Mincheva A - Search Results

1

The human rab GDI beta gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13.

Sedlacek Z, Munstermann E, Mincheva A, Lichter P, Poustka A. Sedlacek Z, et al. Among authors: mincheva a. Mamm Genome. 1998 Jan;9(1):78-80. doi: 10.1007/s003359900685. Mamm Genome. 1998. PMID: 9434952 No abstract available.

2

Assignment of the gene encoding centrosome-associated protein CCD41 to mouse chromosome 2H.

Mincheva A, Rothbarth K, Werner D, Lichter P. Mincheva A, et al. Mamm Genome. 1995 Jun;6(6):444. doi: 10.1007/BF00355652. Mamm Genome. 1995. PMID: 7647473 No abstract available.

3

The human gene for nuclear protein BM28 (CDCL1), a new member of the early S-phase family of proteins, maps to chromosome band 3q21.

Mincheva A, Todorov I, Werner D, Fink TM, Lichter P. Mincheva A, et al. Cytogenet Cell Genet. 1994;65(4):276-7. doi: 10.1159/000133647. Cytogenet Cell Genet. 1994. PMID: 8258304

4

Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1.

Wilgenbus KK, Coy JF, Mincheva A, Nicolai H, Solomon E, Lichter P, Poustka A. Wilgenbus KK, et al. Among authors: mincheva a. Cytogenet Cell Genet. 1996;73(3):240-3. doi: 10.1159/000134347. Cytogenet Cell Genet. 1996. PMID: 8697816

5

Assignment of the human genes for hepatocyte nuclear factor 3-alpha, -beta, and -gamma (HNF3A, HNF3B, HNF3G) to 14q12-q13, 20p11, and 19q13.2-q13.4.

Mincheva A, Lichter P, Schütz G, Kaestner KH. Mincheva A, et al. Genomics. 1997 Feb 1;39(3):417-9. doi: 10.1006/geno.1996.4477. Genomics. 1997. PMID: 9119385 No abstract available.

6

Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.

Wilgenbus KK, Seranski P, Brown A, Leuchs B, Mincheva A, Lichter P, Poustka A. Wilgenbus KK, et al. Among authors: mincheva a. Genomics. 1997 May 15;42(1):1-10. doi: 10.1006/geno.1997.4707. Genomics. 1997. PMID: 9177769

7

Pbx4, a new Pbx family member on mouse chromosome 8, is expressed during spermatogenesis.

Wagner K, Mincheva A, Korn B, Lichter P, Pöpperl H. Wagner K, et al. Among authors: mincheva a. Mech Dev. 2001 May;103(1-2):127-31. doi: 10.1016/s0925-4773(01)00349-5. Mech Dev. 2001. PMID: 11335119 Free article.

8

Assignment of TRADD to human chromosome band 16q22 by in situ hybridization.

Scheuerpflug CG, Lichter P, Debatin KM, Mincheva A. Scheuerpflug CG, et al. Among authors: mincheva a. Cytogenet Cell Genet. 2001;92(3-4):347-8. doi: 10.1159/000056927. Cytogenet Cell Genet. 2001. PMID: 11435712 No abstract available.

9

FARP2, HDLBP and PASK are downregulated in a patient with autism and 2q37.3 deletion syndrome.

Felder B, Radlwimmer B, Benner A, Mincheva A, Tödt G, Beyer KS, Schuster C, Bölte S, Schmötzer G, Klauck SM, Poustka F, Lichter P, Poustka A. Felder B, et al. Among authors: mincheva a. Am J Med Genet A. 2009 May;149A(5):952-9. doi: 10.1002/ajmg.a.32779. Am J Med Genet A. 2009. PMID: 19365831

10

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.

Scheurlen WG, Seranski P, Mincheva A, Kühl J, Sörensen N, Krauss J, Lichter P, Poustka A, Wilgenbus KK. Scheurlen WG, et al. Among authors: mincheva a. Genes Chromosomes Cancer. 1997 Jan;18(1):50-8. doi: 10.1002/(sici)1098-2264(199701)18:1<50::aid-gcc6>3.0.co;2-0. Genes Chromosomes Cancer. 1997. PMID: 8993980

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