Tinlin S - 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: tinlin s. 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

The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.

James PD, Notley C, Hegadorn C, Leggo J, Tuttle A, Tinlin S, Brown C, Andrews C, Labelle A, Chirinian Y, O'Brien L, Othman M, Rivard G, Rapson D, Hough C, Lillicrap D. James PD, et al. Among authors: tinlin s. Blood. 2007 Jan 1;109(1):145-54. doi: 10.1182/blood-2006-05-021105.. Blood. 2007. PMID: 17190853 Free article.

3

The Factor VIII acute phase response requires the participation of NFkappaB and C/EBP.

Begbie M, Notley C, Tinlin S, Sawyer L, Lillicrap D. Begbie M, et al. Among authors: tinlin s. Thromb Haemost. 2000 Aug;84(2):216-22. Thromb Haemost. 2000. PMID: 10959692

4

The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles.

Bowman M, Tuttle A, Notley C, Brown C, Tinlin S, Deforest M, Leggo J, Blanchette VS, Lillicrap D, James P; Association of Hemophilia Clinic Directors of Canada. Bowman M, et al. Among authors: tinlin s. J Thromb Haemost. 2013 Mar;11(3):512-20. doi: 10.1111/jth.12130. J Thromb Haemost. 2013. PMID: 23311757 Free PMC article.

5

Aberrant splicing and premature termination of transcription of the FVIII gene as a cause of severe canine hemophilia A: similarities with the intron 22 inversion mutation in human hemophilia.

Hough C, Kamisue S, Cameron C, Notley C, Tinlin S, Giles A, Lillicrap D. Hough C, et al. Among authors: tinlin s. Thromb Haemost. 2002 Apr;87(4):659-65. Thromb Haemost. 2002. PMID: 12008949

6

Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia A mice.

Brown BD, Shi CX, Rawle FE, Tinlin S, McKinven A, Hough C, Graham FL, Lillicrap D. Brown BD, et al. Among authors: tinlin s. J Thromb Haemost. 2004 Jan;2(1):111-8. doi: 10.1111/j.1538-7836.2004.00552.x. J Thromb Haemost. 2004. PMID: 14717974 Free article.

7

Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs.

Gallo-Penn AM, Shirley PS, Andrews JL, Tinlin S, Webster S, Cameron C, Hough C, Notley C, Lillicrap D, Kaleko M, Connelly S. Gallo-Penn AM, et al. Among authors: tinlin s. Blood. 2001 Jan 1;97(1):107-13. doi: 10.1182/blood.v97.1.107. Blood. 2001. PMID: 11133749 Free article.

8

The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.

Rydz N, Leggo J, Tinlin S, James P, Lillicrap D. Rydz N, et al. Among authors: tinlin s. Am J Hematol. 2013 Dec;88(12):1030-4. doi: 10.1002/ajh.23557. Epub 2013 Sep 9. Am J Hematol. 2013. PMID: 23913812 Free article. Review.

9

Heterogeneity of the immune response to adenovirus-mediated factor VIII gene therapy in different inbred hemophilic mouse strains.

Rawle FE, Shi CX, Brown B, McKinven A, Tinlin S, Graham FL, Hough C, Lillicrap D. Rawle FE, et al. Among authors: tinlin s. J Gene Med. 2004 Dec;6(12):1358-68. doi: 10.1002/jgm.624. J Gene Med. 2004. PMID: 15493040

10

In vivo evaluation of an adenoviral vector encoding canine factor VIII: high-level, sustained expression in hemophiliac mice.

Gallo-Penn AM, Shirley PS, Andrews JL, Kayda DB, Pinkstaff AM, Kaloss M, Tinlin S, Cameron C, Notley C, Hough C, Lillicrap D, Kaleko M, Connelly S. Gallo-Penn AM, et al. Among authors: tinlin s. Hum Gene Ther. 1999 Jul 20;10(11):1791-802. doi: 10.1089/10430349950017473. Hum Gene Ther. 1999. PMID: 10446919

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