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Articles: Basic Science/Genetics |
Prior Articles
Role of immunolglobulin-like transcript family receptors and their ligands in suppressor T-cell–induced dendritic cell tolerization
Human Immunology, 09/16/09
Caveolin-1 and Dopamine-Mediated Internalization of NaKATPase in Human Renal Proximal Tubule Cells
Hypertension, 09/15/09 Amino acid residues 201-205 in C-terminal acidic tail region plays a crucial role in antibacterial activity of HMGB1
BMC: Journal of Biomedical Science, 09/15/09 TLR4-independent and PKR-dependent interleukin 1 receptor antagonist expression upon LPS stimulation
Cellular Immunology, 09/15/09 Nitroglycerin provocation in normal subjects is not a useful human migraine model?
Cephalalgia, 09/15/09 Role of SIP30 in the development and maintenance of peripheral nerve injury-induced neuropathic pain
Pain, 09/15/09 Something New Under the Sun: Lutein's Role in Skin Health
American Journal of Lifestyle Medicine, 09/14/09 Heritabilities for fifteen routine biochemical values: findings in 215 Swedish twin pairs 82 years of age or older
Scandinavian Journal of Clinical and Laboratory Investigation, 09/14/09 HTRA1 Promoter Polymorphism and Risk of Age-Related Macular Degeneration: A Meta-Analysis
Annals of Epidemiology, 09/14/09 Epigenetic programming of diverse glucocorticoid response and inflammatory/immune-mediated disease
Medical Hypotheses, 09/14/09 A threshold level of TLR9 mRNA predicts cellular responsiveness to CpG-ODN in haematological and non-haematological tumour cell lines
Cellular Immunology, 09/14/09 Histidine-rich glycoprotein and concanavalin A synergistically stimulate the phosphatidylinositol 3-kinase-independent signaling pathway in leukocytes leading to increased cell adhesion and changes in cell morphology
Cellular Immunology, 09/14/09 Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis
Nephrology Dialysis Transplantation, 09/14/09 Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus
Human Molecular Genetics, 09/14/09 A genome-wide association study of acenocoumarol maintenance dosage
Human Molecular Genetics, 09/14/09 Generation of an epigenetic signature by chronic hypoxia in prostate cells
Human Molecular Genetics, 09/14/09 A functional genetic study identifies HAND1 mutations in septation defects of the human heart
Human Molecular Genetics, 09/14/09 Inactive X chromosome-specific reduction in placental DNA methylation
Human Molecular Genetics, 09/14/09 Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture
Human Molecular Genetics, 09/14/09 Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanisms
Human Molecular Genetics, 09/14/09
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Indexed Journals: New England Journal of Medicine, The Lancet, Archives of Internal Medicine
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250 Available Pages
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