Bateman JF - Search Results

1

Molecular consequences of dominant Bethlem myopathy collagen VI mutations.

Baker NL, Mörgelin M, Pace RA, Peat RA, Adams NE, Gardner RJ, Rowland LP, Miller G, De Jonghe P, Ceulemans B, Hannibal MC, Edwards M, Thompson EM, Jacobson R, Quinlivan RC, Aftimos S, Kornberg AJ, North KN, Bateman JF, Lamandé SR. Baker NL, et al. Among authors: bateman jf. Ann Neurol. 2007 Oct;62(4):390-405. doi: 10.1002/ana.21213. Ann Neurol. 2007. PMID: 17886299

2

A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV.

Cole WG, Chiodo AA, Lamande SR, Janeczko R, Ramirez F, Dahl HH, Chan D, Bateman JF. Cole WG, et al. Among authors: bateman jf. J Biol Chem. 1990 Oct 5;265(28):17070-7. J Biol Chem. 1990. PMID: 2145268 Free article.

3

The study of collagen structure and function by site-directed mutagenesis of collagen genes.

Bateman JF, Mascara T, Cole WG, Stacey A, Jaenisch R. Bateman JF, et al. Ann N Y Acad Sci. 1990;580:324-9. doi: 10.1111/j.1749-6632.1990.tb17941.x. Ann N Y Acad Sci. 1990. PMID: 2337302 No abstract available.

4

Regulation of procollagen synthesis and processing during ascorbate-induced extracellular matrix accumulation in vitro.

Chan D, Lamande SR, Cole WG, Bateman JF. Chan D, et al. Among authors: bateman jf. Biochem J. 1990 Jul 1;269(1):175-81. doi: 10.1042/bj2690175. Biochem J. 1990. PMID: 2375750 Free PMC article.

5

Detection and localization of base changes in RNA using a chemical cleavage method.

Dahl HH, Lamande SR, Cotton RG, Bateman JF. Dahl HH, et al. Among authors: bateman jf. Anal Biochem. 1989 Dec;183(2):263-8. doi: 10.1016/0003-2697(89)90477-6. Anal Biochem. 1989. PMID: 2483035

6

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. J Biol Chem. 1989 Jul 5;264(19):10960-4. J Biol Chem. 1989. PMID: 2500431 Free article.

7

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

8

Characterization of point mutations in the collagen COL1A1 and COL1A2 genes causing lethal perinatal osteogenesis imperfecta.

Lamande SR, Dahl HH, Cole WG, Bateman JF. Lamande SR, et al. Among authors: bateman jf. J Biol Chem. 1989 Sep 25;264(27):15809-12. J Biol Chem. 1989. PMID: 2777764 Free article.

9

Biochemical heterogeneity of type I collagen mutations in osteogenesis imperfecta.

Bateman JF, Chan D, Lamande S, Mascara T, Cole WG. Bateman JF, et al. Ann N Y Acad Sci. 1988;543:95-105. doi: 10.1111/j.1749-6632.1988.tb55321.x. Ann N Y Acad Sci. 1988. PMID: 3214058 No abstract available.

10

Substitution of arginine for glycine 664 in the collagen alpha 1(I) chain in lethal perinatal osteogenesis imperfecta. Demonstration of the peptide defect by in vitro expression of the mutant cDNA.

Bateman JF, Lamande SR, Dahl HH, Chan D, Cole WG. Bateman JF, et al. J Biol Chem. 1988 Aug 25;263(24):11627-30. J Biol Chem. 1988. PMID: 3403550 Free article.

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