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C P Morris

Showing results (71-80 of 85) with videos related to

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Nature Genetics|December 1, 1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeH S Scott, L Blanch, X H Guo, et al.
BMJ (Clinical Research Ed.)|June 4, 1994
Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experienceE Ranieri, B D Lewis, R L Gerace, et al.
Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HE C Jazwinska, L M Cullen, F Busfield, et al.
The Journal of Clinical Investigation|March 15, 1997
Altered responses of human macrophages to lipopolysaccharide by hydroperoxy eicosatetraenoic acid, hydroxy eicosatetraenoic acid, and arachidonic acid. Inhibition of tumor necrosis factor productionJ V Ferrante, Z H Huang, M Nandoskar, et al.
Human Molecular Genetics|June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patientsS Bunge, W J Kleijer, C Steglich, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotypeJ J Hopwood, A Vellodi, H S Scott, et al.
Journal of Medical Genetics|June 1, 1991
Sanfilippo syndrome type D in two adolescent sistersL Siciliano, A Fiumara, L Pavone, et al.
Acta Psychiatrica Scandinavica|August 11, 2017
Genomewide DNA methylation analysis in combat veterans reveals a novel locus for PTSDD Mehta, D Bruenig, T Carrillo-Roa, et al.
American Journal of Human Genetics|November 1, 1990
Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3H S Scott, L J Ashton, H J Eyre, et al.
Human Molecular Genetics|June 1, 1992
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS geneM L Steén-Bondeson, N Dahl, T Tönnesen, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Nature Genetics|December 1, 1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeH S Scott, L Blanch, X H Guo, et al.
BMJ (Clinical Research Ed.)|June 4, 1994
Neonatal screening for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis: four years' experienceE Ranieri, B D Lewis, R L Gerace, et al.
Nature Genetics|November 1, 1996
Haemochromatosis and HLA-HE C Jazwinska, L M Cullen, F Busfield, et al.
The Journal of Clinical Investigation|March 15, 1997
Altered responses of human macrophages to lipopolysaccharide by hydroperoxy eicosatetraenoic acid, hydroxy eicosatetraenoic acid, and arachidonic acid. Inhibition of tumor necrosis factor productionJ V Ferrante, Z H Huang, M Nandoskar, et al.
Human Molecular Genetics|June 1, 1994
Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patientsS Bunge, W J Kleijer, C Steglich, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotypeJ J Hopwood, A Vellodi, H S Scott, et al.
Journal of Medical Genetics|June 1, 1991
Sanfilippo syndrome type D in two adolescent sistersL Siciliano, A Fiumara, L Pavone, et al.
Acta Psychiatrica Scandinavica|August 11, 2017
Genomewide DNA methylation analysis in combat veterans reveals a novel locus for PTSDD Mehta, D Bruenig, T Carrillo-Roa, et al.
American Journal of Human Genetics|November 1, 1990
Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3H S Scott, L J Ashton, H J Eyre, et al.
Human Molecular Genetics|June 1, 1992
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS geneM L Steén-Bondeson, N Dahl, T Tönnesen, et al.
Pageof 9