✦ LIBER ✦

Identification of two αRYR alleles and characterization of αRYR transcript variants in turkey skeletal muscle

✍ Scribed by Wen Chiang; Chuck P. Allison; John E. Linz; Gale M. Strasburg

Book ID: 116506665
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 605 KB
Volume: 330
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2004.01.023

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Divergent mechanisms in generating molec

Divergent mechanisms in generating molecular variations of αRYR and βRYR in turkey skeletal muscle

✍ Wen Chiang; Hyo-Jung Yoon; John E. Linz; Judith A. Airey; Gale M. Strasburg 📂 Article 📅 2007 🏛 Springer Netherlands 🌐 English ⚖ 890 KB

Two skeletal α-tropomyosin transcripts w

Two skeletal α-tropomyosin transcripts with distinct 3′UTR have different temporal and spatial patterns of expression in the striated muscle lineages of Xenopus laevis

✍ Serge Hardy; Sandra Hamon; Brian Cooper; Tim Mohun; Pierre Thiébaud 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 289 KB

Hb Q-Thailand-Hb H disease in a chinese

Hb Q-Thailand-Hb H disease in a chinese living in Geneva, Switzerland: Characterization of the variant and identification of the two α-thalassemic chromosomes

✍ P. Beris; P. Huber; P. A. Miescher; J. B. Wilson; A. Kutlar; S. S. Chen; Dr. T. 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 402 KB 👁 2 views

Data on a 24-year-old Chinese male with Hb Q-Thailand-Hb H disease are presented. The hemoglobin variant was characterized by fast microprocedures, mainly by reverse-phase high-performance liquid chromatography. Gene mapping analyses identified the a-thalassemia-2, which is associated with the a-Q c

Identification and functional characteri

Identification and functional characterization of two novel mutations in the α-helical loop (residues 484–503) of CYBB/gp91phox resulting in the rare X91+ variant of chronic granulomatous disease

✍ Bernadette Boog; Alex Quach; Maurizio Costabile; Joanne Smart; Patrick Quinn; Ha 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 270 KB

Chronic granulomatous disease (CGD) is mainly caused by mutations in X-linked CYBB that encodes gp91. We have identified two novel mutations in CYBB resulting in the rare X91 + -CGD variant, c.1500T>G (p.Asp500Glu) in two male siblings and c.1463C>A (p.Ala488Asp) in an unrelated male. Zymosan and/or