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G Gyapay

Showing results (21-30 of 48) with videos related to

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Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
Human Molecular Genetics|October 1, 1995
Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear familyN Nadal, M O Rolland, C Tranchant, et al.
Diabetologia|June 1, 1997
Genetic studies of neuropeptide Y and neuropeptide Y receptors Y1 and Y5 regions in morbid obesityC Roche, P Boutin, C Dina, et al.
Oncogene|May 26, 1999
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinomaP Pineau, H Nagai, S Prigent, et al.
Nature Genetics|June 1, 1994
The 1993-94 Généthon human genetic linkage mapG Gyapay, J Morissette, A Vignal, et al.
American Journal of Human Genetics|November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13L Montermini, F Rodius, L Pianese, et al.
Complement and Inflammation|January 1, 1991
Effect of conditioned media of acute myeloid leukemia blast cells on complement synthesis by cultured human cells of monocyte and hepatocyte originG Gyapay, B Schmidt, M Válay, et al.
Genome Research|May 5, 2001
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8C Charlier, K Segers, D Wagenaar, et al.
Nature Genetics|October 1, 1993
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mappingC Ben Hamida, N Doerflinger, S Belal, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Human Genetics|October 1, 1996
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathyP Vicart, J M Dupret, J Hazan, et al.
Human Molecular Genetics|October 1, 1995
Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear familyN Nadal, M O Rolland, C Tranchant, et al.
Diabetologia|June 1, 1997
Genetic studies of neuropeptide Y and neuropeptide Y receptors Y1 and Y5 regions in morbid obesityC Roche, P Boutin, C Dina, et al.
Oncogene|May 26, 1999
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinomaP Pineau, H Nagai, S Prigent, et al.
Nature Genetics|June 1, 1994
The 1993-94 Généthon human genetic linkage mapG Gyapay, J Morissette, A Vignal, et al.
American Journal of Human Genetics|November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13L Montermini, F Rodius, L Pianese, et al.
Complement and Inflammation|January 1, 1991
Effect of conditioned media of acute myeloid leukemia blast cells on complement synthesis by cultured human cells of monocyte and hepatocyte originG Gyapay, B Schmidt, M Válay, et al.
Genome Research|May 5, 2001
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8C Charlier, K Segers, D Wagenaar, et al.
Nature Genetics|October 1, 1993
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mappingC Ben Hamida, N Doerflinger, S Belal, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Pageof 5