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S H Pearce

Showing results (31-40 of 48) with videos related to

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The Journal of Biological Chemistry|August 9, 1996
Expression and characterization of inactivating and activating mutations in the human Ca2+o-sensing receptorM Bai, S Quinn, S Trivedi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Clinical Endocrinology|April 10, 1999
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patientsE H Kemp, R A Ajjan, E S Husebye, et al.
American Journal of Human Genetics|October 16, 1999
Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves diseaseS H Pearce, B Vaidya, H Imrie, et al.
American Journal of Human Genetics|April 14, 2000
Evidence for a new Graves disease susceptibility locus at chromosome 18q21B Vaidya, H Imrie, P Perros, et al.
The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, et al.
Human Molecular Genetics|June 17, 1999
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locusB Vaidya, H Imrie, P Perros, et al.
The New England Journal of Medicine|October 10, 1996
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptorS H Pearce, C Williamson, O Kifor, et al.
Journal of Clinical Pathology|June 3, 2008
Impact of standardised reporting in adrenocortical carcinoma: a single centre clinicopathological reviewA Advani, S Vaikkakara, M S Gill, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
The Journal of Biological Chemistry|August 9, 1996
Expression and characterization of inactivating and activating mutations in the human Ca2+o-sensing receptorM Bai, S Quinn, S Trivedi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.
Clinical Endocrinology|April 10, 1999
A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patientsE H Kemp, R A Ajjan, E S Husebye, et al.
American Journal of Human Genetics|October 16, 1999
Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves diseaseS H Pearce, B Vaidya, H Imrie, et al.
American Journal of Human Genetics|April 14, 2000
Evidence for a new Graves disease susceptibility locus at chromosome 18q21B Vaidya, H Imrie, P Perros, et al.
The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, et al.
Human Molecular Genetics|June 17, 1999
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locusB Vaidya, H Imrie, P Perros, et al.
The New England Journal of Medicine|October 10, 1996
A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptorS H Pearce, C Williamson, O Kifor, et al.
Journal of Clinical Pathology|June 3, 2008
Impact of standardised reporting in adrenocortical carcinoma: a single centre clinicopathological reviewA Advani, S Vaikkakara, M S Gill, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Pageof 5