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- 2024
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Mark
An intronic polymorphism associated with 2,3-bisphosphoglycerate levels in human red cells is linked to expression of RhCE blood groups
2024) In Proceedings of the National Academy of Sciences of the United States of America 121(36). p.1-2(
- Contribution to journal › Letter
- 2023
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Mark
B cell polygenic risk scores associate with anti-dsDNA antibodies and nephritis in systemic lupus erythematosus
(
- Contribution to journal › Article
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Mark
Role of Mannose-binding Lectin and Association with Microbial Sensitization in a Cohort of Patients with Atopic Dermatitis
(
- Contribution to journal › Article
- 2017
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Mark
Do group dynamics affect colour morph clines during a range shift?
(
- Contribution to journal › Article
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Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
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Mark
Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program
(
- Contribution to journal › Article
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Mark
Polymorphism in mtDNA control region of Mizo-Mongloid Breast Cancer samples as revealed by PCR-RFLP analysis
(
- Contribution to journal › Article
- 2015
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Mark
Effect of Gene-Mercury Interactions on Mercury Toxicokinetics and Neurotoxicity
(
- Contribution to journal › Scientific review
- 2014
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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
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Mark
A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
(
- Contribution to journal › Article
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Mark
Unexpected and novel functions of complement proteins
(
- Contribution to journal › Debate/Note/Editorial
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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
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Mark
Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility
(
- Contribution to journal › Article
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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
- 2010
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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
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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
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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
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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
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Mark
The axon reaction : identifying the genes that make a difference
(
- Contribution to journal › Article
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Mark
Detection of oncogenic viruses SV40, BKV, JCV, HCMV, HPV and p53 codon 72 polymorphism in lung carcinoma
(
- Contribution to journal › Article
- 2006
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Mark
The association between common vitamin D receptor gene variations and osteoporosis : a participant-level meta-analysis
(
- Contribution to journal › Article
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Mark
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes : the GENOMOS study
(
- Contribution to journal › Article
- 2005
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Mark
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
(
- Contribution to journal › Article
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Mark
Polymorphisms of the CLCN7 gene are associated with BMD in women
(
- Contribution to journal › Article
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Mark
PTPN11 mutations play a minor role in isolated congenital heart disease
(
- Contribution to journal › Article
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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
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Mark
Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes
(
- Contribution to journal › Article
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Mark
Methylenetetrahydrofolate reductase polymorphism interacts with riboflavin intake to influence bone mineral density
(
- Contribution to journal › Article
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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
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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
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Mark
Effect of a COL1A1 Sp1 binding site polymorphism on arterial pulse wave velocity : an index of compliance
(
- Contribution to journal › Article
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Mark
The NciI polymorphism in the cyclin D1 gene and sporadic primary hyperparathyroidism
(
- Contribution to journal › Article
- 1999
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Mark
Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome
(
- Contribution to journal › Article
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Mark
The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels
(
- Contribution to journal › Article
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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
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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
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Mark
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
(
- Contribution to journal › Article
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Mark
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
(
- Contribution to journal › Article
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Mark
von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura
(
- Contribution to journal › Article