Page last updated: 2024-08-17

adenosine diphosphate and Congenital Hyperinsulinism

adenosine diphosphate has been researched along with Congenital Hyperinsulinism in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Brioudes, E; Grimaldi, M; Karaca, M; Latini, L; Maechler, P; Schalch, T	1
Becker, S; Ganguly, A; Hanna, C; Lin, YW; MacMullen, C; Pinney, SE; Shyng, SL; Stanley, CA; Thornton, P	1

Other Studies

2 other study(ies) available for adenosine diphosphate and Congenital Hyperinsulinism

Article	Year
Identification of the molecular dysfunction caused by glutamate dehydrogenase S445L mutation responsible for hyperinsulinism/hyperammonemia. Human molecular genetics, 2017, 09-15, Volume: 26, Issue:18 Topics: Adenosine Diphosphate; Amino Acids; Animals; Blood Glucose; Congenital Hyperinsulinism; Glucose; Glutamate Dehydrogenase; Glutamine; HEK293 Cells; Humans; Hyperammonemia; Hyperinsulinism; Insulin; Insulin Secretion; Insulin-Secreting Cells; Islets of Langerhans; Mice; Mice, Inbred C57BL; Mutation; Polymorphism, Single Nucleotide	2017
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations. The Journal of clinical investigation, 2008, Volume: 118, Issue:8 Topics: Adenosine Diphosphate; Adult; Aged; Aged, 80 and over; Animals; ATP-Binding Cassette Transporters; Chlorocebus aethiops; Congenital Hyperinsulinism; COS Cells; Diazoxide; Female; Genes, Dominant; Glucose Tolerance Test; Heterozygote; Humans; Hypoglycemia; Insulin; Insulin Secretion; KATP Channels; Male; Middle Aged; Mutation; Patch-Clamp Techniques; Pedigree; Potassium Channels, Inwardly Rectifying; Receptors, Drug; Sulfonylurea Receptors	2008

Article

Year

Identification of the molecular dysfunction caused by glutamate dehydrogenase S445L mutation responsible for hyperinsulinism/hyperammonemia.

Human molecular genetics, 2017, 09-15, Volume: 26, Issue:18

Topics: Adenosine Diphosphate; Amino Acids; Animals; Blood Glucose; Congenital Hyperinsulinism; Glucose; Glutamate Dehydrogenase; Glutamine; HEK293 Cells; Humans; Hyperammonemia; Hyperinsulinism; Insulin; Insulin Secretion; Insulin-Secreting Cells; Islets of Langerhans; Mice; Mice, Inbred C57BL; Mutation; Polymorphism, Single Nucleotide

2017

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

The Journal of clinical investigation, 2008, Volume: 118, Issue:8

Topics: Adenosine Diphosphate; Adult; Aged; Aged, 80 and over; Animals; ATP-Binding Cassette Transporters; Chlorocebus aethiops; Congenital Hyperinsulinism; COS Cells; Diazoxide; Female; Genes, Dominant; Glucose Tolerance Test; Heterozygote; Humans; Hypoglycemia; Insulin; Insulin Secretion; KATP Channels; Male; Middle Aged; Mutation; Patch-Clamp Techniques; Pedigree; Potassium Channels, Inwardly Rectifying; Receptors, Drug; Sulfonylurea Receptors

2008