Zobrazeno 1 - 10
of 25
pro vyhledávání: '"J. C. Lloyd"'
Publikováno v:
Geochronology, Vol 6, Pp 21-36 (2024)
In situ rubidium–strontium (Rb–Sr) geochronology, using laser ablation–inductively coupled plasma–tandem mass spectrometry (LA-ICP-MS/MS) technology, allows rapid dating of K-rich minerals such as micas (e.g. biotite, muscovite, and phlogopit
Externí odkaz:
https://doaj.org/article/654907dc32f54ab7b5faac6d45a95ebe
Publikováno v:
Journal of Medical Genetics. 30:376-380
Ehlers-Danlos syndrome type IV is usually caused by mutations in COL3A1, the gene coding for type III collagen. In a woman with a milder form of this disease, analysis of type III collagen synthesised by her cultured skin fibroblasts showed an appare
Publikováno v:
Human Genetics. 88:325-330
A large family with Ehlers-Danlos syndrome type IV (EDS IV) has previously been described. Unlike most cases of EDS IV, fibroblasts from affected members secreted near normal amounts of type III collagen. We have localized the mutation in this family
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 19
One of every three persons who starts smoking falls ill and dies prematurely because he or she smoked. Smoking has been causally linked to heart disease, cancer, and respiratory diseases and continues to be the number one preventable cause of death i
Publikováno v:
Vaccine. 17(22)
We evaluated the Vaccine Adverse Event Reporting System (VAERS), the spontaneous reporting system for vaccine-associated adverse events in the United States, as a public health surveillance system, using evaluation guidelines from the Centers for Dis
Publikováno v:
Prostate Cancer and Prostatic Diseases. 16:398-398
Publikováno v:
Human mutation. 6(4)
cDNA encoding the C-terminal domain (nt2283 to 3714) of type III collagen was amplified by PCR in five overlapping products and examined for mutations in 13 patients with Ehlers-Danlos syndrome type IV (EDS IV) with uncharacterised lesions and in fiv
Publikováno v:
Genomics. 22(1)
Laminin is a basement membrane glycoprotein composed of three nonidentical chains, A, B1, and B2. Variant chains such as merosin and S-laminin have been found in different tissues. We have isolated a cDNA encoding a novel laminin A variant that hybri
Publikováno v:
Journal of medical genetics. 30(8)
Previous studies have shown that Ehlers-Danlos syndrome type IV (EDS IV) is caused by mutations of type III collagen (COL3A1). Here we have characterised the most amino-terminal glycine substitution so far described in a patient with EDS IV. A combin
Publikováno v:
Human Genetics. 89
Ehlers-Danlos syndrome type IV, an inherited connective tissue disease, is usually caused by mutations in the gene for type III collagen. Here, we describe a glycine to glutamic acid substitution in a patient with this syndrome. Previous studies had