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H Mandel

Showing results (171-180 of 188) with videos related to

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Thyroid : Official Journal of the American Thyroid Association|October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptorD Tiosano, S Pannain, G Vassart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type CV Meiner, S Shpitzen, H Mandel, et al.
The Journal of Clinical Investigation|March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1993
Hypothalamic pituitary adrenal function in the extremely low birth weight infantC E Hanna, L D Keith, M A Colasurdo, et al.
Chemosphere|December 17, 2003
Serum concentrations of perfluorooctanesulfonate and other fluorochemicals in an elderly population from Seattle, WashingtonGeary W Olsen, Timothy R Church, Eric B Larson, et al.
Nucleic Acids Research|February 21, 2024
Pathogenic CANVAS (AAGGG)n repeats stall DNA replication due to the formation of alternative DNA structuresJulia A Hisey, Elina A Radchenko, Nicholas H Mandel, et al.
AIHA Journal : a Journal for the Science of Occupational and Environmental Health and Safety|October 3, 2003
An occupational exposure assessment of a perfluorooctanesulfonyl fluoride production site: biomonitoringGeary W Olsen, Perry W Logan, Kristen J Hansen, et al.
American Journal of Human Genetics|April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23B Annabi, H Hiraiwa, B C Mansfield, et al.
Environmental Research|March 25, 2023
Non-asbestiform elongate mineral particles and mesothelioma risk: Human and experimental evidenceJulie E Goodman, Michael J Becich, David M Bernstein, et al.
American Journal of Human Genetics|November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapyS Gobin-Limballe, F Djouadi, F Aubey, et al.
Pageof 19

Showing results (171-180 of 188) with videos related to

Sort By:
Pageof 19
Thyroid : Official Journal of the American Thyroid Association|October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptorD Tiosano, S Pannain, G Vassart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2001
Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type CV Meiner, S Shpitzen, H Mandel, et al.
The Journal of Clinical Investigation|March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1993
Hypothalamic pituitary adrenal function in the extremely low birth weight infantC E Hanna, L D Keith, M A Colasurdo, et al.
Chemosphere|December 17, 2003
Serum concentrations of perfluorooctanesulfonate and other fluorochemicals in an elderly population from Seattle, WashingtonGeary W Olsen, Timothy R Church, Eric B Larson, et al.
Nucleic Acids Research|February 21, 2024
Pathogenic CANVAS (AAGGG)n repeats stall DNA replication due to the formation of alternative DNA structuresJulia A Hisey, Elina A Radchenko, Nicholas H Mandel, et al.
AIHA Journal : a Journal for the Science of Occupational and Environmental Health and Safety|October 3, 2003
An occupational exposure assessment of a perfluorooctanesulfonyl fluoride production site: biomonitoringGeary W Olsen, Perry W Logan, Kristen J Hansen, et al.
American Journal of Human Genetics|April 16, 1998
The gene for glycogen-storage disease type 1b maps to chromosome 11q23B Annabi, H Hiraiwa, B C Mansfield, et al.
Environmental Research|March 25, 2023
Non-asbestiform elongate mineral particles and mesothelioma risk: Human and experimental evidenceJulie E Goodman, Michael J Becich, David M Bernstein, et al.
American Journal of Human Genetics|November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapyS Gobin-Limballe, F Djouadi, F Aubey, et al.
Pageof 19