Compounds > rubidium
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rubidium and Hyperinsulinism

rubidium has been researched along with Hyperinsulinism in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akrouh, A; Barbetti, F; Colombo, C; de Ville de Goyet, J; Dionisi-Vici, C; Koster, JC; Kurata, HT; Loechner, KJ; Maiorana, A; Nichols, CG; Pizzoferro, M; Rufini, V1
Aguilar-Bryan, L; Bryan, J; Clement, JP; Glaser, B; Gonzalez, G; Nestorowicz, A; Nichols, CG; Permutt, MA; Shyng, SL1
Aguilar-Bryan, L; Bryan, J; Clement, JP; Glaser, B; Inoue, H; Landau, H; Nestorowicz, A; Permutt, MA; Schoor, KP; Stanley, CA; Thornton, PS; Wilson, BA1
LaFranchi, S; Lester, LB; Mougey, A; Shen, S; Shyng, SL; Taschenberger, G1

Other Studies

4 other study(ies) available for rubidium and Hyperinsulinism

ArticleYear
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.
    Diabetes, 2011, Volume: 60, Issue:1

    Topics: Adenosine Triphosphate; Carrier State; Child; DNA; Gas Chromatography-Mass Spectrometry; Gene Amplification; Gene Silencing; Glucose Tolerance Test; Heterozygote; Homozygote; Humans; Hyperinsulinism; Immunoblotting; Insulin; Insulin Secretion; Ion Channel Gating; Islets of Langerhans; Male; Mutation; Phenotype; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Potassium Channels; Potassium Channels, Inwardly Rectifying; Rubidium

2011
Adenosine diphosphate as an intracellular regulator of insulin secretion.
    Science (New York, N.Y.), 1996, Jun-21, Volume: 272, Issue:5269

    Topics: Adenosine Diphosphate; Adenosine Triphosphate; Amino Acid Sequence; Animals; ATP-Binding Cassette Transporters; Cell Line, Transformed; Chlorocebus aethiops; Cricetinae; Diazoxide; Humans; Hyperinsulinism; Hypoglycemia; Insulin; Insulin Secretion; Islets of Langerhans; Molecular Sequence Data; Patch-Clamp Techniques; Point Mutation; Potassium Channels; Potassium Channels, Inwardly Rectifying; Receptors, Drug; Rubidium; Sulfonylurea Receptors; Transfection

1996
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.
    Human molecular genetics, 1996, Volume: 5, Issue:11

    Topics: Animals; ATP-Binding Cassette Transporters; COS Cells; DNA Mutational Analysis; Female; Founder Effect; Gene Frequency; Haplotypes; Hyperinsulinism; Jews; Male; Molecular Sequence Data; Mutation; Point Mutation; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Potassium Channels; Potassium Channels, Inwardly Rectifying; Receptors, Drug; Rubidium; Sequence Deletion; Sulfonylurea Receptors; Transfection

1996
Identification of a familial hyperinsulinism-causing mutation in the sulfonylurea receptor 1 that prevents normal trafficking and function of KATP channels.
    The Journal of biological chemistry, 2002, May-10, Volume: 277, Issue:19

    Topics: Amino Acid Motifs; Animals; Antihypertensive Agents; ATP-Binding Cassette Transporters; Base Sequence; Blotting, Western; COS Cells; Cricetinae; Diazoxide; DNA, Complementary; Endoplasmic Reticulum; Glyburide; Humans; Hyperinsulinism; Hypoglycemic Agents; Immunoblotting; Luminescent Measurements; Lysosomes; Microscopy, Fluorescence; Molecular Sequence Data; Mutation; Patch-Clamp Techniques; Plasmids; Potassium Channels; Potassium Channels, Inwardly Rectifying; Protein Structure, Tertiary; Protein Transport; Receptors, Drug; Rubidium; Signal Transduction; Sulfonylurea Receptors; Time Factors; Transfection

2002