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A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.
Genes (Basel). 2022 Sep 28;13(10):1750. doi: 10.3390/genes13101750.
Genes (Basel). 2022.
PMID: 36292635
Free PMC article.
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.
Myasnikov R, Bukaeva A, Kulikova O, Meshkov A, Kiseleva A, Ershova A, Petukhova A, Divashuk M, Zotova E, Sotnikova E, Kharlap M, Zharikova A, Vyatkin Y, Ramensky V, Abisheva A, Muraveva A, Koretskiy S, Kudryavtseva M, Popov S, Utkina M, Mershina E, Sinitsyn V, Kogan E, Blagova O, Drapkina O.
Myasnikov R, et al.
Genes (Basel). 2022 Feb 7;13(2):309. doi: 10.3390/genes13020309.
Genes (Basel). 2022.
PMID: 35205353
Free PMC article.
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The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Meshkov A, Ershova A, Kiseleva A, Zotova E, Sotnikova E, Petukhova A, Zharikova A, Malyshev P, Rozhkova T, Blokhina A, Limonova A, Ramensky V, Divashuk M, Khasanova Z, Bukaeva A, Kurilova O, Skirko O, Pokrovskaya M, Mikova V, Snigir E, Akinshina A, Mitrofanov S, Kashtanova D, Makarov V, Kukharchuk V, Boytsov S, Yudin S, Drapkina O.
Meshkov A, et al.
Genes (Basel). 2021 Jan 6;12(1):66. doi: 10.3390/genes12010066.
Genes (Basel). 2021.
PMID: 33418990
Free PMC article.
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CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene.
Egorova TV, Zotova ED, Reshetov DA, Polikarpova AV, Vassilieva SG, Vlodavets DV, Gavrilov AA, Ulianov SV, Buchman VL, Deykin AV.
Egorova TV, et al. Among authors: zotova ed.
Dis Model Mech. 2019 Apr 25;12(4):dmm037655. doi: 10.1242/dmm.037655.
Dis Model Mech. 2019.
PMID: 31028078
Free PMC article.
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