Zatz M

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Maria Rita Passos-BuenoDepartamento de Genetica e Biologia Evolutiva, Instituto de Biociências, Universidade de São PauloAdresse e-mail validée de ib.usp.br
Mariz VainzofCentro de Estudos do Genoma Humano e Células Tronco, IBUSPAdresse e-mail validée de usp.br
Suely Kazue Nagahashi MarieProfessor Associado de MedicinaAdresse e-mail validée de usp.br
Natássia VieiraPostdoc FellowAdresse e-mail validée de enders.tch.harvard.edu
Michel S NaslavskyUniversidade de São PauloAdresse e-mail validée de usp.br
Eder ZucconiCo-founder StemCorpAdresse e-mail validée de stemcorp.com.br
Agnes NishimuraKing's College LondonAdresse e-mail validée de kcl.ac.uk
Fernando KokProfessor Titular, Departamento de Neurologia da FMUSPAdresse e-mail validée de mendelics.com.br
Oswaldo Keith OkamotoUniversidade de São PauloAdresse e-mail validée de usp.br
Tatiana JazedjeUniversidade de São Paulo (USP)Adresse e-mail validée de ib.usp.br
João Ricardo Mendes de OliveiraProfessor in Neuropsychiatry, UFPEAdresse e-mail validée de ufpe.br
Miguel Mitne-NetoHuman Genome Research Center / Fleury GroupAdresse e-mail validée de usp.br
Ricardo NitriniProfessor de Neurologia, Faculdade de Medicina da Universidade de Sao PauloAdresse e-mail validée de usp.br
Guilherme Lopes YamamotoMédico geneticista do Instituto da Criança do Hospital das Clínicas da Faculdade de Medicina daAdresse e-mail validée de usp.br
Yeda A O DuarteUniversidade de São PauloAdresse e-mail validée de usp.br
Carlos Eduardo AmbrósioProfessor Anatomia Animal, FZEA, Universidade de São PauloAdresse e-mail validée de usp.br
Silvana Santos/Silvana Cristina dos S...Universidade Estadual da ParaíbaAdresse e-mail validée de ccbs.uepb.edu.br
Vincenzo NigroUniversità della Campania "Luigi Vanvitelli" Dipartimento di Medicina di Precisione, and TIGEMAdresse e-mail validée de unicampania.it
Amanda AssoniAluna de Doutorado, Instituto de Biociências USPAdresse e-mail validée de usp.br
Ernesto GoulartUniversity of Sao PauloAdresse e-mail validée de ib.usp.br

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Zatz M

Universidade de S. Paulo

Adresse e-mail validée de usp.br - Page d'accueil

Genética humana e células-tronco


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis AL Nishimura, M Mitne-Neto, HCA Silva, A Richieri-Costa, S Middleton, ... The American Journal of Human Genetics 75 (5), 822-831, 2004	1253	2004
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A I Richard, O Broux, V Allamand, F Fougerousse, N Chiannilkulchai, ... Cell 81 (1), 27-40, 1995	1184	1995
The genome sequence of the plant pathogen Xylella fastidiosa AJG Simpson, FC Reinach, P Arruda, FA Abreu, M Acencio, R Alvarenga, ... Nature 406 (6792), 151-157, 2000	1132	2000
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B R Bashir, S Britton, T Strachan, S Keers, E Vafiadaki, M Lako, I Richard, ... Nature genetics 20 (1), 37-42, 1998	825	1998
Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018	669	2018
Multipotent stem cells from umbilical cord: cord is richer than blood! M Secco, E Zucconi, NM Vieira, LLQ Fogaça, A Cerqueira, MDF Carvalho, ... Stem cells 26 (1), 146-150, 2008	578	2008
Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene V Nigro, ES Moreira, G Piluso, M Vainzof, A Belsito, L Politano, AA Puca, ... Nature genetics 14 (2), 195-198, 1996	553	1996
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ... Science immunology 6 (62), eabl4340, 2021	544	2021
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin ES Moreira, TJ Wiltshire, G Faulkner, A Nilforoushan, M Vainzof, ... Nature genetics 24 (2), 163-166, 2000	444	2000
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19 T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ... Science immunology 6 (62), eabl4348, 2021	391	2021
Isolation, characterization, and differentiation potential of canine adipose-derived stem cells NM Vieira, V Brandalise, E Zucconi, M Secco, BE Strauss, M Zatz Cell transplantation 19 (3), 279-289, 2010	372	2010
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice A Keller, A Westenberger, MJ Sobrido, M Garcia-Murias, A Domingo, ... Nature genetics 45 (9), 1077-1082, 2013	333	2013
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure … AL Sertié, V Sossi, AMA Camargo, M Zatz, C Brahe, MR Passos-Bueno Human molecular genetics 9 (13), 2051-2058, 2000	326	2000
Calpains and disease M Zatz, A Starling New England Journal of Medicine 352 (23), 2413-2423, 2005	324	2005
Caveolin-3 in muscular dystrophy EM McNally, E de Sá Moreira, DJ Duggan, CG Bönnemann, MP Lisanti, ... Human molecular genetics 7 (5), 871-877, 1998	297	1998
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome GL Yamamoto, M Aguena, M Gos, C Hung, J Pilch, S Fahiminiya, ... Journal of medical genetics 52 (6), 413-421, 2015	287	2015
Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: local or systemic? I Kerkis, CE Ambrosio, A Kerkis, DS Martins, E Zucconi, SAS Fonseca, ... Journal of Translational Medicine 6, 1-13, 2008	271	2008
Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients M Mitne-Neto, M Machado-Costa, MCN Marchetto, MH Bengtson, ... Human molecular genetics 20 (18), 3642-3652, 2011	270	2011
Exomic variants of an elderly cohort of Brazilians in the ABraOM database MS Naslavsky, GL Yamamoto, TF de Almeida, SAM Ezquina, DY Sunaga, ... Human mutation 38 (7), 751-763, 2017	254	2017
Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy MC Silva, ZMA Meira, J Gurgel Giannetti, MM da Silva, ... Journal of the American College of Cardiology 49 (18), 1874-1879, 2007	246	2007

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