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C O Hanemann

Showing results (41-50 of 56) with videos related to

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Gene Therapy|August 24, 1999
Cellular contaminants of adeno-associated virus vector stocks can enhance transductionL Tenenbaum, M Hamdane, M Pouzet, et al.
American Journal of Human Genetics|November 13, 2001
Spinal neurofibromatosis without café-au-lait macules in two families with null mutations of the NF1 geneD Kaufmann, R Müller, B Bartelt, et al.
Journal of Neuroscience Research|April 1, 1994
Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsiesC O Hanemann, G Stoll, D D'Urso, et al.
BMJ Open|June 16, 2026
Repurposing anti-retroviral drugs to treat NF2-related tumours: a protocol for a phase 0 trial (RETREAT)Sarah Campbell, Katherine Beaney, Joanne Hosking, et al.
Nature Genetics|June 1, 1992
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1AN Matsunami, B Smith, L Ballard, et al.
Oncogene|November 10, 2015
The scaffold protein KSR1, a novel therapeutic target for the treatment of Merlin-deficient tumorsL Zhou, J Lyons-Rimmer, S Ammoun, et al.
Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
Neurology|August 25, 2004
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALSC Münch, R Sedlmeier, T Meyer, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
Oncogene|July 11, 2017
Cellular prion protein (PrP<sup>C</sup>) in the development of Merlin-deficient tumoursL Provenzano, Y Ryan, D A Hilton, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Gene Therapy|August 24, 1999
Cellular contaminants of adeno-associated virus vector stocks can enhance transductionL Tenenbaum, M Hamdane, M Pouzet, et al.
American Journal of Human Genetics|November 13, 2001
Spinal neurofibromatosis without café-au-lait macules in two families with null mutations of the NF1 geneD Kaufmann, R Müller, B Bartelt, et al.
Journal of Neuroscience Research|April 1, 1994
Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsiesC O Hanemann, G Stoll, D D'Urso, et al.
BMJ Open|June 16, 2026
Repurposing anti-retroviral drugs to treat NF2-related tumours: a protocol for a phase 0 trial (RETREAT)Sarah Campbell, Katherine Beaney, Joanne Hosking, et al.
Nature Genetics|June 1, 1992
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1AN Matsunami, B Smith, L Ballard, et al.
Oncogene|November 10, 2015
The scaffold protein KSR1, a novel therapeutic target for the treatment of Merlin-deficient tumorsL Zhou, J Lyons-Rimmer, S Ammoun, et al.
Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
Neurology|August 25, 2004
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALSC Münch, R Sedlmeier, T Meyer, et al.
Nature Genetics|June 1, 1992
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplicationV Timmerman, E Nelis, W Van Hul, et al.
Oncogene|July 11, 2017
Cellular prion protein (PrP<sup>C</sup>) in the development of Merlin-deficient tumoursL Provenzano, Y Ryan, D A Hilton, et al.
Pageof 6