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Horsthemke

Showing results (161-170 of 368) with videos related to

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Archives of Orthopaedic and Trauma Surgery|November 12, 2018
The minimalinvasive direct anterior approach in aseptic cup revision hip arthroplasty: a mid-term follow-upMarc Dominique Horsthemke, Christoph Koenig, Georg Gosheger, et al.
American Journal of Human Genetics|May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)|February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locusB Horsthemke, H J Barnert, V Greger, et al.
BMC Bioinformatics|May 3, 2020
wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing dataMarius Wöste, Elsa Leitão, Sandra Laurentino, et al.
Journal of Medical Genetics|April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastomaV Greger, S Kerst, E Messmer, et al.
European Journal of Biochemistry|September 22, 1999
Human TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignmentL Schomburg, S Turwitt, G Prescher, et al.
Journal of Medical Genetics|February 1, 1995
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeG Gillessen-Kaesbach, S Gross, S Kaya-Westerloh, et al.
Neuroscience Letters|March 8, 2014
Methylation analysis of SST and SSTR4 promoters in the neocortex of Alzheimer's disease patientsChristian Grosser, Lisa Neumann, Bernhard Horsthemke, et al.
Human Genetics|April 1, 1992
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresisD Lohmann, B Horsthemke, G Gillessen-Kaesbach, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
Pageof 37

Showing results (161-170 of 368) with videos related to

Sort By:
Pageof 37
Archives of Orthopaedic and Trauma Surgery|November 12, 2018
The minimalinvasive direct anterior approach in aseptic cup revision hip arthroplasty: a mid-term follow-upMarc Dominique Horsthemke, Christoph Koenig, Georg Gosheger, et al.
American Journal of Human Genetics|May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)|February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locusB Horsthemke, H J Barnert, V Greger, et al.
BMC Bioinformatics|May 3, 2020
wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing dataMarius Wöste, Elsa Leitão, Sandra Laurentino, et al.
Journal of Medical Genetics|April 1, 1988
Application of linkage analysis to genetic counselling in families with hereditary retinoblastomaV Greger, S Kerst, E Messmer, et al.
European Journal of Biochemistry|September 22, 1999
Human TRH-degrading ectoenzyme cDNA cloning, functional expression, genomic structure and chromosomal assignmentL Schomburg, S Turwitt, G Prescher, et al.
Journal of Medical Genetics|February 1, 1995
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeG Gillessen-Kaesbach, S Gross, S Kaya-Westerloh, et al.
Neuroscience Letters|March 8, 2014
Methylation analysis of SST and SSTR4 promoters in the neocortex of Alzheimer's disease patientsChristian Grosser, Lisa Neumann, Bernhard Horsthemke, et al.
Human Genetics|April 1, 1992
Detection of small RB1 gene deletions in retinoblastoma by multiplex PCR and high-resolution gel electrophoresisD Lohmann, B Horsthemke, G Gillessen-Kaesbach, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
Pageof 37