Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 97

1.

DYZ1 arrays show sequence variation between the monozygotic males.

Yadav SK, Kumari A, Javed S, Ali S.

BMC Genet. 2014 Feb 4;15:19. doi: 10.1186/1471-2156-15-19.

2.

Organizational variation of DYZ1 repeat sequences on the human Y chromosome and its diagnostic potentials.

Rahman MM, Bashamboo A, Prasad A, Pathak D, Ali S.

DNA Cell Biol. 2004 Sep;23(9):561-71.

PMID:
15383176
3.

Fate of the human Y chromosome linked genes and loci in prostate cancer cell lines DU145 and LNCaP.

Yadav SK, Kumari A, Ali S.

BMC Genomics. 2013 May 11;14:323. doi: 10.1186/1471-2164-14-323.

4.

DYZ1 copy number variation, Y chromosome polymorphism and early recurrent spontaneous abortion/early embryo growth arrest.

Yan J, Fan L, Zhao Y, You L, Wang L, Zhao H, Li Y, Chen ZJ.

Eur J Obstet Gynecol Reprod Biol. 2011 Dec;159(2):371-4. doi: 10.1016/j.ejogrb.2011.07.033. Epub 2011 Aug 9.

PMID:
21831514
5.

Genomic instability of the DYZ1 repeat in patients with Y chromosome anomalies and males exposed to natural background radiation.

Pathak D, Premi S, Srivastava J, Chandy SP, Ali S.

DNA Res. 2006 Jun 30;13(3):103-9. Epub 2006 Sep 16.

6.

Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation.

Razzaghian HR, Shahi MH, Forsberg LA, de Ståhl TD, Absher D, Dahl N, Westerman MP, Dumanski JP.

Am J Med Genet A. 2010 Oct;152A(10):2595-8. doi: 10.1002/ajmg.a.33604.

PMID:
20734341
7.

Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies.

Bashamboo A, Rahman MM, Prasad A, Chandy SP, Ahmad J, Ali S.

Mol Hum Reprod. 2005 Feb;11(2):117-27. Epub 2004 Dec 3.

8.

Genetic integrity of the human Y chromosome exposed to groundwater arsenic.

Ali S, Ali S.

BMC Med Genomics. 2010 Aug 6;3:35. doi: 10.1186/1755-8794-3-35.

9.

Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.

Veenma D, Brosens E, de Jong E, van de Ven C, Meeussen C, Cohen-Overbeek T, Boter M, Eussen H, Douben H, Tibboel D, de Klein A.

Eur J Hum Genet. 2012 Mar;20(3):298-304. doi: 10.1038/ejhg.2011.194. Epub 2011 Nov 9.

10.

Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogram.

Kumari A, Yadav SK, Ali S.

PLoS One. 2012;7(7):e41488. doi: 10.1371/journal.pone.0041488. Epub 2012 Jul 23.

11.

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7.

Wevrick R, Willard VP, Willard HF.

Genomics. 1992 Dec;14(4):912-23.

PMID:
1478672
12.

Radiation-induced DNA breaks in different human satellite DNA sequence areas, analyzed by DNA breakage detection-fluorescence in situ hybridization.

Vázquez-Gundín F, Rivero MT, Gosálvez J, Luis Fernández J.

Radiat Res. 2002 Jun;157(6):711-20.

PMID:
12005551
13.

Development of two highly sensitive forensic sex determination assays based on human DYZ1 and Alu repetitive DNA elements.

Fazi A, Gobeski B, Foran D.

Electrophoresis. 2014 Nov;35(21-22):3028-35. doi: 10.1002/elps.201400103. Epub 2014 Oct 18.

PMID:
25168471
14.

Copy number imbalances in blood and hair in monozygotic twins discordant for amyotrophic lateral sclerosis.

Pamphlett R, Morahan JM.

J Clin Neurosci. 2011 Sep;18(9):1231-4. doi: 10.1016/j.jocn.2010.12.049. Epub 2011 Jul 7.

PMID:
21741244
16.

Evidence of abundant constitutive alkali-labile sites in human 5 bp classical satellite DNA loci by DBD-FISH.

Fernández JL, Vázquez-Gundín F, Rivero MT, Goyanes V, Gosálvez J.

Mutat Res. 2001 Feb 20;473(2):163-8.

PMID:
11166034
17.

Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.

Bruder CE, Piotrowski A, Gijsbers AA, Andersson R, Erickson S, Diaz de Ståhl T, Menzel U, Sandgren J, von Tell D, Poplawski A, Crowley M, Crasto C, Partridge EC, Tiwari H, Allison DB, Komorowski J, van Ommen GJ, Boomsma DI, Pedersen NL, den Dunnen JT, Wirdefeldt K, Dumanski JP.

Am J Hum Genet. 2008 Mar;82(3):763-71. doi: 10.1016/j.ajhg.2007.12.011. Epub 2008 Feb 14.

19.

Very low rate Y-chromosome mosaicism (1:5,400) detectable by a novel probe enzyme combination.

Nakahori Y, Yamada M, Nakagome Y.

Jinrui Idengaku Zasshi. 1989 Sep;34(3):203-8.

PMID:
2634133
20.

Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae).

Haaf T, Schmid M, Steinlein C, Galetti PM Jr, Willard HF.

Chromosome Res. 1993 May;1(1):77-86.

PMID:
8143092
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk