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Horsthemke

Showing results (261-270 of 368) with videos related to

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Genomics|April 1, 1993
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivationR Slim, J Levilliers, H J Lüdecke, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Increased parental ages and uniparental disomy 15: a paternal age effect?W P Robinson, I Lorda-Sanchez, S Malcolm, et al.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 1, 1994
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibraryJ Wienberg, A Jauch, H J Lüdecke, et al.
Genomics|July 1, 1991
New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22W Fiedler, U Claussen, H J Lüdecke, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Clinical utility gene card for: Angelman SyndromeKarin Buiting, Jill Clayton-Smith, Daniel J Driscoll, et al.
Lancet (London, England)|January 25, 1997
Secretion of brain natriuretic peptide in patients with aneurysmal subarachnoid haemorrhageE Berendes, M Walter, P Cullen, et al.
Human Molecular Genetics|August 29, 2003
Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genesBernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Sensors (Basel, Switzerland)|April 13, 2024
Excited-State Lifetime of NV Centers for All-Optical Magnetic Field SensingLudwig Horsthemke, Jens Pogorzelski, Dennis Stiegekötter, et al.
Pageof 37

Showing results (261-270 of 368) with videos related to

Sort By:
Pageof 37
Genomics|April 1, 1993
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivationR Slim, J Levilliers, H J Lüdecke, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Increased parental ages and uniparental disomy 15: a paternal age effect?W P Robinson, I Lorda-Sanchez, S Malcolm, et al.
Prenatal Diagnosis|September 1, 1996
Cytogenetic and age-dependent risk factors associated with uniparental disomy 15W P Robinson, S Langlois, S Schuffenhauer, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 1, 1994
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibraryJ Wienberg, A Jauch, H J Lüdecke, et al.
Genomics|July 1, 1991
New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22W Fiedler, U Claussen, H J Lüdecke, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Clinical utility gene card for: Angelman SyndromeKarin Buiting, Jill Clayton-Smith, Daniel J Driscoll, et al.
Lancet (London, England)|January 25, 1997
Secretion of brain natriuretic peptide in patients with aneurysmal subarachnoid haemorrhageE Berendes, M Walter, P Cullen, et al.
Human Molecular Genetics|August 29, 2003
Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genesBernhard Horsthemke, Hülya Nazlican, Johannes Hüsing, et al.
Human Molecular Genetics|September 1, 1993
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patientsC C Glenn, R D Nicholls, W P Robinson, et al.
Sensors (Basel, Switzerland)|April 13, 2024
Excited-State Lifetime of NV Centers for All-Optical Magnetic Field SensingLudwig Horsthemke, Jens Pogorzelski, Dennis Stiegekötter, et al.
Pageof 37