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hyperinsu-linism due to autosomal dominant Kir6.2 mutation相关文献:
Hyperinsulinism of the newborn.
Glaser B.
Semin Perinatol. 2000 Apr;24(2):150-63. doi: 10.1053/sp.2000.6365.
PMID:10805170
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8.
Nessa A, Aziz QH, Thomas AM, Harmer SC, Tinker A, Hussain K.
Hum Mol Genet. 2015 Sep 15;24(18):5142-53. doi: 10.1093/hmg/ddv233. Epub 2015 Jun 19.
PMID:26092864
Molecular mechanisms of neonatal hyperinsulinism.
Giurgea I, Bellanné-Chantelot C, Ribeiro M, Hubert L, Sempoux C, Robert JJ, Blankenstein O, Hussain K, Brunelle F, Nihoul-Fékété C, Rahier J, Jaubert F, de Lonlay P.
Horm Res. 2006;66(6):289-96. doi: 10.1159/000095938. Epub 2006 Sep 26.
PMID:17003566
Insights in congenital hyperinsulinism.
Hussain K.
Endocr Dev. 2007;11:106-121. doi: 10.1159/000111066.
PMID:17986831
Continuous spectrum of glucose dysmetabolism due to the KCNJ11 gene mutation-Case reports and review of the literature.
He B, Li X, Zhou Z.
J Diabetes. 2021 Jan;13(1):19-32. doi: 10.1111/1753-0407.13114. Epub 2020 Oct 27.
PMID:32935446
Congenital hyperinsulinism: molecular basis of a heterogeneous disease.
Meissner T, Beinbrech B, Mayatepek E.
Hum Mutat. 1999;13(5):351-61. doi: 10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R.
PMID:10338089
Computational Identification of Novel Kir6 Channel Inhibitors.
Chen X, Garon A, Wieder M, Houtman MJC, Zangerl-Plessl EM, Langer T, van der Heyden MAG, Stary-Weinzinger A.
Front Pharmacol. 2019 May 24;10:549. doi: 10.3389/fphar.2019.00549. eCollection 2019.
PMID:31178728
An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus.
Kukuvitis A, Deal C, Arbour L, Polychronakos C.
J Clin Endocrinol Metab. 1997 Apr;82(4):1192-4. doi: 10.1210/jcem.82.4.3904.
PMID:9100595
[From gene to disease; neonatal diabetes mellitus and the KCNJ11 gene].
Slingerland AS, Bruining GJ.
Ned Tijdschr Geneeskd. 2005 Dec 3;149(49):2732-6.
PMID:16375017
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