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Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations.

Urvashi Bhardwaj et al.

American journal of hematology, 78(4), 249-255 (2005-03-30)

beta-Thalassemia is a serious health problem in the United States, especially in California, due to increased Asian immigration. Neonatal screening by using high-performance liquid chromatography (HPLC) or isoelectric focusing (IEF) may lead to confusion due to interactions of various hemoglobinopathies

Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.

Roshan Colah et al.

Blood cells, molecules & diseases, 33(2), 153-157 (2004-08-19)

The beta thalassemias are one of the commonest group of autosomal recessive disorders in India. Although majority of patients are severe and transfusion-dependent, about 10-15% of cases have a milder phenotype. We evaluated the role of beta gene mutations in

Aromatase gene polymorphisms are associated with survival among patients with cardiovascular disease in a sex-specific manner.

Amber L Beitelshees et al.

PloS one, 5(12), e15180-e15180 (2010-12-21)

CYP19A1 encodes aromatase, the enzyme responsible for the conversion of androgens to estrogens, and may play a role in variation in outcomes among men and women with cardiovascular disease. We sought to examine genetic variation in CYP19A1 for its potential

Genetic diversity of beta-thalassemia mutations in Pakistani population.

B Khateeb et al.

JPMA. The Journal of the Pakistan Medical Association, 50(9), 293-296 (2000-10-24)

beta-thalassemia is one of the most common inherited single gene disorder in Pakistan. It is characterized by reduced or absent beta-globin gene expression resulting in abnormal maturation and survival of red blood cells. Due to high prevalence of this disease

Long term clinical impact of successful recanalization of chronic total occlusion in patients with and without type 2 diabetes mellitus.

Chuan-Tsai Tsai et al.

Cardiovascular diabetology, 19(1), 119-119 (2020-08-03)

Diabetes mellitus is one of the risk factors for coronary artery disease and frequently associated with multivessels disease and poor clinical outcomes. Long term outcome of successful revascularization of chronic total occlusions (CTO) in diabetes patients remains controversial. From January

Overexpression of regucalcin suppresses cell death in cloned rat hepatoma H4-II-E cells induced by tumor necrosis factor-alpha or thapsigargin.

Takako Izumi et al.

Journal of cellular biochemistry, 92(2), 296-306 (2004-04-27)

The role of regucalcin, which is a regulatory protein in intracellular signaling pathway, in the regulation of cell death was investigated by using the cloned rat hepatoma H4-II-E cells overexpressing regucalcin. The hepatoma cells (wild-type) and stable regucalcin (RC)/pCXN2 transfectants

Intermolecular Complementation between Two Varicella-Zoster Virus pORF30 Terminase Domains Essential for DNA Encapsidation.

Melissa A Visalli et al.

Journal of virology, 89(19), 10010-10022 (2015-07-24)

The herpesviral terminase complex is part of the intricate machinery that delivers a single viral genome into empty preformed capsids (encapsidation). The varicella-zoster virus (VZV) terminase components (pORF25, pORF30, and pORF45/42) have not been studied as extensively as those of

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