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Annals of Neurology
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March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency
A Hentati, H X Deng, W Y Hung, et al.
Genomics
|
August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2
T Siddique, R McKinney, W Y Hung, et al.
Neurology
|
January 1, 1997
A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis
M S Ahmed, S Afsar, A Hentati, et al.
European Review for Medical and Pharmacological Sciences
|
February 20, 2024
Bark extract of Chaetocarpus castanocarpus (Roxb.) exhibits potent sedative, anxiolytic, and antidepressant effects through an in vivo approach in Swiss albino mice
R Rahman, T Siddique, F A Nipa, et al.
Nature
|
March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D R Rosen, T Siddique, D Patterson, et al.
Neurology
|
July 11, 2006
Paraoxonase cluster polymorphisms are associated with sporadic ALS
M Saeed, N Siddique, W Y Hung, et al.
Neurogenetics
|
May 1, 1997
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis
J S Zu, H X Deng, T P Lo, et al.
Human Molecular Genetics
|
September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31
K Isozumi, R DeLong, J Kaplan, et al.
International Journal of Neurology
|
January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosis
T Siddique, P Hu, A Hentati, et al.
Australian Paediatric Journal
|
January 1, 1988
Systematic gene mapping in man: data management considerations
M A Pericak-Vance, W Y Hung, L Yamaoka, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Annals of Neurology
|
March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency
A Hentati, H X Deng, W Y Hung, et al.
Genomics
|
August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2
T Siddique, R McKinney, W Y Hung, et al.
Neurology
|
January 1, 1997
A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis
M S Ahmed, S Afsar, A Hentati, et al.
European Review for Medical and Pharmacological Sciences
|
February 20, 2024
Bark extract of Chaetocarpus castanocarpus (Roxb.) exhibits potent sedative, anxiolytic, and antidepressant effects through an in vivo approach in Swiss albino mice
R Rahman, T Siddique, F A Nipa, et al.
Nature
|
March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D R Rosen, T Siddique, D Patterson, et al.
Neurology
|
July 11, 2006
Paraoxonase cluster polymorphisms are associated with sporadic ALS
M Saeed, N Siddique, W Y Hung, et al.
Neurogenetics
|
May 1, 1997
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis
J S Zu, H X Deng, T P Lo, et al.
Human Molecular Genetics
|
September 1, 1996
Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31
K Isozumi, R DeLong, J Kaplan, et al.
International Journal of Neurology
|
January 1, 1991
A molecular genetic approach to amyotrophic lateral sclerosis
T Siddique, P Hu, A Hentati, et al.
Australian Paediatric Journal
|
January 1, 1988
Systematic gene mapping in man: data management considerations
M A Pericak-Vance, W Y Hung, L Yamaoka, et al.
Page
of 7