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Results: 13

Select item 218677421.

Chromosome 10 and RET gene copy number alterations in hereditary and sporadic Medullary Thyroid Carcinoma.

Ciampi R, Romei C, Cosci B, Vivaldi A, Bottici V, Renzini G, Ugolini C, Tacito A, Basolo F, Pinchera A, Elisei R.

Mol Cell Endocrinol. 2012 Jan 2;348(1):176-82. doi: 10.1016/j.mce.2011.08.004. Epub 2011 Aug 16.

PMID:: 21867742; [PubMed - indexed for MEDLINE]

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Select item 203345462.

Juvenile polyposis of infancy associated with paracentric inversion and deletion of chromosome 10 in a Hispanic patient: a case report.

Vargas-González R, de la Torre-Mondragón L, Aparicio-Rodríguez JM, Paniagua-Morgan F, López-Hernández G, Garrido-Hernández MA, Nuñez-Barrera S.

Pediatr Dev Pathol. 2010 Nov-Dec;13(6):486-91. doi: 10.2350/10-01-0791-CR.1. Epub 2010 Mar 24.

PMID:: 20334546; [PubMed - indexed for MEDLINE]

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Select item 200141573.

Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10.

Gomez-Rubio P, Meza-Montenegro MM, Cantu-Soto E, Klimecki WT.

J Appl Toxicol. 2010 Apr;30(3):260-70. doi: 10.1002/jat.1492.

PMID:: 20014157; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 199331954.

Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26.

Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D.

Invest Ophthalmol Vis Sci. 2010 Apr;51(4):2191-6. doi: 10.1167/iovs.09-3798. Epub 2009 Nov 20.

PMID:: 19933195; [PubMed - indexed for MEDLINE]

Free Article

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Select item 199216385.

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype.

Sung PL, Chang SP, Wen KC, Chang CM, Yang MJ, Chen LC, Chao KC, Huang CY, Li YC, Lin CC.

Am J Med Genet A. 2009 Dec;149A(12):2768-74. doi: 10.1002/ajmg.a.32878.

PMID:: 19921638; [PubMed - indexed for MEDLINE]

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Select item 196026876.

Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas.

Yadav AK, Renfrow JJ, Scholtens DM, Xie H, Duran GE, Bredel C, Vogel H, Chandler JP, Chakravarti A, Robe PA, Das S, Scheck AC, Kessler JA, Soares MB, Sikic BI, Harsh GR, Bredel M.

JAMA. 2009 Jul 15;302(3):276-89. doi: 10.1001/jama.2009.1022.

PMID:: 19602687; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 195482647.

Recombinant chromosome 10 presenting as a prenatal central nervous system abnormality.

Tritto AT, Myles T, Morris KL, Batanian JR.

Prenat Diagn. 2009 Oct;29(10):986-8. doi: 10.1002/pd.2313. No abstract available.

PMID:: 19548264; [PubMed - indexed for MEDLINE]

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Select item 193063358.

Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.

Arnold S, Pelet A, Amiel J, Borrego S, Hofstra R, Tam P, Ceccherini I, Lyonnet S, Sherman S, Chakravarti A.

Hum Mutat. 2009 May;30(5):771-5. doi: 10.1002/humu.20944.

PMID:: 19306335; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 192414609.

Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.

Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL.

Hum Mutat. 2009 Mar;30(3):463-71. doi: 10.1002/humu.20953.

PMID:: 19241460; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1921303710.

A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population.

Entesarian M, Carlsson B, Mansouri MR, Stattin EL, Holmberg E, Golovleva I, Stefansson H, Klar J, Dahl N.

Am J Med Genet A. 2009 Mar;149A(3):380-6. doi: 10.1002/ajmg.a.32663.

PMID:: 19213037; [PubMed - indexed for MEDLINE]

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Select item 1901233311.

Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation.

Behjati F, Shafeghati Y, Kahrizi K, Firouzabadi SG, Najmabadi H, Dixon N, Davies AF.

Am J Med Genet A. 2008 Dec 15;146A(24):3223-6. doi: 10.1002/ajmg.a.32575. No abstract available.

PMID:: 19012333; [PubMed - indexed for MEDLINE]

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Select item 1893018512.

Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10.

Gelernter J, Kranzler HR, Panhuysen C, Weiss RD, Brady K, Poling J, Farrer L.

Biol Psychiatry. 2009 Jan 15;65(2):111-5. doi: 10.1016/j.biopsych.2008.08.036. Epub 2008 Oct 18.

PMID:: 18930185; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1816342113.

Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease.

Morgan AR, Hamilton G, Turic D, Jehu L, Harold D, Abraham R, Hollingworth P, Moskvina V, Brayne C, Rubinsztein DC, Lynch A, Lawlor B, Gill M, O'Donovan M, Powell J, Lovestone S, Williams J, Owen MJ.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):727-31. doi: 10.1002/ajmg.b.30670.

PMID:: 18163421; [PubMed - indexed for MEDLINE]

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5 free full-text articles in PubMed Central

Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10. [J Appl Toxicol. 2010]
Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10.
Gomez-Rubio P, Meza-Montenegro MM, Cantu-Soto E, Klimecki WT. J Appl Toxicol. 2010 Apr; 30(3):260-70.
Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas. [JAMA. 2009]
Monosomy of chromosome 10 associated with dysregulation of epidermal growth factor signaling in glioblastomas.
Yadav AK, Renfrow JJ, Scholtens DM, Xie H, Duran GE, Bredel C, Vogel H, Chandler JP, Chakravarti A, Robe PA, et al. JAMA. 2009 Jul 15; 302(3):276-89.
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association. [Hum Mutat. 2009]
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
Arnold S, Pelet A, Amiel J, Borrego S, Hofstra R, Tam P, Ceccherini I, Lyonnet S, Sherman S, Chakravarti A. Hum Mutat. 2009 May; 30(5):771-5.

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