Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Brian Harding

Showing results (41-50 of 51) with videos related to

Pageof 6
Sort By:
The Journal of Biological Chemistry|February 27, 2004
Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndromeM Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
Cancer Research|August 24, 2012
MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomasGerard V Walls, Manuel C Lemos, Mahsa Javid, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1Jeremy J O Turner, Poloko D Leotlela, Anna A J Pannett, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
Arthritis and Rheumatism|October 2, 2007
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trialsLucy R Wedderburn, Hemlata Varsani, Charles K C Li, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Human Molecular Genetics|March 17, 2012
Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesFadil M Hannan, M Andrew Nesbit, Chen Zhang, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
Human Molecular Genetics|January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAsif Ali, Paul T Christie, Irina V Grigorieva, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
The Journal of Biological Chemistry|February 27, 2004
Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndromeM Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
Cancer Research|August 24, 2012
MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary adenomasGerard V Walls, Manuel C Lemos, Mahsa Javid, et al.
The Journal of Clinical Investigation|September 17, 2005
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)Ann M Kennedy, Masaki Inada, Stephen M Krane, et al.
The Journal of Clinical Endocrinology and Metabolism|June 7, 2002
Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1Jeremy J O Turner, Poloko D Leotlela, Anna A J Pannett, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
Arthritis and Rheumatism|October 2, 2007
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trialsLucy R Wedderburn, Hemlata Varsani, Charles K C Li, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Human Molecular Genetics|March 17, 2012
Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesFadil M Hannan, M Andrew Nesbit, Chen Zhang, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
Human Molecular Genetics|January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAsif Ali, Paul T Christie, Irina V Grigorieva, et al.
Pageof 6