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1
Human Molecular Genetics
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Revista 		Adicionar ao Meu Espaço

Human Molecular Genetics

ENGLAND Oxford University Press

Acesso online. A biblioteca também possui exemplares impressos.

2
Caveolin-3 in muscular dystrophy
Caveolin-3 in muscular dystrophy
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Artigo 		Adicionar ao Meu Espaço

Caveolin-3 in muscular dystrophy

Elizabeth M McNally Eloísa de Sá Moreira; David J Duggan; Carsten G Bönnemann; Michael P Lisanti; Hart G W Lidov; Mariz Vainzof; Maria Rita Passos-Bueno; Eric P Hoffman; Mayana Zatz; Louis M Kunkel

Human Molecular Genetics v. 7, n. 5, p. 871-877, 1998

Oxford 1998

Item não circula. Consulte sua biblioteca.(Acessar)

3
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 (Knobloch syndrome)
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 (Knobloch syndrome)
Material Type:
Artigo 		Adicionar ao Meu Espaço

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 (Knobloch syndrome)

Andréa Laurato Sertié Vittorio Sossi; Ana Maria A Camargo; Mayana Zatz; Christina Brahe; Maria Rita Passos-Bueno

Human Molecular Genetics v. 9, n. 13, p. 2051-2058, 2000

Oxford 2000

Item não circula. Consulte sua biblioteca.(Acessar)

4
Genomic screening for 'BETA'-sarcoglycan gene mutations missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)
Genomic screening for 'BETA'-sarcoglycan gene mutations missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genomic screening for 'BETA'-sarcoglycan gene mutations missense mutations may cause severe limb-girdle muscular dystrophy type 2e (lgmd 2e)

C G Bonnemann Maria Rita Passos-Bueno; E M Mcnally; Mariz Vainzof; E S Moreira; Suely Kazue Nagahashi Marie; R C M Pavanello; S Noguchi; E Ozawa; Mayana Zatz; L M Kunkel

Oxford v.5 , n.12, p.1953-61, 1996 Human Molecular Genetics

Oxford 1996

Item não circula. Consulte sua biblioteca.(Acessar)

5
A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
Material Type:
Artigo 		Adicionar ao Meu Espaço

A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3

A L Sertié M Quimby; E S Moreira; J Murray; Mayana Zatz; S E Antonarakis; Maria Rita Passos-Bueno

Human Molecular Genetics v. 5, n. 6, p. 843-847, 1996

1996

Item não circula. Consulte sua biblioteca.(Acessar)

6
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 AR LGMD
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 AR LGMD
Material Type:
Artigo 		Adicionar ao Meu Espaço

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 AR LGMD

Maria Rita Passos-Bueno E S Moreira; Mariz Vainzof; Suely Kazue Nagahashi Marie; Mayana Zatz

Human Molecular Genetics v. 5, n. 6, p. 815-820, 1996

1996

Item não circula. Consulte sua biblioteca.(Acessar)

7
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families
Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive duchenne-like muscular dystrophy in brazilian families

Maria Rita Passos-Bueno E Bakker; Suely Kazue Nagahashi Marie; R C M Pavanello; Mariz Vainzof; A. A Carvalho; D Cohen; J S Beckmann; Mayana Zatz

Oxford v.2 , n.2 , p.201-2, 1993 Human Molecular Genetics

Oxford 1993

Item não circula. Consulte sua biblioteca.(Acessar)

8
Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis
Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genetic heterogeneity for duchenne-like muscular dystrophy (dlmd) based on linkage and 50 dag analysis

Maria Rita Passos-Bueno J. R Oliveira; E Bakker; R D Anderson; Suely Kazue Nagahashi Marie; Mariz Vainzof; S Roberds; K P Campbell; Mayana Zatz

Oxford v.2 , n.11, p.1945-7, 1993 Human Molecular Genetics

Oxford 1993

Item não circula. Consulte sua biblioteca.(Acessar)

9
Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype?
Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype?
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Is the maintanance of the c-terminus domain of dystrophin enough to ensure a milder becker muscular dystrophy phenotype?

Mariz Vainzof R I Takata; Maria Rita Passos-Bueno; R C M Pavanello; Mayana Zatz

Oxford v.2 , n.1 , p.39-42, 1993 Human Molecular Genetics

Oxford 1993

Item não circula. Consulte sua biblioteca.(Acessar)

10
Point mutation in a becker muscular dystrophy patient
Point mutation in a becker muscular dystrophy patient
Material Type:
Artigo 		Adicionar ao Meu Espaço

Point mutation in a becker muscular dystrophy patient

R G Roberts Maria Rita Passos-Bueno; M Bobrow; Mariz Vainzof; Mayana Zatz

Oxford v.2 , n.1 , p.75-7, 1993 Human Molecular Genetics

Oxford 1993

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Passos-Bueno, M
  2. Zatz, M
  3. Vainzof, M
  4. Marie, S
  5. Pavanello, R

Neste Assunto:

  1. Genética Médica
  2. Distrofia Muscular
  3. Mutação Genética
  4. Ácidos Nucleicos
  5. Proteínas

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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