINMANN, KARINA;
VAN DER LINDEN, VANESSA;
VAN DER LINDEN, HELIO;
RICARDO DE OLIVEIRA, JOAO MENDES;
MARIA ARRAIS, NIVIA RODRIGUES;
MELO, ADRIANA;
FIGUEIREDO, THALITA;
SANTOS, SILVANA;
GOES MEIRA, JOANNA CASTRO;
PASSOS, SAULO DUARTE;
DE ALMEIDA, ROQUE PACHECO;
BISPO, ANA JOVINABARRETO;
CAVALHEIRO, ESPERABRAO;
KALIL, JORGE;
CUNHA-NETO, EDECIO;
NAKAYA, HELDER;
SANTOS, ROBERT ANDREATA;
DE SOUZA FERREIRA, LUIS CARLOS;
VERJOVSKI-ALMEIDA, SERGIO;
HO, PAULO LEE;
PASSOS-BUENO, MARIA RITA;
ZATZ, MAYANA.
Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells.
NATURE COMMUNICATIONS,
v. 9,
FEB 2 2018.
Citações Web of Science: 9.
MEHRJOUY, MANA M.;
FONSECA, ANA CAROLINA S.;
EHMKE, NADJA;
PASKULIN, GIORGIO;
NOVELLI, ANTONIO;
BENEDICENTI, FRANCESCO;
MENCARELLI, MARIA ANTONIETTA;
RENIERI, ALESSANDRA;
BUSA, TIFFANY;
MISSIRIAN, CHANTAL;
HANSEN, CLAUS;
ABE, KIKUE TERADA;
SPECK-MARTINS, CARLOS EDUARDO;
VIANNA-MORGANTE, ANGELA M.;
BAK, MADS;
TOMMERUP, NIELS.
Regulatory variants of FOXG1 in the context of its topological domain organisation.
European Journal of Human Genetics,
v. 26,
n. 2,
p. 186-196,
FEB 2018.
Citações Web of Science: 4.
GUIMARAES MARQUES, MARCIA J.;
REYES-GARCIA, SELVIN Z.;
MARQUES-CARNEIRO, JOSE E.;
LOPES-SILVA, LEONARDO B.;
ANDERSEN, MONICA L.;
CAVALHEIRO, ESPER A.;
SCORZA, FULVIO A.;
SCORZA, CARLA A.
Long-term Potentiation Decay and Poor Long-lasting Memory Process in the Wild Rodents Proechimys from Brazil's Amazon Rainforest.
FRONTIERS IN BEHAVIORAL NEUROSCIENCE,
v. 12,
JAN 23 2018.
Citações Web of Science: 2.
WHITE, JANSON J.;
MAZZEU, JULIANA F.;
COBAN-AKDEMIR, ZEYNEP;
BAYRAM, YAVUZ;
BAHRAMBEIGI, VAHID;
HOISCHEN, ALEXANDER;
VAN BON, BREGJE W. M.;
GEZDIRICI, ALPER;
GULEC, ELIF YILMAZ;
RAMOND, FRANCIS;
TOURAINE, RENAUD;
THEVENON, JULIEN;
SHINAWI, MARWAN;
BEAVER, ERIN;
HEELEY, JENNIFER;
HOOVER-FONG, JULIE;
DURMAZ, CEREN D.;
KARABULUT, HALIL GURHAN;
MARZIOGLU-OZDEMIR, EBRU;
CAYIR, ATILLA;
DUZ, MEHMET B.;
SEVEN, MEHMET;
PRICE, SUSAN;
FERREIRA, BARBARA MERFORT;
VIANNA-MORGANTE, ANGELA M.;
ELLARD, SIAN;
PARRISH, ANDREW;
STALS, KAREN;
FLORES-DABOUB, JOSUE;
JHANGIANI, SHALINI N.;
GIBBS, RICHARD A.;
BRUNNER, HAN G.;
SUTTON, V. REID;
LUPSKI, JAMES R.;
CARVALHO, CLAUDIA M. B.;
MENDELIAN, BAYLOR-HOPKINS CTR.
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
American Journal of Human Genetics,
v. 102,
n. 1,
p. 27-43,
JAN 4 2018.
Citações Web of Science: 19.
CERONI, JOSE R. M.;
YAMAMOTO, GUILHERME L.;
HONJO, RACHEL S.;
KIM, CHONG A.;
PASSOS-BUENO, MARIA R.;
BERTOLA, DEBORA R.
Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?.
GENETICS AND MOLECULAR BIOLOGY,
v. 41,
n. 1,
p. 85-91,
JAN-MAR 2018.
Citações Web of Science: 0.
MASOTTI, C.;
BRITO, L. A.;
NICA, A. C.;
LUDWIG, K. U.;
NUNES, K.;
SAVASTANO, C. P.;
MALCHER, C.;
FERREIRA, S. G.;
KOBAYASHI, G. S.;
BUENO, D. F.;
ALONSO, N.;
FRANCO, D.;
ROJAS-MARTINEZ, A.;
DOS SANTOS, S. E.;
GALANTE, P. A.;
MEYER, D.;
HUENEMEIER, T.;
MANGOLD, E.;
DERMITZAKIS, E. T.;
PASSOS-BUENO, M. R.
MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach.
JOURNAL OF DENTAL RESEARCH,
v. 97,
n. 1,
p. 33-40,
JAN 2018.
Citações Web of Science: 0.
CARNEIRO, THAISE N. R.;
KREPISCHI, ANA C. V.;
COSTA, SILVIA S.;
DA SILVA, ISRAEL TOJAL;
VIANNA-MORGANTE, ANGELA M.;
VALIERIS, RENAN;
EZQUINA, SUZANA A. M.;
BERTOLA, DEBORA R.;
OTTO, PAULO A.;
ROSENBERG, CARLA.
Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases.
APPLICATION OF CLINICAL GENETICS,
v. 11,
p. 93-98,
2018.
Citações Web of Science: 9.
HOMMA, THAIS K.;
KREPISCHI, ANA C. V.;
FURUYA, TATIANE K.;
HONJO, RACHEL S.;
MALAQUIAS, ALEXSANDRA C.;
BERTOLA, DEBORA R.;
COSTA, SILVIA S.;
CANTON, ANA P.;
ROELA, ROSIMEIRE A.;
FREIRE, BRUNA L.;
KIM, CHONG A.;
ROSENBERG, CARLA;
JORGE, ALEXANDER A. L.
Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause.
Hormone Research in Paediatrics,
v. 89,
n. 1,
p. 13-21,
2018.
Citações Web of Science: 5.
ALVES, LEANDRO U.;
SANTOS, SILVANA;
MUSSO, CAMILA M.;
EZQUINA, SUZANA A. M.;
OPITZ, JOHN M.;
KOK, FERNANDO;
OTTO, PAULO A.;
MINGRONI-NETTO, REGINA C.
Santos syndrome is caused by mutation in the WNT7A gene.
JOURNAL OF HUMAN GENETICS,
v. 62,
n. 12,
p. 1073-1078,
DEC 2017.
Citações Web of Science: 4.
NUNES, BRUNO GHIROTTO;
LOURES, FLAVIO VIEIRA;
SIQUEIRA BUENO, HELOISA MARIA;
CANGUSSU, ERICA BARONI;
GOULART, ERNESTO;
COATTI, GIULIANA CASTELLO;
CALDINI, ELIA GARCIA;
CONDINO-NETO, ANTONIO;
ZATZ, MAYANA.
Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice.
European Journal of Human Genetics,
v. 25,
n. 12,
p. 1388-1396,
DEC 2017.
Citações Web of Science: 0.
MASCHIETTO, MARIANA;
RODRIGUES, TATIANE CRISTINA;
KASHIWABARA, ANDRE YOSHIAKI;
SOUZA DE ARAUJO, ERICA SARA;
MARQUES AGUIAR, TALITA FERREIRA;
LIMA DA COSTA, CECILIA MARIA;
DA CUNHA, ISABELA WERNECK;
VASQUES, LUCIANA DOS REIS;
CYPRIANO, MONICA;
BRENTANI, HELENA;
CAMINADA DE TOLEDO, SILVIA REGINA;
PEARSON, PETER LEES;
CARRARO, DIRCE MARIA;
ROSENBERG, CARLA;
KREPISCHI, ANA C. V.
DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations.
ONCOTARGET,
v. 8,
n. 58,
p. 97871-97889,
NOV 17 2017.
Citações Web of Science: 2.
LEE, CHAE SYNG;
FU, HE;
BARATANG, NISSAN;
ROUSSEAU, JUSTINE;
KUMRA, HEENA;
SUTTON, V. REID;
NICETA, MARCELLO;
CIOLFI, ANDREA;
YAMAMOTO, GUILHERME;
BERTOLA, DEBORA;
MARCELIS, CARLO L.;
LUGTENBERG, DORIEN;
BARTULI, ANDREA;
KIM, CHOEL;
HOOVER-FONG, JULIE;
SOBREIRA, NARA;
PAULI, RICHARD;
BACINO, CARLOS;
KRAKOW, DEBORAH;
PARBOOSINGH, JILLIAN;
YAP, PATRICK;
KARIMINEJAD, ARIANA;
MCDONALD, MARIE T.;
ARACENA, MARIANA I.;
LAUSCH, EKKEHART;
UNGER, SHEILA;
SUPERTI-FURGA, ANDREA;
LU, JAMES T.;
COHN, DAN H.;
TARTAGLIA, MARCO;
LEE, BRENDAN H.;
REINHARDT, DIETER P.;
CAMPEAU, PHILIPPE M.;
MENDELIAN, BAYLOR-HOPKINS CTR.
Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ``Corner Fractures''.
American Journal of Human Genetics,
v. 101,
n. 5,
p. 815-823,
NOV 2 2017.
Citações Web of Science: 9.
BONALDI, ADRIANO;
KASHIWABARA, ANDRE;
DE ARAUJO, ERICA S.;
PEREIRA, LYGIA V.;
PASCHOAL, ALEXANDRE R.;
ANDOZIA, MAYRA B.;
VILLELA, DARINE;
RIVAS, MARIA P.;
SUEMOTO, CLAUDIA K.;
PASQUALUCCI, CARLOS A.;
GRINBERG, LEA T.;
BRENTANI, HELENA;
MARIA-ENGLER, SILVYA S.;
CARRARO, DIRCE M.;
VIANNA-MORGANTE, ANGELA M.;
ROSENBERG, CARLA;
VASQUES, LUCIANA R.;
KREPISCHI, ANA.
Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review.
EPIGENOMES,
v. 1,
n. 2
SEP 2017.
Citações Web of Science: 2.
GOMES, JULIANA P. A.;
ASSONI, AMANDA F.;
PELATTI, MAYRA;
COATTI, GIULIANA;
OKAMOTO, OSWALDO KEITH;
ZATZ, MAYANA.
Deepening a Simple Question: Can MSCs Be Used to Treat Cancer?.
ANTICANCER RESEARCH,
v. 37,
n. 9,
p. 4747-4758,
SEP 2017.
Citações Web of Science: 2.
NASLAVSKY, MICHEL SATYA;
YAMAMOTO, GUILHERME LOPES;
DE ALMEIDA, TATIANA FERREIRA;
EZQUINA, SUZANA A. M.;
SUNAGA, DANIELE YUMI;
PHO, NAM;
BOZOKLIAN, DANIEL;
MILKEWITZ SANDBERG, TATIANA ORLI;
BRITO, LUCIANO ABREU;
LAZAR, MONIZE;
BERNARDO, DANILO VICENSOTTO;
AMARO, JR., EDSON;
DUARTE, YEDA A. O.;
LEBRAO, MARIA LUCIA;
PASSOS-BUENO, MARIA RITA;
ZATZ, MAYANA.
Exomic variants of an elderly cohort of Brazilians in the ABraOM database.
Human mutation,
v. 38,
n. 7,
p. 751-763,
JUL 2017.
Citações Web of Science: 45.
YAGURA, TEITI;
SCHUCH, ANDRE PASSAGLIA;
MACHADO GARCIA, CAMILA CARRIAO;
REILY ROCHA, CLARISSA RIBEIRO;
MORENO, NATALIA CESTARI;
FRIEDMANN ANGELI, JOSE PEDRO;
MENDES, DAVI;
SEVERINO, DIVINOMAR;
SANCHEZ, ANGELICA BIANCHINI;
DI MASCIO, PAOLO;
GENNARI DE MEDEIROS, MARISA HELENA;
MARTINS MENCK, CARLOS FREDERICO.
Direct participation of DNA in the formation of singlet oxygen and base damage under UVA irradiation.
Free Radical Biology and Medicine,
v. 108,
p. 86-93,
JUL 2017.
Citações Web of Science: 7.
MILLER, EMILY E.;
KOBAYASHI, GERSON S.;
MUSSO, CAMILA M.;
ALLEN, MIRANDA;
ISHIY, FELIPE A. A.;
DE CAIRES, JR., LUIZ CARLOS;
GOULART, ERNESTO;
GRIESI-OLIVEIRA, KARINA;
ZECHI-CEIDE, ROSELI M.;
RICHIERI-COSTA, ANTONIO;
BERTOLA, DEBORA R.;
PASSOS-BUENO, MARIA RITA;
SILVER, DEBRA L.
EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome.
Human Molecular Genetics,
v. 26,
n. 12,
p. 2177-2191,
JUN 15 2017.
Citações Web of Science: 5.
ALTMUELLER, FRANZISKA;
LISSEWSKI, CHRISTINA;
BERTOLA, DEBORA;
FLEX, ELISABETTA;
STARK, ZORNITZA;
SPRANGER, STEPHANIE;
BAYNAM, GARETH;
BUSCARILLI, MICHELLE;
DYACK, SARAH;
GILLIS, JANE;
YNTEMA, HELGER G.;
PANTALEONI, FRANCESCA;
VAN LOON, ROSA L. E.;
MACKAY, SARA;
MINA, KYM;
SCHANZE, INA;
TAN, TIONG YANG;
WALSH, MAIE;
WHITE, SUSAN M.;
NIEWISCH, MARENA R.;
GARCIA-MINAUR, SIXTO;
PLAZA, DIEGO;
AHMADIAN, MOHAMMAD REZA;
CAVE, HELENE;
TARTAGLIA, MARCO;
ZENKER, MARTIN.
Genotype and phenotype spectrum of NRAS germline variants.
European Journal of Human Genetics,
v. 25,
n. 7,
p. 823-831,
JUN 2017.
Citações Web of Science: 7.
BERTOLA, DEBORA;
BUSCARILLI, MICHELLE;
STABLEY, DEBORAH L.;
BAKER, LAURA;
DOYLE, DANIEL;
BARTHOLOMEW, DENNIS W.;
SOL-CHURCH, KATIA;
GRIPP, KAREN W.
Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
v. 173,
n. 5,
p. 1309-1318,
MAY 2017.
Citações Web of Science: 8.
MUNFORD, V.;
CASTRO, L. P.;
SOUTO, R.;
LERNER, L. K.;
VILAR, J. B.;
QUAYLE, C.;
ASIF, H.;
SCHUCH, A. P.;
DE SOUZA, T. A.;
IENNE, S.;
ALVES, F. I. A.;
MOURA, L. M. S.;
GALANTE, P. A. F.;
CAMARGO, A. A.;
LIBOREDO, R.;
PENA, S. D. J.;
SARASIN, A.;
CHAIBUB, S. C.;
MENCK, C. F. M.
A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations.
British Journal of Dermatology,
v. 176,
n. 5,
p. 1270-1278,
MAY 2017.
Citações Web of Science: 9.
SAVASTANO, C. P.;
BRITO, L. A.;
FARIA, A. C.;
SETO-SALVIA, N.;
PESKETT, E.;
MUSSO, C. M.;
ALVIZI, L.;
EZQUINA, S. A. M.;
JAMES, C.;
BEALES, P.;
LEES, M.;
MOORE, G. E.;
STANIER, P.;
PASSOS-BUENO, M. R.;
GOSGENE.
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants.
Clinical Genetics,
v. 91,
n. 5,
p. 683-689,
MAY 2017.
Citações Web of Science: 7.
ROMANELLI TAVARES, VANESSA L.;
ZECHI-CEIDE, ROSELI M.;
BERTOLA, DEBORA R.;
GORDON, CHRISTOPHER T.;
FERREIRA, SIMONE G.;
HSIA, GABRIELLA S. P.;
YAMAMOTO, GUILHERME L.;
EZQUINA, SUZANA A. M.;
KOKITSU-NAKATA, NANCY M.;
VENDRAMINI-PITTOLI, SIULAN;
FREITAS, RENATO S.;
SOUZA, JOSIANE;
RAPOSO-AMARAL, CESAR A.;
ZATZ, MAYANA;
AMIEL, JEANNE;
GUION-ALMEIDA, MARIA L.;
PASSOS-BUENO, MARIA RITA.
Targeted Molecular Investigation in Patients within the Clinical Spectrum of Auriculocondylar Syndrome.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
v. 173,
n. 4,
p. 938-945,
APR 2017.
Citações Web of Science: 0.
ASSONI, AMANDA;
COATTI, GIULIANA;
VALADARES, MARCOS C.;
BECCARI, MELINDA;
GOMES, JULIANA;
PELATTI, MAYRA;
MITNE-NETO, MIGUEL;
CARVALHO, VALDEMIR M.;
ZATZ, MAYANA.
Different Donors Mesenchymal Stromal Cells Secretomes Reveal Heterogeneous Profile of Relevance for Therapeutic Use.
STEM CELLS AND DEVELOPMENT,
v. 26,
n. 3,
p. 206-214,
FEB 1 2017.
Citações Web of Science: 12.
GONCALVES DA SILVA, PATRICIA BENITES;
TEIXEIRA DOS SANTOS, MARCIA CRISTINA;
RODINI, CAROLINA OLIVEIRA;
KAID, CAROLINI;
LEITE PEREIRA, MARCIA CRISTINA;
FURUKAWA, GABRIELA;
GIMENES DA CRUZ, DANIEL SANZIO;
GOLDFEDER, MAURICIO BARBUGIANI;
REILY ROCHA, CLARISSA RIBEIRO;
ROSENBERG, CARLA;
OKAMOTO, OSWALDO KEITH.
High OCT4A levels drive tumorigenicity and metastatic potential of medulloblastoma cells.
ONCOTARGET,
v. 8,
n. 12,
p. 19192-19204,
2017.
Citações Web of Science: 3.
GONCALVES DA SILVA, PATRICIA BENITES;
RODINI, CAROLINA OLIVEIRA;
KAID, CAROLINI;
NAKAHATA, ADRIANA MITI;
LEITE PEREIRA, MARCIA CRISTINA;
MATUSHITA, HAMILTON;
DA COSTA, SILVIA SOUZA;
OKAMOTO, OSWALDO KEITH.
Establishment of a novel human medulloblastoma cell line characterized by highly aggressive stem-like cells.
Cytotechnology,
v. 68,
n. 4,
p. 1545-1560,
AUG 2016.
Citações Web of Science: 2.
YEH, ERIKA;
ATIQUE, RODRIGO;
FANGANIELLO, ROBERTO DALTO;
SUNAGA, DANIELE YUMI;
ANDRE ISHIY, FELIPE AUGUSTO;
PASSOS-BUENO, MARIA RITA.
Cell Type-Dependent Nonspecific Fibroblast Growth Factor Signaling in Apert Syndrome.
STEM CELLS AND DEVELOPMENT,
v. 25,
n. 16,
p. 1249-1260,
AUG 2016.
Citações Web of Science: 1.
QUINET, ANNABEL;
MARTINS, DAVI JARDIM;
VESSONI, ALEXANDRE TEIXEIRA;
BIARD, DENIS;
SARASIN, ALAIN;
STARY, ANNE;
MARTINS MENCK, CARLOS FREDERICO.
Translesion synthesis mechanisms depend on the nature of DNA damage in UV-irradiated human cells.
Nucleic Acids Research,
v. 44,
n. 12,
p. 5717-5731,
JUL 8 2016.
Citações Web of Science: 10.
SALGUEIRO BARBONI, MIRELLA TELLES;
GOMES MARTINS, CRISTIANE MARIA;
NAGY, BALAZS VINCE;
TSAI, TINA;
DAMICO, FRANCISCO MAX;
DA COSTA, MARCELO FERNANDES;
PAVANELLO, RITA DE CASSIA M.;
VILACA LOURENCO, NAILA CRISTINA;
PEREIRADE CERQUEIRA, ANTONIA MARIA;
ZATZ, MAYANA;
KREMERS, JAN;
VENTURA, DORA FIX.
Dystrophin Is Required for Proper Functioning of Luminance and Red-Green Cone Opponent Mechanisms in the Human Retina.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE,
v. 57,
n. 8,
p. 3581-3587,
JUL 2016.
Citações Web of Science: 1.
NUNES, KELLY;
PIOVEZAN, BRUNO;
TORRES, MARGARETH A.;
PONTES, GERLANDIA N.;
KIMURA, LILIAN;
CARNAVALLI, JULIANA E. P.;
MINGRONI NETTO, REGINA CELIA;
MORAES, MARIA ELISA;
MEYER, DIOGO.
Population variation of HLA genes in rural communities in Brazil, the Quilombos from the Vale do Ribeira, Sao Paulo - Brazil.
HUMAN IMMUNOLOGY,
v. 77,
n. 6,
p. 447-448,
JUN 2016.
Citações Web of Science: 2.
CALYJUR, PRISCILA CLARA;
ALMEIDA, CAMILA DE FREITAS;
AYUB-GUERRIERI, DANIELLE;
RIBEIRO JUNIOR, ANTONIO FERNANDO;
FERNANDES, STEPHANIE DE ALCANTARA;
ISHIBA, RENATA;
FERNANDES DOS SANTOS, ANDRE LUIS;
ONOFRE-OLIVEIRA, PAULA;
VAINZOF, MARIZ.
The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors.
PLoS One,
v. 11,
n. 3
MAR 8 2016.
Citações Web of Science: 7.
FONTES, MARSHALL I. B.;
SANTOS, ANA P.;
MOLCK, MIRIAM C.;
SIMIONI, MILENA;
NASCIMENTO, DIOGO L. L.;
ANDRADE, ANA K. M.;
ROSENBERG, CARLA;
KREPISCHI, ANA C. V.;
APPENZELLER, SIMONE;
MONLLEO, ISABELLA L.;
GIL-DA-SILVA-LOPES, VERA LUCIA.
Genotype-Phenotype Correlation of 16p13.3 Terminal Duplication and 22q13.33 Deletion: Natural History of a Patient and Review of the Literature.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A,
v. 170,
n. 3,
p. 766-772,
MAR 2016.
Citações Web of Science: 3.
NUNES, KELLY;
ZHENG, XIUWEN;
TORRES, MARGARETH;
MORAES, MARIA ELISA;
PIOVEZAN, BRUNO Z.;
PONTES, GERLANDIA N.;
KIMURA, LILIAN;
CARNAVALLI, JULIANA E. P.;
MINGRONI NETTO, REGINA C.;
MEYER, DIOGO.
HLA imputation in an admixed population: An assessment of the 1000 Genomes data as a training set.
HUMAN IMMUNOLOGY,
v. 77,
n. 3,
p. 307-312,
MAR 2016.
Citações Web of Science: 12.
VILLELA, DARINE;
RAMALHO, RODRIGO F.;
SILVA, ADERBAL R. T.;
BRENTANI, HELENA;
SUEMOTO, CLAUDIA K.;
PASQUALUCCI, CARLOS AUGUSTO;
GRINBERG, LEA T.;
KREPISCHI, ANA C. V.;
ROSENBERG, CARLA.
Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer's Disease Individuals.
NEURAL PLASTICITY,
2016.
Citações Web of Science: 13.
FONSECA, ANA CAROLINA S.;
BONALDI, ADRIANO;
FONSECA, SIMONE A. S.;
OTTO, PAULO A.;
KOK, FERNANDO;
BAK, MADS;
TOMMERUP, NIELS;
VIANNA-MORGANTE, ANGELA M.
The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation.
MOLECULAR CYTOGENETICS,
v. 8,
DEC 30 2015.
Citações Web of Science: 2.
VIEIRA, NATASSIA M.;
ELVERS, INGEGERD;
ALEXANDER, MATTHEW S.;
MOREIRA, YURI B.;
ERAN, ALAL;
GOMES, JULIANA P.;
MARSHALL, JAMIE L.;
KARLSSON, ELINOR K.;
VERJOVSKI-ALMEIDA, SERGIO;
LINDBLAD-TOH, KERSTIN;
KUNKEL, LOUIS M.;
ZATZ, MAYANA.
Jagged 1 Rescues the Duchenne Muscular Dystrophy Phenotype.
Cell,
v. 163,
n. 5,
p. 1204-1213,
NOV 19 2015.
Citações Web of Science: 54.
TEIXEIRA SANTOS, MARCIA CRISTINA;
GONCALVES SILVA, PATRICIA BENITES;
RODINI, CAROLINA OLIVEIRA;
FURUKAWA, GABRIELA;
MARCO ANTONIO, DAVID SANTOS;
ZANOTTO-FILHO, ALFEU;
MOREIRA, JOSE C. F.;
OKAMOTO, OSWALDO KEITH.
Embryonic Stem Cell-Related Protein L1TD1 Is Required for Cell Viability, Neurosphere Formation, and Chemoresistance in Medulloblastoma.
STEM CELLS AND DEVELOPMENT,
v. 24,
n. 22,
p. 2700-2708,
NOV 15 2015.
Citações Web of Science: 4.
BRITO, LUCIANO ABREU;
YAMAMOTO, GUILHERME LOPES;
MELO, SORAIA;
MALCHER, CAROLINA;
FERREIRA, SIMONE GOMES;
FIGUEIREDO, JOANA;
ALVIZI, LUCAS;
KOBAYASHI, GERSON SHIGERU;
NASLAVSKY, MICHEL SATYA;
ALONSO, NIVALDO;
FELIX, TEMIS MARIA;
ZATZ, MAYANA;
SERUCA, RAQUEL;
PASSOS-BUENO, MARIA RITA.
Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate.
Human mutation,
v. 36,
n. 11,
p. 1029-1033,
NOV 2015.
Citações Web of Science: 19.
KAID, CAROLINI;
SILVA, PATRICIA B. G.;
CORTEZ, BEATRIZ A.;
RODINI, CAROLINA O.;
SEMEDO-KURIKI, PATRICIA;
OKAMOTO, OSWALDO K.
miR-367 promotes proliferation and stem-like traits in medulloblastoma cells.
Cancer Science,
v. 106,
n. 9,
p. 1188-1195,
SEP 2015.
Citações Web of Science: 23.
VIEIRA, NATASSIA M.;
GUO, LING T.;
ESTRELA, ELICIA;
KUNKEL, LOUIS M.;
ZATZ, MAYANA;
SHELTON, G. DIANE.
Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype.
Neuromuscular Disorders,
v. 25,
n. 5,
p. 363-370,
MAY 2015.
Citações Web of Science: 16.
ZATZ, M.;
VIEIRA, N. M.;
ZUCCONI, E.;
PELATTI, M.;
GOMES, J.;
VAINZOF, M.;
MARTINS-BACH, A. B.;
GARCIA OTADUY, M. C.;
BENTO DOS SANTOS, G.;
AMARO, JR., E.;
LANDINI, V.;
ANDRADE, T.
A normal life without muscle dystrophin.
Neuromuscular Disorders,
v. 25,
n. 5,
p. 371-374,
MAY 2015.
Citações Web of Science: 11.
MARTINS-BACH, AUREA B.;
MALHEIROS, JACKELINE;
MATOT, BEATRICE;
MARTINS, POLIANA C. M.;
ALMEIDA, CAMILA F.;
CALDEIRA, WALDIR;
RIBEIRO, ALBERTO F.;
DE SOUSA, PAULO LOUREIRO;
AZZABOU, NOURA;
TANNSUS, ALBERTO;
CARLIER, PIERRE G.;
VAINZOF, MARIZ.
Quantitative T2 Combined with Texture Analysis of Nuclear Magnetic Resonance Images Identify Different Degrees of Muscle Involvement in Three Mouse Models of Muscle Dystrophy: mdx, Large(myd) and mdx/Large(myd).
PLoS One,
v. 10,
n. 2
FEB 24 2015.
Citações Web of Science: 5.
MOREIRA, DANIELLE P.;
GRIESI-OLIVEIRA, KARINA;
BOSSOLANI-MARTINS, ANA L.;
LOURENCO, NAILA C. V.;
TAKAHASHI, VANESSA N. O.;
DA ROCHA, KATIA M.;
MOREIRA, ELOISA S.;
VADASZ, ESTEVAO;
CASTRO MEIRA, JOANNA GOES;
BERTOLA, DEBORA;
O' HALLORAN, EOGHAN;
MAGALHAES, TIAGO R.;
FETT-CONTE, AGNES C.;
PASSOS-BUENO, MARIA RITA.
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy.
PLoS One,
v. 9,
n. 9
SEP 25 2014.
Citações Web of Science: 12.
VICTORINO KREPISCHI, ANA CRISTINA;
CAPELLI, LEONARDO PIRES;
SILVA, AMANDA GONCALVES;
SOUZA DE ARAUJO, ERICA SARA;
PEARSON, PETER LEES;
HECK, BENJAMIN;
LIMA DA COSTA, CECILIA MARIA;
DE CAMARGO, BEATRIZ;
ROSENBERG, CARLA.
Large germline copy number variations as predisposing factor in childhood neoplasms.
FUTURE ONCOLOGY,
v. 10,
n. 9,
p. 1627-1633,
JUL 2014.
Citações Web of Science: 2.
RODRIGUES, TATIANE CRISTINA;
FIDALGO, FELIPE;
LIMA DA COSTA, CECILIA MARIA;
FERREIRA, ELISA NAPOLITANO;
DA CUNHA, ISABELA WERNECK;
CARRARO, DIRCE MARIA;
VICTORINO KREPISCHI, ANA CRISTINA;
ROSENBERG, CARLA.
Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas.
FUTURE ONCOLOGY,
v. 10,
n. 15,
p. 2449-2457,
2014.
Citações Web of Science: 5.
Patente(s) depositada(s) como resultado deste projeto de pesquisa