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M Frydman

Showing results (161-170 of 172) with videos related to

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Human Molecular Genetics|January 1, 1995
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndromeH J Lüdecke, M J Wagner, J Nardmann, et al.
Molecular Cancer Therapeutics|May 21, 2020
Targeting Casein Kinase 1 Delta Sensitizes Pancreatic and Bladder Cancer Cells to Gemcitabine Treatment by Upregulating Deoxycytidine KinaseFrancesca Vena, Simon Bayle, Ainhoa Nieto, et al.
Human Genetics|March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeY Ziv, M Frydman, E Lange, et al.
Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.
American Journal of Human Genetics|December 5, 1998
Mutation analysis of LMX1B gene in nail-patella syndrome patientsI McIntosh, S D Dreyer, M V Clough, et al.
Cancer Research|October 30, 2025
Targeting CDK12/13 Drives Mitotic Arrest to Overcome Resistance to KRASG12C InhibitorsYaakov E Stern, Pompom Ghosh, John Peroza, et al.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Molecular Syndromology|April 20, 2013
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and MicrocephalyJ A Rosenfeld, K H Kim, B Angle, et al.
Journal of Medical Genetics|November 25, 2003
Identification of eight novel NSD1 mutations in Sotos syndromeJ Kamimura, Y Endo, N Kurotaki, et al.
Pageof 18

Showing results (161-170 of 172) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|January 1, 1995
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndromeH J Lüdecke, M J Wagner, J Nardmann, et al.
Molecular Cancer Therapeutics|May 21, 2020
Targeting Casein Kinase 1 Delta Sensitizes Pancreatic and Bladder Cancer Cells to Gemcitabine Treatment by Upregulating Deoxycytidine KinaseFrancesca Vena, Simon Bayle, Ainhoa Nieto, et al.
Human Genetics|March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeY Ziv, M Frydman, E Lange, et al.
Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.
American Journal of Human Genetics|December 5, 1998
Mutation analysis of LMX1B gene in nail-patella syndrome patientsI McIntosh, S D Dreyer, M V Clough, et al.
Cancer Research|October 30, 2025
Targeting CDK12/13 Drives Mitotic Arrest to Overcome Resistance to KRASG12C InhibitorsYaakov E Stern, Pompom Ghosh, John Peroza, et al.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Molecular Syndromology|April 20, 2013
Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and MicrocephalyJ A Rosenfeld, K H Kim, B Angle, et al.
Journal of Medical Genetics|November 25, 2003
Identification of eight novel NSD1 mutations in Sotos syndromeJ Kamimura, Y Endo, N Kurotaki, et al.
Pageof 18