Found: 38
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Identification of a new mutation in the α4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.
- Published in:
- Nephrology Dialysis Transplantation, 2001, v. 16, n. 10, p. 2008, doi. 10.1093/ndt/16.10.2008
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- Article
Linkage and association to candidate regions in Swedish atopic dermatitis families.
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- Human Genetics, 2001, v. 109, n. 2, p. 129, doi. 10.1007/s004390100556
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- Article
No evidence for a familial breast cancer susceptibility gene at chromosome 13q21 in Swedish breast cancer families.
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- International Journal of Cancer, 2002, v. 98, n. 5, p. 799, doi. 10.1002/ijc.10318
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- Article
No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22.
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- International Journal of Cancer, 2002, v. 98, n. 4, p. 638, doi. 10.1002/ijc.10214
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- Article
Genetic Regulation of Bone Traits Is Influenced by Sex and Reciprocal Cross in F2 Progeny From GK and F344 Rats.
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- Journal of Bone & Mineral Research, 2009, v. 24, n. 6, p. 1066, doi. 10.1359/jbmr.081252
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- Article
Interaction and association analysis of a type 1 diabetes susceptibility locus on chromosome 5q11-q13 and the 7q32 chromosomal region in Scandinavian families.
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- 2004
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- journal article
Phenotyping of Individual Pancreatic Islets Locates Genetic Defects in Stimulus Secretion Coupling to Niddm1i Within the Major Diabetes Locus in GK Rats.
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- Diabetes, 2001, v. 50, n. 12, p. 2737, doi. 10.2337/diabetes.50.12.2737
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- Article
Increased mRNA levels of Mn-SOD and catalase in embryos of diabetic rats from a malformation-resistant strain.
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- 2000
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- journal article
Pathophysiological and genetic characterization of the major diabetes locus in GK rats.
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- 1999
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- journal article
Glucose potentiation of arginine-induced insulin secretion is impaired in subjects with a glucokinase Glu256Lys mutation.
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- 1994
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- journal article
Impact of diabetic inheritance on glucose tolerance and insulin secretion in spontaneously diabetic GK-Wistar rats.
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- 1994
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- journal article
Differences in the ratio of RNA encoding two isoforms of the insulin receptor between control and NIDDM patients. The RNA variant without Exon 11 predominates in both groups.
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- 1993
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- journal article
No Evidence for Linkage in Swedish Multiplex T1DM Families to IL12B on Chromosome 5q33-34.
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- Annals of the New York Academy of Sciences, 2003, v. 1005, n. 1, p. 352, doi. 10.1196/annals.1288.057
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- Article
Spatial distribution of active genes implicated in the regulation of insulin-like growth factor stimulatory loops in human decidual and placental tissue of first-trimester pregnancy.
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- Molecular Reproduction & Development, 1992, v. 33, n. 1, p. 7, doi. 10.1002/mrd.1080330103
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- Article
Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.
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- Journal of Human Genetics, 2012, v. 57, n. 2, p. 115, doi. 10.1038/jhg.2011.137
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- Article
Novel Congenic Strain of the Goto-Kakizaki Rat Reveals Nuclear-Mitochondrial Interactions in Type 2 Diabetes.
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- Diabetes, 2007, v. 56, p. A305
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- Publication type:
- Article
Separately Inherited Defects in Insulin Exocytosis and β-Cell Glucose Metabolism Contribute to Type 2 Diabetes.
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- Diabetes, 2006, v. 55, n. 12, p. 3494, doi. 10.2337/db06-0796
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- Article
Altered transcapillary escape of albumin and microalbuminuria reflects two different pathogenetic mechanisms.
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- 2005
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- journal article
Variation in the BMP2 gene: bone mineral density and ultrasound in young adult and elderly women.
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- 2007
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- journal article
A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
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- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 783, doi. 10.1038/ejhg.2012.4
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- Article
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
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- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1117, doi. 10.1038/ejhg.2008.62
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- Article
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction.
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- Nature Genetics, 2005, v. 37, n. 5, p. 486, doi. 10.1038/ng1544
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- Article
Variation in the PTH2R gene is associated with age-related degenerative changes in the lumbar spine.
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- Journal of Bone & Mineral Metabolism, 2015, v. 33, n. 1, p. 9, doi. 10.1007/s00774-013-0550-x
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- Article
Effect of growth hormone treatment on insulin action in adipocytes from children with Prader-Willi syndrome.
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- European Journal of Endocrinology, 1998, v. 138, n. 5, p. 510, doi. 10.1530/eje.0.1380510
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- Article
Variation in the <i>MC4R</i> Gene Is Associated with Bone Phenotypes in Elderly Swedish Women.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088565
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- Article
HTR1A a Novel Type 1 Diabetes Susceptibility Gene on Chromosome 5p13-q13.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0035439
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- Article
Identification of Candidate Gene Regions in the Rat by Co-Localization of QTLs for Bone Density, Size, Structure and Strength.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022462
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- Article
Comparative Sequence Analysis of the Non-Protein- Coding Mitochondrial DNA of Inbred Rat Strains.
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- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0008148
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- Article
Synergistic effect of partially inactivating mutations in steroid 21-hydroxylase deficiency.
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- 1997
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- Publication type:
- journal article
Variations in apolipoprotein D and sigma non-opioid intracellular receptor 1 genes with relation to risk, severity and outcome of ischemic stroke.
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- BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/s12883-014-0191-2
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- Article
Variations in apolipoprotein D and sigma non-opioid intracellular receptor 1 genes with relation to risk, severity and outcome of ischemic stroke.
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- 2014
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- Publication type:
- journal article
Quantitative trait loci disposing for both experimental arthritis and encephalomyelitis in the DA rat; impact on severity of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis and antibody isotype pattern.
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- European Journal of Immunology, 1998, v. 28, n. 7, p. 2188, doi. 10.1002/(SICI)1521-4141(199807)28:07<2188::AID-IMMU2188>3.0.CO;2-B
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- Article
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
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- Cerebrovascular Diseases, 2005, v. 20, n. 5, p. 381, doi. 10.1159/000088668
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- Article
High-Resolution Quantitative Trait Locus Analysis Reveals Multiple Diabetes Susceptibility Loci Mapped to Intervals\800 kb in the Species-Conserved Niddm1i of the GK Rat.
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- Genetics, 2006, v. 174, n. 3, p. 1565, doi. 10.1534/genetics.106.062208
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- Article
High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes.
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- Human Molecular Genetics, 2003, v. 12, n. 17, p. 2087, doi. 10.1093/hmg/ddg224
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- Article
Rats made congenic for Oia3 on chromosome 10 become susceptible to squalene-induced arthritis.
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- Human Molecular Genetics, 2001, v. 10, n. 6, p. 565, doi. 10.1093/hmg/10.6.565
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- Article
Linkage analysis of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis in the rat identifies a locus controlling demyelination on chromosome 18.
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- Human Molecular Genetics, 1999, v. 8, n. 12, p. 2183, doi. 10.1093/hmg/8.12.2183
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- Article
Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations.
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- Human Molecular Genetics, 1993, v. 2, n. 5, p. 499
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- Publication type:
- Article