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Articles: Basic Science/Genetics |
Prior Articles
Bioresonance hypothesis: A new mechanism on the pathogenesis of trigeminal neuralgia
Medical Hypotheses, 11/13/09
Defects in IL-2R signaling contribute to diminished maintenance of FOXP3 expression in CD4+CD25+ regulatory T cells of T1D subjects
Diabetes, 11/13/09 RD Lawrence Lecture 2009 Old genes, new tricks: learning about blood glucose regulation from naturally occurring genetic variation in humans
Diabetic Medicine, 11/13/09 Modulation of phenotypic expression of APOA5 Q97X and L242P mutations
Atherosclerosis, 11/13/09 Rejuvenation in distinct cell populations – What does it mean?
Experimental Gerontology, 11/12/09
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Microarray analysis of senescent vascular smooth muscle cells: A link to atherosclerosis and vascular calcification
Experimental Gerontology, 11/12/09 CYP3A4 and CYP3A5 Polymorphisms and Blood Pressure Response to Amlodipine among African-American Men and Women with Early Hypertensive Renal Disease
American Journal of Nephrology, 11/12/09 Crigler-Najjar syndrome in The Netherlands: Identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants
Human Mutation, 11/12/09 Vitamin B-6 Intake Is Inversely Related to, and the Requirement Is Affected by, Inflammation Status
The Journal of Nutrition, 11/12/09 The relationship between ACE gene ID polymorphism and aerobic capacity in Asian rugby players
Singapore Medical Journal, 11/11/09
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Homozygous loss of BHD causes early embryonic lethality and kidney tumor development with activation of mTORC1 and mTORC2
Proceedings of the National Academy of Sciences of the United States of America, 11/11/09 CSD, BBB and MMP-9 elevations: animal experiments versus clinical phenomena in migraine
Expert Review of Neurotherapeutics, 11/11/09 Long-term depression of pain-related cerebral activation in healthy man: An fMRI study
European Journal of Pain, 11/10/09 Molecular analysis of Pericentrin gene (PCNT) in a series of 24 Seckel/ MOPD II families
Journal of Medical Genetics, 11/10/09 Clinical and Molecular Characterization of Bardet-Biedl Syndrome in Consanguineous Populations: The Power of Homozygosity Mapping
Journal of Medical Genetics, 11/10/09 Phenotypic Spectrum of MFN2 Mutations in the Spanish Population
Journal of Medical Genetics, 11/10/09 Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis
Journal of Medical Genetics, 11/10/09 Mutations of FUS Gene in Sporadic Amyotrophic Lateral Sclerosis
Journal of Medical Genetics, 11/10/09 Karyomapping: a Universal Method for Genome Wide Analysis of Genetic Disease based on Mapping Crossovers between Parental Haplotypes
Journal of Medical Genetics, 11/10/09 Renal tumor suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin
Journal of Medical Genetics, 11/10/09
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Indexed Journals: New England Journal of Medicine, The Lancet, Archives of Internal Medicine
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