Mapping, cloning and genetic characterization of the region containing the Wilson disease gene
Gilliam, T.C, Matseoane, D, Parano, E, Sternlieb, I, Evgrafov, O, Boukhgalter, B, Russo, J. J, Brzustowicz, L. M, Wasco, W, Pirastu, M, Penchaszadeh, G. K, Fischer, S. G, Cayanis, E, Scheinberg, I. H, Cao, A, Figus, A. L, Loudianos, J, Vitale, E, Petrukhin, K, Warburton, D, Ott, J, Pavone, L, Devoto, M, Tanzi, R.E, Chernov, I
Published in Nature genetics (01.12.1993)
Published in Nature genetics (01.12.1993)
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Journal Article
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
Tanzi, R.E, Petrukhin, K, Chernov, I, Pellequer, J.L, Wasco, W, Ross, B, Romano, D.M, Parano, E, Pavone, L, Brzustowicz, L.M, Devoto, M, Peppercorn, J, Bush, A.I, Sternlieb, I, Pirastu, M, Gusella, J.F, Evgrafov, O, Penchaszadeh, G.K, Honig, B, Edelman, I.S, Soares, M.B, Scheinberg, I.H, Gilliam, T.C
Published in Nature genetics (01.12.1993)
Published in Nature genetics (01.12.1993)
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Journal Article
Pig kidney Na +,K +-ATPase : Primary structure and spatial organization
Ovchinnikov, Yu.A., Modyanov, N.N., Broude, N.E., Petrukhin, K.E., Grishin, A.V., Arzamazova, N.M., Aldanova, N.A., Monastyrskaya, G.S., Sverdlov, E.D.
Published in FEBS letters (09.06.1986)
Published in FEBS letters (09.06.1986)
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Journal Article
Efficient Construction of a Physical Map by Fiber-Fish of the CLN5 Region: Refined Assignment and Long-Range Contig Covering the Critical Region on 13q22
Klockars, T., Savukoski, M., Isosomppi, J., Laan, M., Järvelä, I., Petrukhin, K., Palotie, A., Peltonen, L.
Published in Genomics (San Diego, Calif.) (01.07.1996)
Published in Genomics (San Diego, Calif.) (01.07.1996)
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Journal Article
Development of a picosecond MCP based particle detector
Barnyakov, A.Yu, Barnyakov, M.Yu, Blinov, V.E., Bobrovnikov, V.S., Bykov, A.V., Ivanov, V.Ya, Katcin, A.A., Mamoshkina, E.V., Ovtin, I.V., Petrukhin, K.G., Pivovarov, S.G., Prisekin, V.G., Pyata, E.E.
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.02.2020)
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.02.2020)
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Journal Article
A Microsatellite Genetic Linkage Map of Human Chromosome 13
Petrukhin, Konstantin E., Speer, Marcy C., Cayanis, Eftihia, Bonaldo, Maria de Fátima, Tantravahi, Umadevi, Soares, Marcelo Bento, Fischer, Stuart G., Warburton, Dorothy, Gilliam, T.Conrad, Ott, Jurg
Published in Genomics (San Diego, Calif.) (1993)
Published in Genomics (San Diego, Calif.) (1993)
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Journal Article
Bestrophin, the Product of the Best Vitelliform Macular Dystrophy Gene (VMD2), Localizes to the Basolateral Plasma Membrane of the Retinal Pigment Epithelium
Marmorstein, Alan D., Marmorstein, Lihua Y., Rayborn, Mary, Wang, Xinxing, Hollyfield, Joe G., Petrukhin, Konstantin
Published in Proceedings of the National Academy of Sciences - PNAS (07.11.2000)
Published in Proceedings of the National Academy of Sciences - PNAS (07.11.2000)
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Journal Article
The family of human Na,K-ATPase genes ATP1AL1 gene is transcriptionally competent and probably encodes the related ion transport ATPase
Modyanov, N.N., Petrukhin, K.E., Sverdlov, V.E., Grishin, A.V., Orlova, M.Y., Kostina, M.B., Makarevich, O.I., Broude, N.E., Monastyrskaya, G.S., Sverdlov, E.D.
Published in FEBS letters (14.01.1991)
Published in FEBS letters (14.01.1991)
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Journal Article
The family of human Na +,K +-ATPase genes No less than five genes and/or pseudogenes related to the α-subunit
Sverdlov, E.D., Monastyrskaya, G.S., Broude, N.E., Ushkaryov, Yu.A., Allikmets, R.L., Melkov, A.M., Smirnov, Yu.V., Malyshev, I.V., Dulobova, I.E., Petrukhin, K.E., Grishin, A.V., Kijatkin, N.I., Kostina, M.B., Sverdlov, V.E., Modyanov, N.N., Ovchnikov, Yu.A.
Published in FEBS letters (15.06.1987)
Published in FEBS letters (15.06.1987)
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Journal Article
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
Petrukhin, Konstantin, Zhang, Kang, Kniazeva, Marina, Han, Min, Li, Wen, Yu, Zhengya, Yang, Zhenglin, Li, Yang, Metzker, Michael L, Allikmets, Rando, Zack, Donald J, Kakuk, Laura E, Lagali, Pamela S, Wong, Paul W, MacDonald, Ian M, Sieving, Paul A, Figueroa, David J, Austin, Christopher P, Gould, Robert J, Ayyagari, Radha
Published in Nature genetics (01.01.2001)
Published in Nature genetics (01.01.2001)
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Journal Article
Na +, K +-ATPase: Tissue-specific expression of genes coding for α-subunit in diverse human tissues
Sverdlov, E.D., Akopyanz, N.S., Petrukhin, K.E., Broude, N.E., Monastyrskaya, G.S., Modyanov, N.N.
Published in FEBS letters (24.10.1988)
Published in FEBS letters (24.10.1988)
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Journal Article
Identification of the gene responsible for Best macular dystrophy
Petrukhin, Konstantin, Wadelius, Claes, Koisti, Markus J, Bakall, Benjamin, Li, Wen, Xie, Guochun, Marknell, Towa, Sandgren, Ola, Forsman, Kristina, Holmgren, Gösta, Andreasson, Sten, Vujic, Mihailo, Bergen, Arthur A. B, McGarty-Dugan, Valarie, Figueroa, David, Austin, Christopher P, Metzker, Michael L, Caskey, C.Thomas
Published in Nature genetics (01.07.1998)
Published in Nature genetics (01.07.1998)
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Journal Article
Diverse Macular Dystrophy Phenotype Caused by a Novel Complex Mutation in the ELOVL4 Gene
Bernstein, Paul S, Tammur, Jaana, Singh, Nanda, Hutchinson, Amy, Dixon, Missy, Pappas, Chris M, Zabriskie, Norman A, Zhang, Kang, Petrukhin, Konstantin, Leppert, Mark, Allikmets, Rando
Published in Investigative ophthalmology & visual science (01.12.2001)
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Published in Investigative ophthalmology & visual science (01.12.2001)
Journal Article
Human Na +, K + -ATPase genes : β-Subunit gene family contains at least one gene and one pseudogene
Ushkaryov, Yu.A., Monastyrskaya, G.S., Broude, N.E., Nikiforova, N.N., Bessarab, D.A., Orlova, M.Yu, Petrukhin, K.E., Modyanov, N.N., Sverdlov, E.D.
Published in FEBS Letters (06.11.1989)
Published in FEBS Letters (06.11.1989)
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Assessment of mutations in the best macular dystrophy ( VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull’s-eye maculopathy
Seddon, Johanna M, Afshari, Mehran A, Sharma, Sanjay, Bernstein, Paul S, Chong, Sandy, Hutchinson, Amy, Petrukhin, Konstantin, Allikmets, Rando
Published in Ophthalmology (Rochester, Minn.) (01.11.2001)
Published in Ophthalmology (Rochester, Minn.) (01.11.2001)
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