Zatz M
TitleCited byYear
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
9801995
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, 2000
9582000
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
8892004
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, 1998
6601998
Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, ...
Nature genetics 14 (2), 195, 1996
4891996
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
4582008
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, 2000
3502000
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
2582000
Calpains and disease
M Zatz, A Starling
New England Journal of Medicine 352 (23), 2413-2423, 2005
2562005
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
2532010
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
2471998
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), 35, 2008
2092008
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
1982011
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ...
Human molecular genetics 5 (12), 1963-1969, 1996
1981996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
EM McNally, MR Passos-Bueno, CG Bönnemann, M Vainzof, ...
American journal of human genetics 59 (5), 1040, 1996
1831996
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
A Keller, A Westenberger, MJ Sobrido, M García-Murias, A Domingo, ...
Nature genetics 45 (9), 1077, 2013
1772013
The 10 autosomal recessive limb-girdle muscular dystrophies
M Zatz, F de Paula, A Starling, M Vainzof
Neuromuscular disorders 13 (7-8), 532-544, 2003
1732003
Myocardial delayed enhancement by magnetic resonance imaging in patients with muscular dystrophy
MC Silva, ZMA Meira, JG Giannetti, MM da Silva, AFO Campos, ...
Journal of the American College of Cardiology 49 (18), 1874-1879, 2007
1662007
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
PN Valdmanis, IA Meijer, A Reynolds, A Lei, P MacLeod, D Schlesinger, ...
The American Journal of Human Genetics 80 (1), 152-161, 2007
1572007
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours
TS Zorick, Z Mustacchi, SY Bando, M Zatz, CA Moreira-Filho, BÈ Olsen, ...
European Journal of Human Genetics 9 (11), 811, 2001
1512001
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