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Results: 1 to 20 of 437

1.

A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia.

Othman MA, Rincic M, Melo JB, Carreira IM, Alhourani E, Hunstig F, Glaser A, Liehr T.

Leuk Res Treatment. 2014;2014:357123. doi: 10.1155/2014/357123. Epub 2014 Oct 8.

PMID:
25374696
[PubMed]
Free PMC Article
2.

Small supernumerary marker chromosomes and the nuclear architecture of sperm - a study in a fertile and an infertile brother.

Karamysheva T, Kosyakova N, Guediche N, Liehr T.

Syst Biol Reprod Med. 2014 Nov 6:1-5. [Epub ahead of print]

PMID:
25374326
[PubMed - as supplied by publisher]
3.

Small supernumerary marker chromosomes detected in connection with infertility.

Liehr T.

Zhonghua Nan Ke Xue. 2014 Sep;20(9):771-80.

PMID:
25306802
[PubMed - in process]
4.

Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case.

Bispo AV, Burégio-Frota P, Oliveira dos Santos L, Leal GF, Duarte AR, Araújo J, Cavalcante da Silva V, Muniz MT, Liehr T, Santos N.

Reprod Fertil Dev. 2014 Oct;26(8):1176-82. doi: 10.1071/RD13207.

PMID:
25294360
[PubMed - in process]
5.

An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations.

Al-Achkar W, Wafa A, Othman MA, Moassass F, Aljapawe A, Liehr T.

Mol Cytogenet. 2014 Sep 10;7(1):60. doi: 10.1186/s13039-014-0060-0. eCollection 2014.

PMID:
25254075
[PubMed]
Free PMC Article
6.

Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - A long term in vitro study.

Hussein SS, Kreskowski K, Ziegler M, Klein E, Hamid AB, Kosyakova N, Volleth M, Liehr T, Fan X, Piaszinski K.

Gene. 2014 Dec 1;552(2):246-8. doi: 10.1016/j.gene.2014.09.041. Epub 2014 Sep 20.

PMID:
25245454
[PubMed - in process]
7.

Application of BAC-probes to visualize copy number variants (CNVs).

Weise A, Othman MA, Bhatt S, Löhmer S, Liehr T.

Methods Mol Biol. 2015;1227:299-307. doi: 10.1007/978-1-4939-1652-8_16.

PMID:
25239754
[PubMed - in process]
8.

BAC-probes applied for characterization of fragile sites (FS).

Mrasek K, Wilhelm K, Quintana LG, Theuss L, Liehr T, Leskovac A, Filipovic J, Joksic G, Joksic I, Weise A.

Methods Mol Biol. 2015;1227:289-98. doi: 10.1007/978-1-4939-1652-8_15.

PMID:
25239753
[PubMed - in process]
9.

New BAC probe set to narrow down chromosomal breakpoints in small and large derivative chromosomes, especially suited for mosaic conditions.

Hamid AB, Fan X, Kosyakova N, Radhakrishnan G, Liehr T, Karamysheva T.

Methods Mol Biol. 2015;1227:279-87. doi: 10.1007/978-1-4939-1652-8_14.

PMID:
25239752
[PubMed - in process]
10.

Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathway.

Roediger J, Hessenkemper W, Bartsch S, Manvelyan M, Huettner SS, Liehr T, Esmaeili M, Foller S, Petersen I, Grimm MO, Baniahmad A.

Mol Cancer. 2014 Sep 12;13:214. doi: 10.1186/1476-4598-13-214.

PMID:
25216853
[PubMed - in process]
Free PMC Article
11.

Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae).

Yano CF, Bertollo LA, Molina WF, Liehr T, Cioffi Mde B.

Comp Cytogenet. 2014 Jul 14;8(2):139-51. doi: 10.3897/CompCytogen.v8i2.7597. eCollection 2014.

PMID:
25147625
[PubMed]
Free PMC Article
12.

Partial monosomy 3q26.33-3q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case report.

Şahin Y, Kiper PÖ, Alanay Y, Liehr T, Utine GE, Boduroğlu K.

Clin Dysmorphol. 2014 Oct;23(4):147-51. doi: 10.1097/MCD.0000000000000042. No abstract available.

PMID:
25144152
[PubMed - in process]
13.

Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies.

Natiq A, Elalaoui SC, Liehr T, Amzazi S, Sefiani A.

Indian J Hum Genet. 2014 Jan;20(1):89-91. doi: 10.4103/0971-6866.132767.

PMID:
24959023
[PubMed]
Free PMC Article
14.

Small supernumerary marker chromosomes - an update.

Liehr T.

Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I11. doi: 10.1186/1755-8166-7-S1-I11. eCollection 2014. No abstract available.

PMID:
24940369
[PubMed]
Free PMC Article
15.

Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes.

Liehr T.

Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I21. doi: 10.1186/1755-8166-7-S1-I21. eCollection 2014. No abstract available.

PMID:
24940361
[PubMed]
Free PMC Article
16.

Molecular Cytogenetic Characterization of an inv(Y)(p11.2q11.221∼q11.222) in a Syrian Family.

Al-Achkar W, Wafa A, Al-Ablog A, Moassass F, Liehr T.

Balkan J Med Genet. 2013 Dec;16(2):73-6. doi: 10.2478/bjmg-2013-0035.

PMID:
24778567
[PubMed]
Free PMC Article
17.

Molecular Cytogenetic Study of the NF2 Gene Deletion in Meningioma in Sudanese Patients.

Abdelmontalab FY, Fadl EI, Abushama H, Kreskowski K, Liehr T.

Balkan J Med Genet. 2013 Dec;16(2):29-32. doi: 10.2478/bjmg-2013-0028.

PMID:
24778560
[PubMed]
Free PMC Article
18.

An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review.

Vlaikou AM, Manolakos E, Noutsopoulos D, Markopoulos G, Liehr T, Vetro A, Ziegler M, Weise A, Kreskowski K, Papoulidis I, Thomaidis L, Syrrou M.

Cytogenet Genome Res. 2014;142(4):227-38. doi: 10.1159/000361001. Epub 2014 Apr 9. Review.

PMID:
24733116
[PubMed - indexed for MEDLINE]
19.

Mitotic stability of small supernumerary marker chromosomes: a study based on 93 immortalized cell lines.

Spittel H, Kubek F, Kreskowski K, Ziegler M, Klein E, Hamid AB, Kosyakova N, Radhakrishnan G, Junge A, Kozlowski P, Schulze B, Martin T, Huhle D, Mehnert K, Rodríguez L, Ergun MA, Sarri C, Militaru M, Stipoljev F, Tittelbach H, Vasheghani F, de Bello Cioffi M, Hussein SS, Fan X, Volleth M, Liehr T.

Cytogenet Genome Res. 2014;142(3):151-60. doi: 10.1159/000360776. Epub 2014 Apr 1.

PMID:
24714101
[PubMed - indexed for MEDLINE]
Free Article
20.

Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements.

Sahoo T, Wang JC, Elnaggar MM, Sanchez-Lara P, Ross LP, Mahon LW, Hafezi K, Deming A, Hinman L, Bruno Y, Bartley JA, Liehr T, Anguiano A, Jones M.

Eur J Hum Genet. 2014 Apr 9. doi: 10.1038/ejhg.2014.53. [Epub ahead of print]

PMID:
24713661
[PubMed - as supplied by publisher]
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