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Items: 1 to 50 of 66

1.

Generation of functional cardiomyocytes from rat embryonic and induced pluripotent stem cells using feeder-free expansion and differentiation in suspension culture.

Dahlmann J, Awad G, Dolny C, Weinert S, Richter K, Fischer KD, Munsch T, Leßmann V, Volleth M, Zenker M, Chen Y, Merkl C, Schnieke A, Baraki H, Kutschka I, Kensah G.

PLoS One. 2018 Mar 7;13(3):e0192652. doi: 10.1371/journal.pone.0192652. eCollection 2018.

2.

Chromosomal Evolution in Chiroptera.

Sotero-Caio CG, Baker RJ, Volleth M.

Genes (Basel). 2017 Oct 13;8(10). pii: E272. doi: 10.3390/genes8100272. Review.

3.

Demonstration of 5-Methylcytosine-Rich DNA Sequences in Chiroptera.

Schmid M, Steinlein C, Lomb C, Volleth M.

Cytogenet Genome Res. 2017;152(1):38-45. doi: 10.1159/000475740. Epub 2017 May 18.

PMID:
28514774
4.
5.

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.

6.
7.

A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndrome.

Wieland I, Schanze D, Schanze I, Volleth M, Muschke P, Zenker M.

Am J Med Genet A. 2014 Dec;164A(12):3213-4. doi: 10.1002/ajmg.a.36765. Epub 2014 Sep 23. No abstract available.

PMID:
25251057
8.

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
9.

Karyotype evolution in the horseshoe bat Rhinolophus sedulus by whole-arm reciprocal translocation (WART).

Volleth M, Heller KG, Yong HS, Müller S.

Cytogenet Genome Res. 2014;143(4):241-50. doi: 10.1159/000365824. Epub 2014 Aug 16.

PMID:
25139053
10.

Deletions in the 3' part of the NFIX gene including a recurrent Alu-mediated deletion of exon 6 and 7 account for previously unexplained cases of Marshall-Smith syndrome.

Schanze D, Neubauer D, Cormier-Daire V, Delrue MA, Dieux-Coeslier A, Hasegawa T, Holmberg EE, Koenig R, Krueger G, Schanze I, Seemanova E, Shaw AC, Vogt J, Volleth M, Reis A, Meinecke P, Hennekam RC, Zenker M.

Hum Mutat. 2014 Sep;35(9):1092-100. doi: 10.1002/humu.22603. Epub 2014 Jul 8.

PMID:
24924640
11.

Taxonomic, bioacoustic and faunistic data on a collection of Tettigonioidea from Eastern Congo (Insecta: Orthoptera).

Heller KG, Hemp C, Liu C, Volleth M.

Zootaxa. 2014 Apr 4;3785:343-76. doi: 10.11646/zootaxa.3785.3.2.

PMID:
24872232
12.

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.

13.

Chromosomal evolution among leaf-nosed nectarivorous bats--evidence from cross-species chromosome painting (Phyllostomidae, Chiroptera).

Sotero-Caio CG, Volleth M, Gollahon LS, Fu B, Cheng W, Ng BL, Yang F, Baker RJ.

BMC Evol Biol. 2013 Dec 26;13:276. doi: 10.1186/1471-2148-13-276.

14.

Human Ring Chromosomes - New Insights for their Clinical Significance.

Guilherme R, Klein E, Hamid A, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen M, Manolakos E, Kosyakova N, Liehr T.

Balkan J Med Genet. 2013 Jun;16(1):13-20. doi: 10.2478/bjmg-2013-0013.

15.

Complex small supernumerary marker chromosomes - an update.

Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB.

Mol Cytogenet. 2013 Oct 31;6:46. doi: 10.1186/1755-8166-6-46. eCollection 2013.

16.

Evidence for two karyotypic variants of the lesser horseshoe bat ( Rhinolophus hipposideros , Chiroptera, Mammalia) in Central Europe.

Volleth M, Biedermann M, Schorcht W, Heller KG.

Cytogenet Genome Res. 2013;140(1):55-61. doi: 10.1159/000350693. Epub 2013 Apr 25.

PMID:
23635426
17.

Heteromorphic variants of chromosome 9.

Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner RD, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Mde B, Ergul E.

Mol Cytogenet. 2013 Apr 1;6(1):14. doi: 10.1186/1755-8166-6-14.

18.

Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?

Guilherme RS, Klein E, Venner C, Hamid AB, Bhatt S, Melaragno MI, Volleth M, Polityko A, Kulpanovich A, Kosyakova N, Liehr T.

Chromosome Res. 2012 Oct;20(7):825-35. doi: 10.1007/s10577-012-9316-x. Epub 2012 Oct 18.

PMID:
23076733
19.

16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.

Barber JC, Hall V, Maloney VK, Huang S, Roberts AM, Brady AF, Foulds N, Bewes B, Volleth M, Liehr T, Mehnert K, Bateman M, White H.

Eur J Hum Genet. 2013 Feb;21(2):182-9. doi: 10.1038/ejhg.2012.144. Epub 2012 Jul 25.

20.

Chromosome evolution in bats as revealed by FISH: the ongoing search for the ancestral chiropteran karyotype.

Volleth M, Eick G.

Cytogenet Genome Res. 2012;137(2-4):165-73. doi: 10.1159/000338929. Epub 2012 Jun 2.

PMID:
22678038
21.

Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.

Klein E, Rocchi M, Ovens-Raeder A, Kosyakova N, Weise A, Ziegler M, Meins M, Morlot S, Fischer W, Volleth M, Polityko A, Ogilvie CM, Kraus C, Liehr T.

Cytogenet Genome Res. 2012;136(3):163-6. doi: 10.1159/000336648. Epub 2012 Mar 1.

PMID:
22377933
22.

Comparative chromosome painting of four Siberian Vespertilionidae species with Aselliscus stoliczkanus and human probes.

Kulemzina AI, Nie W, Trifonov VA, Staroselec Y, Vasenkov DA, Volleth M, Yang F, Graphodatsky AS.

Cytogenet Genome Res. 2011;134(3):200-5. doi: 10.1159/000328834. Epub 2011 Jun 29.

PMID:
21709413
23.

High-resolution chromosome painting reveals the first genetic signature for the chiropteran suborder Pteropodiformes (Mammalia: Chiroptera).

Volleth M, Yang F, Müller S.

Chromosome Res. 2011 May;19(4):507-19. doi: 10.1007/s10577-011-9196-5. Epub 2011 Mar 11.

PMID:
21394511
24.

The human genome puzzle - the role of copy number variation in somatic mosaicism.

Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Bhatt S, Thoma K, Gebhart E, Wilhelm S, Fahsold R, Volleth M, Weise A.

Curr Genomics. 2010 Sep;11(6):426-31. doi: 10.2174/138920210793176047.

25.

A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation.

Argyriou L, Hiort O, Meinecke P, Wünsch L, Volleth M, Hinrichs F, Caliebe A, Gillessen-Kaesbach G.

Clin Dysmorphol. 2010 Oct;19(4):190-4. doi: 10.1097/MCD.0b013e32833c8ba1.

PMID:
20671549
26.

Translocation and deletion around SOX9 in a patient with acampomelic campomelic dysplasia and sex reversal.

Jakubiczka S, Schröder C, Ullmann R, Volleth M, Ledig S, Gilberg E, Kroisel P, Wieacker P.

Sex Dev. 2010;4(3):143-9. doi: 10.1159/000302403. Epub 2010 May 4.

PMID:
20453475
27.

Early embryonic chromosome instability results in stable mosaic pattern in human tissues.

Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Volleth M, Weise A.

PLoS One. 2010 Mar 9;5(3):e9591. doi: 10.1371/journal.pone.0009591.

28.

Comparative cytogenetics of moles (Eulipotyphla, Talpidae): chromosomal differences in Talpa romana and T. europaea.

Gornung E, Volleth M, Capanna E, Castiglia R.

Cytogenet Genome Res. 2008;121(3-4):249-54. doi: 10.1159/000138892. Epub 2008 Aug 29.

PMID:
18758166
29.

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.

Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazaurik ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T.

Int J Mol Med. 2008 Jun;21(6):705-14.

30.
31.

Familial translocation t(1;9) associated with macromastia: molecular cloning of the breakpoints.

Wieacker P, Apeshiotis N, Jakubiczka S, Volleth M, Wieland I.

Sex Dev. 2007;1(1):35-41. doi: 10.1159/000096237.

32.

Chromosome number reduction accompanied by extensive heterochromatin addition in the bat Glauconycteris beatrix (Mammalia; Chiroptera, Vespertilionidae).

Volleth M, Heller KG.

Cytogenet Genome Res. 2007;119(3-4):245-7. doi: 10.1159/000112069. Epub 2008 Feb 1.

PMID:
18253037
33.

Prenatal diagnosis of Roberts syndrome and detection of an ESCO2 frameshift mutation in a Pakistani family.

Schulz S, Gerloff C, Ledig S, Langer D, Volleth M, Shirneshan K, Wieacker P.

Prenat Diagn. 2008 Jan;28(1):42-5. doi: 10.1002/pd.1904.

PMID:
18186147
34.
35.

Karyotypic differences in two sibling species of Scotophilus from South Africa (Vespertilionidae, Chiroptera, Mammalia).

Eick GN, Jacobs DS, Yang F, Volleth M.

Cytogenet Genome Res. 2007;118(1):72-7.

PMID:
17901703
36.

Karyotype evolution in Rhinolophus bats (Rhinolophidae, Chiroptera) illuminated by cross-species chromosome painting and G-banding comparison.

Mao X, Nie W, Wang J, Su W, Ao L, Feng Q, Wang Y, Volleth M, Yang F.

Chromosome Res. 2007;15(7):835-48. Epub 2007 Oct 1.

PMID:
17899409
37.

The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophy.

Cortese R, Eckhardt F, Volleth M, Wehnert M, Koelsch U, Wieacker P, Brune T.

J Mol Endocrinol. 2007 Jun;38(6):663-71.

PMID:
17556535
38.

New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.

Tönnies H, Pietrzak J, Bocian E, MacDermont K, Kuechler A, Belitz B, Trautmann U, Schmidt A, Schulze B, Rodríguez L, Binkert F, Yardin C, Kosyakova N, Volleth M, Mkrtchyan H, Schreyer I, von Eggeling F, Weise A, Mrasek K, Liehr T.

J Histochem Cytochem. 2007 Jun;55(6):651-60. Epub 2007 Mar 6.

PMID:
17341473
39.

Karyotypic evolution and phylogenetic relationships in the order Chiroptera as revealed by G-banding comparison and chromosome painting.

Ao L, Mao X, Nie W, Gu X, Feng Q, Wang J, Su W, Wang Y, Volleth M, Yang F.

Chromosome Res. 2007;15(3):257-67. Epub 2007 May 10.

PMID:
17310301
40.

Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC.

Jakubiczka S, Bettecken T, Mohnike K, Schneppenheim R, Stumm M, Tönnies H, Volleth M, Wieacker P.

Eur J Pediatr. 2007 Jul;166(7):743-5. Epub 2006 Nov 8.

PMID:
17091258
41.
42.

Karyotype relationships of six bat species (Chiroptera, Vespertilionidae) from China revealed by chromosome painting and G-banding comparison.

Ao L, Gu X, Feng Q, Wang J, O'Brien PC, Fu B, Mao X, Su W, Wang Y, Volleth M, Yang F, Nie W.

Cytogenet Genome Res. 2006;115(2):145-53.

PMID:
17065796
43.

High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).

Wieland I, Muschke P, Volleth M, Röpke A, Pelz AF, Stumm M, Wieacker P.

Genes Chromosomes Cancer. 2006 Oct;45(10):945-9.

PMID:
16845657
44.

Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome.

Bartsch O, Rasi S, Delicado A, Dyack S, Neumann LM, Seemanová E, Volleth M, Haaf T, Kalscheuer VM.

Hum Genet. 2006 Sep;120(2):179-86. Epub 2006 Jun 17.

PMID:
16783566
45.

Intrachromosomal triplication 12p11.22-p12.3 and gonadal mosaicism of partial tetrasomy 12p.

Eckel H, Wimmer R, Volleth M, Jakubiczka S, Muschke P, Wieacker P.

Am J Med Genet A. 2006 Jun 1;140(11):1219-22.

PMID:
16652358
46.

Are molecular cytogenetics and bioinformatics suggesting diverging models of ancestral mammalian genomes?

Froenicke L, Caldés MG, Graphodatsky A, Müller S, Lyons LA, Robinson TJ, Volleth M, Yang F, Wienberg J.

Genome Res. 2006 Mar;16(3):306-10. No abstract available.

47.

Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14.

Volleth M, Stumm M, Bürger J, Muschke P, Wieacker P.

Cytogenet Genome Res. 2005;108(4):283-6.

PMID:
15627746
49.

The imbalanced mixed lymphocyte reaction between maternal and fetal lymphocytes as well as between the lymphocytes of adult children and their parents is mediated by activated CD8+ T cells.

Brune T, Masjoshusmann K, Reinhold D, Steinhardt J, Exeler R, Volleth M, Louwen F.

Am J Reprod Immunol. 2004 Oct;52(4):284-9.

PMID:
15494050
50.

Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.

Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M.

Am J Med Genet A. 2004 Sep 1;129A(3):261-4.

PMID:
15326625

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