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- 2004
-
Mark
Association of the Collagen Type 1 (COL1A 1) Sp1 Binding Site Polymorphism to Femoral Neck Bone Mineral Density and Wrist Fracture in 1044 Elderly Swedish Women.
(
- Contribution to journal › Article
-
Mark
Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes
(
- Contribution to journal › Article
-
Mark
Methylenetetrahydrofolate reductase polymorphism interacts with riboflavin intake to influence bone mineral density
(
- Contribution to journal › Article
-
Mark
Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Heparan sulfate synthesized by mouse embryonic stem cells deficient in NDST1 and NDST2 is 6-O-sulfated but contains no N-sulfate groups
(
- Contribution to journal › Article
- 2003
-
Mark
Genes and erectile function
(
- Contribution to journal › Scientific review
-
Mark
Discrete gene loci regulate neurodegeneration, lymphocyte infiltration, and major histocompatibility complex class II expression in the CNS
2003) In The Journal of Neuroscience : the official journal of the Society for Neuroscience 23(30). p.23-9817(
- Contribution to journal › Article
-
Mark
Finnish and Swedish genotypes and risk of cancer in Sweden
(
- Contribution to journal › Letter
- 2002
-
Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
-
Mark
HLA-DQ genotypes in classic type 1 diabetes and in latent autoimmune diabetes of the adult.
(
- Contribution to journal › Article
-
Mark
Genetic links between the acute-phase response and arthritis development in rats.
(
- Contribution to journal › Article
-
Mark
Genetic variability in hepatitis B viruses.
(
- Contribution to journal › Scientific review
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
Thrifty genotypes and phenotypes in the pathogenesis of early-onset obesity.
(
- Contribution to journal › Letter
-
Mark
Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Effects of harvest time and storage on dietary fibre components in various cultivars of white cabbage (Brassica oleracea var capitata)
(
- Contribution to journal › Article
-
Mark
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
(
- Contribution to journal › Article
-
Mark
Food-borne outbreak of gastroenteritis associated with genogroup I calicivirus.
(
- Contribution to journal › Article
-
Mark
Multiple endocrine neoplasia type 1 polymorphism D418D is associated with sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2001
-
Mark
Genetic factors related to racial variation in plasma levels of insulin-like growth factor-1: implications for premenopausal breast cancer risk
(
- Contribution to journal › Article
-
Mark
CYP gene polymorphisms and early menarche
(
- Contribution to journal › Article
-
Mark
Gene-expression profiles in hereditary breast cancer
(
- Contribution to journal › Article
-
Mark
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden--an evolutionary advantage?
(
- Contribution to journal › Letter
-
Mark
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
(
- Contribution to journal › Article
-
Mark
Prediction of osteoporotic fractures by bone densitometry and COLIA1 genotyping : a prospective, population-based study in men and women
(
- Contribution to journal › Article
-
Mark
COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss
(
- Contribution to journal › Article
-
Mark
Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
(
- Contribution to journal › Article
-
Mark
Clinical expressions of juvenile hereditary retinal degenerations and macular dystrophies: Electrophysiological and genetic studies
2001)(
- Thesis › Doctoral thesis (compilation)
-
Mark
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2000
-
Mark
Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion
(
- Contribution to journal › Article
- 1999
-
Mark
Prenatal diagnosis of haemophilia
(
- Contribution to journal › Scientific review
-
Mark
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
(
- Contribution to journal › Article
-
Mark
The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels
(
- Contribution to journal › Article
-
Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
(
- Contribution to journal › Article
- 1998
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
(
- Contribution to journal › Article
-
Mark
Inverse relationship between GAD65 antibody levels and severe retinopathy in younger type 1 diabetic patients
(
- Contribution to journal › Article
-
Mark
Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women
(
- Contribution to journal › Article
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
-
Mark
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families
(
- Contribution to journal › Letter
- 1997
-
Mark
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
(
- Contribution to journal › Article
-
Mark
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
(
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
- 1996
-
Mark
HLA-DQB1*0201/0302 is associated with severe retinopathy in patients with IDDM
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
(
- Contribution to journal › Article
- 1995
-
Mark
Hepatitis C superinfection in hepatitis C virus (HCV)-infected patients transplanted with an HCV-infected kidney
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
- 1994
-
Mark
Typing of hepatitis C virus isolates by DNA enzyme immunoassay
(
- Contribution to journal › Article
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