Kerrebrock AW - Search Results

1

Serrate2 is disrupted in the mouse limb-development mutant syndactylism.

Sidow A, Bulotsky MS, Kerrebrock AW, Bronson RT, Daly MJ, Reeve MP, Hawkins TL, Birren BW, Jaenisch R, Lander ES. Sidow A, et al. Among authors: kerrebrock aw. Nature. 1997 Oct 16;389(6652):722-5. doi: 10.1038/39587. Nature. 1997. PMID: 9338782

2

Disruption of the nuclear hormone receptor RORalpha in staggerer mice.

Hamilton BA, Frankel WN, Kerrebrock AW, Hawkins TL, FitzHugh W, Kusumi K, Russell LB, Mueller KL, van Berkel V, Birren BW, Kruglyak L, Lander ES. Hamilton BA, et al. Among authors: kerrebrock aw. Nature. 1996 Feb 22;379(6567):736-9. doi: 10.1038/379736a0. Nature. 1996. PMID: 8602221

3

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

Kusumi K, Sun ES, Kerrebrock AW, Bronson RT, Chi DC, Bulotsky MS, Spencer JB, Birren BW, Frankel WN, Lander ES. Kusumi K, et al. Among authors: kerrebrock aw. Nat Genet. 1998 Jul;19(3):274-8. doi: 10.1038/961. Nat Genet. 1998. PMID: 9662403

4

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant.

Sidow A, Bulotsky MS, Kerrebrock AW, Birren BW, Altshuler D, Jaenisch R, Johnson KR, Lander ES. Sidow A, et al. Among authors: kerrebrock aw. Nat Genet. 1999 Sep;23(1):104-7. doi: 10.1038/12709. Nat Genet. 1999. PMID: 10471509

5

The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression.

Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, Daly MJ, Kruglyak L, Reeve MP, Nemhauser JL, Hawkins TL, Rubin EM, Lander ES. Hamilton BA, et al. Among authors: kerrebrock aw. Neuron. 1997 May;18(5):711-22. doi: 10.1016/s0896-6273(00)80312-8. Neuron. 1997. PMID: 9182797 Free article.

6

Identification of the Finnish founder mutation for diastrophic dysplasia (DTD).

Hästbacka J, Kerrebrock A, Mokkala K, Clines G, Lovett M, Kaitila I, de la Chapelle A, Lander ES. Hästbacka J, et al. Eur J Hum Genet. 1999 Sep;7(6):664-70. doi: 10.1038/sj.ejhg.5200361. Eur J Hum Genet. 1999. PMID: 10482955

7

Mei-S332, a Drosophila protein required for sister-chromatid cohesion, can localize to meiotic centromere regions.

Kerrebrock AW, Moore DP, Wu JS, Orr-Weaver TL. Kerrebrock AW, et al. Cell. 1995 Oct 20;83(2):247-56. doi: 10.1016/0092-8674(95)90166-3. Cell. 1995. PMID: 7585942 Free article.

8

The Drosophila mei-S332 gene promotes sister-chromatid cohesion in meiosis following kinetochore differentiation.

Kerrebrock AW, Miyazaki WY, Birnby D, Orr-Weaver TL. Kerrebrock AW, et al. Genetics. 1992 Apr;130(4):827-41. doi: 10.1093/genetics/130.4.827. Genetics. 1992. PMID: 1582560 Free PMC article.

9

The cohesion protein MEI-S332 localizes to condensed meiotic and mitotic centromeres until sister chromatids separate.

Moore DP, Page AW, Tang TT, Kerrebrock AW, Orr-Weaver TL. Moore DP, et al. Among authors: kerrebrock aw. J Cell Biol. 1998 Mar 9;140(5):1003-12. doi: 10.1083/jcb.140.5.1003. J Cell Biol. 1998. PMID: 9490715 Free PMC article.

10

Isolation and characterization of ribosomal DNA variants from Sciara coprophila.

Kerrebrock AW, Srivastava R, Gerbi SA. Kerrebrock AW, et al. J Mol Biol. 1989 Nov 5;210(1):1-13. doi: 10.1016/0022-2836(89)90286-6. J Mol Biol. 1989. PMID: 2555520

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