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PubMed 15867855 Genetic variants of the T-cell immunoglobulin mucin 1 but not the T-cell immunoglobulin mucin 3 gene are associated with asthma in an African American population. BACKGROUND: The T-cell immunoglobulin 1.71 KB 2025-10-02 46 26 2021-12-05
PubMed 15770495 New mutations, hotspots, and founder effects in Brazilian patients with steroid 5alpha-reductase deficiency type 2. Mutations of the steroid 5alpha-reductase type 2 (SRD5A2) gene in 46,XY subjects cau 1.78 KB 2015-11-19 26 37 2021-12-05
PubMed 15755837 Common dihydrofolate reductase 19-base pair deletion allele: a novel risk factor for preterm delivery. BACKGROUND: Folate is critical for cell division, a major feature of in utero development. Dihydr 1.64 KB 2015-11-22 24 28 2021-12-05
PubMed 15754732 Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics. Primary hyperparathyroidism (pHPT) is a common endocrine disease that in more 1.92 KB 2015-11-19 43 36 2021-12-05
PubMed 15749661 Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis. BACKGROUND AND OBJECTIVES: The low prevalence of the C282Y mutation of the HFE gene 1.64 KB 2015-11-19 28 50 2021-12-05
PubMed 15668505 Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers. The HH genotype of the nonconservative amino acid substitution polymorphism N372H in the BRCA2 gene 1.55 KB 2015-11-18 27 25 2021-12-05
PubMed 15485686 A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia. OBJECTIVE: Congenital long QT syndrome (LQTS) with in utero onset of the rhyth 1.77 KB 2015-11-19 34 30 2021-12-05
PubMed 15464247 Influence of interleukin 12B (IL12B) polymorphisms on spontaneous and treatment-induced recovery from hepatitis C virus infection. BACKGROUND/AIMS: Interleukin-12 (IL-12) governs the Th1-type immune r 1.49 KB 2015-11-19 26 26 2021-12-05
PubMed 15461822 Vaccine candidates derived from a novel infectious cDNA clone of an American genotype dengue virus type 2. BACKGROUND: A dengue virus type 2 (DEN-2 Tonga/74) isolated from a 1974 epidemic was characte 1.59 KB 2015-11-19 27 47 2021-12-05
PubMed 15033202 Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly. The Nijmegen breakage syndrome is a rare autosomal recessive chromosomal instability disorder characterized b 2.03 KB 2015-11-18 25 29 2021-12-05