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Rahul Mittal

Showing results (181-190 of 195) with videos related to

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Human Molecular Genetics|January 21, 2015
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulationM'hamed Grati, Imen Chakchouk, Qi Ma, et al.
Plos One|August 17, 2022
The impact of COVID-19 on individuals with ASD in the US: Parent perspectives on social and support concernsEmily Furar, Florence Wang, Jennifer S Durocher, et al.
Gene|January 15, 2018
Genetic basis of hearing loss in Spanish, Hispanic and Latino populationsRahul Mittal, Amit P Patel, Desiree Nguyen, et al.
Journal of Medical Microbiology|August 8, 2015
Current concepts in the pathogenesis and treatment of chronic suppurative otitis mediaRahul Mittal, Christopher V Lisi, Robert Gerring, et al.
The Journal of Gene Medicine|November 26, 2016
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic interventionSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Molecular Genetics and Genomics : MGG|January 31, 2015
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53Imen Chakchouk, M'hamed Grati, Guney Bademci, et al.
Frontiers in Cellular and Infection Microbiology|December 26, 2017
Zika Virus: An Emerging Global Health ThreatRahul Mittal, Desiree Nguyen, Luca H Debs, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Molecular Cancer Therapeutics|August 5, 2017
Combination Therapy with c-Met and Src Inhibitors Induces Caspase-Dependent Apoptosis of Merlin-Deficient Schwann Cells and Suppresses Growth of Schwannoma CellsMarisa A Fuse, Stephani Klingeman Plati, Sarah S Burns, et al.
Pageof 20

Showing results (181-190 of 195) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|January 21, 2015
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulationM'hamed Grati, Imen Chakchouk, Qi Ma, et al.
Plos One|August 17, 2022
The impact of COVID-19 on individuals with ASD in the US: Parent perspectives on social and support concernsEmily Furar, Florence Wang, Jennifer S Durocher, et al.
Gene|January 15, 2018
Genetic basis of hearing loss in Spanish, Hispanic and Latino populationsRahul Mittal, Amit P Patel, Desiree Nguyen, et al.
Journal of Medical Microbiology|August 8, 2015
Current concepts in the pathogenesis and treatment of chronic suppurative otitis mediaRahul Mittal, Christopher V Lisi, Robert Gerring, et al.
The Journal of Gene Medicine|November 26, 2016
Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic interventionSo Young Kim, Ah Reum Kim, Nayoung K D Kim, et al.
Human Mutation|February 4, 2016
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 IsoformM'hamed Grati, Denise Yan, Manmeet H Raval, et al.
Molecular Genetics and Genomics : MGG|January 31, 2015
Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53Imen Chakchouk, M'hamed Grati, Guney Bademci, et al.
Frontiers in Cellular and Infection Microbiology|December 26, 2017
Zika Virus: An Emerging Global Health ThreatRahul Mittal, Desiree Nguyen, Luca H Debs, et al.
Plos One|March 9, 2017
Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approachDenise Yan, Guangxin Xiang, Xingping Chai, et al.
Molecular Cancer Therapeutics|August 5, 2017
Combination Therapy with c-Met and Src Inhibitors Induces Caspase-Dependent Apoptosis of Merlin-Deficient Schwann Cells and Suppresses Growth of Schwannoma CellsMarisa A Fuse, Stephani Klingeman Plati, Sarah S Burns, et al.
Pageof 20