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Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons
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Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons

Griesi-Oliveira, K ; Acab, A ; Gupta, A R ; Sunaga, D Y ; Chailangkarn, T ; Nicol, X ; Nunez, Y ; Walker, M F ; Murdoch, J D ; Sanders, S J ; Fernandez, T V ; Ji, W ; Lifton, R P ; Vadasz, E ; Dietrich, A ; Pradhan, D ; Song, H ; Ming, G-L ; Gu, X ; Haddad, G ; Marchetto, M C N ; Spitzer, N ; Passos-Bueno, M R ; State, M W ; Muotri, A R

Molecular psychiatry, 2015-11, Vol.20 (11), p.1350-1365 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Selective Pharmacological Inhibition of NOX2 by GSK2795039 Improves Bladder Dysfunction in Cyclophosphamide-Induced Cystitis in Mice
Selective Pharmacological Inhibition of NOX2 by GSK2795039 Improves Bladder Dysfunction in Cyclophosphamide-Induced Cystitis in Mice
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Selective Pharmacological Inhibition of NOX2 by GSK2795039 Improves Bladder Dysfunction in Cyclophosphamide-Induced Cystitis in Mice

de Oliveira, Mariana G ; Monica, Fabíola Z ; Passos, Gabriela R ; Victorio, Jamaira A ; Davel, Ana Paula ; Oliveira, Anna Lethicia Lima ; Parada, Carlos A ; D'Ancona, Carlos A L ; Hill, Warren G ; Antunes, Edson

Antioxidants, 2022-12, Vol.12 (1), p.92 [Periódico revisado por pares]

Switzerland: MDPI AG

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3
Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?
Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?
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Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?

Ceroni, José Rm ; Yamamoto, Guilherme L ; Honjo, Rachel S ; Kim, Chong A ; Passos-Bueno, Maria R ; Bertola, Débora R

Genetics and molecular biology, 2018-01, Vol.41 (1), p.85-91 [Periódico revisado por pares]

Brazil: Sociedade Brasileira de Genética

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4
Osteogenesis imperfecta in Brazilian patients
Osteogenesis imperfecta in Brazilian patients
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Osteogenesis imperfecta in Brazilian patients

Trancozo, Maira ; Moraes, Marcos V D ; Silva, Dalila A ; Soares, Jéssica A M ; Barbirato, Clara ; Almeida, Márcio G ; Santos, Lígia R ; Rebouças, Maria R G O ; Akel, Jr, Akel N ; Sipolatti, Valentim ; Nunes, Vanda R R ; Errera, Flavia I V ; Aguena, Meire ; Passos-Bueno, Maria R ; Paula, Flavia de

Genetics and molecular biology, 2019-04, Vol.42 (2), p.344-350 [Periódico revisado por pares]

Brazil: Sociedade Brasileira de Genética

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5
Pharmacological Inhibition of NAPDH Oxidase NOX2 Improves Bladder Dysfunction in Murine Cyclophosphamide‐Induced Cystitis
Pharmacological Inhibition of NAPDH Oxidase NOX2 Improves Bladder Dysfunction in Murine Cyclophosphamide‐Induced Cystitis
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Pharmacological Inhibition of NAPDH Oxidase NOX2 Improves Bladder Dysfunction in Murine Cyclophosphamide‐Induced Cystitis

Oliveira, Mariana G. ; Monica, Fabiola Z. ; Passos, Gabriela R. ; Oliveira, Akila L. ; Oliveira, Anna Lethicia L. ; Antunes, Edson

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a [Periódico revisado por pares]

The Federation of American Societies for Experimental Biology

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6
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)
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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)

SERTIE, A. L ; SOSSI, V ; CAMARGO, A. A ; ZATZ, M ; BRAHE, C ; PASSOS-BUENO, M. R

Human molecular genetics, 2000-08, Vol.9 (13), p.2051-2058 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder
Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder
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Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder

Griesi-Oliveira, K ; Fogo, M S ; Pinto, B G G ; Alves, A Y ; Suzuki, A M ; Morales, A G ; Ezquina, S ; Sosa, O J ; Sutton, G J ; Sunaga-Franze, D Y ; Bueno, A P ; Seabra, G ; Sardinha, L ; Costa, S S ; Rosenberg, C ; Zachi, E C ; Sertie, A L ; Martins-de-Souza, D ; Reis, E M ; Voineagu, I ; Passos-Bueno, M R

Molecular psychiatry, 2021-05, Vol.26 (5), p.1589-1605 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Ability of HMGB1 protein to bind to intrinsically bent and non-bent DNA sites in the AMPD2 gene amplicon
Ability of HMGB1 protein to bind to intrinsically bent and non-bent DNA sites in the AMPD2 gene amplicon
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Ability of HMGB1 protein to bind to intrinsically bent and non-bent DNA sites in the AMPD2 gene amplicon

Passos, K J R ; Fiorini, A ; Rosado, F R ; Freitas, D V B ; Lima Neto, Q A ; Pattaro Junior, J R ; Gaspar, V P ; Fernandez, M A

Genetics and molecular research, 2016-06, Vol.15 (2) [Periódico revisado por pares]

Brazil

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9
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease
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The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease

OLIVEIRA, J. R. M ; GALLINDO, R. M ; MAIA, L. G. S ; BRITO-MARQUES, P. R ; OTTO, P. A ; PASSOS-BUENOS, M. R ; MORAIS, M. A ; ZATZ, M

Molecular psychiatry, 1998-09, Vol.3 (5), p.438-441 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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10
Caveolin-3 in Muscular Dystrophy
Caveolin-3 in Muscular Dystrophy
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Caveolin-3 in Muscular Dystrophy

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

Human molecular genetics, 1998-05, Vol.7 (5), p.871-877 [Periódico revisado por pares]

Oxford: Oxford University Press

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