Swank RT - Search Results

1

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.

Keller SA, Jones JM, Boyle A, Barrow LL, Killen PD, Green DG, Kapousta NV, Hitchcock PF, Swank RT, Meisler MH. Keller SA, et al. Among authors: swank rt. Genomics. 1994 Sep 15;23(2):309-20. doi: 10.1006/geno.1994.1506. Genomics. 1994. PMID: 7835879 Free article.

2

Identification of genes within the Krd deletion on mouse chromosome 19.

Ji W, Herron B, Jones JM, Jenkins NA, Gilbert DJ, Copeland NG, Swank R, Flaherty L, Meisler MH. Ji W, et al. Mamm Genome. 1999 Apr;10(4):399-401. doi: 10.1007/s003359901010. Mamm Genome. 1999. PMID: 10087301 Free article. No abstract available.

3

Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm.

O'Brien EP, Novak EK, Keller SA, Poirier C, Guénet JL, Swank RT. O'Brien EP, et al. Among authors: swank rt. Mamm Genome. 1994 Jun;5(6):356-60. doi: 10.1007/BF00356554. Mamm Genome. 1994. PMID: 8043950 Free article.

4

Pigmentation and lysosome function in mice homozygous for both pale ear and beige-J pigment genes.

Novak EK, Swank RT, Meisler MH. Novak EK, et al. Among authors: swank rt. Genet Res. 1980 Apr;35(2):195-204. doi: 10.1017/s001667230001404x. Genet Res. 1980. PMID: 7390156 No abstract available.

5

The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene.

Suzuki T, Li W, Zhang Q, Novak EK, Sviderskaya EV, Wilson A, Bennett DC, Roe BA, Swank RT, Spritz RA. Suzuki T, et al. Among authors: swank rt. Genomics. 2001 Nov;78(1-2):30-7. doi: 10.1006/geno.2001.6644. Genomics. 2001. PMID: 11707070

6

An integrated genetic map of the pearl locus of mouse chromosome 13.

Seymour AB, Yanak BL, O'Brien EP, Rusiniak ME, Novak EK, Pinto LH, Swank RT, Gorin MB. Seymour AB, et al. Among authors: swank rt. Genome Res. 1996 Jun;6(6):538-44. doi: 10.1101/gr.6.6.538. Genome Res. 1996. PMID: 8828042 Free article.

7

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. Among authors: swank rt. 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.

8

Genomic structure of the mouse Ap3b1 gene in normal and pearl mice.

Feng L, Rigatti BW, Novak EK, Gorin MB, Swank RT. Feng L, et al. Among authors: swank rt. Genomics. 2000 Nov 1;69(3):370-9. doi: 10.1006/geno.2000.6350. Genomics. 2000. PMID: 11056055

9

The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation.

Suzuki T, Oiso N, Gautam R, Novak EK, Panthier JJ, Suprabha PG, Vida T, Swank RT, Spritz RA. Suzuki T, et al. Among authors: swank rt. Proc Natl Acad Sci U S A. 2003 Feb 4;100(3):1146-50. doi: 10.1073/pnas.0237292100. Epub 2003 Jan 21. Proc Natl Acad Sci U S A. 2003. PMID: 12538872 Free PMC article.

10

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: swank rt. Blood. 1994 Jun 1;83(11):3225-31. Blood. 1994. PMID: 8193357 Free article.

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