X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (89) 89
index medicus (85) 85
diabetes mellitus, type 2 - genetics (54) 54
endocrinology & metabolism (51) 51
male (49) 49
adult (45) 45
female (45) 45
genetic aspects (45) 45
genetics (42) 42
type 2 diabetes (38) 38
diabetes (37) 37
middle aged (32) 32
mutation (31) 31
abridged index medicus (30) 30
life sciences (28) 28
research (28) 28
human genetics (26) 26
polymorphism, single nucleotide (24) 24
risk factors (22) 22
pedigree (20) 20
aged (19) 19
diabetes mellitus - genetics (19) 19
adolescent (18) 18
child (18) 18
physiological aspects (18) 18
genotype (17) 17
genome-wide association (15) 15
glucokinase - genetics (15) 15
hyperglycemia (15) 15
mellitus (15) 15
cohort studies (14) 14
genetic linkage (14) 14
infant, newborn (14) 14
insulin (14) 14
potassium channels, inwardly rectifying - genetics (14) 14
base sequence (13) 13
france (13) 13
genetic predisposition to disease (13) 13
genetics & heredity (13) 13
health aspects (13) 13
linkage (13) 13
diabetes mellitus (12) 12
european continental ancestry group - genetics (12) 12
gene (12) 12
glucose (12) 12
molecular sequence data (12) 12
obesity (12) 12
transcription factors - genetics (12) 12
analysis (11) 11
biochemistry & molecular biology (11) 11
diabetes mellitus, type 2 (11) 11
genes (11) 11
insulin resistance (11) 11
mutations (11) 11
chromosome mapping (10) 10
insulin - metabolism (10) 10
activating mutations (9) 9
animals (9) 9
atp-binding cassette transporters - genetics (9) 9
expression (9) 9
genetic variation (9) 9
glucokinase (9) 9
infant (9) 9
insulin secretion (9) 9
internal medicine (9) 9
pancreatic beta cells (9) 9
receptors, drug - genetics (9) 9
sulfonylurea receptors (9) 9
alleles (8) 8
blood glucose - metabolism (8) 8
diabetes-mellitus (8) 8
diagnosis (8) 8
exons (8) 8
gene frequency (8) 8
gene mutations (8) 8
genome-wide association study (8) 8
hepatocyte nuclear factor 1-alpha (8) 8
hyperglycemia - genetics (8) 8
infants (8) 8
kir6.2 (8) 8
polymerase chain reaction (8) 8
polymorphism, genetic (8) 8
case-control studies (7) 7
cell line (7) 7
child, preschool (7) 7
diabetes mellitus, type 2 - blood (7) 7
diabetes mellitus, type 2 - epidemiology (7) 7
diabetes mellitus, type 2 - metabolism (7) 7
dna-binding proteins (7) 7
european continental ancestry group (7) 7
genetic polymorphisms (7) 7
genetic research (7) 7
hepatocyte nuclear factor 1 (7) 7
hepatocyte nuclear factor 1-beta (7) 7
insulin resistance - genetics (7) 7
insulin-secretion (7) 7
lod score (7) 7
mice (7) 7
mody (7) 7
pancreas (7) 7
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Diabetes, ISSN 1753-0393, 11/2016, Volume 8, Issue 6, pp. 782 - 795
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2012, Volume 44, Issue 3, pp. 297 - 301
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2006, Volume 355, Issue 5, pp. 456 - 466
In this study, mutations in the gene encoding the sulfonylurea receptor, a component of the beta-cell ATP-sensitive potassium channel, are described in infants... 
IMMUNE DYSREGULATION | KIR6.2 MUTATIONS | NUCLEOTIDES | REGULATOR | MEDICINE, GENERAL & INTERNAL | MECHANISM | K-ATP CHANNELS | INSULIN-SECRETION | STOICHIOMETRY | SULFONYLUREA RECEPTOR | TRANSIENT | Tolbutamide - pharmacology | Diabetes Complications | Diabetes Mellitus - genetics | Receptors, Drug - genetics | Humans | Male | Mutation, Missense | Sulfonylurea Receptors | Potassium Channels - metabolism | Insulin-Secreting Cells - metabolism | ATP-Binding Cassette Transporters - genetics | ATP-Binding Cassette Transporters - metabolism | Female | Potassium Channels, Inwardly Rectifying - antagonists & inhibitors | Infant, Newborn | Hypoglycemic Agents - therapeutic use | Sulfonylurea Compounds - therapeutic use | Diabetes Mellitus - drug therapy | Diabetes Mellitus - metabolism | Potassium Channels, Inwardly Rectifying - genetics | Receptors, Drug - metabolism | Potassium Channels - genetics | Birth Weight | Insulin-Secreting Cells - drug effects | Pedigree | Heterozygote | Developmental Disabilities - complications | Potassium Channels, Inwardly Rectifying - metabolism | Receptors, Drug - antagonists & inhibitors | ATP-Binding Cassette Transporters - antagonists & inhibitors | Infants (Newborn) | Genetic aspects | Diabetes | Research | Gene mutations | Diseases | Mutation | Pancreas | Genes | Adenosine triphosphatase | Index Medicus | Abridged Index Medicus | Life Sciences | Genetics | Human genetics
Journal Article
04/2017, Frontiers in Diabetes, ISBN 3318060240, Volume 25, 23
Monogenic diabetes is defined as diabetes resulting from a rare causal deleterious mutation of a single gene that usually impairs pancreatic β-cell function.... 
Chapter
Book Chapter
Nature Genetics, ISSN 1061-4036, 10/2009, Volume 41, Issue 10, pp. 1110 - 1115
Journal Article
Diabetes Care, ISSN 0149-5992, 10/2008, Volume 31, Issue 10, pp. 2056 - 2061
Predicting Diabetes: Clinical, Biological, and Genetic Approaches Data from the Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Beverley... 
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2009, Volume 41, Issue 1, pp. 89 - 94
Journal Article
Journal Article
Science, ISSN 0036-8075, 5/2008, Volume 320, Issue 5879, pp. 1085 - 1088
Journal Article