Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
about
Hyperinsulinemic Hypoglycemia - The Molecular MechanismsDysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutationsUnbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11Genetics of neonatal hyperinsulinism.Ions, genes and insulin release: from basic science to clinical disease. Based on the 1998 R. D. Lawrence Lecture.Congenital hyperinsulinism: current status and future perspectives.Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism.Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.K(ATP) channels and insulin secretion disorders.Hyperinsulinism in infancy: from basic science to clinical disease.Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism DisordersNovel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescenceUpdate of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI.Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening.Congenital hyperinsulinism: global and Japanese perspectives.Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations.p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas
P2860
Q26749617-9DBE7BDB-2800-497B-9FC0-B5EF363A7518Q28361461-07407BBB-913B-4691-A88D-B1DB46A8F4B4Q28366519-88D85805-C02C-4123-B033-36C7E8EE8BDAQ33844326-3D2839EE-E3DD-4880-B3CC-231A372C555EQ33880824-229124E9-9494-4FC7-96D8-25CD0D376C6EQ33964788-210019E3-CFA7-4D8B-BD2C-695D1635D452Q34117318-61846541-B831-446D-8803-41792EF6B027Q34448663-57E711AF-D00D-4EED-B09A-36FD04D5D9C8Q34731579-DD72C46A-8CF8-43C2-926E-7D82BC95C270Q35625609-866DDCE7-B600-427B-9F33-379E5E3B4CF1Q36716020-3DFFC9CD-4919-474D-9351-81D8BADC9D36Q36756556-8CEB848C-5ED7-4EC6-8097-E337021DE46CQ37259401-965357CC-409E-4FA0-BD78-1AC002942FF7Q37270892-3C441007-5DE5-4723-BEC4-3E9AAD714FFEQ37878248-DC6185B1-4207-46CE-80A2-7459E99A18FAQ48332523-841A0D60-4343-46E1-9E7A-608A1DA08FF8Q51127204-D37C0BB2-5689-4B5C-8294-0F5B351FF95CQ51261501-FB74344F-E88B-46CF-8AEE-301233643F62Q51293958-9D66DBD1-A6E0-4FBF-9BCD-5F60D44CF698Q57499701-5A939E7F-9FA5-44C2-A962-20C0F4A83AD3
P2860
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@en
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@nl
type
label
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@en
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@nl
prefLabel
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@en
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@nl
P2093
P1433
P1476
Hyperinsulinism caused by pate ...... he sulfonylurea-receptor gene.
@en
P2093
P304
P356
10.2337/DIABETES.48.8.1652
P407
P577
1999-08-01T00:00:00Z