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P Cochaux

Showing results (31-40 of 57) with videos related to

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Clinical Endocrinology|April 1, 1984
Iodide organification defect in a cold thyroid nodule: absence of iodide effect on cyclic AMP accumulationN Demeester-Mirkine, J Van Sande, P Dor, et al.
The Journal of Clinical Investigation|December 1, 1991
A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidismT Ieiri, P Cochaux, H M Targovnik, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messengerH M Targovnik, G Medeiros-Neto, V Varela, et al.
Hemoglobin|March 18, 2000
Hb Ube-2 [alpha68(E17)Asn-Asp] and Hb Hafnia [beta116(G18)His-->Gln] observed during neonatal screening in BrusselsF Cotton, V Hansen, C Lin, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
AIDS (London, England)|February 19, 1998
Induction of specific T-cell responses in HIV infectionA C Leandersson, G Bratt, J Hinkula, et al.
Nature|October 14, 1993
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomasJ Parma, L Duprez, J Van Sande, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1988
Pathogenesis of autonomous thyroid nodules: in vitro study of iodine and adenosine 3',5'-monophosphate metabolismJ Van Sande, F Lamy, R Lecocq, et al.
Thyroid : Official Journal of the American Thyroid Association|May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidismH M Targovnik, G D Frechtel, F M Mendive, et al.
Gastrointestinal Endoscopy|July 1, 1998
Relative contribution of Ki-ras gene analysis and brush cytology during ERCP for the diagnosis of biliary and pancreatic diseasesJ L Van Laethem, V Bourgeois, J Parma, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Clinical Endocrinology|April 1, 1984
Iodide organification defect in a cold thyroid nodule: absence of iodide effect on cyclic AMP accumulationN Demeester-Mirkine, J Van Sande, P Dor, et al.
The Journal of Clinical Investigation|December 1, 1991
A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidismT Ieiri, P Cochaux, H M Targovnik, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1993
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messengerH M Targovnik, G Medeiros-Neto, V Varela, et al.
Hemoglobin|March 18, 2000
Hb Ube-2 [alpha68(E17)Asn-Asp] and Hb Hafnia [beta116(G18)His-->Gln] observed during neonatal screening in BrusselsF Cotton, V Hansen, C Lin, et al.
Ophthalmic Genetics|September 1, 1995
Neurological disorders in members of families with Leber's hereditary optic neuropathy (LHON) caused by different mitochondrial mutationsF M Meire, R Van Coster, P Cochaux, et al.
AIDS (London, England)|February 19, 1998
Induction of specific T-cell responses in HIV infectionA C Leandersson, G Bratt, J Hinkula, et al.
Nature|October 14, 1993
Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomasJ Parma, L Duprez, J Van Sande, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1988
Pathogenesis of autonomous thyroid nodules: in vitro study of iodine and adenosine 3',5'-monophosphate metabolismJ Van Sande, F Lamy, R Lecocq, et al.
Thyroid : Official Journal of the American Thyroid Association|May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidismH M Targovnik, G D Frechtel, F M Mendive, et al.
Gastrointestinal Endoscopy|July 1, 1998
Relative contribution of Ki-ras gene analysis and brush cytology during ERCP for the diagnosis of biliary and pancreatic diseasesJ L Van Laethem, V Bourgeois, J Parma, et al.
Pageof 6