Harrison WR - Search Results

1

Smcy transgene does not rescue spermatogenesis in sex-reversed mice.

Agulnik AI, Harrison WR, Bishop CE. Agulnik AI, et al. Among authors: harrison wr. Mamm Genome. 2001 Feb;12(2):112-6. doi: 10.1007/s003350010249. Mamm Genome. 2001. PMID: 11210179

2

A transgenic insertion upstream of sox9 is associated with dominant XX sex reversal in the mouse.

Bishop CE, Whitworth DJ, Qin Y, Agoulnik AI, Agoulnik IU, Harrison WR, Behringer RR, Overbeek PA. Bishop CE, et al. Among authors: harrison wr. Nat Genet. 2000 Dec;26(4):490-4. doi: 10.1038/82652. Nat Genet. 2000. PMID: 11101852

3

Generation of rat mutants using a coat color-tagged Sleeping Beauty transposon system.

Lu B, Geurts AM, Poirier C, Petit DC, Harrison W, Overbeek PA, Bishop CE. Lu B, et al. Mamm Genome. 2007 May;18(5):338-46. doi: 10.1007/s00335-007-9025-5. Epub 2007 Jun 8. Mamm Genome. 2007. PMID: 17557177

4

A transgenic insertion causing cryptorchidism in mice.

Overbeek PA, Gorlov IP, Sutherland RW, Houston JB, Harrison WR, Boettger-Tong HL, Bishop CE, Agoulnik AI. Overbeek PA, et al. Among authors: harrison wr. Genesis. 2001 May;30(1):26-35. doi: 10.1002/gene.1029. Genesis. 2001. PMID: 11353515

5

A transgenic insertion on mouse chromosome 17 inactivates a novel immunoglobulin superfamily gene potentially involved in sperm-egg fusion.

Lorenzetti D, Poirier C, Zhao M, Overbeek PA, Harrison W, Bishop CE. Lorenzetti D, et al. Mamm Genome. 2014 Apr;25(3-4):141-8. doi: 10.1007/s00335-013-9491-x. Epub 2013 Nov 26. Mamm Genome. 2014. PMID: 24275887

6

YAC rescue of downless locus mutations in mice.

Majumder K, Shawlot W, Schuster G, Harrison W, Elder FF, Overbeek PA. Majumder K, et al. Mamm Genome. 1998 Nov;9(11):863-8. doi: 10.1007/s003359900884. Mamm Genome. 1998. PMID: 9799834

7

A mutation in the inner mitochondrial membrane peptidase 2-like gene (Immp2l) affects mitochondrial function and impairs fertility in mice.

Lu B, Poirier C, Gaspar T, Gratzke C, Harrison W, Busija D, Matzuk MM, Andersson KE, Overbeek PA, Bishop CE. Lu B, et al. Biol Reprod. 2008 Apr;78(4):601-10. doi: 10.1095/biolreprod.107.065987. Epub 2007 Dec 19. Biol Reprod. 2008. PMID: 18094351

8

Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3.

Robinson ML, Allen CE, Davy BE, Durfee WJ, Elder FF, Elliott CS, Harrison WR. Robinson ML, et al. Among authors: harrison wr. Mamm Genome. 2002 Nov;13(11):625-32. doi: 10.1007/s00335-002-2201-8. Mamm Genome. 2002. PMID: 12461648

9

exma: an X-linked insertional mutation that disrupts forebrain and eye development.

Cunningham D, Xiao Q, Chatterjee A, Sulik K, Juriloff D, Elder F, Harrison W, Schuster G, Overbeek PA, Herman GE. Cunningham D, et al. Mamm Genome. 2002 Apr;13(4):179-85. doi: 10.1007/s00335-001-2121-z. Mamm Genome. 2002. PMID: 11956759

10

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al. Hecht JT, et al. Among authors: harrison wr. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

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