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Human Mutation
|
July 20, 2001
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
S Masmoudi, S E Antonarakis, T Schwede, et al.
Human Genetics
|
April 3, 2001
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains
M Wattenhofer, K Shibuya, J Kudoh, et al.
Genomics
|
August 22, 2000
C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning
M Guipponi, K Brunschwig, Z Chamoun, et al.
The Journal of Biological Chemistry
|
June 23, 2010
Airway surface liquid volume regulation determines different airway phenotypes in liddle compared with betaENaC-overexpressing mice
Marcus A Mall, Brian Button, Bjarki Johannesson, et al.
Blood
|
July 13, 2000
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia
M Neerman-Arbez, P de Moerloose, C Bridel, et al.
Genomics
|
August 22, 2000
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region
A Berry, H S Scott, J Kudoh, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
March 16, 2005
[Induced abortion in France: results of the COCON study]
N Lelong, C Moreau, M Kaminski, et al.
Genomics
|
December 9, 2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency
L Bartoloni, M Wattenhofer, J Kudoh, et al.
Human Mutation
|
January 15, 1999
Mutation analyses of North American APS-1 patients
M Heino, H S Scott, Q Chen, et al.
The EMBO Journal
|
October 29, 2004
Small proline-rich protein 1A is a gp130 pathway- and stress-inducible cardioprotective protein
Sylvain Pradervand, Hideo Yasukawa, Olivier G Muller, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 295) with videos related to
Sort By:
Page
of 30
Human Mutation
|
July 20, 2001
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
S Masmoudi, S E Antonarakis, T Schwede, et al.
Human Genetics
|
April 3, 2001
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains
M Wattenhofer, K Shibuya, J Kudoh, et al.
Genomics
|
August 22, 2000
C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning
M Guipponi, K Brunschwig, Z Chamoun, et al.
The Journal of Biological Chemistry
|
June 23, 2010
Airway surface liquid volume regulation determines different airway phenotypes in liddle compared with betaENaC-overexpressing mice
Marcus A Mall, Brian Button, Bjarki Johannesson, et al.
Blood
|
July 13, 2000
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia
M Neerman-Arbez, P de Moerloose, C Bridel, et al.
Genomics
|
August 22, 2000
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region
A Berry, H S Scott, J Kudoh, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction
|
March 16, 2005
[Induced abortion in France: results of the COCON study]
N Lelong, C Moreau, M Kaminski, et al.
Genomics
|
December 9, 2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency
L Bartoloni, M Wattenhofer, J Kudoh, et al.
Human Mutation
|
January 15, 1999
Mutation analyses of North American APS-1 patients
M Heino, H S Scott, Q Chen, et al.
The EMBO Journal
|
October 29, 2004
Small proline-rich protein 1A is a gp130 pathway- and stress-inducible cardioprotective protein
Sylvain Pradervand, Hideo Yasukawa, Olivier G Muller, et al.
Page
of 30