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Human Molecular Genetics
|
June 1, 1992
Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype
M Town, J M Bautista, P J Mason, et al.
British Journal of Pharmacology
|
May 1, 1982
Ulcerative colitis: effect of sulphasalazine, its metabolites and indomethacin on the ability of human colonic mucosa to metabolize prostaglandins in vitro
K Hillier, P J Mason, S Pacheco, et al.
Blood
|
October 6, 1997
Skewed X-inactivation in carriers of X-linked dyskeratosis congenita
T J Vulliamy, S W Knight, I Dokal, et al.
European Journal of Biochemistry
|
March 30, 2001
Glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase. A novel bifunctional enzyme in malaria parasites
J L Clarke, D A Scopes, O Sodeinde, et al.
Blood Cells, Molecules & Diseases
|
March 22, 2001
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
T J Vulliamy, S W Knight, P J Mason, et al.
Blood Cells, Molecules & Diseases
|
August 1, 2015
Variations in reactive oxygen species between mouse strains
D A Reeves, B W Gu, M Bessler, et al.
Clinical and Experimental Immunology
|
August 11, 1998
Recombinant alpha-chains of type IV collagen demonstrate that the amino terminal of the Goodpasture autoantigen is crucial for antibody recognition
J J Ryan, P J Mason, C D Pusey, et al.
Blood
|
December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
K Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics
|
May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21
M Bessler, P Hillmen, L Longo, et al.
Journal of Molecular Biology
|
March 25, 1982
Evolutionary implications of a complex pattern of DNA sequence homology extending far upstream of the hsp70 genes at loci 87A7 and 87C1 in Drosophila melanogaster
P J Mason, I Török, I Kiss, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 80) with videos related to
Sort By:
Page
of 8
Human Molecular Genetics
|
June 1, 1992
Both mutations in G6PD A- are necessary to produce the G6PD deficient phenotype
M Town, J M Bautista, P J Mason, et al.
British Journal of Pharmacology
|
May 1, 1982
Ulcerative colitis: effect of sulphasalazine, its metabolites and indomethacin on the ability of human colonic mucosa to metabolize prostaglandins in vitro
K Hillier, P J Mason, S Pacheco, et al.
Blood
|
October 6, 1997
Skewed X-inactivation in carriers of X-linked dyskeratosis congenita
T J Vulliamy, S W Knight, I Dokal, et al.
European Journal of Biochemistry
|
March 30, 2001
Glucose-6-phosphate dehydrogenase-6-phosphogluconolactonase. A novel bifunctional enzyme in malaria parasites
J L Clarke, D A Scopes, O Sodeinde, et al.
Blood Cells, Molecules & Diseases
|
March 22, 2001
Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita
T J Vulliamy, S W Knight, P J Mason, et al.
Blood Cells, Molecules & Diseases
|
August 1, 2015
Variations in reactive oxygen species between mouse strains
D A Reeves, B W Gu, M Bessler, et al.
Clinical and Experimental Immunology
|
August 11, 1998
Recombinant alpha-chains of type IV collagen demonstrate that the amino terminal of the Goodpasture autoantigen is crucial for antibody recognition
J J Ryan, P J Mason, C D Pusey, et al.
Blood
|
December 15, 1995
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
K Nafa, P J Mason, P Hillmen, et al.
Human Molecular Genetics
|
May 1, 1994
Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21
M Bessler, P Hillmen, L Longo, et al.
Journal of Molecular Biology
|
March 25, 1982
Evolutionary implications of a complex pattern of DNA sequence homology extending far upstream of the hsp70 genes at loci 87A7 and 87C1 in Drosophila melanogaster
P J Mason, I Török, I Kiss, et al.
Page
of 8