Maria Rita Passos-Bueno
Maria Rita Passos-Bueno
Departamento de Genetica e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo
Verified email at ib.usp.br
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
9831995
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
6611998
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
4901996
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
Clinical spectrum of fibroblast growth factor receptor mutations
MR Passos‐Bueno, WR Wilcox, EW Jabs, AL Sertie, LG Alonso, H Kitoh
Human mutation 14 (2), 115-125, 1999
3301999
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
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
2491998
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity
D Jenkins, D Seelow, FS Jehee, CA Perlyn, LG Alonso, DF Bueno, ...
The American Journal of Human Genetics 80 (6), 1162-1170, 2007
2262007
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
Reconstruction of large cranial defects in nonimmunosuppressed experimental design with human dental pulp stem cells
A de Mendonça Costa, DF Bueno, MT Martins, I Kerkis, A Kerkis, ...
Journal of Craniofacial Surgery 19 (1), 204-210, 2008
1932008
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
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22. 3
AL Sertie, M Quimby, ES Moreira, J Murray, M Zatz, SE Antonarakis, ...
Human molecular genetics 5 (6), 843-847, 1996
157*1996
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
Stem cell proliferation under low intensity laser irradiation: a preliminary study
FP Eduardo, DF Bueno, PM de Freitas, MM Marques, MR Passos‐Bueno, ...
Lasers in Surgery and Medicine: The Official Journal of the American Society …, 2008
1502008
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations
MR Passos-Bueno, AL Sertié, FS Jehee, R Fanganiello, E Yeh
Craniofacial Sutures 12, 107-143, 2008
1502008
Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)
CG Bönnemann, MR Passos-Bueno, EM McNally, M Vainzof, ES Moreira, ...
Human molecular genetics 5 (12), 1953-1961, 1996
1351996
The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12
ES Moreira, M Vainzof, SK Marie, AL Sertie, M Zatz, MR Passos-Bueno
The American Journal of Human Genetics 61 (1), 151-159, 1997
1341997
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes
M Zatz, M Vainzof, MR Passos-Bueno
Current opinion in neurology 13 (5), 511-517, 2000
1332000
The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females
M Zatz, SK Marie, A Cerqueira, M Vainzof, RCM Pavanello, ...
American journal of medical genetics 77 (2), 155-161, 1998
1291998
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33–34 (LGMD2F) and indicates that there is at least one more subtype of …
MR Passos-Bueno, ES Moreira, M Vainzof, SK Marie, M Zatz
Human molecular genetics 5 (6), 815-820, 1996
1281996
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