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Horsthemke

Showing results (131-140 of 368) with videos related to

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Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Biochemical Society Transactions|April 1, 1987
Recombinant DNA technology and low-density lipoprotein receptor defectsJ Davison, B Horsthemke, A Dunning, et al.
European Journal of Human Genetics : EJHG|October 23, 2008
Low frequency of imprinting defects in ICSI children born small for gestational ageDeniz Kanber, Karin Buiting, Michael Zeschnigk, et al.
Biochemical and Biophysical Research Communications|May 29, 1981
Degradation of luteinizing hormone - releasing hormone and analogs by adenohypophyseal peptidasesB Horsthemke, H Knisatschek, J Rivier, et al.
American Journal of Human Genetics|December 1, 1992
A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma geneB Brandt, V Greger, D Yandell, et al.
Chaos (Woodbury, N.Y.)|April 3, 2021
Nonlinear waves in a quintic FitzHugh-Nagumo model with cross diffusion: Fronts, pulses, and wave trainsEvgeny P Zemskov, Mikhail A Tsyganov, Klaus Kassner, et al.
Journal of Visualized Experiments : Jove|November 6, 2018
Time-lapse 3D Imaging of Phagocytosis by Mouse MacrophagesMarkus Horsthemke, Janine Wilden, Anne C Bachg, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 26, 2011
Genetic aspects of familial Ménière's diseaseDiana Arweiler-Harbeck, Bernhard Horsthemke, Klaus Jahnke, et al.
Human Genetics|November 27, 2004
Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndromeMaren Runte, Raymonda Varon, Denise Horn, et al.
European Journal of Pediatrics|November 1, 1992
Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 familiesD Strumberg, B P Hauffa, B Horsthemke, et al.
Pageof 37

Showing results (131-140 of 368) with videos related to

Sort By:
Pageof 37
Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Biochemical Society Transactions|April 1, 1987
Recombinant DNA technology and low-density lipoprotein receptor defectsJ Davison, B Horsthemke, A Dunning, et al.
European Journal of Human Genetics : EJHG|October 23, 2008
Low frequency of imprinting defects in ICSI children born small for gestational ageDeniz Kanber, Karin Buiting, Michael Zeschnigk, et al.
Biochemical and Biophysical Research Communications|May 29, 1981
Degradation of luteinizing hormone - releasing hormone and analogs by adenohypophyseal peptidasesB Horsthemke, H Knisatschek, J Rivier, et al.
American Journal of Human Genetics|December 1, 1992
A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma geneB Brandt, V Greger, D Yandell, et al.
Chaos (Woodbury, N.Y.)|April 3, 2021
Nonlinear waves in a quintic FitzHugh-Nagumo model with cross diffusion: Fronts, pulses, and wave trainsEvgeny P Zemskov, Mikhail A Tsyganov, Klaus Kassner, et al.
Journal of Visualized Experiments : Jove|November 6, 2018
Time-lapse 3D Imaging of Phagocytosis by Mouse MacrophagesMarkus Horsthemke, Janine Wilden, Anne C Bachg, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 26, 2011
Genetic aspects of familial Ménière's diseaseDiana Arweiler-Harbeck, Bernhard Horsthemke, Klaus Jahnke, et al.
Human Genetics|November 27, 2004
Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndromeMaren Runte, Raymonda Varon, Denise Horn, et al.
European Journal of Pediatrics|November 1, 1992
Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 familiesD Strumberg, B P Hauffa, B Horsthemke, et al.
Pageof 37