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J L Mandel

Showing results (181-190 of 257) with videos related to

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Genomics|May 1, 1997
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathyJ Laporte, P Kioschis, L J Hu, et al.
Human Molecular Genetics|May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell cultureE W Khandjian, A Fortin, A Thibodeau, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
Journal of Molecular Biology|May 15, 1977
Amanitin binding to RNA polymerase II in alpha-amanitin-resistant rat myoblast mutantsM M Crerar, S J Andrews, E S David, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
American Journal of Human Genetics|April 1, 1995
Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26N Dahl, J Laporte, L Hu, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Human Molecular Genetics|October 1, 1995
Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear familyN Nadal, M O Rolland, C Tranchant, et al.
Biochemistry|September 3, 2003
The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA bindingS Adinolfi, A Ramos, S R Martin, et al.
Nature Genetics|June 1, 1994
FRAXAC2 instabilityR I Richards, K Holman, K Friend, et al.
Pageof 26

Showing results (181-190 of 257) with videos related to

Sort By:
Pageof 26
Genomics|May 1, 1997
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathyJ Laporte, P Kioschis, L J Hu, et al.
Human Molecular Genetics|May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell cultureE W Khandjian, A Fortin, A Thibodeau, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
Journal of Molecular Biology|May 15, 1977
Amanitin binding to RNA polymerase II in alpha-amanitin-resistant rat myoblast mutantsM M Crerar, S J Andrews, E S David, et al.
Neurobiology of Disease|March 9, 1999
Heterogeneous intracellular localization and expression of ataxin-3Y Trottier, G Cancel, I An-Gourfinkel, et al.
American Journal of Human Genetics|April 1, 1995
Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26N Dahl, J Laporte, L Hu, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Human Molecular Genetics|October 1, 1995
Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear familyN Nadal, M O Rolland, C Tranchant, et al.
Biochemistry|September 3, 2003
The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA bindingS Adinolfi, A Ramos, S R Martin, et al.
Nature Genetics|June 1, 1994
FRAXAC2 instabilityR I Richards, K Holman, K Friend, et al.
Pageof 26