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J H Smith

Showing results (441-450 of 588) with videos related to

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Molecular and Cellular Biology|February 18, 2004
Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in miceE Tse, A J H Smith, S Hunt, et al.
Clinical Genetics|February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutationM S Hildebrand, N P Thorne, C J Bromhead, et al.
The Laryngoscope|March 11, 2009
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing lossA Eliot Shearer, Michael S Hildebrand, Jennifer A Webster, et al.
Kidney International|November 26, 2023
Renin and renin blockade have no role in complement activityYuzhou Zhang, Bertha Martin, M Ashley Spies, et al.
Gut|April 6, 2007
Experimental acute pancreatitis in PAP/HIP knock-out miceMeritxell Gironella, Emma Folch-Puy, Aude LeGoffic, et al.
American Journal of Medical Genetics. Part A|June 28, 2012
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf populationZohreh Fattahi, A Eliot Shearer, Mojgan Babanejad, et al.
Genetic Testing and Molecular Biomarkers|April 9, 2010
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effectsMariem Ben Saïd, Mounira Hmani-Aifa, Imen Amar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2008
Advances in molecular and cellular therapies for hearing lossMichael S Hildebrand, Stephen S Newton, Samuel P Gubbels, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
GJB2 mutations: passage through IranHossein Najmabadi, Carla Nishimura, Kimia Kahrizi, et al.
Pageof 59

Showing results (441-450 of 588) with videos related to

Sort By:
Pageof 59
Molecular and Cellular Biology|February 18, 2004
Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in miceE Tse, A J H Smith, S Hunt, et al.
Clinical Genetics|February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutationM S Hildebrand, N P Thorne, C J Bromhead, et al.
The Laryngoscope|March 11, 2009
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing lossA Eliot Shearer, Michael S Hildebrand, Jennifer A Webster, et al.
Kidney International|November 26, 2023
Renin and renin blockade have no role in complement activityYuzhou Zhang, Bertha Martin, M Ashley Spies, et al.
Gut|April 6, 2007
Experimental acute pancreatitis in PAP/HIP knock-out miceMeritxell Gironella, Emma Folch-Puy, Aude LeGoffic, et al.
American Journal of Medical Genetics. Part A|June 28, 2012
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf populationZohreh Fattahi, A Eliot Shearer, Mojgan Babanejad, et al.
Genetic Testing and Molecular Biomarkers|April 9, 2010
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effectsMariem Ben Saïd, Mounira Hmani-Aifa, Imen Amar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2003
Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical GeneticsRaye L Alford, Thomas B Friedman, Bronya J B Keats, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2008
Advances in molecular and cellular therapies for hearing lossMichael S Hildebrand, Stephen S Newton, Samuel P Gubbels, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
GJB2 mutations: passage through IranHossein Najmabadi, Carla Nishimura, Kimia Kahrizi, et al.
Pageof 59