Nolan P - Search Results

1

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

Alavizadeh A, Kiernan AE, Nolan P, Lo C, Steel KP, Bucan M. Alavizadeh A, et al. Among authors: nolan p. Dev Biol. 2001 Jun 1;234(1):244-60. doi: 10.1006/dbio.2001.0241. Dev Biol. 2001. PMID: 11356033 Free article.

2

Heterozygosity mapping of partially congenic lines: mapping of a semidominant neurological mutation, Wheels (Whl), on mouse chromosome 4.

Nolan PM, Sollars PJ, Bohne BA, Ewens WJ, Pickard GE, Bućan M. Nolan PM, et al. Genetics. 1995 May;140(1):245-54. doi: 10.1093/genetics/140.1.245. Genetics. 1995. PMID: 7635289 Free PMC article.

3

Cloning of a complementary deoxyribonucleic acid encoding the murine homolog of the very low density lipoprotein/apolipoprotein-E receptor: expression pattern and assignment of the gene to mouse chromosome 19.

Gåfvels ME, Paavola LG, Boyd CO, Nolan PM, Wittmaack F, Chawla A, Lazar MA, Bucan M, Angelin BO, Strauss JF 3rd. Gåfvels ME, et al. Among authors: nolan pm. Endocrinology. 1994 Jul;135(1):387-94. doi: 10.1210/endo.135.1.8013374. Endocrinology. 1994. PMID: 8013374

4

Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse.

Bućan M, Gatalica B, Nolan P, Chung A, Leroux A, Grossman MH, Nadeau JH, Emanuel BS, Budarf M. Bućan M, et al. Among authors: nolan p. Hum Mol Genet. 1993 Aug;2(8):1245-52. doi: 10.1093/hmg/2.8.1245. Hum Mol Genet. 1993. PMID: 8401507

5

Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels.

Pickard GE, Sollars PJ, Rinchik EM, Nolan PM, Bucan M. Pickard GE, et al. Among authors: nolan pm. Brain Res. 1995 Dec 24;705(1-2):255-66. doi: 10.1016/0006-8993(95)01171-4. Brain Res. 1995. PMID: 8821757 Free article.

6

Random mutagenesis screen for dominant behavioral mutations in mice.

Nolan PM, Kapfhamer D, Bućan M. Nolan PM, et al. Methods. 1997 Dec;13(4):379-95. doi: 10.1006/meth.1997.0545. Methods. 1997. PMID: 9480783 Free article. Review.

7

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson JA, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher EM, Martin J, Rastan S, Brown SD, Hunter J. Nolan PM, et al. Nat Genet. 2000 Aug;25(4):440-3. doi: 10.1038/78140. Nat Genet. 2000. PMID: 10932191

8

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.

Kiernan AE, Erven A, Voegeling S, Peters J, Nolan P, Hunter J, Bacon Y, Steel KP, Brown SD, Guénet JL. Kiernan AE, et al. Among authors: nolan p. Mamm Genome. 2002 Mar;13(3):142-8. doi: 10.1007/BF02684018. Mamm Genome. 2002. PMID: 11919684

9

Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse.

Kapfhamer D, Valladares O, Sun Y, Nolan PM, Rux JJ, Arnold SE, Veasey SC, Bućan M. Kapfhamer D, et al. Nat Genet. 2002 Oct;32(2):290-5. doi: 10.1038/ng991. Epub 2002 Sep 16. Nat Genet. 2002. PMID: 12244319

10

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.

Curtin JA, Quint E, Tsipouri V, Arkell RM, Cattanach B, Copp AJ, Henderson DJ, Spurr N, Stanier P, Fisher EM, Nolan PM, Steel KP, Brown SD, Gray IC, Murdoch JN. Curtin JA, et al. Among authors: nolan pm. Curr Biol. 2003 Jul 1;13(13):1129-33. doi: 10.1016/s0960-9822(03)00374-9. Curr Biol. 2003. PMID: 12842012 Free article.

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