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Uta Francke

Showing results (1-10 of 47) with videos related to

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American Journal of Human Genetics|March 12, 2013
2012 William Allan Award: Adventures in cytogeneticsUta Francke
EMBO Molecular Medicine|January 1, 2010
On the bumpy road towards 'personalized medicine'Uta Francke
Nature Clinical Practice. Neurology|August 26, 2006
Mechanisms of disease: neurogenetics of MeCP2 deficiencyUta Francke
Molecular Genetics & Genomic Medicine|February 6, 2014
How will genomic information become integrated into the health care system?Uta Francke
Human Molecular Genetics|June 7, 2006
Ube3a expression is not altered in Mecp2 mutant miceCharandle Jordan, Uta Francke
Human Molecular Genetics|April 15, 2006
Identification of cis-regulatory elements for MECP2 expressionJinglan Liu, Uta Francke
BMC Medical Genetics|November 7, 2002
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutationsJeff Traynor, Priyanka Agarwal, Laura Lazzeroni, et al.
American Journal of Human Genetics|August 3, 2002
Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndromeRenata C Gallagher, Birgit Pils, Mohammed Albalwi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 23, 2018
Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. <i>Cell</i>. 1994. 78: 635-644Jonathan M J Derry, Hans D Ochs, Uta Francke
American Journal of Medical Genetics. Part A|July 16, 2024
Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorderJorge L Rodriguez-Gil, Peter L Nagy, Uta Francke
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|March 12, 2013
2012 William Allan Award: Adventures in cytogeneticsUta Francke
EMBO Molecular Medicine|January 1, 2010
On the bumpy road towards 'personalized medicine'Uta Francke
Nature Clinical Practice. Neurology|August 26, 2006
Mechanisms of disease: neurogenetics of MeCP2 deficiencyUta Francke
Molecular Genetics & Genomic Medicine|February 6, 2014
How will genomic information become integrated into the health care system?Uta Francke
Human Molecular Genetics|June 7, 2006
Ube3a expression is not altered in Mecp2 mutant miceCharandle Jordan, Uta Francke
Human Molecular Genetics|April 15, 2006
Identification of cis-regulatory elements for MECP2 expressionJinglan Liu, Uta Francke
BMC Medical Genetics|November 7, 2002
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutationsJeff Traynor, Priyanka Agarwal, Laura Lazzeroni, et al.
American Journal of Human Genetics|August 3, 2002
Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndromeRenata C Gallagher, Birgit Pils, Mohammed Albalwi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 23, 2018
Pillars Article: Isolation of a Novel Gene Mutated in Wiskott-Aldrich Syndrome. <i>Cell</i>. 1994. 78: 635-644Jonathan M J Derry, Hans D Ochs, Uta Francke
American Journal of Medical Genetics. Part A|July 16, 2024
Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorderJorge L Rodriguez-Gil, Peter L Nagy, Uta Francke
Pageof 5