1 – 42 of 42
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2023
-
Mark
B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus
(
- Contribution to journal › Article
-
Mark
Role of Mannose-binding Lectin and Association with Microbial Sensitization in a Cohort of Patients with Atopic Dermatitis
(
- Contribution to journal › Article
- 2017
-
Mark
Do group dynamics affect colour morph clines during a range shift?
(
- Contribution to journal › Article
-
Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
-
Mark
Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program
(
- Contribution to journal › Article
-
Mark
Polymorphism in mtDNA control region of Mizo-Mongloid Breast Cancer samples as revealed by PCR-RFLP analysis
(
- Contribution to journal › Article
- 2015
-
Mark
Effect of Gene-Mercury Interactions on Mercury Toxicokinetics and Neurotoxicity
(
- Contribution to journal › Scientific review
- 2014
-
Mark
Unexpected and novel functions of complement proteins
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
(
- Contribution to journal › Article
-
Mark
The 'extremely ancient' chromosome that isn't : a forensic bioinformatic investigation of Albert Perry's X-degenerate portion of the Y chromosome
(
- Contribution to journal › Article
-
Mark
Mitochondrial D-loop and cytochrome oxidase C subunit I polymorphisms among the breast cancer patients of Mizoram, Northeast India
(
- Contribution to journal › Article
- 2011
-
Mark
A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
(
- Contribution to journal › Article
-
Mark
Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility
(
- Contribution to journal › Article
- 2010
-
Mark
Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease : large-scale collaborative study
(
- Contribution to journal › Article
-
Mark
Association between vitamin D receptor gene polymorphisms, falls, balance and muscle power : results from two independent studies (APOSS and OPUS)
(
- Contribution to journal › Article
-
Mark
Demographic histories of four spruce (Picea) species of the Qinghai-Tibetan Plateau and neighboring areas inferred from multiple nuclear loci
(
- Contribution to journal › Article
- 2008
-
Mark
Vitamin K1 intake is associated with higher bone mineral density and reduced bone resorption in early postmenopausal Scottish women : no evidence of gene-nutrient interaction with apolipoprotein E polymorphisms
(
- Contribution to journal › Article
- 2007
-
Mark
The axon reaction : identifying the genes that make a difference
(
- Contribution to journal › Article
-
Mark
Detection of oncogenic viruses SV40, BKV, JCV, HCMV, HPV and p53 codon 72 polymorphism in lung carcinoma
(
- Contribution to journal › Article
- 2006
-
Mark
The association between common vitamin D receptor gene variations and osteoporosis : a participant-level meta-analysis
(
- Contribution to journal › Article
-
Mark
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes : the GENOMOS study
(
- Contribution to journal › Article
- 2005
-
Mark
PTPN11 mutations play a minor role in isolated congenital heart disease
(
- Contribution to journal › Article
-
Mark
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
(
- Contribution to journal › Article
-
Mark
Polymorphisms of the CLCN7 gene are associated with BMD in women
(
- Contribution to journal › Article
-
Mark
Human neuropeptide Y signal peptide gain-of-function polymorphism is associated with increased body mass index : possible mode of function
(
- Contribution to journal › Article
- 2004
-
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 between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in women
(
- Contribution to journal › Article
- 2002
-
Mark
Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
(
- Contribution to journal › Article
-
Mark
Multiple endocrine neoplasia type 1 polymorphism D418D is associated with sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 2001
-
Mark
Association between COLIA1 Sp1 alleles and femoral neck geometry
(
- Contribution to journal › Article
-
Mark
Estrogen receptor alpha gene polymorphisms and bone mineral density : haplotype analysis in women from the United Kingdom
(
- 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
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 1999
-
Mark
Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome
(
- 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
-
Mark
The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels
(
- Contribution to journal › Article
- 1998
-
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
- 1997
-
Mark
von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
(
- Contribution to journal › Article
-
Mark
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
(
- Contribution to journal › Article
-
Mark
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
(
- Contribution to journal › Article