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Annals of the New York Academy of Sciences
|
December 10, 1999
A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female
G S Lin, J D Glass, S Shumas, et al.
Cell and Tissue Research
|
August 22, 2001
Internodal specializations of myelinated axons in the central nervous system
E J Arroyo, T Xu, S Poliak, et al.
Journal of Neuroscience Research
|
December 8, 1998
Maturation-dependent apoptotic cell death of oligodendrocytes in myelin-deficient rats
J B Grinspan, M Coulalaglou, J S Beesley, et al.
Metabolic Brain Disease
|
May 22, 2007
Supplementation with vitamins E plus C or soy isoflavones in ovariectomized rats: effect on the activities of Na(+), K (+)-ATPase and cholinesterases
Siomara C Monteiro, Cristiane B Mattos, Emilene B S Scherer, et al.
Tissue Antigens
|
November 10, 2007
Identification and characterization of three novel HLA alleles, HLA-A*240214, HLA-A*3215 and HLA-DQB1*060302
A Heinold, M Bauer, G Opelz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2003
Connexins are critical for normal myelination in the CNS
Daniela M Menichella, Daniel A Goodenough, Erich Sirkowski, et al.
Human Immunology
|
November 13, 2001
Human leukocyte antigen class II allele frequencies and haplotype association in Iranian normal population
A Amirzargar, J Mytilineos, S Farjadian, et al.
Glia
|
August 5, 2004
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes
Kleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, et al.
Neuron
|
November 1, 1994
Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease
R Bruzzone, T W White, S S Scherer, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
October 20, 1998
HLA class II (DRB1, DQA1 and DQB1) associated genetic susceptibility in Iranian multiple sclerosis (MS) patients
A Amirzargar, J Mytilineos, A Yousefipour, et al.
Page
of 52
Search research articles
Search
Showing results (231-240 of 519) with videos related to
Sort By:
Page
of 52
Annals of the New York Academy of Sciences
|
December 10, 1999
A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female
G S Lin, J D Glass, S Shumas, et al.
Cell and Tissue Research
|
August 22, 2001
Internodal specializations of myelinated axons in the central nervous system
E J Arroyo, T Xu, S Poliak, et al.
Journal of Neuroscience Research
|
December 8, 1998
Maturation-dependent apoptotic cell death of oligodendrocytes in myelin-deficient rats
J B Grinspan, M Coulalaglou, J S Beesley, et al.
Metabolic Brain Disease
|
May 22, 2007
Supplementation with vitamins E plus C or soy isoflavones in ovariectomized rats: effect on the activities of Na(+), K (+)-ATPase and cholinesterases
Siomara C Monteiro, Cristiane B Mattos, Emilene B S Scherer, et al.
Tissue Antigens
|
November 10, 2007
Identification and characterization of three novel HLA alleles, HLA-A*240214, HLA-A*3215 and HLA-DQB1*060302
A Heinold, M Bauer, G Opelz, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2003
Connexins are critical for normal myelination in the CNS
Daniela M Menichella, Daniel A Goodenough, Erich Sirkowski, et al.
Human Immunology
|
November 13, 2001
Human leukocyte antigen class II allele frequencies and haplotype association in Iranian normal population
A Amirzargar, J Mytilineos, S Farjadian, et al.
Glia
|
August 5, 2004
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes
Kleopas A Kleopa, Jennifer L Orthmann, Alan Enriquez, et al.
Neuron
|
November 1, 1994
Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease
R Bruzzone, T W White, S S Scherer, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics
|
October 20, 1998
HLA class II (DRB1, DQA1 and DQB1) associated genetic susceptibility in Iranian multiple sclerosis (MS) patients
A Amirzargar, J Mytilineos, A Yousefipour, et al.
Page
of 52