Gilliam TC - Search Results

1

Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases).

Lutsenko S, Petrukhin K, Gilliam TC, Kaplan JH. Lutsenko S, et al. Among authors: gilliam tc. Ann N Y Acad Sci. 1997 Nov 3;834:155-7. doi: 10.1111/j.1749-6632.1997.tb52246.x. Ann N Y Acad Sci. 1997. PMID: 9405803 No abstract available.

2

Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments.

Yang XL, Miura N, Kawarada Y, Terada K, Petrukhin K, Gilliam T, Sugiyama T. Yang XL, et al. Biochem J. 1997 Sep 15;326 ( Pt 3)(Pt 3):897-902. doi: 10.1042/bj3260897. Biochem J. 1997. PMID: 9307043 Free PMC article.

3

Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions.

Petrukhin K, Lutsenko S, Chernov I, Ross BM, Kaplan JH, Gilliam TC. Petrukhin K, et al. Among authors: gilliam tc. Hum Mol Genet. 1994 Sep;3(9):1647-56. doi: 10.1093/hmg/3.9.1647. Hum Mol Genet. 1994. PMID: 7833924

4

Genetic disorders of copper metabolism.

Petrukhin K, Gilliam TC. Petrukhin K, et al. Among authors: gilliam tc. Curr Opin Pediatr. 1994 Dec;6(6):698-701. doi: 10.1097/00008480-199412000-00015. Curr Opin Pediatr. 1994. PMID: 7849817 Review.

5

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.

Shah AB, Chernov I, Zhang HT, Ross BM, Das K, Lutsenko S, Parano E, Pavone L, Evgrafov O, Ivanova-Smolenskaya IA, Annerén G, Westermark K, Urrutia FH, Penchaszadeh GK, Sternlieb I, Scheinberg IH, Gilliam TC, Petrukhin K. Shah AB, et al. Among authors: gilliam tc. Am J Hum Genet. 1997 Aug;61(2):317-28. doi: 10.1086/514864. Am J Hum Genet. 1997. PMID: 9311736 Free PMC article.

6

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.

Buiakova OI, Xu J, Lutsenko S, Zeitlin S, Das K, Das S, Ross BM, Mekios C, Scheinberg IH, Gilliam TC. Buiakova OI, et al. Among authors: gilliam tc. Hum Mol Genet. 1999 Sep;8(9):1665-71. doi: 10.1093/hmg/8.9.1665. Hum Mol Genet. 1999. PMID: 10441329

7

Dinucleotide repeat polymorphism at the D1S182 locus.

Petrukhin KE, Gilliam TC. Petrukhin KE, et al. Among authors: gilliam tc. Hum Mol Genet. 1992 Sep;1(6):454. Hum Mol Genet. 1992. PMID: 1301921 No abstract available.

8

Dinucleotide repeat polymorphism at the D19S206 locus.

Petrukhin KE, Gilliam TC. Petrukhin KE, et al. Among authors: gilliam tc. Hum Mol Genet. 1992 Sep;1(6):454. Hum Mol Genet. 1992. PMID: 1301922 No abstract available.

9

Dinucleotide repeat polymorphism at the D4S251 locus.

Petrukhin KE, Modyanov NN, Gilliam TC. Petrukhin KE, et al. Among authors: gilliam tc. Hum Mol Genet. 1992 Aug;1(5):349. doi: 10.1093/hmg/1.5.349. Hum Mol Genet. 1992. PMID: 1303215 No abstract available.

10

A microsatellite genetic linkage map of human chromosome 13.

Petrukhin KE, Speer MC, Cayanis E, Bonaldo MF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J. Petrukhin KE, et al. Among authors: gilliam tc. Genomics. 1993 Jan;15(1):76-85. doi: 10.1006/geno.1993.1012. Genomics. 1993. PMID: 8432553

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