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Showing results (241-250 of 368) with videos related to

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Clinical Epigenetics|May 8, 2020
The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesisElsa Leitão, Sara Di Persio, Sandra Laurentino, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Plos One|October 2, 2014
Pre- and postovulatory aging of murine oocytes affect the transcript level and poly(A) tail length of maternal effect genesDebora Dankert, Hannah Demond, Tom Trapphoff, et al.
American Journal of Human Genetics|May 23, 2002
Intracytoplasmic sperm injection may increase the risk of imprinting defectsGerald F Cox, Joachim Bürger, Va Lip, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Nature Genetics|May 10, 2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchB Bielinska, S M Blaydes, K Buiting, et al.
Neuroendocrinology|June 1, 1984
Characterization of a neutral endopeptidase localized in the mitochondrial matrix of rat anterior pituitary tissue with GnRH as a substrateP Leblanc, A L'Heritier, C Kordon, et al.
Clinical Genetics|April 7, 2005
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qterT Eggermann, D Meschede, H Schüler, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 1, 1997
Isolation of DNA from the centromere of human chromosome 7 by microdissectionF Behrens, U Claussen, L M Iyer, et al.
European Journal of Human Genetics : EJHG|December 11, 2008
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeDeniz Kanber, Jacques Giltay, Dagmar Wieczorek, et al.
Pageof 37

Showing results (241-250 of 368) with videos related to

Sort By:
Pageof 37
Clinical Epigenetics|May 8, 2020
The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesisElsa Leitão, Sara Di Persio, Sandra Laurentino, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Plos One|October 2, 2014
Pre- and postovulatory aging of murine oocytes affect the transcript level and poly(A) tail length of maternal effect genesDebora Dankert, Hannah Demond, Tom Trapphoff, et al.
American Journal of Human Genetics|May 23, 2002
Intracytoplasmic sperm injection may increase the risk of imprinting defectsGerald F Cox, Joachim Bürger, Va Lip, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Nature Genetics|May 10, 2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switchB Bielinska, S M Blaydes, K Buiting, et al.
Neuroendocrinology|June 1, 1984
Characterization of a neutral endopeptidase localized in the mitochondrial matrix of rat anterior pituitary tissue with GnRH as a substrateP Leblanc, A L'Heritier, C Kordon, et al.
Clinical Genetics|April 7, 2005
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qterT Eggermann, D Meschede, H Schüler, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 1, 1997
Isolation of DNA from the centromere of human chromosome 7 by microdissectionF Behrens, U Claussen, L M Iyer, et al.
European Journal of Human Genetics : EJHG|December 11, 2008
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeDeniz Kanber, Jacques Giltay, Dagmar Wieczorek, et al.
Pageof 37