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11
The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies
The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies
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The Sarcoglycan Complex in the Six Autosomal Recessive Limb-Girdle Muscular Dystrophies

Vainzof, M. ; Passos-Bueno, M. R. ; Canovas, M. ; Moreira, E. S. ; Pavanello, R. C. M. ; Marie, S. K. ; Anderson, L. V. B. ; Bonnemann, C. G. ; McNally, E. M. ; Nigro, V. ; Kunkel, L. M. ; Zatz, M.

Human molecular genetics, 1996-12, Vol.5 (12), p.1963-1969 [Periódico revisado por pares]

Oxford: Oxford University Press

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12
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
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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

Passos-Bueno, M. R. ; Moreira, E. S. ; Vainzof, M. ; Marie, S. K. ; Zatz, M.

Human molecular genetics, 1996-06, Vol.5 (6), p.815-820 [Periódico revisado por pares]

Oxford: Oxford University Press

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13
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours
High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours
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High serum endostatin levels in Down syndrome: implications for improved treatment and prevention of solid tumours

Zorick, T S ; Mustacchi, Z ; Bando, S Y ; Zatz, M ; Moreira-Filho, C A ; Olsen, B ; Passos-Bueno, M R

European journal of human genetics : EJHG, 2001-11, Vol.9 (11), p.811-814 [Periódico revisado por pares]

England: Nature Publishing Group

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14
Dysferlin protein analysis in limb-girdle muscular dystrophies
Dysferlin protein analysis in limb-girdle muscular dystrophies
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Dysferlin protein analysis in limb-girdle muscular dystrophies

Vainzof, M ; Anderson, L V ; McNally, E M ; Davis, D B ; Faulkner, G ; Valle, G ; Moreira, E S ; Pavanello, R C ; Passos-Bueno, M R ; Zatz, M

Journal of molecular neuroscience, 2001-08, Vol.17 (1), p.71-80 [Periódico revisado por pares]

United States: Springer Nature B.V

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15
A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3
A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3
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A Gene Which Causes Severe Ocular Alterations and Occipital Encephalocele (Knobloch Syndrome) is Mapped to 21q22.3

Sertié, A. L. ; Quimby, M. ; Moreira, E. S. ; Murray, J. ; Zatz, M. ; Antonarakis, S. E. ; Passos-Bueno, M. R.

Human molecular genetics, 1996-06, Vol.5 (6), p.843-847 [Periódico revisado por pares]

Oxford: Oxford University Press

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16
Molecular combing in the analysis of developmentally regulated amplified segments of Bradysia hygida
Molecular combing in the analysis of developmentally regulated amplified segments of Bradysia hygida
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Molecular combing in the analysis of developmentally regulated amplified segments of Bradysia hygida

Passos, K J R ; Togoro, S Y ; Carignon, S ; Koundrioukoff, S ; Lachages, A-M ; Debatisse, M ; Fernandez, M A

Genetics and molecular research, 2012-01, Vol.11 (3), p.2060-2070 [Periódico revisado por pares]

Brazil

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17
Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder
Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder
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Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder

Oliveira, J R ; Carvalho, D R ; Pontual, D ; Gallindo, R M ; Sougey, E B ; Gentil, V ; Lafer, B ; Maia, L G ; Morais, Jr, M A ; Matioli, S ; Vallada, H ; Moreno, R A ; Nishimura, A ; Otto, P A ; Passos-Bueno, M R ; Zatz, M

Molecular psychiatry, 2000-07, Vol.5 (4), p.348-349 [Periódico revisado por pares]

England: Nature Publishing Group

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18
Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)
Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)
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Genomic Screening for β-Sarcoglycan Gene Mutations: Missense Mutations May Cause Severe Limb-girdle Muscular Dystrophy Type 2E (LGMD 2E)

Bönnemann, Carsten G. ; Passos-Bueno, M. Rita ; McNally, Elizabeth M. ; Vainzof, Mariz ; Moreira, Eloísa de Sá ; Marie, Suely K. ; Pavanello, Rita C. M. ; Noguchi, Satoru ; Ozawa, Eijiro ; Zatz, Mayana ; Kunkel, Louis M.

Human molecular genetics, 1996-12, Vol.5 (12), p.1953-1961 [Periódico revisado por pares]

Oxford: Oxford University Press

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19
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
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Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex

Vainzof, M ; Moreira, E S ; Ferraz, G ; Passos-Bueno, M R ; Marie, S K ; Zatz, M

European journal of human genetics : EJHG, 1999-02, Vol.7 (2), p.251-254 [Periódico revisado por pares]

England

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20
Biological treatment of kraft pulp mill foul condensates at high temperatures using a membrane bioreactor
Biological treatment of kraft pulp mill foul condensates at high temperatures using a membrane bioreactor
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Biological treatment of kraft pulp mill foul condensates at high temperatures using a membrane bioreactor

Dias, João Carlos Teixeira ; Rezende, Rachel Passos ; Silva, Cláudio M. ; Linardi, Valter R.

Process biochemistry (1991), 2005-03, Vol.40 (3), p.1125-1129 [Periódico revisado por pares]

Elsevier Ltd

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