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1
A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay
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Artigo
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A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay

Santos-Rebouças, Cíntia B. ; Fintelman-Rodrigues, Natalia ; Jensen, Lars R. ; Kuss, Andreas W. ; Ribeiro, Márcia G. ; Campos, Mário ; Santos, Jussara M. ; Pimentel, Márcia M.G.

Neuroscience letters, 2011-07, Vol.498 (1), p.67-71 [Periódico revisado por pares]

Shannon: Elsevier Ireland Ltd

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2
Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome
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Artigo
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Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome

Reinius, Björn ; Johansson, Martin M ; Radomska, Katarzyna J ; Morrow, Edward H ; Pandey, Gaurav K ; Kanduri, Chandrasekhar ; Sandberg, Rickard ; Williams, Robert W ; Jazin, Elena

BMC genomics, 2012, Vol.13 (1), p.607-607 [Periódico revisado por pares]

England: BioMed Central

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3
Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome
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Artigo
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Abundance of female-biased and paucity of male-biased somatically expressed genes on the mouse X-chromosome

Reinius, Björn ; Johansson, Martin ; Radomska, Katarzyna ; Morrow, Edward H ; Pandey, Gaurav Kumar ; Chandrasekhar, Kanduri ; Sandberg, Rickard ; Williams, Robert W ; Jazin, Elena

Genomik 2012

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4
The von Hippel-Lindau tumor suppressor protein regulates gene expression and tumor growth through histone demethylase JARID1C
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Artigo
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The von Hippel-Lindau tumor suppressor protein regulates gene expression and tumor growth through histone demethylase JARID1C

Niu, X ; Zhang, T ; Liao, L ; Zhou, L ; Lindner, D J ; Zhou, M ; Rini, B ; Yan, Q ; Yang, H

Oncogene, 2012-02, Vol.31 (6), p.776-786 [Periódico revisado por pares]

England: Nature Publishing Group

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5
A novel c.2T > C mutation of the KDM5C / JARID1C gene in one large family with X-linked intellectual disability
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Artigo
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A novel c.2T > C mutation of the KDM5C / JARID1C gene in one large family with X-linked intellectual disability

Õunap, Katrin ; Puusepp-Benazzouz, Helen ; Peters, Maire ; Vaher, Ulvi ; Rein, Reet ; Proos, Anne ; Field, Mike ; Reimand, Tiia

European journal of medical genetics, 2012-03, Vol.55 (3), p.178-184 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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6
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C
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Artigo
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Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C

Grafodatskaya, Daria ; Chung, Barian H Y ; Butcher, Darci T ; Turinsky, Andrei L ; Goodman, Sarah J ; Choufani, Sana ; Chen, Yi-An ; Lou, Youliang ; Zhao, Chunhua ; Rajendram, Rageen ; Abidi, Fatima E ; Skinner, Cindy ; Stavropoulos, James ; Bondy, Carolyn A ; Hamilton, Jill ; Wodak, Shoshana ; Scherer, Stephen W ; Schwartz, Charles E ; Weksberg, Rosanna

BMC medical genomics, 2013-01, Vol.6 (1), p.1-1, Article 1 [Periódico revisado por pares]

England: BioMed Central

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7
Aberrant promoter hypermethylation of PBRM1, BAP1, SETD2, KDM6A and other chromatin-modifying genes is absent or rare in clear cell RCC
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Report
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Aberrant promoter hypermethylation of PBRM1, BAP1, SETD2, KDM6A and other chromatin-modifying genes is absent or rare in clear cell RCC

Ibragimova, Ilsiya ; Maradeo, Marie E. ; Dulaimi, Essel ; Cairns, Paul

Epigenetics, 2013, Vol.8 (5), p.486-493

Taylor & Francis

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8
Aberrant promoter hypermethylation of PBRM1, BAP1, SETD2, KDM6A and other chromatin-modifying genes is absent or rare in clear cell RCC
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Artigo
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Aberrant promoter hypermethylation of PBRM1, BAP1, SETD2, KDM6A and other chromatin-modifying genes is absent or rare in clear cell RCC

Ibragimova, Ilsiya ; Maradeo, Marie E ; Dulaimi, Essel ; Cairns, Paul

Epigenetics, 2013-05, Vol.8 (5), p.486-493 [Periódico revisado por pares]

United States: Landes Bioscience

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9
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature
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Artigo
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KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature

Gonçalves, Thainá Fernandez ; Gonçalves, Andressa Pereira ; Fintelman Rodrigues, Natalia ; dos Santos, Jussara Mendonça ; Pimentel, Márcia Mattos Gonçalves ; Santos-Rebouças, Cíntia Barros

European journal of medical genetics, 2014-03, Vol.57 (4), p.138-144 [Periódico revisado por pares]

Netherlands: Elsevier Masson SAS

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10
Methamphetamine-Associated Memory Is Regulated by a Writer and an Eraser of Permissive Histone Methylation
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Artigo
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Methamphetamine-Associated Memory Is Regulated by a Writer and an Eraser of Permissive Histone Methylation

Aguilar-Valles, Argel ; Vaissière, Thomas ; Griggs, Erica M ; Mikaelsson, Mikael A ; Takács, Irma F ; Young, Erica J ; Rumbaugh, Gavin ; Miller, Courtney A

Biological psychiatry (1969), 2014-07, Vol.76 (1), p.57-65 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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Deste Autor:

  1. Leal, G
  2. Oliveira, J
  3. Oliveira Santos, J
  4. Oliveira, D
  5. Krepischi, A

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