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Results: 1-16 |
Results: 16

Authors: PETRUKHIN K KOISTI MJ BAKALL B LI W XIE GC MARKNELL T SANDGREN O FORSMAN K HOLMGREN G ANDREASSON S VUJIC M BERGEN AAB MCGARTYDUGAN V FIGUEROA D AUSTIN CP METZKER ML CASKEY CT WADELIUS C
Citation: K. Petrukhin et al., IDENTIFICATION OF THE GENE RESPONSIBLE FOR BEST MACULAR DYSTROPHY, Nature genetics, 19(3), 1998, pp. 241-247

Authors: NOLL M PETRUKHIN K LUTSENKO S
Citation: M. Noll et al., IDENTIFICATION OF A NOVEL TRANSCRIPTION REGULATOR FROM PROTEUS-MIRABILIS, PMTR, REVEALED A POSSIBLE ROLE OF YJAI PROTEIN IN BALANCING ZINC IN ESCHERICHIA-COLI, The Journal of biological chemistry, 273(33), 1998, pp. 21393-21401

Authors: YANG XL MIURA N KAWARADA Y TERADA K PETRUKHIN K GILLIAM TC SUGIYAMA T
Citation: Xl. Yang et al., 2 FORMS OF WILSON-DISEASE PROTEIN PRODUCED BY ALTERNATIVE SPLICING ARE LOCALIZED IN DISTINCT CELLULAR COMPARTMENTS, Biochemical journal, 326, 1997, pp. 897-902

Authors: LUTSENKO S PETRUKHIN K COOPER MJ GILLIAM CT KAPLAN JH
Citation: S. Lutsenko et al., N-TERMINAL DOMAINS OF HUMAN COPPER-TRANSPORTING ADENOSINE TRIPHOSPHATASES (THE WILSONS AND MENKES DISEASE PROTEINS) BIND COPPER SELECTIVELYIN-VIVO AND IN-VITRO WITH STOICHIOMETRY OF ONE COPPER PER METAL-BINDING REPEAT, The Journal of biological chemistry, 272(30), 1997, pp. 18939-18944

Authors: NOLL M PETRUKHIN K LUTSENKO S
Citation: M. Noll et al., ZN-DEPENDENT PROTEOLYTIC CLEAVAGE OF F188 GENE-PRODUCT IS ASSOCIATED WITH AN INCREASE IN ZN-RESISTANCE IN BACTERIA, Biophysical journal, 72(2), 1997, pp. 368-368

Authors: LUTSENKO S PETRUKHIN K GILLIAM TC KAPLAN JH
Citation: S. Lutsenko et al., CHARACTERIZATION OF METAL-BINDING PROPERTIES OF THE N-TERMINAL DOMAINS OF THE MENKES AND WILSON DISEASE PROTEINS, Biophysical journal, 72(2), 1997, p.

Authors: SHAH AB CHERNOV I ZHANG HT ROSS BM DAS K LUTSENKO S PARANO E PAVONE L EVGRAFOV O IVANOVASMOLENSKAYA IA ANNEREN G WESTERMARK K URRUTIA FH PENCHASZADEH GK STERNLIEB I SCHEINBERG IH GILLIAM TC PETRUKHIN K
Citation: Ab. Shah et al., IDENTIFICATION AND ANALYSIS OF MUTATIONS IN THE WILSON-DISEASE GENE (ATP7B) - POPULATION FREQUENCIES, GENOTYPE-PHENOTYPE CORRELATION, AND FUNCTIONAL ANALYSES, American journal of human genetics, 61(2), 1997, pp. 317-328

Authors: KLOCKARS T SAVUKOSKI M ISOSOMPPI J LAAN M JARVELA I PETRUKHIN K PALOTIE A PELTONEN L
Citation: T. Klockars et al., 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, Genomics, 35(1), 1996, pp. 71-78

Authors: KLOCKARS T LAAN M FISCHER S PETRUKHIN K JARVELA I VARILO T SAVUKOSKI M PELTONEN L
Citation: T. Klockars et al., PHYSICAL MAPPING OF THE REGION CONTAINING THE CLN5 GENE AT CHROMOSOME13Q22, Cytogenetics and cell genetics, 75(2-3), 1996, pp. 107-107

Authors: PETRUKHIN K FISCHER SG LIEBMAN JM CAYANIS E KALACHIKOV S ZHANG HT RITCH R GILLIAM TC
Citation: K. Petrukhin et al., MAPPING THE JUVENILE GLAUCOMA GENE, Investigative ophthalmology & visual science, 37(3), 1996, pp. 149-149

Authors: SHAH AB PETRUKHIN K CHERNOV I ZHANG HT ROSS BM PARANO E PAVANO L EVGRAFOV O IVANOVASMOLENKAYA IA ANNEREN G WESTERMARK K PENCHASZADEH GK STERNLIEB I SCHEINBERG IH GILLIAM TC
Citation: Ab. Shah et al., MUTATION ANALYSIS OF THE WILSON DISEASE GENE IN VARIOUS ETHNIC POPULATIONS, American journal of human genetics, 57(4), 1995, pp. 982-982

Authors: PETRUKHIN K LUTSENKO S CHERNOV I ROSS BM KAPLAN JH GILLIAM TC
Citation: K. Petrukhin et al., CHARACTERIZATION OF THE WILSON-DISEASE GENE ENCODING A P-TYPE COPPER TRANSPORTING ATPASE - GENOMIC ORGANIZATION, ALTERNATIVE SPLICING, AND STRUCTURE FUNCTION PREDICTIONS/, Human molecular genetics, 3(9), 1994, pp. 1647-1656

Authors: LUTSENKO S GENCO M PETRUKHIN K GILLIAM TC KAPLAN JH
Citation: S. Lutsenko et al., ARCHITECTURE OF P-TYPE ATPASES - CORE STRUCTURE - SPECIFIC DOMAINS, DOMAIN-DOMAIN INTERACTIONS, The FASEB journal, 8(7), 1994, pp. 10001449-10001449

Authors: PETRUKHIN K FISCHER SG PIRASTU M TANZI RE CHERNOV I DEVOTO M BRZUSTOWICZ LM CAYANIS E VITALE E RUSSO JJ MATSEOANE D BOUKHGALTER B WASCO W FIGUS AL LOUDIANOS J CAO A STERNLIEB I EVGRAFOV O PARANO E PAVONE L WARBURTON D OTT J PENCHASZADEH GK SCHEINBERG IH GILLIAM TC
Citation: K. Petrukhin et al., MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE, Nature genetics, 5(4), 1993, pp. 338-343

Authors: TANZI RE PETRUKHIN K CHERNOV I PELLEQUER JL WASCO W ROSS B ROMANO DM PARANO E PAVONE L BRZUSTOWICZ LM DEVOTO M PEPPERCORN J BUSH AI STERNLIEB I PIRASTU M GUSELLA JF EVGRAFOV O PENCHASZADEH GK HONIG B EDELMAN IS SOARES MB SCHEINBERG IH GILLIAM TC
Citation: Re. Tanzi et al., THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGYTO THE MENKES DISEASE GENE, Nature genetics, 5(4), 1993, pp. 344-350

Authors: BROWN S RUSSO J TAN DF PETRUKHIN K CHITAYAT D ROSE T WINDSOR E WEKSBERG R MCKENZIE J WARBURTON D
Citation: S. Brown et al., THE 13Q-SYNDROME - THE MOLECULAR DEFINITION OF A CRITICAL DELETION REGION IN BAND 13Q32, American journal of human genetics, 53(3), 1993, pp. 219-219
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