Bidwell J - Search Results

1

Type 2N von Willebrand disease: rapid genetic diagnosis of G2811A (R854Q), C2696T (R816W), T2701A (H817Q) and G2823T (C858F)--detection of a novel candidate type 2N mutation: C2810T (R854W).

Bowen DJ, Standen GR, Mazurier C, Gaucher C, Cumming A, Keeney S, Bidwell J. Bowen DJ, et al. Among authors: bidwell j. Thromb Haemost. 1998 Jul;80(1):32-6. Thromb Haemost. 1998. PMID: 9684781 Clinical Trial.

2

UHG-based mutation screening in type 2B von Willebrand's disease: detection of a candidate mutation Ser547Phe.

Wood N, Standen GR, Bowen DJ, Cumming A, Lush C, Lee R, Bidwell J. Wood N, et al. Among authors: bidwell j. Thromb Haemost. 1996 Feb;75(2):363-7. Thromb Haemost. 1996. PMID: 8815591

3

Genetic diagnosis of factor V Leiden using heteroduplex technology.

Bowen DJ, Standen GR, Granville S, Bowley S, Wood NA, Bidwell J. Bowen DJ, et al. Among authors: bidwell j. Thromb Haemost. 1997 Jan;77(1):119-22. Thromb Haemost. 1997. PMID: 9031460

4

Rapid genotypic diagnosis of type 2A von Willebrand's disease by heteroduplex analysis.

Culpan D, Goodeve A, Bowen DJ, Standen G, Bidwell J. Culpan D, et al. Among authors: bidwell j. Clin Lab Haematol. 1998 Jun;20(3):177-8. doi: 10.1046/j.1365-2257.1998.00111.x. Clin Lab Haematol. 1998. PMID: 9681234

5

Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generator.

Wood N, Standen GR, Murray EW, Lillicrap D, Holmberg L, Peake IR, Bidwell J. Wood N, et al. Among authors: bidwell j. Br J Haematol. 1995 Jan;89(1):152-6. doi: 10.1111/j.1365-2141.1995.tb08922.x. Br J Haematol. 1995. PMID: 7833255

6

Rapid mutation screening in type 2A von Willebrand's disease using universal heteroduplex generators.

Culpan D, Standen G, Wood N, Mazurier C, Gaucher C, Bidwell J. Culpan D, et al. Among authors: bidwell j. Br J Haematol. 1997 Mar;96(3):464-9. doi: 10.1046/j.1365-2141.1997.d01-2054.x. Br J Haematol. 1997. PMID: 9054649 Free article.

7

A new (K1518E) candidate mutation detected by universal heteroduplex generator analysis in a patient with type 2A (phenotype IIA) von Willebrand disease.

Enayat MS, Theophilus BD, Hill FG, Rose PE, Culpan D, Bidwell J, Standen GR. Enayat MS, et al. Among authors: bidwell j. Thromb Haemost. 1998 Jan;79(1):240. Thromb Haemost. 1998. PMID: 9459358 No abstract available.

8

Diagnosis of sickle-cell disease with a universal heteroduplex generator.

Wood N, Standen G, Hows J, Bradley B, Bidwell J. Wood N, et al. Among authors: bidwell j. Lancet. 1993 Dec 18-25;342(8886-8887):1519-20. doi: 10.1016/s0140-6736(05)80086-8. Lancet. 1993. PMID: 7902902

9

RT-PCR permits simultaneous genotyping of thiopurine S-methyltransferase allelic variants by multiplex induced heteroduplex analysis.

Wood N, Fraser A, Bidwell J, Standen G. Wood N, et al. Among authors: bidwell j. Hum Mutat. 2004 Jul;24(1):93-9. doi: 10.1002/humu.20057. Hum Mutat. 2004. PMID: 15221793

10

Optimisation and properties of a UHG for genotyping of hemoglobins S and C.

Wood N, Standen G, Old J, Bidwell J. Wood N, et al. Among authors: bidwell j. Hum Mutat. 1995;5(2):166-72. doi: 10.1002/humu.1380050210. Hum Mutat. 1995. PMID: 7749414

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