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Horsthemke

Showing results (211-220 of 368) with videos related to

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Genes, Chromosomes & Cancer|March 1, 1991
Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locusI Newsham, U Claussen, H J Lüdecke, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouseR D Nicholls, W Gottlieb, L B Russell, et al.
Genome Biology and Evolution|June 14, 2014
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouseKatrin Rademacher, Christopher Schröder, Deniz Kanber, et al.
American Journal of Human Genetics|August 1, 1997
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastomaD R Lohmann, M Gerick, B Brandt, et al.
Bone Marrow Transplantation|November 21, 2012
Allostimulatory activity of CD133+ hematopoietic cellsP Patel, J Abbasian, D Mahmud, et al.
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Plos One|September 10, 2016
Preovulatory Aging In Vivo and In Vitro Affects Maturation Rates, Abundance of Selected Proteins, Histone Methylation Pattern and Spindle Integrity in Murine OocytesHannah Demond, Tom Trapphoff, Deborah Dankert, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
European Journal of Human Genetics : EJHG|January 21, 2010
An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistanceAmla Kuechler, Berthold P Hauffa, Angela Köninger, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
FTO levels affect RNA modification and the transcriptomeTea Berulava, Matthias Ziehe, Ludger Klein-Hitpass, et al.
Pageof 37

Showing results (211-220 of 368) with videos related to

Sort By:
Pageof 37
Genes, Chromosomes & Cancer|March 1, 1991
Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locusI Newsham, U Claussen, H J Lüdecke, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouseR D Nicholls, W Gottlieb, L B Russell, et al.
Genome Biology and Evolution|June 14, 2014
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouseKatrin Rademacher, Christopher Schröder, Deniz Kanber, et al.
American Journal of Human Genetics|August 1, 1997
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastomaD R Lohmann, M Gerick, B Brandt, et al.
Bone Marrow Transplantation|November 21, 2012
Allostimulatory activity of CD133+ hematopoietic cellsP Patel, J Abbasian, D Mahmud, et al.
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Plos One|September 10, 2016
Preovulatory Aging In Vivo and In Vitro Affects Maturation Rates, Abundance of Selected Proteins, Histone Methylation Pattern and Spindle Integrity in Murine OocytesHannah Demond, Tom Trapphoff, Deborah Dankert, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
European Journal of Human Genetics : EJHG|January 21, 2010
An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistanceAmla Kuechler, Berthold P Hauffa, Angela Köninger, et al.
European Journal of Human Genetics : EJHG|August 9, 2012
FTO levels affect RNA modification and the transcriptomeTea Berulava, Matthias Ziehe, Ludger Klein-Hitpass, et al.
Pageof 37