Evgrafov OV - Search Results

1

Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia.

Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakov AV, Lebedev VM, Kuznetzova TV, Shlykova SN, et al. Baranov VS, et al. Among authors: evgrafov ov. Prenat Diagn. 1993 May;13(5):323-33. doi: 10.1002/pd.1970130503. Prenat Diagn. 1993. PMID: 8101987

2

Prenatal diagnosis of spinal muscular atrophy in Russia.

Shagina I, Dadali HL, Sitnikov VP, Pugachev VV, Malygina NA, Evgrafov OV. Shagina I, et al. Among authors: evgrafov ov. Prenat Diagn. 1995 Jan;15(1):27-34. doi: 10.1002/pd.1970150107. Prenat Diagn. 1995. PMID: 7739994

3

[Analysis of deletions in the dystrophin gene by the multiplex amplification method in patients suffering from Duchenne's muscular dystrophy].

Malysheva OV, Poliakov AV, Zaĭtseva SP, Malygina NA, Gorbunova VN, Evgrafov OV, Makarov VG, Krasil'nikov VV, Baranov VS, Vadalian LO. Malysheva OV, et al. Among authors: evgrafov ov. Mol Gen Mikrobiol Virusol. 1992 May-Jun;(5-6):27-31. Mol Gen Mikrobiol Virusol. 1992. PMID: 1454081 Russian.

4

[Expression of the human dystrophin gene in mdx mouse muscle fibers after transfection using liposomes and synthetic oligopeptides].

Baranov VS, Tarasenko OV, Baranov VS, Tarasenko OV, Baranov AN, Kiselev AV, Ivashchenko TE, Evgrafov OV, Mikhailov Vm, Dickson G. Baranov VS, et al. Among authors: evgrafov ov. Genetika. 1998 Jul;34(7):876-82. Genetika. 1998. PMID: 9749328 Russian.

5

Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia.

Evgrafov OV, Polyakov AV, Dzenis IG, Baharev VA. Evgrafov OV, et al. Hum Mutat. 1995;5(2):131-6. doi: 10.1002/humu.1380050206. Hum Mutat. 1995. PMID: 7749411

6

A novel IVS2 -2A>T splicing mutation in the GH-1 gene in familial isolated growth hormone deficiency type II in the spectrum of other splicing mutations in the Russian population.

Fofanova OV, Evgrafov OV, Polyakov AV, Poltaraus AB, Peterkova VA, Dedov II. Fofanova OV, et al. Among authors: evgrafov ov. J Clin Endocrinol Metab. 2003 Feb;88(2):820-6. doi: 10.1210/jc.2002-020269. J Clin Endocrinol Metab. 2003. PMID: 12574219

7

High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect.

Polyakov AV, Dzenis IG, Baharev VA, Evgrafov OV. Polyakov AV, et al. Among authors: evgrafov ov. Hum Mutat. 1998;Suppl 1:S53-4. doi: 10.1002/humu.1380110118. Hum Mutat. 1998. PMID: 9452039 No abstract available.

8

Bacterial beta-galactosidase and human dystrophin genes are expressed in mouse skeletal muscle fibers after ballistic transfection.

Zelenin AV, Kolesnikov VA, Tarasenko OA, Shafei RA, Zelenina IA, Mikhailov VV, Semenova ML, Kovalenko DV, Artemyeva OV, Ivaschenko TE, Evgrafov OV, Dickson G, Baranovand VS. Zelenin AV, et al. Among authors: evgrafov ov. FEBS Lett. 1997 Sep 8;414(2):319-22. doi: 10.1016/s0014-5793(97)01019-3. FEBS Lett. 1997. PMID: 9315710 Free article.

9

GH-1 gene splicing mutations: molecular basis of hereditary isolated growth hormone deficiency in children.

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II. Fofanova OV, et al. Among authors: evgrafov ov. Bull Exp Biol Med. 2006 Mar;141(3):347-52. doi: 10.1007/s10517-006-0168-2. Bull Exp Biol Med. 2006. PMID: 17073157

10

A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency.

Fofanova OV, Evgrafov OV, Polyakov AV, Peterkova VA, Dedov II. Fofanova OV, et al. Among authors: evgrafov ov. Hormones (Athens). 2006 Oct-Dec;5(4):288-94. doi: 10.14310/horm.2002.11194. Hormones (Athens). 2006. PMID: 17178704 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

99 results

Search Page