Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 428

1.

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(1):214. [Epub ahead of print]

PMID:
25216853
[PubMed - as supplied by publisher]
Free Article
2.

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
3.

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

Sahin Y, Kiper PO, 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]
4.

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
5.

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
6.

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
7.

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
8.

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
9.

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]
10.

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
11.

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]
12.

Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.

Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I.

Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):284-93. doi: 10.1002/bdra.23213. Epub 2014 Feb 12.

PMID:
24677675
[PubMed - in process]
13.

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature.

Manolakos E, Vetro A, Garas A, Thomaidis L, Kefalas K, Kitsos G, Ziegler M, Liehr T, Zuffardi O, Papoulidis I.

Exp Ther Med. 2014 Apr;7(4):953-957. Epub 2014 Feb 6.

PMID:
24669257
[PubMed]
Free PMC Article
14.

Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents.

De Souza MT, Hassan R, Liehr T, Marques-Salles TJ, Boulhosa AM, Abdelhay E, Ribeiro RC, Silva ML.

Pediatr Blood Cancer. 2014 Aug;61(8):1422-6. doi: 10.1002/pbc.25030. Epub 2014 Mar 26.

PMID:
24668946
[PubMed - indexed for MEDLINE]
15.

Chromosomal mapping of repetitive DNAs in Triportheus trifurcatus (Characidae, Characiformes): insights into the differentiation of the Z and W chromosomes.

Yano CF, Poltronieri J, Bertollo LA, Artoni RF, Liehr T, de Bello Cioffi M.

PLoS One. 2014 Mar 14;9(3):e90946. doi: 10.1371/journal.pone.0090946. eCollection 2014.

PMID:
24632562
[PubMed - in process]
Free PMC Article
16.

X chromosome aneuploidy in the Alzheimer's disease brain.

Yurov YB, Vorsanova SG, Liehr T, Kolotii AD, Iourov IY.

Mol Cytogenet. 2014 Mar 6;7(1):20. doi: 10.1186/1755-8166-7-20.

PMID:
24602248
[PubMed]
Free PMC Article
17.

Monitoring of gas station attendants exposure to benzene, toluene, xylene (BTX) using three-color chromosome painting.

Santiago F, Alves G, Otero UB, Tabalipa MM, Scherrer LR, Kosyakova N, Ornellas MH, Liehr T.

Mol Cytogenet. 2014 Feb 27;7(1):15. doi: 10.1186/1755-8166-7-15.

PMID:
24576355
[PubMed]
Free PMC Article
18.

Reviewer acknowledgement 2014.

Liehr T, Heng H, Yurov Y.

Mol Cytogenet. 2014 Feb 14;7(1):11. doi: 10.1186/1755-8166-7-11.

PMID:
24529454
[PubMed]
Free PMC Article
19.
20.

Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study.

Sheth FJ, Liehr T, Kumari P, Akinde R, Sheth HJ, Sheth JJ.

Indian J Hum Genet. 2013 Oct;19(4):415-22. doi: 10.4103/0971-6866.124369.

PMID:
24497706
[PubMed]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk