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Human Molecular Genetics
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September 1, 1992
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2)
J A Trofatter, M L Sytsma, J F Gusella, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 10, 2010
Genotype at polymorphism rs11200638 and HTRA1 expression level
Gaofeng Wang, William K Scott, Jonathan L Haines, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Clinical, neuropathological and genetic aspects of the tuberous sclerosis complex
M P Short, E P Richardson, J L Haines, et al.
Genomics
|
November 15, 1994
Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3)
W L Yan, T J Lerner, J L Haines, et al.
Journal of Cell Science
|
August 14, 2008
Btn1 affects cytokinesis and cell-wall deposition by independent mechanisms, one of which is linked to dysregulation of vacuole pH
Sandra Codlin, Rebecca L Haines, J Jemima E Burden, et al.
Epilepsia
|
November 1, 1985
Altered amino acid levels in multiply affected sibships with seizures
J L Haines, S S Rich, M Y Tsai, et al.
Genomics
|
August 1, 1994
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetrance
S K Kim, J L Haines, E L Berson, et al.
Blood
|
July 1, 1990
Human erythropoietin receptor: cloning, expression, and biologic characterization
S S Jones, A D D'Andrea, L L Haines, et al.
Annals of Neurology
|
September 27, 2002
Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12
William K Scott, Jeffery M Vance, Jonathan L Haines, et al.
Lancet (London, England)
|
June 1, 1996
Presenilin-1 polymorphism and Alzheimer's disease
W K Scott, A D Roses, J L Haines, et al.
Page
of 100
Search research articles
Search
Showing results (111-120 of 993) with videos related to
Sort By:
Page
of 100
Human Molecular Genetics
|
September 1, 1992
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2)
J A Trofatter, M L Sytsma, J F Gusella, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 10, 2010
Genotype at polymorphism rs11200638 and HTRA1 expression level
Gaofeng Wang, William K Scott, Jonathan L Haines, et al.
Brain Pathology (Zurich, Switzerland)
|
April 1, 1995
Clinical, neuropathological and genetic aspects of the tuberous sclerosis complex
M P Short, E P Richardson, J L Haines, et al.
Genomics
|
November 15, 1994
Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3)
W L Yan, T J Lerner, J L Haines, et al.
Journal of Cell Science
|
August 14, 2008
Btn1 affects cytokinesis and cell-wall deposition by independent mechanisms, one of which is linked to dysregulation of vacuole pH
Sandra Codlin, Rebecca L Haines, J Jemima E Burden, et al.
Epilepsia
|
November 1, 1985
Altered amino acid levels in multiply affected sibships with seizures
J L Haines, S S Rich, M Y Tsai, et al.
Genomics
|
August 1, 1994
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetrance
S K Kim, J L Haines, E L Berson, et al.
Blood
|
July 1, 1990
Human erythropoietin receptor: cloning, expression, and biologic characterization
S S Jones, A D D'Andrea, L L Haines, et al.
Annals of Neurology
|
September 27, 2002
Linkage of Parkinsonism and Alzheimer's disease with Lewy body pathology to chromosome 12
William K Scott, Jeffery M Vance, Jonathan L Haines, et al.
Lancet (London, England)
|
June 1, 1996
Presenilin-1 polymorphism and Alzheimer's disease
W K Scott, A D Roses, J L Haines, et al.
Page
of 100