𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The association of a codon 136 PrP gene variant with the occurrence of natural scrapie

✍ Scribed by N. Hunter; W. Goldmann; G. Smith; J. Hope

Publisher
Springer Vienna
Year
1994
Tongue
English
Weight
533 KB
Volume
137
Category
Article
ISSN
1432-8798

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Association of a polymorphic variant of
Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population
✍ Ye, Lin; Miki, Tetsuro; Nakura, Jun; Oshima, Junko; Kamino, Kouzin; Rakugi, Hiro πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 594 KB

The Werner syndrome (WS) is a rare autosomal recessive progeroid syndrome characterized by the premature onset of multiple age-related disorders, including atherosclerosis, cancer, non-insulin-dependent diabetes mellitus (NIDDM), ocular cataracts and osteoporosis [Epstein et al., 1966]. The major ca

Association of a variant in the muscarin
Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction
✍ A. Mobascher; D. Rujescu; K. Mittelstraß; I. Giegling; C. Lamina; B. Nitz; H. Br πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 124 KB πŸ‘ 2 views

## Abstract Genetic factors contribute to the overall risk of developing nicotine addiction, which is the major cause of preventable deaths in western countries. However, knowledge regarding specific polymorphisms influencing smoking phenotypes remains scarce. In the present study we provide eviden

A variant of the myosin light chain kina
A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans
✍ Carlos Flores; Shwu-Fan Ma; Karen Maresso; Carole Ober; Joe G. N. Garcia πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 159 KB πŸ‘ 1 views

## Abstract Asthma is a complex phenotype influenced by environmental and genetic factors for which severe irreversible structural airway alterations are more frequently observed in African Americans. In addition to a multitude of factors contributing to its pathobiology, increased amounts of myosi

A common variant located in the 3β€²UTR of
A common variant located in the 3β€²UTR of the RET gene is associated with protection from Hirschsprung disease
✍ Paola Griseri; Francesca Lantieri; Francesca Puppo; Tiziana Bachetti; Marco Di D πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 381 KB

Complex diseases are common genetic disorders showing familial aggregation but no typical Mendelian inheritance. Hirschsprung disease (HSCR), a developmental disorder characterized by the absence of enteric neurons in distal segments of the gut, shows a complex pattern of inheritance, with the RET p