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L A Everett

Showing results (1-10 of 15) with videos related to

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Human Molecular Genetics|September 2, 1999
A family of mammalian anion transporters and their involvement in human genetic diseasesL A Everett, E D Green
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner earL A Everett, H Morsli, D K Wu, et al.
Genomics|December 1, 1992
A panel of human chromosome 22-specific sequence tagged sitesJ E Collins, L A Everett, D R Bentley, et al.
Journal of Strength and Conditioning Research|October 16, 2020
Changes in Loaded Countermovement Jumps During Precompetition and Competition Training Mesocycles in Elite RowersKirsten L A Everett, Dale W Chapman, John A Mitchell, et al.
Journal of Strength and Conditioning Research|September 18, 2020
Effects of Westbound Trans-meridian Travel on Countermovement Jump Performance in International-Level RowersKirsten L A Everett, Dale W Chapman, John A Mitchell, et al.
Endocrinology|January 29, 2000
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cellsI E Royaux, K Suzuki, A Mori, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2001
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretionI E Royaux, S M Wall, L P Karniski, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 30, 1998
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndromeW R Cremers, C Bolder, R J Admiraal, et al.
International Journal of Pediatric Otorhinolaryngology|December 16, 1998
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndromeC W Cremers, R J Admiraal, P L Huygen, et al.
Human Molecular Genetics|January 12, 2001
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndromeL A Everett, I A Belyantseva, K Noben-Trauth, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|September 2, 1999
A family of mammalian anion transporters and their involvement in human genetic diseasesL A Everett, E D Green
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner earL A Everett, H Morsli, D K Wu, et al.
Genomics|December 1, 1992
A panel of human chromosome 22-specific sequence tagged sitesJ E Collins, L A Everett, D R Bentley, et al.
Journal of Strength and Conditioning Research|October 16, 2020
Changes in Loaded Countermovement Jumps During Precompetition and Competition Training Mesocycles in Elite RowersKirsten L A Everett, Dale W Chapman, John A Mitchell, et al.
Journal of Strength and Conditioning Research|September 18, 2020
Effects of Westbound Trans-meridian Travel on Countermovement Jump Performance in International-Level RowersKirsten L A Everett, Dale W Chapman, John A Mitchell, et al.
Endocrinology|January 29, 2000
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cellsI E Royaux, K Suzuki, A Mori, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2001
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretionI E Royaux, S M Wall, L P Karniski, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 30, 1998
Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndromeW R Cremers, C Bolder, R J Admiraal, et al.
International Journal of Pediatric Otorhinolaryngology|December 16, 1998
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndromeC W Cremers, R J Admiraal, P L Huygen, et al.
Human Molecular Genetics|January 12, 2001
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndromeL A Everett, I A Belyantseva, K Noben-Trauth, et al.
Pageof 2