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Results: 1 to 20 of 67

1.

Phenotypic connections in surprising places.

Linghu B, DeLisi C.

Genome Biol. 2010;11(4):116. doi: 10.1186/gb-2010-11-4-116. Epub 2010 Apr 28.

PMID:
20423531
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Complications associated with genetic background effects in models of experimental epilepsy.

Schauwecker PE.

Prog Brain Res. 2002;135:139-48. Review.

PMID:
12143336
[PubMed - indexed for MEDLINE]
3.

Systematic analysis, comparison, and integration of disease based human genetic association data and mouse genetic phenotypic information.

Zhang Y, De S, Garner JR, Smith K, Wang SA, Becker KG.

BMC Med Genomics. 2010 Jan 21;3:1. doi: 10.1186/1755-8794-3-1.

PMID:
20092628
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

DNA-based animal models of human disease: from genotype to phenotype.

Schook LB, Kuzmuk K, Adam S, Rund L, Chen K, Rogatcheva M, Mazur M, Pollock C, Counter C.

Dev Biol (Basel). 2008;132:15-25.

PMID:
18817282
[PubMed - indexed for MEDLINE]
5.

Domain interplay concept in animal models of neuropsychiatric disorders: a new strategy for high-throughput neurophenotyping research.

Kalueff AV, Ren-Patterson RF, LaPorte JL, Murphy DL.

Behav Brain Res. 2008 Apr 9;188(2):243-9. doi: 10.1016/j.bbr.2007.11.011. Epub 2007 Nov 22. Review.

PMID:
18164476
[PubMed - indexed for MEDLINE]
6.

Environmental epigenomics and disease susceptibility.

Jirtle RL, Skinner MK.

Nat Rev Genet. 2007 Apr;8(4):253-62. Review.

PMID:
17363974
[PubMed - indexed for MEDLINE]
7.

Mutant models for genes associated with schizophrenia.

Desbonnet L, Waddington JL, O'Tuathaigh CM.

Biochem Soc Trans. 2009 Feb;37(Pt 1):308-12. doi: 10.1042/BST0370308. Review.

PMID:
19143653
[PubMed - indexed for MEDLINE]
8.

Murine models of human acute myeloid leukemia.

Fortier JM, Graubert TA.

Cancer Treat Res. 2010;145:183-96. doi: 10.1007/978-0-387-69259-3_11. Review.

PMID:
20306252
[PubMed - indexed for MEDLINE]
9.

Genetic defects in muscular dystrophy.

Chandrasekharan K, Martin PT.

Methods Enzymol. 2010;479:291-322. doi: 10.1016/S0076-6879(10)79017-0. Review.

PMID:
20816173
[PubMed - indexed for MEDLINE]
10.

Poliovirus neurovirulence and attenuation, a conceptual framework.

John TJ.

Dev Biol Stand. 1993;78:117-9. Review. No abstract available.

PMID:
8388822
[PubMed - indexed for MEDLINE]
11.

The complexity of the genotype-phenotype relationship and the limitations of using genetic "markers" at the individual level.

Templeton AR.

Sci Context. 1998 Autumn-Winter;11(3-4):373-89.

PMID:
15168668
[PubMed - indexed for MEDLINE]
12.

Beyond Mendel: an evolving view of human genetic disease transmission.

Badano JL, Katsanis N.

Nat Rev Genet. 2002 Oct;3(10):779-89. Review.

PMID:
12360236
[PubMed - indexed for MEDLINE]
13.

Animal models for genetic neuromuscular diseases.

Vainzof M, Ayub-Guerrieri D, Onofre PC, Martins PC, Lopes VF, Zilberztajn D, Maia LS, Sell K, Yamamoto LU.

J Mol Neurosci. 2008 Mar;34(3):241-8. doi: 10.1007/s12031-007-9023-9. Epub 2008 Jan 18. Review.

PMID:
18202836
[PubMed - indexed for MEDLINE]
14.

[Malignancy risk and Wiedemann-Beckwith syndrome: what follow-up to provide?].

Santiago J, Muszlak M, Samson C, Goulois E, Glorion A, Atale A, Ranaivoarivony V, Hebert JC, Bouvier R, Cordier MP.

Arch Pediatr. 2008 Sep;15(9):1498-502. doi: 10.1016/j.arcped.2008.06.009. Epub 2008 Jul 31. French.

PMID:
18674889
[PubMed - indexed for MEDLINE]
15.

Genetic and environmental modifiers of Alzheimer's disease phenotypes in the mouse.

Ryman D, Lamb BT.

Curr Alzheimer Res. 2006 Dec;3(5):465-73. Review.

PMID:
17168645
[PubMed - indexed for MEDLINE]
16.

NHEJ deficiency and disease.

Pierce AJ, Jasin M.

Mol Cell. 2001 Dec;8(6):1160-1.

PMID:
11885597
[PubMed - indexed for MEDLINE]
Free Article
17.

Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions.

Gardiner K, Fortna A, Bechtel L, Davisson MT.

Gene. 2003 Oct 30;318:137-47.

PMID:
14585506
[PubMed - indexed for MEDLINE]
18.

Animal models for the genetic study of human alcohol phenotypes.

Phillips T.

Alcohol Res Health. 2002;26(3):202-7.

PMID:
12875048
[PubMed - indexed for MEDLINE]
Free Article
19.

Sex-specific variability and a 'cage effect' independently mask a neuropathic pain quantitative trait locus detected in a whole genome scan.

Devor M, Gilad A, Arbilly M, Nissenbaum J, Yakir B, Raber P, Minert A, Pisanté A, Darvasi A.

Eur J Neurosci. 2007 Aug;26(3):681-8.

PMID:
17686043
[PubMed - indexed for MEDLINE]
20.

Is there a need for animal models of human genetic disorders in the post-genome era?

van Zutphen LF.

Comp Med. 2000 Feb;50(1):10-1. No abstract available.

PMID:
10987660
[PubMed - indexed for MEDLINE]

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