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Items: 4

1.
Genotype and phenotype analysis of a cohort of patients with congenital hyperinsulinism based on DOPA-PET CT scanning
Jinwen Ni, Jingjie Ge, Miaoying Zhang, Khalid Hussain, Yihui Guan, Ruoqian Cheng, Li Xi, Zhangqian Zheng, Shuhua Ren, Feihong Luo
Eur J Pediatr. 2019; 178(8): 1161–1169. Published online 2019 Jun 19. doi: 10.1007/s00431-019-03408-6
PMCID:
PMC6647509
AbstractArticlePDF–2.9M
2.
Association of KCNJ11 rs5219 gene polymorphism with type 2 diabetes mellitus in a population of Syria: a case-control study
Osama Makhzoom, Younes Kabalan, Faizeh AL-Quobaili
BMC Med Genet. 2019; 20: 107. Published online 2019 Jun 13. doi: 10.1186/s12881-019-0846-3
PMCID:
PMC6567472
AbstractArticlePDF–685K
3.
ATP binding without hydrolysis switches sulfonylurea receptor 1 (SUR1) to outward-facing conformations that activate KATP channels
Jelena Sikimic, Timothy S. McMillen, Cita Bleile, Frank Dastvan, Ulrich Quast, Peter Krippeit-Drews, Gisela Drews, Joseph Bryan
J Biol Chem. 2019 Mar 8; 294(10): 3707–3719. Published online 2018 Dec 26. doi: 10.1074/jbc.RA118.005236
PMCID:
PMC6416425
AbstractArticlePDF–2.0M
4.
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.
P M Thomas, G J Cote, D M Hallman, P M Mathew
Am J Hum Genet. 1995 Feb; 56(2): 416–421.
PMCID:
PMC1801118
SummaryPage BrowsePDF–1.0M

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