Mohlke KL - Search Results

1

von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.

Nichols WC, Cooney KA, Mohlke KL, Ballew JD, Yang A, Bruck ME, Reddington M, Novak EK, Swank RT, Ginsburg D. Nichols WC, et al. Among authors: mohlke kl. Blood. 1994 Jun 1;83(11):3225-31. Blood. 1994. PMID: 8193357 Free article.

2

von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.

Nichols WC, Cooney KA, Mohlke KL, Ballew JD, Yang A, Bruck ME, Reddington M, Novak EK, Swank RT, Ginsburg D. Nichols WC, et al. Among authors: mohlke kl. Blood. 1995 Sep 15;86(6):2461. Blood. 1995. PMID: 7662996 Free article. No abstract available.

3

Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse chromosome 6.

Barrow LL, Simin K, Mohlke K, Nichols WC, Ginsburg D, Meisler MH. Barrow LL, et al. Mamm Genome. 1993;4(6):343-5. doi: 10.1007/BF00357095. Mamm Genome. 1993. PMID: 8318738 Free article. No abstract available.

4

A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processing.

Mohlke KL, Nichols WC, Rehemtulla A, Kaufman RJ, Fagerström HM, Ritvanen KL, Kekomăki R, Ginsburg D. Mohlke KL, et al. Br J Haematol. 1996 Oct;95(1):184-91. doi: 10.1046/j.1365-2141.1996.7572377.x. Br J Haematol. 1996. PMID: 8857958

5

A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11.

Mohlke KL, Nichols WC, Westrick RJ, Novak EK, Cooney KA, Swank RT, Ginsburg D. Mohlke KL, et al. Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15352-7. doi: 10.1073/pnas.93.26.15352. Proc Natl Acad Sci U S A. 1996. PMID: 8986815 Free PMC article.

6

von Willebrand disease and quantitative variation in von Willebrand factor.

Mohlke KL, Ginsburg D. Mohlke KL, et al. J Lab Clin Med. 1997 Sep;130(3):252-61. doi: 10.1016/s0022-2143(97)90019-6. J Lab Clin Med. 1997. PMID: 9341984 Review. No abstract available.

7

Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.

Mohlke KL, Purkayastha AA, Westrick RJ, Ginsburg D. Mohlke KL, et al. Genomics. 1998 Nov 15;54(1):19-30. doi: 10.1006/geno.1998.5553. Genomics. 1998. PMID: 9806826

8

Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase.

Mohlke KL, Purkayastha AA, Westrick RJ, Smith PL, Petryniak B, Lowe JB, Ginsburg D. Mohlke KL, et al. Cell. 1999 Jan 8;96(1):111-20. doi: 10.1016/s0092-8674(00)80964-2. Cell. 1999. PMID: 9989502 Free article.

9

The molecular basis of von Willebrand disease.

Mohlke KL, Nichols WC, Ginsburg D. Mohlke KL, et al. Int J Clin Lab Res. 1999;29(1):1-7. doi: 10.1007/s005990050054. Int J Clin Lab Res. 1999. PMID: 10356656 Review.

10

Spontaneous Irs1 passenger mutation linked to a gene-targeted SerpinB2 allele.

Westrick RJ, Mohlke KL, Korepta LM, Yang AY, Zhu G, Manning SL, Winn ME, Dougherty KM, Ginsburg D. Westrick RJ, et al. Among authors: mohlke kl. Proc Natl Acad Sci U S A. 2010 Sep 28;107(39):16904-9. doi: 10.1073/pnas.1012050107. Epub 2010 Sep 13. Proc Natl Acad Sci U S A. 2010. PMID: 20837540 Free PMC article.

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