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A P Jackson

Showing results (81-90 of 91) with videos related to

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The Journal of Physiology|December 18, 2001
The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heartA I Fahmi, M Patel, E B Stevens, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Journal of Medical Genetics|March 8, 2003
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolismY J Crow, D N Black, M Ali, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 26, 2000
beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kineticsK Morgan, E B Stevens, B Shah, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Science (New York, N.Y.)|March 8, 2014
Molecular gas clumps from the destruction of icy bodies in the β Pictoris debris diskW R F Dent, M C Wyatt, A Roberge, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Journal of Medical Genetics|May 24, 2005
A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21M Ali, L J Highet, D Lacombe, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
The Journal of Physiology|December 18, 2001
The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heartA I Fahmi, M Patel, E B Stevens, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31L J Pulleyn, A P Jackson, E Roberts, et al.
Journal of Medical Genetics|March 8, 2003
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolismY J Crow, D N Black, M Ali, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 26, 2000
beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kineticsK Morgan, E B Stevens, B Shah, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2E Roberts, A P Jackson, A C Carradice, et al.
American Journal of Human Genetics|July 31, 1998
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterA P Jackson, D P McHale, D A Campbell, et al.
Science (New York, N.Y.)|March 8, 2014
Molecular gas clumps from the destruction of icy bodies in the β Pictoris debris diskW R F Dent, M C Wyatt, A Roberge, et al.
Nature Genetics|July 5, 2001
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia diseaseA R Curtis, C Fey, C M Morris, et al.
Journal of Medical Genetics|May 24, 2005
A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21M Ali, L J Highet, D Lacombe, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Pageof 10