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Horsthemke

Showing results (191-200 of 368) with videos related to

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Lancet (London, England)|May 4, 1996
Prognostic implications of monosomy 3 in uveal melanomaG Prescher, N Bornfeld, H Hirche, et al.
Human Genetics|July 1, 1989
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeH J Lüdecke, R Burdiek, G Senger, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defectG Gillessen-Kaesbach, S Demuth, H Thiele, et al.
Comparative and Functional Genomics|July 17, 2008
Methylation analysis of several tumour suppressor genes shows a low frequency of methylation of CDKN2A and RARB in uveal melanomasMichael Zeschnigk, Frank Tschentscher, Christina Lich, et al.
Human Molecular Genetics|June 15, 2012
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated proteinLisa C Neumann, Yolanda Markaki, Emil Mladenov, et al.
The Journal of Biological Chemistry|July 30, 2003
The RING finger protein RNF4, a co-regulator of transcription, interacts with the TRPS1 transcription factorFrank J Kaiser, Tarik Möröy, Glenn T G Chang, et al.
European Journal of Human Genetics : EJHG|December 4, 2004
Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndromeEva Wey, Deborah Bartholdi, Mariluce Riegel, et al.
Plos One|November 28, 2013
The origin of the RB1 imprintDeniz Kanber, Karin Buiting, Christian Roos, et al.
Heliyon|February 6, 2020
A human somatic cell culture system for modelling gene silencing by transcriptional interferenceTheresa Kühnel, Helena Sophie Barbara Heinz, Nadja Utz, et al.
Journal of Visualized Experiments : Jove|April 21, 2020
Time-lapse Imaging of Mouse Macrophage ChemotaxisEsther van den Bos, Stefan Walbaum, Markus Horsthemke, et al.
Pageof 37

Showing results (191-200 of 368) with videos related to

Sort By:
Pageof 37
Lancet (London, England)|May 4, 1996
Prognostic implications of monosomy 3 in uveal melanomaG Prescher, N Bornfeld, H Hirche, et al.
Human Genetics|July 1, 1989
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndromeH J Lüdecke, R Burdiek, G Senger, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defectG Gillessen-Kaesbach, S Demuth, H Thiele, et al.
Comparative and Functional Genomics|July 17, 2008
Methylation analysis of several tumour suppressor genes shows a low frequency of methylation of CDKN2A and RARB in uveal melanomasMichael Zeschnigk, Frank Tschentscher, Christina Lich, et al.
Human Molecular Genetics|June 15, 2012
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated proteinLisa C Neumann, Yolanda Markaki, Emil Mladenov, et al.
The Journal of Biological Chemistry|July 30, 2003
The RING finger protein RNF4, a co-regulator of transcription, interacts with the TRPS1 transcription factorFrank J Kaiser, Tarik Möröy, Glenn T G Chang, et al.
European Journal of Human Genetics : EJHG|December 4, 2004
Mosaic imprinting defect in a patient with an almost typical expression of the Prader-Willi syndromeEva Wey, Deborah Bartholdi, Mariluce Riegel, et al.
Plos One|November 28, 2013
The origin of the RB1 imprintDeniz Kanber, Karin Buiting, Christian Roos, et al.
Heliyon|February 6, 2020
A human somatic cell culture system for modelling gene silencing by transcriptional interferenceTheresa Kühnel, Helena Sophie Barbara Heinz, Nadja Utz, et al.
Journal of Visualized Experiments : Jove|April 21, 2020
Time-lapse Imaging of Mouse Macrophage ChemotaxisEsther van den Bos, Stefan Walbaum, Markus Horsthemke, et al.
Pageof 37