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Brian Harding

Showing results (31-40 of 51) with videos related to

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Annals of Neurology|May 31, 2023
Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome SpectrumElizabeth M McCormick, Kierstin Keller, Julie P Taylor, et al.
Journal of Neuro-Oncology|January 7, 2010
Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisationSamantha J Ward, Katherine Karakoula, Kim P Phipps, et al.
Acta Neuropathologica|May 17, 2018
Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activationPayal Jain, Lea F Surrey, Joshua Straka, et al.
Genes, Chromosomes & Cancer|July 30, 2008
Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13Katherine Karakoula, Blanca Suarez-Merino, Samantha Ward, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2013
Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patientsCaroline M Gorvin, Martijn J Wilmer, Sian E Piret, et al.
The Journal of Endocrinology|July 10, 2009
Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiersManuel C Lemos, Brian Harding, Anita A C Reed, et al.
Clinical Endocrinology|October 24, 2006
Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral densityBrian Harding, Alan J Curley, Fadil M Hannan, et al.
Acta Neuropathologica|March 31, 2010
Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cellShireena A Yasin, Kate Latak, Francesca Becherini, et al.
Endocrine-Related Cancer|July 22, 2009
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemiaBrian Harding, Manuel C Lemos, Anita A C Reed, et al.
Neoplasia (New York, N.Y.)|August 2, 2008
Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytomaNicola Potter, Aikaterini Karakoula, Kim P Phipps, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Annals of Neurology|May 31, 2023
Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome SpectrumElizabeth M McCormick, Kierstin Keller, Julie P Taylor, et al.
Journal of Neuro-Oncology|January 7, 2010
Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisationSamantha J Ward, Katherine Karakoula, Kim P Phipps, et al.
Acta Neuropathologica|May 17, 2018
Novel FGFR2-INA fusion identified in two low-grade mixed neuronal-glial tumors drives oncogenesis via MAPK and PI3K/mTOR pathway activationPayal Jain, Lea F Surrey, Joshua Straka, et al.
Genes, Chromosomes & Cancer|July 30, 2008
Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13Katherine Karakoula, Blanca Suarez-Merino, Samantha Ward, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2013
Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patientsCaroline M Gorvin, Martijn J Wilmer, Sian E Piret, et al.
The Journal of Endocrinology|July 10, 2009
Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiersManuel C Lemos, Brian Harding, Anita A C Reed, et al.
Clinical Endocrinology|October 24, 2006
Functional characterization of calcium sensing receptor polymorphisms and absence of association with indices of calcium homeostasis and bone mineral densityBrian Harding, Alan J Curley, Fadil M Hannan, et al.
Acta Neuropathologica|March 31, 2010
Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cellShireena A Yasin, Kate Latak, Francesca Becherini, et al.
Endocrine-Related Cancer|July 22, 2009
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemiaBrian Harding, Manuel C Lemos, Anita A C Reed, et al.
Neoplasia (New York, N.Y.)|August 2, 2008
Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytomaNicola Potter, Aikaterini Karakoula, Kim P Phipps, et al.
Pageof 6