Lillicrap D - Search Results

1

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.

James PD, Paterson AD, Notley C, Cameron C, Hegadorn C, Tinlin S, Brown C, O'Brien L, Leggo J, Lillicrap D; ASSOCIATION OF HEMOPHILIA CLINIC DIRECTORS OF CANADA. James PD, et al. Among authors: lillicrap d. J Thromb Haemost. 2006 Apr;4(4):783-92. doi: 10.1111/j.1538-7836.2006.01860.x. J Thromb Haemost. 2006. PMID: 16634747 Free article.

2

Differential termination of primer extension: a novel, quantifiable method for detection of point mutations.

Picketts DJ, Cameron C, Taylor SA, Deugau KV, Lillicrap DP. Picketts DJ, et al. Among authors: lillicrap dp. Hum Genet. 1992 May;89(2):155-7. doi: 10.1007/BF00217115. Hum Genet. 1992. PMID: 1587524

3

Characterization of the original Christmas disease mutation (cysteine 206----serine): from clinical recognition to molecular pathogenesis.

Taylor SA, Duffin J, Cameron C, Teitel J, Garvey B, Lillicrap DP. Taylor SA, et al. Among authors: lillicrap dp. Thromb Haemost. 1992 Jan 23;67(1):63-5. Thromb Haemost. 1992. PMID: 1615485

4

Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemia.

Shepherd L, Cameron C, Galbraith P, Windsor S, Lillicrap D. Shepherd L, et al. Among authors: lillicrap d. Leuk Res. 1991;15(5):297-303. doi: 10.1016/0145-2126(91)90004-d. Leuk Res. 1991. PMID: 1675299

5

Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.

Murray EW, Giles AR, Lillicrap D. Murray EW, et al. Among authors: lillicrap d. Am J Hum Genet. 1992 Jan;50(1):199-207. Am J Hum Genet. 1992. PMID: 1729889 Free PMC article.

6

Recurring mutations at CpG dinucleotides in the region of the von Willebrand factor gene encoding the glycoprotein Ib binding domain, in patients with type IIB von Willebrand's disease.

Lillicrap D, Murray EW, Benford K, Blanchette VS, Rivard GE, Wensley R, Giles AR. Lillicrap D, et al. Br J Haematol. 1991 Dec;79(4):612-7. doi: 10.1111/j.1365-2141.1991.tb08089.x. Br J Haematol. 1991. PMID: 1772783

7

Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease.

Murray EW, Giles AR, Bridge PJ, Peake IR, Lillicrap DP. Murray EW, et al. Among authors: lillicrap dp. Blood. 1991 Apr 1;77(7):1476-83. Blood. 1991. PMID: 2009368 Free article.

8

Role of the liver-enriched transcription factor hepatocyte nuclear factor 1 in transcriptional regulation of the factor V111 gene.

McGlynn LK, Mueller CR, Begbie M, Notley CR, Lillicrap D. McGlynn LK, et al. Among authors: lillicrap d. Mol Cell Biol. 1996 May;16(5):1936-45. doi: 10.1128/MCB.16.5.1936. Mol Cell Biol. 1996. PMID: 8628260 Free PMC article.

9

von Willebrand disease: pathogenesis, classification, and management.

Murray EW, Lillicrap D. Murray EW, et al. Among authors: lillicrap d. Transfus Med Rev. 1996 Apr;10(2):93-110. doi: 10.1016/s0887-7963(96)80086-1. Transfus Med Rev. 1996. PMID: 8721967 Review. No abstract available.

10

The canine factor VIII cDNA and 5' flanking sequence.

Cameron C, Notley C, Hoyle S, McGlynn L, Hough C, Kamisue S, Giles A, Lillicrap D. Cameron C, et al. Among authors: lillicrap d. Thromb Haemost. 1998 Feb;79(2):317-22. Thromb Haemost. 1998. PMID: 9493583

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