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Items: 1 to 50 of 100

1.

Identification of an HMGB3 frameshift mutation in a family with an X-linked colobomatous microphthalmia syndrome using whole-genome and X-exome sequencing.

Scott AF, Mohr DW, Kasch LM, Barton JA, Pittiglio R, Ingersoll R, Craig B, Marosy BA, Doheny KF, Bromley WC, Roderick TH, Chassaing N, Calvas P, Prabhu SS, Jabs EW.

JAMA Ophthalmol. 2014 Oct;132(10):1215-20. doi: 10.1001/jamaophthalmol.2014.1731.

PMID:
24993872
2.

Mouse models of ocular diseases.

Chang B, Hawes NL, Hurd RE, Wang J, Howell D, Davisson MT, Roderick TH, Nusinowitz S, Heckenlively JR.

Vis Neurosci. 2005 Sep-Oct;22(5):587-93.

PMID:
16332269
3.

Heritability of life span in mice and its implication for direct and indirect selection for longevity.

Klebanov S, Flurkey K, Roderick TH, Archer JR, Astle MC, Chen J, Harrison DE.

Genetica. 2000;110(3):209-18.

PMID:
11766841
4.

Maximum life spans in mice are extended by wild strain alleles.

Klebanov S, Astle CM, Roderick TH, Flurkey K, Archer JR, Chen J, Harrison DE.

Exp Biol Med (Maywood). 2001 Oct;226(9):854-9.

PMID:
11568309
5.

Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.

Cook SA, Akeson EC, Calvano C, Johnson KR, Mandell J, Hawes NL, Bronson RT, Roderick TH, Davisson MT.

Cytogenet Cell Genet. 2001;93(1-2):77-82.

PMID:
11474184
6.

Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.

Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR.

Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57.

PMID:
10967077
7.

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.

Akhmedov NB, Piriev NI, Chang B, Rapoport AL, Hawes NL, Nishina PM, Nusinowitz S, Heckenlively JR, Roderick TH, Kozak CA, Danciger M, Davisson MT, Farber DB.

Proc Natl Acad Sci U S A. 2000 May 9;97(10):5551-6.

8.

Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract.

Smith RS, Hawes NL, Chang B, Roderick TH, Akeson EC, Heckenlively JR, Gong X, Wang X, Davisson MT.

Genomics. 2000 Feb 1;63(3):314-20.

PMID:
10704279
9.

Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse.

Chang B, Hawes NL, Roderick TH, Smith RS, Heckenlively JR, Horwitz J, Davisson MT.

Mol Vis. 1999 Sep 10;5:21.

10.

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

Chang B, Smith RS, Hawes NL, Anderson MG, Zabaleta A, Savinova O, Roderick TH, Heckenlively JR, Davisson MT, John SW.

Nat Genet. 1999 Apr;21(4):405-9.

PMID:
10192392
11.

Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice.

John SW, Smith RS, Savinova OV, Hawes NL, Chang B, Turnbull D, Davisson M, Roderick TH, Heckenlively JR.

Invest Ophthalmol Vis Sci. 1998 May;39(6):951-62. Erratum in: Invest Ophthalmol Vis Sci 1998 Aug;39(9):1641.

PMID:
9579474
12.

A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse.

Roderick TH, Chang B, Hawes NL, Heckenlively JR.

Genomics. 1997 Jun 15;42(3):393-6.

PMID:
9205110
13.

Selection for maximum longevity in mice.

Harrison DE, Roderick TH.

Exp Gerontol. 1997 Jan-Apr;32(1-2):65-78. Review.

PMID:
9088903
14.

Chromosomal localization of a new mouse lens opacity gene (lop18)

Chang B, Hawes NL, Smith RS, Heckenlively JR, Davisson MT, Roderick TH.

Genomics. 1996 Aug 15;36(1):171-3. Erratum in: Genomics 1997 Jan 15;39(2):237.

PMID:
8812430
15.

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.

Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, Vidgen D, Hoover F, Goldman D, Kalnins VI, Roderick TH, Taylor BA, Hankin MH, McInnes RR.

Nat Genet. 1996 Apr;12(4):376-84.

PMID:
8630490
16.

Corn1: a mouse model for corneal surface disease and neovascularization.

Smith RS, Hawes NL, Kuhlmann SD, Heckenlively JR, Chang B, Roderick TH, Sundberg JP.

Invest Ophthalmol Vis Sci. 1996 Feb;37(2):397-404.

PMID:
8603845
17.

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Heckenlively JR, Chang B, Erway LC, Peng C, Hawes NL, Hageman GS, Roderick TH.

Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11100-4.

18.

Allele capture by selection for flanking markers: a new method for analyzing multigenic traits.

Harrison DE, Roderick TH, Paigen K.

Growth Dev Aging. 1995 Fall;59(3):73-6. No abstract available.

PMID:
8675370
19.

Microphthalmia and associated abnormalities in inbred black mice.

Smith RS, Roderick TH, Sundberg JP.

Lab Anim Sci. 1994 Dec;44(6):551-60. Review.

PMID:
7898027
20.

Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis.

Chang B, Bronson RT, Hawes NL, Roderick TH, Peng C, Hageman GS, Heckenlively JR.

Invest Ophthalmol Vis Sci. 1994 Mar;35(3):1071-6.

PMID:
8125718
21.

New mouse primary retinal degeneration (rd-3).

Chang B, Heckenlively JR, Hawes NL, Roderick TH.

Genomics. 1993 Apr;16(1):45-9.

PMID:
8486383
22.

Inference of order in genetic systems.

Guidi JN, Roderick TH.

Proc Int Conf Intell Syst Mol Biol. 1993;1:163-71.

PMID:
7584332
23.

Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes.

Runge PE, Hawes NL, Heckenlively JR, Langley SH, Roderick TH.

Invest Ophthalmol Vis Sci. 1992 Oct;33(11):3202-8. Review.

PMID:
1399425
24.

Genetic linkage analysis of the murine developmental mutant velvet coat (Ve) and the distal chromosome 15 developmental genes Hox-3.1, Rar-g, Wnt-1, and Krt-2.

Hart CP, Compton JG, Langley SH, Hunihan L, LeClair KP, Zelent A, Roderick TH, Ruddle FH.

J Exp Zool. 1992 Aug 1;263(1):83-95.

PMID:
1379621
25.

Comparative map for mice and humans.

Nadeau JH, Davisson MT, Doolittle DP, Grant P, Hillyard AL, Kosowsky MR, Roderick TH.

Mamm Genome. 1992;3(9):480-536. Review. No abstract available.

PMID:
1392257
26.

FVB/N: an inbred mouse strain preferable for transgenic analyses.

Taketo M, Schroeder AC, Mobraaten LE, Gunning KB, Hanten G, Fox RR, Roderick TH, Stewart CL, Lilly F, Hansen CT, et al.

Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2065-9.

27.

Comparative map for mice and humans.

Nadeau JH, Davisson MT, Doolittle DP, Grant P, Hillyard AL, Kosowsky M, Roderick TH.

Mamm Genome. 1991;1 Spec No:S461-515. Review. No abstract available.

PMID:
1799811
28.

Mouse chromosome 1.

Seldin MF, Roderick TH, Paigen B.

Mamm Genome. 1991;1 Spec No:S1-17. Review. No abstract available.

PMID:
1799793
29.

The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15.

Davisson MT, Roderick TH, Akeson EC, Hawes NL, Sweet HO.

Genet Res. 1990 Oct-Dec;56(2-3):167-78.

PMID:
2272507
30.

The use of comparative mapping to identify loci involved in human carcinogenesis.

Roderick TH, Hillyard AL, Doolittle DP, Davisson MT.

Birth Defects Orig Artic Ser. 1990;26(1):141-78. Review. No abstract available.

PMID:
2224076
31.

Screening for mouse retinal degenerations. II. Molossinus MOLC and MOLD strains.

Winston JV, Heckenlively JR, Roderick TH.

Doc Ophthalmol. 1989 Mar;71(3):241-52.

PMID:
2776629
32.

Screening for mouse retinal degenerations. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology.

Heckenlively JR, Winston JV, Roderick TH.

Doc Ophthalmol. 1989 Mar;71(3):229-39.

PMID:
2776628
33.
34.

Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice.

Schiffer SP, Prochazka M, Jezyk PF, Roderick TH, Yudkoff M, Patterson DF.

Biochem Genet. 1989 Feb;27(1-2):47-58.

PMID:
2712823
35.

Report of the committee on comparative mapping.

Lalley PA, Davison MT, Graves JA, O'Brien SJ, Womack JE, Roderick TH, Creau-Goldberg N, Hillyard AL, Doolittle DP, Rogers JA.

Cytogenet Cell Genet. 1989;51(1-4):503-32. Review. No abstract available.

PMID:
2676382
36.

Juvenile spermatogonial depletion (jsd): a genetic defect of germ cell proliferation of male mice.

Beamer WG, Cunliffe-Beamer TL, Shultz KL, Langley SH, Roderick TH.

Biol Reprod. 1988 May;38(4):899-908.

PMID:
3401545
37.

The Hox-2 homeo box gene complex on mouse chromosome 11 is closely linked to Re.

Hart CP, Dalton DK, Nichols L, Hunihan L, Roderick TH, Langley SH, Taylor BA, Ruddle FH.

Genetics. 1988 Feb;118(2):319-27.

38.

Report of the committee on comparative mapping.

Lalley PA, Davisson MT, Graves JA, O'Brien SJ, Roderick TH, Doolittle DP, Hillyard AL.

Cytogenet Cell Genet. 1988;49(1-3):227-35. No abstract available.

PMID:
3203543
39.

Mapping X-linked ophthalmic diseases. III. Provisional assignment of the locus for blue cone monochromacy to Xq28.

Lewis RA, Holcomb JD, Bromley WC, Wilson MC, Roderick TH, Hejtmancik JF.

Arch Ophthalmol. 1987 Aug;105(8):1055-9.

PMID:
2888453
40.

Different genes specify hyporesponsiveness to seizures induced by caffeine and the benzodiazepine inverse agonist, DMCM.

Seale TW, Abla KA, Roderick TH, Rennert OM, Carney JM.

Pharmacol Biochem Behav. 1987 Jul;27(3):451-6.

PMID:
2821552
41.
42.

Report on the committee on comparative mapping.

Lalley PA, O'Brien SJ, Créau-Goldberg N, Davisson MT, Roderick TH, Echard G, Womack JE, Graves JM, Doolittle DP, Guidi JN.

Cytogenet Cell Genet. 1987;46(1-4):367-89. No abstract available.

PMID:
3507284
43.

Twenty-five years in medical genetics and experimental mammalian genetics with particular reference to the gene map of mouse and man.

McKusick VA, Roderick TH.

Birth Defects Orig Artic Ser. 1987;23(3):1-17. Review. No abstract available.

PMID:
3307931
44.

Electroretinograms in carriers of blue cone monochromatism.

Berson EL, Sandberg MA, Maguire A, Bromley WC, Roderick TH.

Am J Ophthalmol. 1986 Aug 15;102(2):254-61.

PMID:
3488684
45.

Complex genetic determinants of susceptibility to methylxanthine-induced locomotor activity changes.

Seale TW, Roderick TH, Johnson P, Logan L, Rennert OM, Carney JM.

Pharmacol Biochem Behav. 1986 May;24(5):1333-41.

PMID:
3725837
46.

Mouse chromosome fragility.

Sanz MM, Jenkins EC, Brown WT, Davisson MT, Kevin MJ, Roderick TH, Silverman WP, Wisniewski HM.

Am J Med Genet. 1986 Jan-Feb;23(1-2):491-509.

PMID:
2937303
47.

Rapid mutations in mice?

Green MC, Bailey DW, Green EL, Roderick TH, Russell ES.

Science. 1985 Dec 20;230(4732):1407-8. No abstract available.

PMID:
17749681
48.

A single gene difference determines relative susceptibility to caffeine-induced lethality in SWR and CBA inbred mice.

Seale TW, Johnson P, Roderick TH, Carney JM, Rennert OM.

Pharmacol Biochem Behav. 1985 Aug;23(2):275-8.

PMID:
4059313
49.

Genetic and developmental studies of a new mouse mutation that produces otocephaly.

Juriloff DM, Sulik KK, Roderick TH, Hogan BK.

J Craniofac Genet Dev Biol. 1985;5(2):121-45.

PMID:
4019727
50.

Some unusual genetic characteristics of BALB/c and evidence for genetic variation among BALB/c substrains.

Roderick TH, Langley SH, Leiter EH.

Curr Top Microbiol Immunol. 1985;122:9-18. Review. No abstract available.

PMID:
3899524

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