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American Journal of Human Genetics
|
August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome
Saima Riazuddin, Saima Anwar, Martin Fischer, et al.
Journal of Translational Medicine
|
December 11, 2014
Melanoma expression of matrix metalloproteinase-23 is associated with blunted tumor immunity and poor responses to immunotherapy
Duane Moogk, Ines Pires da Silva, Michelle W Ma, et al.
Journal of Translational Medicine
|
August 4, 2012
Serum microRNAs as biomarkers for recurrence in melanoma
Erica B Friedman, Shulian Shang, Eleazar Vega-Saenz de Miera, et al.
Science Advances
|
October 9, 2024
SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac
Hyun Jae Lee, Cristina Fenollar-Ferrer, Kevin Isgrig, et al.
American Journal of Human Genetics
|
July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus
Sadaf Naz, Chantal M Giguere, David C Kohrman, et al.
Journal of Clinical and Translational Science
|
December 10, 2024
Evaluation and lessons learned from the dissemination and implementation science scholars program in the national cancer prevention and control research network
Daniela B Friedman, Cam Escoffery, Elaine H Morrato, et al.
Clinical Genetics
|
August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiers
Sadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
JBMR Plus
|
April 3, 2025
How neighborhood socioeconomic status, green space, and walkability are associated with risk for fracture among postmenopausal women
Marilyn E Wende, Matthew C Lohman, Daniela B Friedman, et al.
Journal of Medical Genetics
|
August 7, 2017
A common <i>SLC26A4</i>-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct
Parna Chattaraj, Tina Munjal, Keiji Honda, et al.
Human Molecular Genetics
|
September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells
Eva L Morozko, Ayako Nishio, Neil J Ingham, et al.
Page
of 97
Search research articles
Search
Showing results (871-880 of 968) with videos related to
Sort By:
Page
of 97
American Journal of Human Genetics
|
August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome
Saima Riazuddin, Saima Anwar, Martin Fischer, et al.
Journal of Translational Medicine
|
December 11, 2014
Melanoma expression of matrix metalloproteinase-23 is associated with blunted tumor immunity and poor responses to immunotherapy
Duane Moogk, Ines Pires da Silva, Michelle W Ma, et al.
Journal of Translational Medicine
|
August 4, 2012
Serum microRNAs as biomarkers for recurrence in melanoma
Erica B Friedman, Shulian Shang, Eleazar Vega-Saenz de Miera, et al.
Science Advances
|
October 9, 2024
SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac
Hyun Jae Lee, Cristina Fenollar-Ferrer, Kevin Isgrig, et al.
American Journal of Human Genetics
|
July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus
Sadaf Naz, Chantal M Giguere, David C Kohrman, et al.
Journal of Clinical and Translational Science
|
December 10, 2024
Evaluation and lessons learned from the dissemination and implementation science scholars program in the national cancer prevention and control research network
Daniela B Friedman, Cam Escoffery, Elaine H Morrato, et al.
Clinical Genetics
|
August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiers
Sadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
JBMR Plus
|
April 3, 2025
How neighborhood socioeconomic status, green space, and walkability are associated with risk for fracture among postmenopausal women
Marilyn E Wende, Matthew C Lohman, Daniela B Friedman, et al.
Journal of Medical Genetics
|
August 7, 2017
A common <i>SLC26A4</i>-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct
Parna Chattaraj, Tina Munjal, Keiji Honda, et al.
Human Molecular Genetics
|
September 14, 2014
ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells
Eva L Morozko, Ayako Nishio, Neil J Ingham, et al.
Page
of 97