UP - logo

Rezultati iskanja

Osnovno iskanje    Izbirno iskanje   
Iskalna
zahteva
Knjižnica

Trenutno NISTE avtorizirani za dostop do e-virov UPUK. Za polni dostop se PRIJAVITE.

1 2 3 4 5
zadetkov: 130
1.
  • Overlap of Endocrine Hormon... Overlap of Endocrine Hormone Expression in the Mouse Intestine Revealed by Transcriptional Profiling and Flow Cytometry
    Habib, Abdella M; Richards, Paul; Cairns, Lynne S ... Endocrinology (Philadelphia), 7/2012, Letnik: 153, Številka: 7
    Journal Article
    Recenzirano
    Odprti dostop

    The intestine secretes a range of hormones with important local and distant actions, including the control of insulin secretion and appetite. A number of enteroendocrine cell types have been ...
Celotno besedilo
2.
  • A Cryptochrome 2 mutation y... A Cryptochrome 2 mutation yields advanced sleep phase in humans
    Hirano, Arisa; Shi, Guangsen; Jones, Christopher R ... eLife, 08/2016, Letnik: 5
    Journal Article
    Recenzirano
    Odprti dostop

    Familial Advanced Sleep Phase (FASP) is a heritable human sleep phenotype characterized by very early sleep and wake times. We identified a missense mutation in the human Cryptochrome 2 (CRY2) gene ...
Celotno besedilo
3.
  • Hyperglycemia and Adverse P... Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study: Common Genetic Variants in GCK and TCF7L2 Are Associated With Fasting and Postchallenge Glucose Levels in Pregnancy and With the New Consensus Definition of Gestational Diabetes Mellitus From the International Association of Diabetes and Pregnancy Study Groups
    FREATHY, Rachel M; HAYES, M. Geoffrey; HATTERSLEY, Andrew T ... Diabetes (New York, N.Y.), 2010, 2010-Oct, 2010-10-00, 20101001, 2010-08-01, 20101000, Letnik: 59, Številka: 10
    Journal Article
    Recenzirano
    Odprti dostop

    Common genetic variants in GCK and TCF7L2 are associated with higher fasting glucose and type 2 diabetes in nonpregnant populations. However, their associations with glucose levels from oral glucose ...
Celotno besedilo
4.
  • Genetic Risk Reclassificati... Genetic Risk Reclassification for Type 2 Diabetes by Age Below or Above 50 Years Using 40 Type 2 Diabetes Risk Single Nucleotide Polymorphisms
    DE MIGUEL-YANES, Jose M; SHRADER, Peter; MEIGS, James B ... Diabetes care, 2011, 2011-Jan, 2011-01-01, 20110101, 2010-10-01, 20110100, Letnik: 34, Številka: 1
    Journal Article
    Recenzirano
    Odprti dostop

    To test if knowledge of type 2 diabetes genetic variants improves disease prediction. We tested 40 single nucleotide polymorphisms (SNPs) associated with diabetes in 3,471 Framingham Offspring Study ...
Celotno besedilo
5.
  • Variation in Maturity-Onset... Variation in Maturity-Onset Diabetes of the Young Genes Influence Response to Interventions for Diabetes Prevention
    Billings, Liana K; Jablonski, Kathleen A; Warner, A Sofia ... The journal of clinical endocrinology and metabolism, 2017-August, 2017-Aug-01, 2017-08-01, 20170801, 2017-04-01, Letnik: 102, Številka: 8
    Journal Article
    Recenzirano
    Odprti dostop

    Variation in genes that cause maturity-onset diabetes of the young (MODY) has been associated with diabetes incidence and glycemic traits. This study aimed to determine whether genetic variation in ...
Celotno besedilo
6.
  • Common Variants at 10 Genom... Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways
    Soranzo, N; Sanna, S; Wheeler, E ... Diabetes (New York, N.Y.), 2010, 2010-12-01, 2010-11-29, 2010-01-01, 2010-09-01, 20101200, Letnik: 59, Številka: 12
    Journal Article, Publication
    Recenzirano
    Odprti dostop

    Glycated hemoglobin (HbA₁(c)), used to monitor and diagnose diabetes, is influenced by average glycemia over a 2- to 3-month period. Genetic factors affecting expression, turnover, and abnormal ...
Celotno besedilo
7.
  • Transethnic meta‐analysis o... Transethnic meta‐analysis of genomewide association studies
    Morris, Andrew P Genetic epidemiology, December 2011, 2011-Dec, 20111201, 2011-11-01, 20111200, Letnik: 35, Številka: 8
    Journal Article
    Recenzirano
    Odprti dostop

    The detection of loci contributing effects to complex human traits, and their subsequent fine‐mapping for the location of causal variants, remains a considerable challenge for the genetics research ...
Celotno besedilo
8.
  • Genetics of Type 1 Diabetes... Genetics of Type 1 Diabetes: What's Next?
    POCIOT, Flemming; AKOLKAR, Beena; CONCANNON, Patrick ... Diabetes (New York, N.Y.), 2010, 2010-Jul, 2010-07-01, 20100701, 2010-01-01, 20100700, Letnik: 59, Številka: 7
    Journal Article
    Recenzirano
    Odprti dostop
Celotno besedilo
9.
  • Genetics of type 2 diabetes... Genetics of type 2 diabetes: the GWAS era and future perspectives [Review]
    Imamura, Minako; Maeda, Shiro Endocrine journal, 2011, 2011-00-00, 20110101, Letnik: 58, Številka: 9
    Journal Article
    Recenzirano
    Odprti dostop

    Genome-wide association studies (GWAS) have facilitated a substantial and rapid rise in the number of confirmed genetic susceptibility variants for type 2 diabetes (T2D). Approximately 40 variants ...
Celotno besedilo
10.
  • AKT1 polymorphisms are asso... AKT1 polymorphisms are associated with risk for metabolic syndrome
    Devaney, Joseph M; Devaney, Joseph M; Gordish-Dressman, Heather ... Human genetics, 02/2011, Letnik: 129, Številka: 2
    Journal Article
    Recenzirano
    Odprti dostop

    Converging lines of evidence suggest that AKT1 is a major mediator of the responses to insulin, insulin-like growth factor 1 (IGF1), and glucose. AKT1 also plays a key role in the regulation of both ...
Celotno besedilo
1 2 3 4 5
zadetkov: 130

Nalaganje filtrov