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Items: 1 to 20 of 495

1.

Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens.

Fan X, Supiwong W, Weise A, Mrasek K, Kosyakova N, Tanomtong A, Pinthong K, Trifonov VA, Cioffi Mde B, Grothmann P, Liehr T, Oliveira EH.

Heliyon. 2015 Nov 24;1(3):e00042. doi: 10.1016/j.heliyon.2015.e00042. eCollection 2015 Nov.

2.

Alpha-fetoprotein and its value for predicting pregnancy outcomes - a re-evaluation.

Darouich AA, Liehr T, Weise A, Schlembach D, Schleußner E, Kiehntopf M, Schreyer I.

J Prenat Med. 2015 Jul-Dec;9(3-4):18-23. doi: 10.11138/jpm/2015.9.3.018.

3.

Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytes.

Hovhannisyan G, Aroutiounian R, Babayan N, Harutyunyan T, Liehr T.

Mol Cytogenet. 2016 Jun 21;9:49. doi: 10.1186/s13039-016-0258-4. eCollection 2016.

4.

Interphase Molecular Cytogenetic Detection Rates of Chronic Lymphocytic Leukemia-Specific Aberrations Are Higher in Cultivated Cells Than in Blood or Bone Marrow Smears.

Alhourani E, Aroutiounian R, Harutyunyan T, Glaser A, Schlie C, Pohle B, Liehr T.

J Histochem Cytochem. 2016 Aug;64(8):495-501. doi: 10.1369/0022155416655086. Epub 2016 Jun 17.

PMID:
27315825
5.

Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.

Ney Garcia DR, de Souza MT, de Figueiredo AF, Othman MA, Rittscher K, Abdelhay E, Capela de Matos RR, Meyer C, Marschalek R, Land MG, Liehr T, Ribeiro RC, Silva ML.

Hematol Oncol. 2016 Jun 10. doi: 10.1002/hon.2299. [Epub ahead of print]

PMID:
27282883
6.

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Amasdl S, Natiq A, Elalaoui SC, Sbiti A, Liehr T, Sefiani A.

J Med Case Rep. 2016 May 13;10(1):122. doi: 10.1186/s13256-016-0830-x.

7.

BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients.

Alhourani E, Othman MA, Melo JB, Carreira IM, Grygalewicz B, Vujić D, Zecević Z, Joksić G, Glaser A, Pohle B, Schlie C, Hauke S, Liehr T.

Oncol Lett. 2016 May;11(5):3240-3246. Epub 2016 Mar 29.

8.

Chromosomes in a genome-wise order: evidence for metaphase architecture.

Weise A, Bhatt S, Piaszinski K, Kosyakova N, Fan X, Altendorf-Hofmann A, Tanomtong A, Chaveerach A, de Cioffi MB, de Oliveira E, Walther JU, Liehr T, Chaudhuri JP.

Mol Cytogenet. 2016 Apr 27;9:36. doi: 10.1186/s13039-016-0243-y. eCollection 2016.

9.

Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensis.

Portela-Bens S, Merlo MA, Rodríguez ME, Cross I, Manchado M, Kosyakova N, Liehr T, Rebordinos L.

Chromosoma. 2016 Apr 14. [Epub ahead of print]

PMID:
27080536
10.

W Chromosome Dynamics in Triportheus Species (Characiformes, Triportheidae): An Ongoing Process Narrated by Repetitive Sequences.

Yano CF, Bertollo LA, Liehr T, Troy WP, Cioffi Mde B.

J Hered. 2016 Jul;107(4):342-8. doi: 10.1093/jhered/esw021. Epub 2016 Apr 1.

PMID:
27036509
11.

A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.

Othman MA, Grygalewicz B, Pienkowska-Grela B, Rygier J, Ejduk A, Rincic M, Melo JB, Carreira IM, Meyer B, Liehr T.

Oncol Lett. 2016 Mar;11(3):2117-2122. Epub 2016 Jan 29.

12.

Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors.

Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T.

Mol Syndromol. 2016 Feb;6(5):210-21. doi: 10.1159/000441408. Epub 2015 Oct 31.

13.

Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.

Rincic M, Rados M, Krsnik Z, Gotovac K, Borovecki F, Liehr T, Brecevic L.

Mol Cytogenet. 2016 Feb 20;9:19. doi: 10.1186/s13039-016-0221-4. eCollection 2016.

14.

Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing.

Zlotina A, Kulikova T, Kosyakova N, Liehr T, Krasikova A.

BMC Genomics. 2016 Feb 20;17:126. doi: 10.1186/s12864-016-2437-4.

15.

Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus.

Sangpakdee W, Tanomtong A, Fan X, Pinthong K, Weise A, Liehr T.

Mol Cytogenet. 2016 Feb 17;9:17. doi: 10.1186/s13039-016-0228-x. eCollection 2016.

16.

Reviewer acknowledgement 2016.

Liehr T, Heng H, Yurov Y, Meloni-Ehrig A, Iourov I.

Mol Cytogenet. 2016 Feb 10;9:14. doi: 10.1186/s13039-016-0226-z. eCollection 2016.

17.

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes.

Coci EG, Koehler U, Liehr T, Stelzner A, Fink C, Langen H, Riedel J.

Mol Cytogenet. 2016 Feb 3;9:10. doi: 10.1186/s13039-016-0219-y. eCollection 2016.

18.

A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findings.

Wannenmacher B, Mitter D, Kießling F, Liehr T, Weise A, Siekmeyer M, Kiess W.

J Pediatr Endocrinol Metab. 2016 May 1;29(5):611-6. doi: 10.1515/jpem-2015-0375.

PMID:
26824977
19.
20.

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.

Amasdl S, Natiq A, Sbiti A, Zerkaoui M, Lyahyai J, Amzazi S, Liehr T, Sefiani A.

BMC Res Notes. 2016 Jan 2;9:5. doi: 10.1186/s13104-015-1828-y.

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