Cole W - Search Results

1

Perinatal lethal osteogenesis imperfecta in transgenic mice bearing an engineered mutant pro-alpha 1(I) collagen gene.

Stacey A, Bateman J, Choi T, Mascara T, Cole W, Jaenisch R. Stacey A, et al. Among authors: cole w. Nature. 1988 Mar 10;332(6160):131-6. doi: 10.1038/332131a0. Nature. 1988. PMID: 2450280

2

Correlation of clinical and molecular biological abnormalities in osteogenesis imperfecta.

Cole W, Chan D, Lamande S, Mascara T, Rogers J, Bateman J. Cole W, et al. Connect Tissue Res. 1989;21(1-4):91-5; discussion 95-7. doi: 10.3109/03008208909049999. Connect Tissue Res. 1989. PMID: 2605955

3

Collagen defects in lethal perinatal osteogenesis imperfecta.

Bateman JF, Chan D, Mascara T, Rogers JG, Cole WG. Bateman JF, et al. Among authors: cole wg. Biochem J. 1986 Dec 15;240(3):699-708. doi: 10.1042/bj2400699. Biochem J. 1986. PMID: 3827862 Free PMC article.

4

Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta.

Bateman JF, Mascara T, Chan D, Cole WG. Bateman JF, et al. Among authors: cole wg. Biochem J. 1984 Jan 1;217(1):103-15. doi: 10.1042/bj2170103. Biochem J. 1984. PMID: 6421277 Free PMC article.

5

The phenotypic features of osteogenesis imperfecta resulting from a mutation of the carboxyl-terminal pro alpha 1 (I) propeptide that impairs the assembly of type I procollagen and formation of the extracellular matrix.

Cole WG, Chow CW, Bateman JF, Sillence DO. Cole WG, et al. J Med Genet. 1996 Nov;33(11):965-7. doi: 10.1136/jmg.33.11.965. J Med Genet. 1996. PMID: 8950680 Free PMC article.

6

Lethal perinatal osteogenesis imperfecta due to a type I collagen alpha 2(I) Gly to Arg substitution detected by chemical cleavage of an mRNA:cDNA sequence mismatch.

Bateman JF, Moeller I, Hannagan M, Chan D, Cole WG. Bateman JF, et al. Among authors: cole wg. Hum Mutat. 1992;1(1):55-62. doi: 10.1002/humu.1380010109. Hum Mutat. 1992. PMID: 1284475

7

The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissues.

Cole WG, Campbell PE, Rogers JG, Bateman JF. Cole WG, et al. J Med Genet. 1990 Sep;27(9):545-51. doi: 10.1136/jmg.27.9.545. J Med Genet. 1990. PMID: 2121988 Free PMC article.

8

The clinical features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by arginine in the pro alpha 1(I) chain of type I procollagen.

Cole WG, Chow CW, Rogers JG, Bateman JF. Cole WG, et al. J Med Genet. 1990 Apr;27(4):228-35. doi: 10.1136/jmg.27.4.228. J Med Genet. 1990. PMID: 2325102 Free PMC article.

9

A frameshift mutation results in a truncated nonfunctional carboxyl-terminal pro alpha 1(I) propeptide of type I collagen in osteogenesis imperfecta.

Bateman JF, Lamande SR, Dahl HH, Chan D, Mascara T, Cole WG. Bateman JF, et al. Among authors: cole wg. J Biol Chem. 1989 Jul 5;264(19):10960-4. J Biol Chem. 1989. PMID: 2500431 Free article.

F., Chan, D., Mascara, T., Rogers, J. G., and Cole, W. G. (1986) Biochem. J. 240, 699-708)....

10

Collagen protein abnormalities produced by site-directed mutagenesis of the pro alpha 1(I) gene.

Bateman JF, Mascara T, Cole WG, Stacey A, Jaenisch R. Bateman JF, et al. Among authors: cole wg. Connect Tissue Res. 1989;20(1-4):205-12; discussion 261-3. doi: 10.3109/03008208909023889. Connect Tissue Res. 1989. PMID: 2612152

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