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C Polychronakos

Showing results (71-80 of 82) with videos related to

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Molecular Psychiatry|May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental diseaseC S Ku, C Polychronakos, E K Tan, et al.
Journal of the Neurological Sciences|October 25, 2016
Central nervous system involvement in multiple symmetric lipomatosisV K Kimiskidis, V Papaliagkas, S Papagiannopoulos, et al.
Nature Genetics|March 1, 1997
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locusP Vafiadis, S T Bennett, J A Todd, et al.
Diabetes & Metabolism|October 13, 2007
Minor contribution of SMAD7 and KLF10 variants to genetic susceptibility of type 2 diabetesR Gutierrez-Aguilar, Y Benmezroua, B Balkau, et al.
Human Molecular Genetics|March 4, 2000
An imprinted locus associated with transient neonatal diabetes mellitusR J Gardner, D J Mackay, A J Mungall, et al.
Journal of Pediatric Surgery|August 1, 1987
Management of thyroid nodules in children: a 20-year experienceJ G Desjardins, A H Khan, P Montupet, et al.
Diabetologia|December 14, 2004
Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndromeJ Mitchell, Z Punthakee, B Lo, et al.
Journal of Medical Genetics|July 15, 2005
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?M-C Tessier, H-Q Qu, R Fréchette, et al.
Genes and Immunity|December 4, 2009
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotypeA K Steck, E E Baschal, J M Jasinski, et al.
Nature Genetics|November 14, 1997
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB GroupS T Bennett, A J Wilson, L Esposito, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Molecular Psychiatry|May 30, 2012
A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental diseaseC S Ku, C Polychronakos, E K Tan, et al.
Journal of the Neurological Sciences|October 25, 2016
Central nervous system involvement in multiple symmetric lipomatosisV K Kimiskidis, V Papaliagkas, S Papagiannopoulos, et al.
Nature Genetics|March 1, 1997
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locusP Vafiadis, S T Bennett, J A Todd, et al.
Diabetes & Metabolism|October 13, 2007
Minor contribution of SMAD7 and KLF10 variants to genetic susceptibility of type 2 diabetesR Gutierrez-Aguilar, Y Benmezroua, B Balkau, et al.
Human Molecular Genetics|March 4, 2000
An imprinted locus associated with transient neonatal diabetes mellitusR J Gardner, D J Mackay, A J Mungall, et al.
Journal of Pediatric Surgery|August 1, 1987
Management of thyroid nodules in children: a 20-year experienceJ G Desjardins, A H Khan, P Montupet, et al.
Diabetologia|December 14, 2004
Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndromeJ Mitchell, Z Punthakee, B Lo, et al.
Journal of Medical Genetics|July 15, 2005
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype?M-C Tessier, H-Q Qu, R Fréchette, et al.
Genes and Immunity|December 4, 2009
rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotypeA K Steck, E E Baschal, J M Jasinski, et al.
Nature Genetics|November 14, 1997
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB GroupS T Bennett, A J Wilson, L Esposito, et al.
Pageof 9