Zinchenko R - Search Results

1

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.

Kazantseva A, Goltsov A, Zinchenko R, Grigorenko AP, Abrukova AV, Moliaka YK, Kirillov AG, Guo Z, Lyle S, Ginter EK, Rogaev EI. Kazantseva A, et al. Among authors: zinchenko r. Science. 2006 Nov 10;314(5801):982-5. doi: 10.1126/science.1133276. Science. 2006. PMID: 17095700

2

Evaluation of orphan diseases global burden.

Makarova EV, Krysanov IS, Valilyeva TP, Vasiliev MD, Zinchenko RA. Makarova EV, et al. Eur J Transl Myol. 2021 May 14;31(2):9610. doi: 10.4081/ejtm.2021.9610. Eur J Transl Myol. 2021. PMID: 33985324 Free PMC article.

3

[Molecular and genetic aspects of age-related macular degeneration and glaucoma].

Efendieva MH, Budzinskaya MV, Kadyshev VV, Zinchenko RA, Savochkina OA, Pupysheva AD. Efendieva MH, et al. Among authors: zinchenko ra. Vestn Oftalmol. 2019;135(3):121-127. doi: 10.17116/oftalma2019135031121. Vestn Oftalmol. 2019. PMID: 31393456 Review. Russian.

4

The Presentation of Two Unrelated Clinical Cases from the Republic of North Ossetia-Alania with the Same Previously Undescribed Variant in the COL6A2 Gene.

Ionova SA, Murtazina AF, Tebieva IS, Getoeva ZK, Dadali EL, Chausova PA, Shchagina OA, Marakhonov AV, Kutsev SI, Zinchenko RA. Ionova SA, et al. Int J Mol Sci. 2022 Oct 12;23(20):12127. doi: 10.3390/ijms232012127. Int J Mol Sci. 2022. PMID: 36292982 Free PMC article.

5

[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)].

Zolnikova IV, Milash SV, Zinchenko RA, Polyakov AV, Stepanova AA, Chernyak AB, Sianosyan AA, Egorova IV, Kadyshev VV. Zolnikova IV, et al. Among authors: zinchenko ra. Vestn Oftalmol. 2022;138(5):80-86. doi: 10.17116/oftalma202213805180. Vestn Oftalmol. 2022. PMID: 36288421 Russian.

6

Clinical and Functional Characteristics of the E92K CFTR Gene Variant in the Russian and Turkish Population of People with Cystic Fibrosis.

Kondratyeva E, Melyanovskaya Y, Bulatenko N, Davydenko K, Filatova A, Efremova A, Skoblov M, Bukharova T, Sherman V, Voronkova A, Zhekaite E, Krasovskiy S, Amelina E, Petrova N, Polyakov A, Adyan T, Starinova M, Krasnova M, Vasilyev A, Makhnach O, Zinchenko R, Kutsev S, Gokdemir Y, Karadag B, Goldshtein D. Kondratyeva E, et al. Among authors: zinchenko r. Int J Mol Sci. 2023 Mar 28;24(7):6351. doi: 10.3390/ijms24076351. Int J Mol Sci. 2023. PMID: 37047318 Free PMC article.

7

[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy].

Vasilyeva TA, Kadyshev VV, Marakhonov AV, Kanivets IV, Korostelev SA, Koshkin PA, Pyankov DV, Petrova NV, Kutsev SI, Zinchenko RA. Vasilyeva TA, et al. Among authors: zinchenko ra. Vestn Oftalmol. 2023;139(1):69-74. doi: 10.17116/oftalma202313901169. Vestn Oftalmol. 2023. PMID: 36924516 Russian.

8

Study of The Molecular Nature of Congenital Cataracts in Patients from The Volga-Ural Region.

Khidiyatova I, Khidiyatova I, Zinchenko R, Marakhonov A, Karunas A, Avkhadeeva S, Aznzbaev M, Khusnutdinova E. Khidiyatova I, et al. Among authors: zinchenko r. Curr Issues Mol Biol. 2023 Jun 15;45(6):5145-5163. doi: 10.3390/cimb45060327. Curr Issues Mol Biol. 2023. PMID: 37367076 Free PMC article.

9

Clinical and Genetic Characteristics of a Patient with Cystic Fibrosis with a Complex Allele [E217G;G509D] and Functional Evaluation of the CFTR Channel.

Kondratyeva E, Melyanovskaya Y, Efremova A, Krasnova M, Mokrousova D, Bulatenko N, Petrova N, Polyakov A, Adyan T, Kovalskaia V, Bukharova T, Marakhonov A, Zinchenko R, Zhekaite E, Buhonin A, Goldshtein D. Kondratyeva E, et al. Among authors: zinchenko r. Genes (Basel). 2023 Aug 28;14(9):1705. doi: 10.3390/genes14091705. Genes (Basel). 2023. PMID: 37761847 Free PMC article.

10

Total hypotrichosis: genetic form of alopecia not linked to hairless gene.

Rogaev EI, Zinchenko RA, Dvoryachikov G, Sherbatich T, Ginter EK. Rogaev EI, et al. Among authors: zinchenko ra. Lancet. 1999 Sep 25;354(9184):1097-8. doi: 10.1016/s0140-6736(99)02816-0. Lancet. 1999. PMID: 10509509

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

114 results

Search Page