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Items: 17

1.

Loss of chromosome 13 material in cellular angiofibromas indicates pathogenetic similarity with spindle cell lipomas.

Panagopoulos I, Gorunova L, Bjerkehagen B, Andersen K, Lund-Iversen M, Heim S.

Diagn Pathol. 2017 Feb 13;12(1):17. doi: 10.1186/s13000-017-0607-6.

2.

Prenatal Detection and Postnatal Follow-Up of Segmental Aneusomies of Chromosome 13 in 4 Consecutive Pregnancies in an Ethnic South Indian Family With a Maternally Inherited Balanced Translocation.

Francis A, Meleyil SM, Pullely JP, Koshy T, Batra MP, Kottukkal BB, Kannoly GK.

Lab Med. 2015 Fall;46(4):343-6. doi: 10.1309/LMQN1TOPPK11FVIH.

PMID:
26489681
4.

Acquired isodisomy on chromosome 13 at diagnosis results in impaired overall survival in patients with FLT3-ITD mutant acute myeloid leukaemia.

Loke JC, Akiki S, Borrow J, Ewing J, Bokhari SW, Chandra D, Arrazi J, Hazlewood P, Arthur K, Walsh J, Membwange Y, Wandroo FA, Watts A, Borg A, Brock K, Ferguson P, Craddock C, Griffiths M, Raghavan M.

Leukemia. 2015 Dec;29(12):2404-7. doi: 10.1038/leu.2015.148. Epub 2015 Jun 19. No abstract available.

PMID:
26172402
5.

Endothelial chromosome 13 deletion in congenital heart disease-associated pulmonary arterial hypertension dysregulates SMAD9 signaling.

Drake KM, Comhair SA, Erzurum SC, Tuder RM, Aldred MA.

Am J Respir Crit Care Med. 2015 Apr 1;191(7):850-4. doi: 10.1164/rccm.201411-1985LE. No abstract available.

6.

An infertile 45,X male with a SRY-bearing chromosome 13: a clinical case report and literature review.

Peng D, Zhang YS, Zhang XY, Hu C, Liu MH, Liu RZ.

J Assist Reprod Genet. 2015 Jan;32(1):107-9. doi: 10.1007/s10815-014-0376-z. Epub 2014 Nov 6.

7.

De novo LINE-1 retrotransposition in HepG2 cells preferentially targets gene poor regions of chromosome 13.

Bojang P Jr, Anderton MJ, Roberts RA, Ramos KS.

Genomics. 2014 Aug;104(2):96-104. doi: 10.1016/j.ygeno.2014.07.001. Epub 2014 Jul 17.

8.

Chromosome 13 deletion and hypodiploidy on conventional cytogenetics are robust prognostic factors in Korean multiple myeloma patients: web-based multicenter registry study.

Oh S, Koo DH, Kwon MJ, Kim K, Suh C, Min CK, Yoon SS, Shin HJ, Jo DY, Kwak JY, Kim JS, Sohn SK, Joo YD, Eom HS, Kim SH, Kim YS, Kim C, Mun YC, Kim H, Lee DS, Lee JH; Korean Multiple Myeloma Working Party (KMMWP)..

Ann Hematol. 2014 Aug;93(8):1353-61. doi: 10.1007/s00277-014-2057-5. Epub 2014 Mar 27.

PMID:
24671365
9.

Genetic mapping of high caries experience on human chromosome 13.

Küchler EC, Deeley K, Ho B, Linkowski S, Meyer C, Noel J, Kouzbari MZ, Bezamat M, Granjeiro JM, Antunes LS, Antunes LA, de Abreu FV, Costa MC, Tannure PN, Seymen F, Koruyucu M, Patir A, Mereb JC, Poletta FA, Castilla EE, Orioli IM, Marazita ML, Vieira AR.

BMC Med Genet. 2013 Nov 5;14:116. doi: 10.1186/1471-2350-14-116.

10.

Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.

Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W.

Gene. 2013 Oct 15;529(1):163-8. doi: 10.1016/j.gene.2013.07.050. Epub 2013 Aug 8.

PMID:
23933417
11.

Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: a possible recurrent chromosome aberration.

Plaja A, Lloveras E, Martinez-Bouzas C, Barreña B, Del Campo M, Fernández A, Herrero M, Barranco L, Palau N, López-Aríztegui MA, Català V, Tejada MI.

Am J Med Genet A. 2013 Sep;161A(9):2363-8. doi: 10.1002/ajmg.a.36102. Epub 2013 Jul 25.

PMID:
23894094
12.

Genome association study of human chromosome 13 and susceptibility to coronary artery disease in a Chinese population.

Jie P, Xing C, Tingting L, Yi X, Jianning Z, Tingting J, Tianjiao L, Gang C, Yuan G.

J Genet. 2013 Apr;92(1):85-91. No abstract available.

13.

Duplication of isodicentric chromosome 13, idic(13)(p11.2), leading to pentasomy 13q in acute myeloid leukemia without maturation.

Kjeldsen E, Kallenbach M.

Cytogenet Genome Res. 2013;140(1):21-8. doi: 10.1159/000350694. Epub 2013 Apr 23.

PMID:
23615042
14.

Nodal marginal zone B cell lymphoma with prominent follicular colonization with deletion of chromosome 13.

Tabata R, Tabata C, Nagai T, Yasumizu R, Kojima M.

Pathol Res Pract. 2012 Nov 15;208(11):679-82. doi: 10.1016/j.prp.2012.07.009. Epub 2012 Sep 7.

PMID:
22963839
15.

Cognitive and behavioral phenotype of a young man with a chromosome 13 deletion del(13)(q21.32q31.1).

Matute E, Inozemtseva O, Aguilar-Lemarroy A, Jave-Suarez LF, Della Mina E, Zuffardi O, Rivera H.

Cogn Behav Neurol. 2012 Sep;25(3):154-8. doi: 10.1097/WNN.0b013e31826dfd3c.

PMID:
22960441
16.

Origin of a prenatal mosaic supernumerary neocentromeric derivative chromosome 13 determined by QF-PCR.

Dawson AJ, Hryshko M, Konkin D, Bal S, Bernier D, Tomiuk M, Burnett S, Frosk P, Chodirker BN, Chun K.

Fetal Diagn Ther. 2013;33(1):75-8. doi: 10.1159/000337537. Epub 2012 May 17.

PMID:
22614064
17.

Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study.

Rice TK, Sarzynski MA, Sung YJ, Argyropoulos G, Stütz AM, Teran-Garcia M, Rao DC, Bouchard C, Rankinen T.

Eur J Appl Physiol. 2012 Aug;112(8):2969-78. doi: 10.1007/s00421-011-2274-8. Epub 2011 Dec 15.

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