Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
Wnt signaling genes of murine chromosome 15 are involved in sex-affected pathways of inflammatory arthritis.
Kudryavtseva E, Forde TS, Pucker AD, Adarichev VA.
Arthritis Rheum. 2012 Apr;64(4):1057-68. doi: 10.1002/art.33414. Epub 2011 Oct 17.
Related citations
Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.
Sakazume S, Ohashi H, Sasaki Y, Harada N, Nakanishi K, Sato H, Emi M, Endoh K, Sohma R, Kido Y, Nagai T, Kubota T.
Hum Genet. 2012 Jan;131(1):121-30. doi: 10.1007/s00439-011-1051-4. Epub 2011 Jul 7.
Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.
Chen Y, Liu YJ, Pei YF, Yang TL, Deng FY, Liu XG, Li DY, Deng HW.
Obesity (Silver Spring). 2011 Jun;19(6):1229-34. doi: 10.1038/oby.2010.323. Epub 2011 Jan 13.
Frequent loss of heterozygosity in the β2-microglobulin region of chromosome 15 in primary human tumors.
Maleno I, Aptsiauri N, Cabrera T, Gallego A, Paschen A, López-Nevot MA, Garrido F.
Immunogenetics. 2011 Feb;63(2):65-71. doi: 10.1007/s00251-010-0494-4. Epub 2010 Nov 18.
Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15.
Sharp AJ, Migliavacca E, Dupre Y, Stathaki E, Sailani MR, Baumer A, Schinzel A, Mackay DJ, Robinson DO, Cobellis G, Cobellis L, Brunner HG, Steiner B, Antonarakis SE.
Genome Res. 2010 Sep;20(9):1271-8. doi: 10.1101/gr.108597.110. Epub 2010 Jul 14.
Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.
Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K.
Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857.
Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity.
Koç A, Onur SO, Ergün MA, Perçin EF.
Asian J Androl. 2009 Sep;11(5):617-22. doi: 10.1038/aja.2009.37. Epub 2009 Aug 24.
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15.
Keskitalo K, Broms U, Heliövaara M, Ripatti S, Surakka I, Perola M, Pitkäniemi J, Peltonen L, Aromaa A, Kaprio J.
Hum Mol Genet. 2009 Oct 15;18(20):4007-12. doi: 10.1093/hmg/ddp322. Epub 2009 Jul 23.
Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15.
Jovanović-Privrodski JD, Kavecan II, Obrenović MR, Buonadonna LA, Bukvić NM.
Pediatr Neurol. 2009 Jul;41(1):65-7. doi: 10.1016/j.pediatrneurol.2009.02.004.
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.
Manolakos E, Vetro A, Kitmirides S, Papoulidis I, Kosyakova N, Mrasek K, Weise A, Agapitos E, Orru S, Peitsidis P, Liehr T, Petersen MB.
Prenat Diagn. 2009 Sep;29(9):884-8. doi: 10.1002/pd.2295. No abstract available.
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on