Ivaschenko T - Search Results

1

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Among authors: ivaschenko t. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353

2

Two new mutations detected by single-strand conformation polymorphism analysis in cystic fibrosis from Russia.

Ivaschenko TE, Baranov VS, Dean M. Ivaschenko TE, et al. Hum Genet. 1993 Mar;91(1):63-5. doi: 10.1007/BF00230224. Hum Genet. 1993. PMID: 7681034

3

Novel frameshift mutation in exon 4 of CFTR gene.

Ivaschenko T, Bakay M, Baranov V. Ivaschenko T, et al. Hum Mutat. 1995;5(2):184-5. doi: 10.1002/humu.1380050215. Hum Mutat. 1995. PMID: 7538377 No abstract available.

4

Rapid and efficient PCR/StyI test for identification of common mutation R408W in phenylketonuria patients.

Ivaschenko T, Baranov VS. Ivaschenko T, et al. J Med Genet. 1993 Feb;30(2):153-4. doi: 10.1136/jmg.30.2.153. J Med Genet. 1993. PMID: 8445621 Free PMC article. No abstract available.

5

Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR.

Baranov VS, Ivaschenko TE, Gorbunova VN, Livshitz LA, Venozinskis MT, Gembovskaya SA, Kalinin VN, Romanenko OP, Gembitzkaya TE, Orlov AV, et al. Baranov VS, et al. Among authors: ivaschenko te. Hum Genet. 1991 May;87(1):61-4. doi: 10.1007/BF01213094. Hum Genet. 1991. PMID: 2037283

6

Proportion of the GSTM1 0/0 genotype in some Slavic populations and its correlation with cystic fibrosis and some multifactorial diseases.

Baranov VS, Ivaschenko T, Bakay B, Aseev M, Belotserkovskaya R, Baranova H, Malet P, Perriot J, Mouraire P, Baskakov VN, Savitskyi GA, Gorbushin S, Deyneka SI, Michnin E, Barchuck A, Vakharlovsky V, Pavlov G, Shilko VI, Guembitzkaya T, Kovaleva L. Baranov VS, et al. Among authors: ivaschenko t. Hum Genet. 1996 Apr;97(4):516-20. doi: 10.1007/BF02267078. Hum Genet. 1996. PMID: 8834254

7

A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death.

Ivaschenko TE, White MB, Dean M, Baranov VS. Ivaschenko TE, et al. Genomics. 1991 May;10(1):298-9. doi: 10.1016/0888-7543(91)90517-i. Genomics. 1991. PMID: 1710601 No abstract available.

8

Peculiarities of the GSTM1 0/0 genotype in French heavy smokers with various types of chronic bronchitis.

Baranova H, Perriot J, Albuisson E, Ivaschenko T, Baranov VS, Hemery B, Mouraire P, Riol N, Malet P. Baranova H, et al. Among authors: ivaschenko t. Hum Genet. 1997 Jun;99(6):822-6. doi: 10.1007/s004390050455. Hum Genet. 1997. PMID: 9187680

9

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT).

White MB, Krueger LJ, Holsclaw DS Jr, Gerrard BC, Stewart C, Quittell L, Dolganov G, Baranov V, Ivaschenko T, Kapronov NI, et al. White MB, et al. Among authors: ivaschenko t. Genomics. 1991 May;10(1):266-9. doi: 10.1016/0888-7543(91)90510-l. Genomics. 1991. PMID: 1710600

10

Five years' experience of prenatal diagnosis of cystic fibrosis in the former U.S.S.R.

Baranov VS, Gorbunova VN, Ivaschenko TE, Shwed NYu, Osinovskaya NS, Kascheeva TK, Lebedev VM, Mikhailov AV, Vakharlovsky VG, Kuznetzova TV. Baranov VS, et al. Among authors: ivaschenko te. Prenat Diagn. 1992 Jul;12(7):575-86. doi: 10.1002/pd.1970120703. Prenat Diagn. 1992. PMID: 1354866

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