Shedlovsky A - Search Results

1

Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse.

Symula DJ, Shedlovsky A, Dove WF. Symula DJ, et al. Among authors: shedlovsky a. Mamm Genome. 1997 Feb;8(2):98-101. doi: 10.1007/s003359900366. Mamm Genome. 1997. PMID: 9060407

2

Meiotic mapping of murine chromosome 17: the string of loci around l(17)-2Pas.

King TR, Dove WF, Guénet JL, Herrmann BG, Shedlovsky A. King TR, et al. Among authors: shedlovsky a. Mamm Genome. 1991;1(1):37-46. doi: 10.1007/BF00350844. Mamm Genome. 1991. PMID: 1794044

3

Pahhph-5: a mouse mutant deficient in phenylalanine hydroxylase.

McDonald JD, Bode VC, Dove WF, Shedlovsky A. McDonald JD, et al. Among authors: shedlovsky a. Proc Natl Acad Sci U S A. 1990 Mar;87(5):1965-7. doi: 10.1073/pnas.87.5.1965. Proc Natl Acad Sci U S A. 1990. PMID: 2308957 Free PMC article.

4

Mapping to molecular resolution in the T to H-2 region of the mouse genome with a nested set of meiotic recombinants.

King TR, Dove WF, Herrmann B, Moser AR, Shedlovsky A. King TR, et al. Among authors: shedlovsky a. Proc Natl Acad Sci U S A. 1989 Jan;86(1):222-6. doi: 10.1073/pnas.86.1.222. Proc Natl Acad Sci U S A. 1989. PMID: 2911572 Free PMC article.

5

Saturation germ line mutagenesis of the murine t region including a lethal allele at the quaking locus.

Shedlovsky A, King TR, Dove WF. Shedlovsky A, et al. Proc Natl Acad Sci U S A. 1988 Jan;85(1):180-4. doi: 10.1073/pnas.85.1.180. Proc Natl Acad Sci U S A. 1988. PMID: 3422415 Free PMC article.

6

Detailed physical and genetic mapping in the region of plasminogen, D17Rp17e, and quaking.

Cox RD, Whittington J, Shedlovsky A, Connelly CS, Dove WF, Goldsworthy M, Larin Z, Lehrach H. Cox RD, et al. Among authors: shedlovsky a. Mamm Genome. 1993 Dec;4(12):687-94. doi: 10.1007/BF00357791. Mamm Genome. 1993. PMID: 8111116

7

Mouse models of human phenylketonuria.

Shedlovsky A, McDonald JD, Symula D, Dove WF. Shedlovsky A, et al. Genetics. 1993 Aug;134(4):1205-10. doi: 10.1093/genetics/134.4.1205. Genetics. 1993. PMID: 8375656 Free PMC article.

8

A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport.

Symula DJ, Shedlovsky A, Guillery EN, Dove WF. Symula DJ, et al. Among authors: shedlovsky a. Mamm Genome. 1997 Feb;8(2):102-7. doi: 10.1007/s003359900367. Mamm Genome. 1997. PMID: 9060408

9

Identification of Mom7, a novel modifier of Apc(Min/+) on mouse chromosome 18.

Kwong LN, Shedlovsky A, Biehl BS, Clipson L, Pasch CA, Dove WF. Kwong LN, et al. Among authors: shedlovsky a. Genetics. 2007 Jun;176(2):1237-44. doi: 10.1534/genetics.107.071217. Epub 2007 Apr 15. Genetics. 2007. PMID: 17435219 Free PMC article.

10

A strategy to identify dominant point mutant modifiers of a quantitative trait.

Dove WF, Shedlovsky A, Clipson L, Amos-Landgraf JM, Halberg RB, Krentz KJ, Boehm FJ, Newton MA, Adams DJ, Keane TM. Dove WF, et al. Among authors: shedlovsky a. G3 (Bethesda). 2014 Apr 17;4(6):1113-21. doi: 10.1534/g3.114.010595. G3 (Bethesda). 2014. PMID: 24747760 Free PMC article.

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