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H S Scott

Showing results (21-30 of 84) with videos related to

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Human Molecular Genetics|September 1, 1993
Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeH S Scott, P V Nelson, T Litjens, et al.
Genomics|April 15, 1997
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3L Mittaz, H S Scott, C Rossier, et al.
Cell Transplantation|July 1, 1996
Long-term correction of albumin levels in the Nagase analbuminemic rat: repopulation of the liver by transplanted normal hepatocytes under a regeneration responseA D Moscioni, J Rozga, S Chen, et al.
Leukemia|February 13, 2004
No evidence for core-binding factor CBFbeta as a leukemia predisposing factor in chromosome 16q22-linked familial AMLR Escher, F Hagos, J Michaud, et al.
Human Mutation|August 29, 2001
APECED mutations in the autoimmune regulator (AIRE) geneM Heino, P Peterson, J Kudoh, et al.
Human Mutation|January 1, 1995
Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implicationsH S Scott, S Bunge, A Gal, et al.
Human Mutation|January 1, 1992
alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotypeH S Scott, T Litjens, P V Nelson, et al.
Human Genetics|March 1, 1992
Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major alleleH S Scott, P V Nelson, A Cooper, et al.
The Journal of Clinical Endocrinology and Metabolism|October 21, 2011
CBG Santiago: a novel CBG mutationD J Torpy, B Ardesjö Lundgren, J T Ho, et al.
Human Genetics|December 22, 1999
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and YH Chen, C Rossier, M A Morris, et al.
Pageof 9

Showing results (21-30 of 84) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|September 1, 1993
Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeH S Scott, P V Nelson, T Litjens, et al.
Genomics|April 15, 1997
Cloning of a human RNA editing deaminase (ADARB1) of glutamate receptors that maps to chromosome 21q22.3L Mittaz, H S Scott, C Rossier, et al.
Cell Transplantation|July 1, 1996
Long-term correction of albumin levels in the Nagase analbuminemic rat: repopulation of the liver by transplanted normal hepatocytes under a regeneration responseA D Moscioni, J Rozga, S Chen, et al.
Leukemia|February 13, 2004
No evidence for core-binding factor CBFbeta as a leukemia predisposing factor in chromosome 16q22-linked familial AMLR Escher, F Hagos, J Michaud, et al.
Human Mutation|August 29, 2001
APECED mutations in the autoimmune regulator (AIRE) geneM Heino, P Peterson, J Kudoh, et al.
Human Mutation|January 1, 1995
Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implicationsH S Scott, S Bunge, A Gal, et al.
Human Mutation|January 1, 1992
alpha-L-iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotypeH S Scott, T Litjens, P V Nelson, et al.
Human Genetics|March 1, 1992
Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major alleleH S Scott, P V Nelson, A Cooper, et al.
The Journal of Clinical Endocrinology and Metabolism|October 21, 2011
CBG Santiago: a novel CBG mutationD J Torpy, B Ardesjö Lundgren, J T Ho, et al.
Human Genetics|December 22, 1999
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and YH Chen, C Rossier, M A Morris, et al.
Pageof 9