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Results: 17

Select item 230003371.

Haploidentical hematopoietic stem cell transplantation for lymphoma with monosomy of chromosome 6 (loss of heterozygosity in the HLA region)--who should be a donor?

Ikegame K, Kaida K, Lakoma L, Ishii S, Inoue T, Kato R, Soma T, Okada M, Ogawa H.

Transpl Immunol. 2012 Dec;27(4):162-5. doi: 10.1016/j.trim.2012.09.002. Epub 2012 Sep 19.

PMID:: 23000337; [PubMed - indexed for MEDLINE]

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Select item 226394452.

Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.

Huang B, Pearle P, Rauen KA, Cotter PD.

Am J Med Genet A. 2012 Jul;158A(7):1568-73. doi: 10.1002/ajmg.a.35385. Epub 2012 May 25.

PMID:: 22639445; [PubMed - indexed for MEDLINE]

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Select item 226166183.

New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6.

Tassano E, Tavella E, Valli R, Micalizzi C, Cuoco C, Maserati E, Pasquali F, Morerio C.

Leuk Lymphoma. 2012 Dec;53(12):2434-8. doi: 10.3109/10428194.2012.695778. Epub 2012 Jun 13.

PMID:: 22616618; [PubMed - indexed for MEDLINE]

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Select item 225377504.

Ancestry markers from the human chromosome 6: Alu repeats from the MHC in autochthonous Basques.

García-Obregón S, Alfonso-Sánchez MA, Pérez-Miranda AM, Gómez-Pérez L, de Parcorbo MM, Peña JA.

Hum Immunol. 2012 Jul;73(7):720-5. doi: 10.1016/j.humimm.2012.04.010. Epub 2012 Apr 23.

PMID:: 22537750; [PubMed - indexed for MEDLINE]

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Select item 220166885.

False homozygosity results in HLA genotyping due to loss of chromosome 6 in a patient with acute lymphoblastic leukemia.

Park H, Hyun J, Park SS, Park MH, Song EY.

Korean J Lab Med. 2011 Oct;31(4):302-6. doi: 10.3343/kjlm.2011.31.4.302. Epub 2011 Oct 3.

PMID:: 22016688; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 219894836.

Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant.

Goumy C, Kemeny S, Eymard-Pierre E, Richard C, Gouas L, Combes P, Gay-Bellile M, Gallot D, Tchirkov A, Vago P.

Gene. 2011 Dec 15;490(1-2):15-7. doi: 10.1016/j.gene.2011.09.008. Epub 2011 Oct 1.

PMID:: 21989483; [PubMed - indexed for MEDLINE]

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Select item 214888537.

A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6.

Cummings AC, Lee SL, McCauley JL, Jiang L, Crunk A, McFarland LL, Gallins PJ, Fuzzell D, Knebusch C, Jackson CE, Scott WK, Pericak-Vance MA, Haines JL.

Ann Hum Genet. 2011 May;75(3):351-8. doi: 10.1111/j.1469-1809.2011.00643.x.

PMID:: 21488853; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 211667878.

Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome.

Sasaki K, Okamoto N, Kosaki K, Yorifuji T, Shimokawa O, Mishima H, Yoshiura KI, Harada N.

Clin Genet. 2011 Nov;80(5):478-83. doi: 10.1111/j.1399-0004.2010.01599.x. Epub 2010 Dec 20.

PMID:: 21166787; [PubMed - indexed for MEDLINE]

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Select item 208857929.

Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.

Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, Vance JM, Slifer MA, Gwirtsman HE, Gilbert JR, Haines JL, Buxbaum JD, Pericak-Vance MA.

PLoS Genet. 2010 Sep 23;6(9). doi:pii: e1001130. 10.1371/journal.pgen.1001130.

PMID:: 20885792; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2068398610.

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation.

Krepischi AC, Rosenberg C, Costa SS, Crolla JA, Huang S, Vianna-Morgante AM.

Am J Med Genet A. 2010 Sep;152A(9):2376-8. doi: 10.1002/ajmg.a.33554. No abstract available.

PMID:: 20683986; [PubMed - indexed for MEDLINE]

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Select item 2058316411.

Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate.

Salahshourifar I, Halim AS, Sulaiman WA, Zilfalil BA.

Am J Med Genet A. 2010 Jul;152A(7):1818-21. doi: 10.1002/ajmg.a.33526.

PMID:: 20583164; [PubMed - indexed for MEDLINE]

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Select item 2041211012.

Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia.

Suzuki S, Fujisawa D, Hashimoto K, Asano T, Maimaiti M, Matsuo K, Tanahashi Y, Mukai T, Fujieda K.

Clin Genet. 2010 Dec;78(6):580-4. doi: 10.1111/j.1399-0004.2010.01433.x.

PMID:: 20412110; [PubMed - indexed for MEDLINE]

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Select item 2018679413.

Paternal uniparental isodisomy of chromosome 6 causing a complex syndrome including complete IFN-gamma receptor 1 deficiency.

Prando C, Boisson-Dupuis S, Grant AV, Kong XF, Bustamante J, Feinberg J, Chapgier A, Rose Y, Jannière L, Rizzardi E, Zhang Q, Shanahan CM, Viollet L, Lyonnet S, Abel L, Ruga EM, Casanova JL.

Am J Med Genet A. 2010 Mar;152A(3):622-9. doi: 10.1002/ajmg.a.33291. Review.

PMID:: 20186794; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 2003406614.

Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: a four-break model.

Wang JC, Dang L, Fisker T.

Am J Med Genet A. 2010 Jan;152A(1):209-11. doi: 10.1002/ajmg.a.33161. No abstract available.

PMID:: 20034066; [PubMed - indexed for MEDLINE]

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Select item 2003162415.

A common copy number variation on chromosome 6 association with the gene expression level of endothelin 1 in transformed B lymphocytes from three racial groups.

Sun YV, Peyser PA, Kardia SL.

Circ Cardiovasc Genet. 2009 Oct;2(5):483-8. doi: 10.1161/CIRCGENETICS.109.848754. Epub 2009 Aug 2.

PMID:: 20031624; [PubMed - indexed for MEDLINE]

Free PMC Article

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Select item 1948093816.

Association between acute promyelocytic leukemia and ring chromosome 6.

Park TS, Kim J, Song J, Song S, Suh B, Choi JR, Kim SJ, Lee HW, Min YH.

Cancer Genet Cytogenet. 2009 Jul;192(1):48-50. doi: 10.1016/j.cancergencyto.2009.02.009. No abstract available.

PMID:: 19480938; [PubMed - indexed for MEDLINE]

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Select item 1938291417.

Chromosome 6 encoded RNaseT2 protein is a cell growth regulator.

Liu J, Zhawar VK, Kaur G, Kaur GP, Deriel JK, Kandpal RP, Athwal RS.

J Cell Mol Med. 2010 May;14(5):1146-55. doi: 10.1111/j.1582-4934.2009.00749.x. Epub 2009 Mar 27.

PMID:: 19382914; [PubMed - indexed for MEDLINE]

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5 free full-text articles in PubMed Central

False homozygosity results in HLA genotyping due to loss of chromosome 6 in a patient with acute lymphoblastic leukemia. [Korean J Lab Med. 2011]
False homozygosity results in HLA genotyping due to loss of chromosome 6 in a patient with acute lymphoblastic leukemia.
Park H, Hyun J, Park SS, Park MH, Song EY. Korean J Lab Med. 2011 Oct; 31(4):302-6. Epub 2011 Oct 3.
A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6. [Ann Hum Genet. 2011]
A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6.
Cummings AC, Lee SL, McCauley JL, Jiang L, Crunk A, McFarland LL, Gallins PJ, Fuzzell D, Knebusch C, Jackson CE, et al. Ann Hum Genet. 2011 May; 75(3):351-8.
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. [PLoS Genet. 2010]
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.
Naj AC, Beecham GW, Martin ER, Gallins PJ, Powell EH, Konidari I, Whitehead PL, Cai G, Haroutunian V, Scott WK, et al. PLoS Genet. 2010 Sep 23; 6(9). Epub 2010 Sep 23.

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