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Human Molecular Genetics
|
September 2, 1999
A family of mammalian anion transporters and their involvement in human genetic diseases
L 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 ear
L A Everett, H Morsli, D K Wu, et al.
Genomics
|
December 1, 1992
A panel of human chromosome 22-specific sequence tagged sites
J 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 Rowers
Kirsten 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 Rowers
Kirsten 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 cells
I 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 secretion
I 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 syndrome
W 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 syndrome
C 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 syndrome
L A Everett, I A Belyantseva, K Noben-Trauth, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Human Molecular Genetics
|
September 2, 1999
A family of mammalian anion transporters and their involvement in human genetic diseases
L 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 ear
L A Everett, H Morsli, D K Wu, et al.
Genomics
|
December 1, 1992
A panel of human chromosome 22-specific sequence tagged sites
J 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 Rowers
Kirsten 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 Rowers
Kirsten 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 cells
I 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 secretion
I 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 syndrome
W 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 syndrome
C 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 syndrome
L A Everett, I A Belyantseva, K Noben-Trauth, et al.
Page
of 2