L Colleaux - JoVE Visualize

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Yeast (Chichester, England)|November 1, 1992

The sequence of a 9.3 kb segment located on the left arm of the yeast chromosome XI reveals five open reading frames including the CCE1 gene and putative products related to MYO2 and to the ribosomal protein L10S Pascolo, M Ghazvini, J Boyer, et al.

European Journal of Human Genetics : EJHG|April 26, 2000

The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disordersC Cardoso, C Mignon, G Hetet, et al.

Human Molecular Genetics|May 16, 1998

Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 proteinC Cardoso, S Timsit, L Villard, et al.

Journal of Medical Genetics|May 1, 1996

Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbandsL Colleaux, M May, J Belougne, et al.

Cell|February 28, 1986

Universal code equivalent of a yeast mitochondrial intron reading frame is expressed into E. coli as a specific double strand endonucleaseL Colleaux, L d'Auriol, M Betermier, et al.

American Journal of Medical Genetics|April 6, 1999

Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.

Genomics|July 15, 1997

Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.

Journal of Medical Genetics|October 4, 2000

ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X proteinC Cardoso, Y Lutz, C Mignon, et al.

American Journal of Medical Genetics. Part A|February 26, 2005

Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocationN Philip, L Colleaux, S Sigaudy, et al.

European Journal of Medical Genetics|October 8, 2013

A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.

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Showing results (11-20 of 41) with videos related to

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Pageof 5

Yeast (Chichester, England)|November 1, 1992

The sequence of a 9.3 kb segment located on the left arm of the yeast chromosome XI reveals five open reading frames including the CCE1 gene and putative products related to MYO2 and to the ribosomal protein L10S Pascolo, M Ghazvini, J Boyer, et al.

European Journal of Human Genetics : EJHG|April 26, 2000

The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disordersC Cardoso, C Mignon, G Hetet, et al.

Human Molecular Genetics|May 16, 1998

Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 proteinC Cardoso, S Timsit, L Villard, et al.

Journal of Medical Genetics|May 1, 1996

Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbandsL Colleaux, M May, J Belougne, et al.

Cell|February 28, 1986

Universal code equivalent of a yeast mitochondrial intron reading frame is expressed into E. coli as a specific double strand endonucleaseL Colleaux, L d'Auriol, M Betermier, et al.

American Journal of Medical Genetics|April 6, 1999

Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one familyN Ronce, M Raynaud, A Toutain, et al.

Genomics|July 15, 1997

Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicaseL Villard, A M Lossi, C Cardoso, et al.

Journal of Medical Genetics|October 4, 2000

ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X proteinC Cardoso, Y Lutz, C Mignon, et al.

American Journal of Medical Genetics. Part A|February 26, 2005

Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocationN Philip, L Colleaux, S Sigaudy, et al.

European Journal of Medical Genetics|October 8, 2013

A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.

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