Flynn G - Search Results

1

Clinical, cytogenetic, and molecular analysis of three families with FRAXE.

Barnicoat AJ, Wang Q, Turk J, Green E, Mathew CG, Flynn G, Buckle V, Hirst M, Davies K, Bobrow M. Barnicoat AJ, et al. Among authors: flynn g. J Med Genet. 1997 Jan;34(1):13-7. doi: 10.1136/jmg.34.1.13. J Med Genet. 1997. PMID: 9032643 Free PMC article.

2

The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.

Hirst MC, Barnicoat A, Flynn G, Wang Q, Daker M, Buckle VJ, Davies KE, Bobrow M. Hirst MC, et al. Among authors: flynn g. Hum Mol Genet. 1993 Feb;2(2):197-200. doi: 10.1093/hmg/2.2.197. Hum Mol Genet. 1993. PMID: 8499907

3

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

Flynn GA, Hirst MC, Knight SJ, Macpherson JN, Barber JC, Flannery AV, Davies KE, Buckle VJ. Flynn GA, et al. J Med Genet. 1993 Feb;30(2):97-100. doi: 10.1136/jmg.30.2.97. J Med Genet. 1993. PMID: 8445629 Free PMC article.

4

High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE. Morrison KE, et al. Among authors: flynn ga. Am J Hum Genet. 1992 Mar;50(3):520-7. Am J Hum Genet. 1992. PMID: 1539593 Free PMC article.

5

A YAC contig across the fragile X site defines the region of fragility.

Hirst MC, Rack K, Nakahori Y, Roche A, Bell MV, Flynn G, Christadoulou Z, MacKinnon RN, Francis M, Littler AJ, et al. Hirst MC, et al. Among authors: flynn g. Nucleic Acids Res. 1991 Jun 25;19(12):3283-8. doi: 10.1093/nar/19.12.3283. Nucleic Acids Res. 1991. PMID: 2062644 Free PMC article.

6

Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V, et al. Morrison KE, et al. Among authors: flynn ga. Hum Genet. 1993 Sep;92(2):133-8. doi: 10.1007/BF00219680. Hum Genet. 1993. PMID: 8370578

7

Identification of a novel mutation in a non-Jewish factor XI deficient kindred.

Alhaq A, Mitchell M, Sethi M, Rahman S, Flynn G, Boulton P, Caeno G, Smith M, Savidge G. Alhaq A, et al. Among authors: flynn g. Br J Haematol. 1999 Jan;104(1):44-9. doi: 10.1046/j.1365-2141.1999.01150.x. Br J Haematol. 1999. PMID: 10027710 Free article.

8

Modulation of RGD sequence motifs regulates disintegrin recognition of alphaIIb beta3 and alpha5 beta1 integrin complexes. Replacement of elegantin alanine-50 with proline, N-terminal to the RGD sequence, diminishes recognition of the alpha5 beta1 complex with restoration induced by Mn2+ cation.

Rahman S, Aitken A, Flynn G, Formstone C, Savidge GF. Rahman S, et al. Among authors: flynn g. Biochem J. 1998 Oct 15;335 ( Pt 2)(Pt 2):247-57. doi: 10.1042/bj3350247. Biochem J. 1998. PMID: 9761721 Free PMC article.

9

Differential recognition of snake venom proteins expressing specific Arg-Gly-Asp (RGD) sequence motifs by wild-type and variant integrin alphaIIbbeta3: further evidence for distinct sites of RGD ligand recognition exhibiting negative allostery.

Rahman S, Flynn G, Aitken A, Patel Y, Hussain F, Lu X, Loftus JC, French D, Wijelath E, Strand K, Savidge GF. Rahman S, et al. Among authors: flynn g. Biochem J. 2000 Feb 1;345 Pt 3(Pt 3):701-9. Biochem J. 2000. PMID: 10642531 Free PMC article.

10

Evidence for a role for Galphai1 in mediating weak agonist-induced platelet aggregation in human platelets: reduced Galphai1 expression and defective Gi signaling in the platelets of a patient with a chronic bleeding disorder.

Patel YM, Patel K, Rahman S, Smith MP, Spooner G, Sumathipala R, Mitchell M, Flynn G, Aitken A, Savidge G. Patel YM, et al. Among authors: flynn g. Blood. 2003 Jun 15;101(12):4828-35. doi: 10.1182/blood-2002-10-3080. Epub 2003 Feb 27. Blood. 2003. PMID: 12609843 Free article.

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