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Showing results (291-300 of 295) with videos related to

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The Journal of Clinical Investigation|December 18, 2003
Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5Joost G J Hoenderop, Johannes P T M van Leeuwen, Bram C J van der Eerden, et al.
Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Human Molecular Genetics|October 24, 2002
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroMichel Guipponi, Grégoire Vuagniaux, Marie Wattenhofer, et al.
Molecular Endocrinology (Baltimore, Md.)|August 26, 1998
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different originsH S Scott, M Heino, P Peterson, et al.
Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.
Pageof 30

Showing results (291-300 of 295) with videos related to

Sort By:
Pageof 30
You have reached the last page of results.This site can display upto 295 results.
The Journal of Clinical Investigation|December 18, 2003
Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5Joost G J Hoenderop, Johannes P T M van Leeuwen, Bram C J van der Eerden, et al.
Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Human Molecular Genetics|October 24, 2002
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroMichel Guipponi, Grégoire Vuagniaux, Marie Wattenhofer, et al.
Molecular Endocrinology (Baltimore, Md.)|August 26, 1998
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different originsH S Scott, M Heino, P Peterson, et al.
Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.
Pageof 30