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Cell|February 10, 1995
A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesisY Li, D A Lacerda, M L Warman, et al.
Biochemical and Biophysical Research Communications|May 19, 1997
Two forms of avian(chicken) TATA-binding protein mRNA generated by alternative polyadenylationJ Yamauchi, A Sugita, M Fujiwara, et al.
Kidney International|September 12, 1998
A model of autosomal recessive Alport syndrome in English cocker spaniel dogsG E Lees, R G Helman, C E Kashtan, et al.
The American Journal of Physiology|May 1, 1994
Enhancement of gustatory nerve fibers to NaCl and formation of ion channels by commercial novobiocinA M Feigin, Y Ninomiya, S M Bezrukov, et al.
American Journal of Human Genetics|April 16, 1998
Topoisomerase I and II consensus sequences in a 17-kb deletion junction of the COL4A5 and COL4A6 genes and immunohistochemical analysis of esophageal leiomyomatosis associated with Alport syndromeY Ueki, I Naito, T Oohashi, et al.
Investigative Ophthalmology & Visual Science|May 1, 1996
Extracellular matrix alterations in human corneas with bullous keratopathyA V Ljubimov, R E Burgeson, R J Butkowski, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|December 1, 1996
Basement membrane abnormalities in human eyes with diabetic retinopathyA V Ljubimov, R E Burgeson, R J Butkowski, et al.
The Journal of Biological Chemistry|August 15, 1989
The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organizationT Kimura, K S Cheah, S D Chan, et al.
Journal of Medical Genetics|August 1, 1996
Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adultI Matsuda, T Matsuura, A Nishiyori, et al.
Journal of the American College of Cardiology|January 1, 1996
Coronary angioplasty ameliorates hypoperfusion-induced endothelial dysfunction in patients with stable angina pectorisT Komaru, S Isoyama, N Sekiguchi, et al.
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