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Horsthemke

Showing results (291-300 of 368) with videos related to

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Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Human Molecular Genetics|May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19pM Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
Orvosi Hetilap|January 9, 2018
[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]Orsolya Dóra Ács, Bálint Péterfia, Péter Hollósi, et al.
International Journal of Molecular Medicine|January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell levelA Weise, M Gross, K Mrasek, et al.
American Journal of Human Genetics|August 1, 1997
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndromeJ M Conroy, T A Grebe, L A Becker, et al.
The Journal of Biological Chemistry|April 26, 2020
Knockout mouse models reveal the contributions of G protein subunits to complement C5a receptor-mediated chemotaxisEsther van den Bos, Benjamin Ambrosy, Markus Horsthemke, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell lineH F Schoenmakers, P F Kools, B Kazmierczak, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Genomics|January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14W Bardenheuer, S Szymanski, A Lux, et al.
Differentiation; Research in Biological Diversity|November 28, 2007
Light optical precision measurements of the active and inactive Prader-Willi syndrome imprinted regions in human cell nucleiJoachim Rauch, Tobias A Knoch, Irina Solovei, et al.
Pageof 37

Showing results (291-300 of 368) with videos related to

Sort By:
Pageof 37
Nature|September 10, 1987
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European familiesC Van Broeckhoven, A M Genthe, A Vandenberghe, et al.
Human Molecular Genetics|May 1, 1994
A gene for hereditary multiple exostoses maps to chromosome 19pM Le Merrer, L Legeai-Mallet, P M Jeannin, et al.
Orvosi Hetilap|January 9, 2018
[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]Orsolya Dóra Ács, Bálint Péterfia, Péter Hollósi, et al.
International Journal of Molecular Medicine|January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell levelA Weise, M Gross, K Mrasek, et al.
American Journal of Human Genetics|August 1, 1997
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndromeJ M Conroy, T A Grebe, L A Becker, et al.
The Journal of Biological Chemistry|April 26, 2020
Knockout mouse models reveal the contributions of G protein subunits to complement C5a receptor-mediated chemotaxisEsther van den Bos, Benjamin Ambrosy, Markus Horsthemke, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell lineH F Schoenmakers, P F Kools, B Kazmierczak, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Genomics|January 15, 1994
Characterization of a microdissection library from human chromosome region 3p14W Bardenheuer, S Szymanski, A Lux, et al.
Differentiation; Research in Biological Diversity|November 28, 2007
Light optical precision measurements of the active and inactive Prader-Willi syndrome imprinted regions in human cell nucleiJoachim Rauch, Tobias A Knoch, Irina Solovei, et al.
Pageof 37