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Blood
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November 9, 2000
Cytoskeletal regulation of the platelet glycoprotein Ib/V/IX-von willebrand factor interaction
N Mistry, S L Cranmer, Y Yuan, et al.
Cell Death and Differentiation
|
February 4, 2014
The granzyme B-Serpinb9 axis controls the fate of lymphocytes after lysosomal stress
C H Bird, M E Christensen, M S J Mangan, et al.
Journal of Genetics
|
June 17, 2011
The first genetic map of pigeon pea based on diversity arrays technology (DArT) markers
Shi Ying Yang, Rachit K Saxena, Pawan L Kulwal, et al.
The British Journal of Dermatology
|
January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild disease
J E Mellerio, L Pulkkinen, J R McMillan, et al.
Human Mutation
|
April 29, 1998
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex
L D Corden, J E Mellerio, M J Gratian, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
March 9, 2023
Lower-limb resistance training reduces exertional dyspnea and intrinsic neuromuscular fatigability in individuals with chronic obstructive pulmonary disease
Nicole M Brunton, David J Barbour, Jinelle C Gelinas, et al.
Malaria Journal
|
November 15, 2017
Yeast interfering RNA larvicides targeting neural genes induce high rates of Anopheles larval mortality
Keshava Mysore, Limb K Hapairai, Longhua Sun, et al.
Nature Genetics
|
March 30, 2001
Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci
W O Cookson, B Ubhi, R Lawrence, et al.
The Journal of Investigative Dermatology
|
January 1, 1994
Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE)
W H McLean, R A Eady, P J Dopping-Hepenstal, et al.
Nature Genetics
|
September 7, 2001
Gene polymorphism in Netherton and common atopic disease
A J Walley, S Chavanas, M F Moffatt, et al.
Page
of 21
Search research articles
Search
Showing results (161-170 of 202) with videos related to
Sort By:
Page
of 21
Blood
|
November 9, 2000
Cytoskeletal regulation of the platelet glycoprotein Ib/V/IX-von willebrand factor interaction
N Mistry, S L Cranmer, Y Yuan, et al.
Cell Death and Differentiation
|
February 4, 2014
The granzyme B-Serpinb9 axis controls the fate of lymphocytes after lysosomal stress
C H Bird, M E Christensen, M S J Mangan, et al.
Journal of Genetics
|
June 17, 2011
The first genetic map of pigeon pea based on diversity arrays technology (DArT) markers
Shi Ying Yang, Rachit K Saxena, Pawan L Kulwal, et al.
The British Journal of Dermatology
|
January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild disease
J E Mellerio, L Pulkkinen, J R McMillan, et al.
Human Mutation
|
April 29, 1998
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex
L D Corden, J E Mellerio, M J Gratian, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|
March 9, 2023
Lower-limb resistance training reduces exertional dyspnea and intrinsic neuromuscular fatigability in individuals with chronic obstructive pulmonary disease
Nicole M Brunton, David J Barbour, Jinelle C Gelinas, et al.
Malaria Journal
|
November 15, 2017
Yeast interfering RNA larvicides targeting neural genes induce high rates of Anopheles larval mortality
Keshava Mysore, Limb K Hapairai, Longhua Sun, et al.
Nature Genetics
|
March 30, 2001
Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci
W O Cookson, B Ubhi, R Lawrence, et al.
The Journal of Investigative Dermatology
|
January 1, 1994
Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE)
W H McLean, R A Eady, P J Dopping-Hepenstal, et al.
Nature Genetics
|
September 7, 2001
Gene polymorphism in Netherton and common atopic disease
A J Walley, S Chavanas, M F Moffatt, et al.
Page
of 21