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Select item 232755301.

Homozygous leptin receptor mutation due to uniparental disomy of chromosome 1: response to bariatric surgery.

Le Beyec J, Cugnet-Anceau C, Pépin D, Alili R, Cotillard A, Lacorte JM, Basdevant A, Laville M, Clément K.

J Clin Endocrinol Metab. 2013 Feb;98(2):E397-402. doi: 10.1210/jc.2012-2779. Epub 2012 Dec 28.

PMID:: 23275530; [PubMed - indexed for MEDLINE]

Select item 231682432.

Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML.

Beach DF, Barnoski BL, Aviv H, Patel V, Schwarting R, Strair R, Lachant NA.

Cancer Genet. 2012 Dec;205(12):665-8. doi: 10.1016/j.cancergen.2012.09.004. Epub 2012 Nov 16.

PMID:: 23168243; [PubMed - indexed for MEDLINE]

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Select item 230940743.

Association of the IL-10 gene family locus on chromosome 1 with juvenile idiopathic arthritis (JIA).

Omoyinmi E, Forabosco P, Hamaoui R, Bryant A, Hinks A, Ursu S; Childhood Arthritis Prospective Study (CAPS); BSPAR study group; Childhood Arthritis Response to Medication Study (CHARMS), Wedderburn LR, Thomson W, Lewis CM, Woo P.

PLoS One. 2012;7(10):e47673. doi: 10.1371/journal.pone.0047673. Epub 2012 Oct 18.

PMID:: 23094074; [PubMed - indexed for MEDLINE]

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Select item 226926844.

Loss of function of Ifi202b by a microdeletion on chromosome 1 of C57BL/6J mice suppresses 11β-hydroxysteroid dehydrogenase type 1 expression and development of obesity.

Vogel H, Scherneck S, Kanzleiter T, Benz V, Kluge R, Stadion M, Kryvych S, Blüher M, Klöting N, Joost HG, Schürmann A.

Hum Mol Genet. 2012 Sep 1;21(17):3845-57. doi: 10.1093/hmg/dds213. Epub 2012 Jun 12.

PMID:: 22692684; [PubMed - indexed for MEDLINE]

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Select item 225581315.

Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration.

Cantsilieris S, White SJ, Richardson AJ, Guymer RH, Baird PN.

PLoS One. 2012;7(4):e35255. doi: 10.1371/journal.pone.0035255. Epub 2012 Apr 25.

PMID:: 22558131; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 223916216.

Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature.

Manolakos E, Sifakis S, Sotiriou S, Peitsidis P, Eleftheriades M, Mersinias V, Liehr T, Thomaidis L, Kitsos G, Papoulidis I, Petersen MB, Orru S.

Clin Dysmorphol. 2012 Apr;21(2):101-5. doi: 10.1097/MCD.0b013e32834e9279. Review. No abstract available.

PMID:: 22391621; [PubMed - indexed for MEDLINE]

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Select item 223516947.

MAPKAP kinase 2 overexpression influences prognosis in gastrointestinal stromal tumors and associates with copy number variations on chromosome 1 and expression of p38 MAP kinase and ETV1.

Birner P, Beer A, Vinatzer U, Stary S, Höftberger R, Nirtl N, Wrba F, Streubel B, Schoppmann SF.

Clin Cancer Res. 2012 Apr 1;18(7):1879-87. doi: 10.1158/1078-0432.CCR-11-2364. Epub 2012 Feb 20.

PMID:: 22351694; [PubMed - indexed for MEDLINE]

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Select item 221160718.

Meiotic recombination, synapsis, meiotic inactivation and sperm aneuploidy in a chromosome 1 inversion carrier.

Kirkpatrick G, Chow V, Ma S.

Reprod Biomed Online. 2012 Jan;24(1):91-100. doi: 10.1016/j.rbmo.2011.09.013. Epub 2011 Oct 7.

PMID:: 22116071; [PubMed - indexed for MEDLINE]

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