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Rahul Mittal

Showing results (191-200 of 195) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
Oncotarget|April 22, 2017
Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cellsAlejandra M Petrilli, Jeanine Garcia, Marga Bott, et al.
Human Genetics|March 30, 2016
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60Mariem Ben Said, M'hamed Grati, Takahiro Ishimoto, et al.
Neuro-Oncology|January 8, 2019
Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2-associated schwannomas reveals differences in efficacy and drug resistance developmentMarisa A Fuse, Christine T Dinh, Jeremie Vitte, et al.
Human Genetics|June 27, 2016
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continentsDenise Yan, Demet Tekin, Guney Bademci, et al.
Pageof 20

Showing results (191-200 of 195) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 195 results.
Proceedings of the National Academy of Sciences of the United States of America|June 25, 2014
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearingOscar Diaz-Horta, Asli Subasioglu-Uzak, M'hamed Grati, et al.
Oncotarget|April 22, 2017
Ponatinib promotes a G1 cell-cycle arrest of merlin/NF2-deficient human schwann cellsAlejandra M Petrilli, Jeanine Garcia, Marga Bott, et al.
Human Genetics|March 30, 2016
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60Mariem Ben Said, M'hamed Grati, Takahiro Ishimoto, et al.
Neuro-Oncology|January 8, 2019
Preclinical assessment of MEK1/2 inhibitors for neurofibromatosis type 2-associated schwannomas reveals differences in efficacy and drug resistance developmentMarisa A Fuse, Christine T Dinh, Jeremie Vitte, et al.
Human Genetics|June 27, 2016
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continentsDenise Yan, Demet Tekin, Guney Bademci, et al.
Pageof 20