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K D Smith

Showing results (181-190 of 211) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1994
Bw4-reactive and Bw6-reactive antibodies recognize multiple distinct HLA structures that partially overlap in the alpha-1 helixC T Lutz, K D Smith, N S Greazel, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Human Molecular Genetics|March 21, 1998
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsL T Braiterman, S Zheng, P A Watkins, et al.
Annals of Neurology|April 20, 2001
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screeningL Bezman, A B Moser, G V Raymond, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 28, 2003
American Association of Clinical Endocrinologists medical guidelines for the clinical practice for the diagnosis and treatment of hyperandrogenic disordersN F Goodman, M B Bledsoe, R H Cobin, et al.
Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.
Nature Medicine|November 11, 1998
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophyS Kemp, H M Wei, J F Lu, et al.
Molecular and Cellular Biology|January 2, 2003
Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophyM C McGuinness, J-F Lu, H-P Zhang, et al.
Journal of Neuropathology and Experimental Neurology|October 9, 2001
Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentationM Ito, B M Blumberg, D J Mock, et al.
Annals of Human Genetics|March 30, 2000
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotypingA W Bergen, C Y Wang, J Tsai, et al.
Pageof 22

Showing results (181-190 of 211) with videos related to

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Pageof 22
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1994
Bw4-reactive and Bw6-reactive antibodies recognize multiple distinct HLA structures that partially overlap in the alpha-1 helixC T Lutz, K D Smith, N S Greazel, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Human Molecular Genetics|March 21, 1998
Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteinsL T Braiterman, S Zheng, P A Watkins, et al.
Annals of Neurology|April 20, 2001
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screeningL Bezman, A B Moser, G V Raymond, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 28, 2003
American Association of Clinical Endocrinologists medical guidelines for the clinical practice for the diagnosis and treatment of hyperandrogenic disordersN F Goodman, M B Bledsoe, R H Cobin, et al.
Human Genetics|February 1, 1992
The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditismG D Berkovitz, P Y Fechner, S M Marcantonio, et al.
Nature Medicine|November 11, 1998
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophyS Kemp, H M Wei, J F Lu, et al.
Molecular and Cellular Biology|January 2, 2003
Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophyM C McGuinness, J-F Lu, H-P Zhang, et al.
Journal of Neuropathology and Experimental Neurology|October 9, 2001
Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentationM Ito, B M Blumberg, D J Mock, et al.
Annals of Human Genetics|March 30, 2000
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotypingA W Bergen, C Y Wang, J Tsai, et al.
Pageof 22