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Items: 18


Genetic architecture of atherosclerosis dissected by QTL analyses in three F2 intercrosses of apolipoprotein E-null mice on C57BL6/J, DBA/2J and 129S6/SvEvTac backgrounds.

Makhanova N, Morgan AP, Kayashima Y, Makhanov A, Hiller S, Zhilicheva S, Xu L, Pardo-Manuel de Villena F, Maeda N.

PLoS One. 2017 Aug 24;12(8):e0182882. doi: 10.1371/journal.pone.0182882. eCollection 2017.


Prader-Willi Syndrome: Clinical and Genetic Findings.

Butler MG, Thompson T.

Endocrinologist. 2000 Jul;10(4 Suppl 1):3S-16S.


Chronic exposure to ethanol in male mice may be associated with hearing loss in offspring.

Liang F, Diao L, Jiang N, Zhang J, Wang HJ, Zhou WH, Huang GY, Ma D.

Asian J Androl. 2015 Nov-Dec;17(6):985-90. doi: 10.4103/1008-682X.160267.


Identification of novel imprinted differentially methylated regions by global analysis of human-parthenogenetic-induced pluripotent stem cells.

Stelzer Y, Ronen D, Bock C, Boyle P, Meissner A, Benvenisty N.

Stem Cell Reports. 2013 Jun 4;1(1):79-89. doi: 10.1016/j.stemcr.2013.03.005. eCollection 2013.


Sex bias in copy number variation of olfactory receptor gene family depends on ethnicity.

Shadravan F.

Front Genet. 2013 Mar 14;4:32. doi: 10.3389/fgene.2013.00032. eCollection 2013.


Advanced paternal age increases the risk of schizophrenia and obsessive-compulsive disorder in a Chinese Han population.

Wu Y, Liu X, Luo H, Deng W, Zhao G, Wang Q, Zhang L, Ma X, Liu X, Murray RA, Collier DA, Li T.

Psychiatry Res. 2012 Aug 15;198(3):353-9. doi: 10.1016/j.psychres.2012.01.020. Epub 2012 Mar 16.


Epigenetic transgenerational actions of endocrine disruptors.

Skinner MK, Manikkam M, Guerrero-Bosagna C.

Reprod Toxicol. 2011 Apr;31(3):337-43. doi: 10.1016/j.reprotox.2010.10.012. Epub 2010 Nov 3.


Epigenetic transgenerational actions of environmental factors in disease etiology.

Skinner MK, Manikkam M, Guerrero-Bosagna C.

Trends Endocrinol Metab. 2010 Apr;21(4):214-22. doi: 10.1016/j.tem.2009.12.007. Epub 2010 Jan 14. Review.


Schizophrenia and birthplace of paternal and maternal grandfather in the Jerusalem perinatal cohort prospective study.

Harlap S, Perrin MC, Deutsch L, Kleinhaus K, Fennig S, Nahon D, Teitelbaum A, Friedlander Y, Malaspina D.

Schizophr Res. 2009 Jun;111(1-3):23-31. doi: 10.1016/j.schres.2009.03.022. Epub 2009 Apr 9.


Imprinting disorders and assisted reproductive technology.

Manipalviratn S, DeCherney A, Segars J.

Fertil Steril. 2009 Feb;91(2):305-15. doi: 10.1016/j.fertnstert.2009.01.002. Review.


Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E, Blasi F, Maestrini E, Broxholme J, Tzenova J, Weeks D, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC).

J Med Genet. 2005 Feb;42(2):132-7.


A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting.

Karason A, Gudjonsson JE, Upmanyu R, Antonsdottir AA, Hauksson VB, Runasdottir EH, Jonsson HH, Gudbjartsson DF, Frigge ML, Kong A, Stefansson K, Valdimarsson H, Gulcher JR.

Am J Hum Genet. 2003 Jan;72(1):125-31. Epub 2002 Dec 9.


RNA hairpins in noncoding regions of human brain and Caenorhabditis elegans mRNA are edited by adenosine deaminases that act on RNA.

Morse DP, Aruscavage PJ, Bass BL.

Proc Natl Acad Sci U S A. 2002 Jun 11;99(12):7906-11. Epub 2002 Jun 4.


A functional role for Tsix transcription in blocking Xist RNA accumulation but not in X-chromosome choice.

Stavropoulos N, Lu N, Lee JT.

Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10232-7. Epub 2001 Jul 31.


The ubiquitin-proteasome pathway and proteasome inhibitors.

Myung J, Kim KB, Crews CM.

Med Res Rev. 2001 Jul;21(4):245-73. Review.


Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.

Pujana MA, Nadal M, Gratacòs M, Peral B, Csiszar K, González-Sarmiento R, Sumoy L, Estivill X.

Genome Res. 2001 Jan;11(1):98-111.


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