Kalchman M - Search Results

1

The influence of huntingtin protein size on nuclear localization and cellular toxicity.

Hackam AS, Singaraja R, Wellington CL, Metzler M, McCutcheon K, Zhang T, Kalchman M, Hayden MR. Hackam AS, et al. Among authors: kalchman m. J Cell Biol. 1998 Jun 1;141(5):1097-105. doi: 10.1083/jcb.141.5.1097. J Cell Biol. 1998. PMID: 9606203 Free PMC article.

2

HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain.

Kalchman MA, Koide HB, McCutcheon K, Graham RK, Nichol K, Nishiyama K, Kazemi-Esfarjani P, Lynn FC, Wellington C, Metzler M, Goldberg YP, Kanazawa I, Gietz RD, Hayden MR. Kalchman MA, et al. Nat Genet. 1997 May;16(1):44-53. doi: 10.1038/ng0597-44. Nat Genet. 1997. PMID: 9140394

3

Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract.

Goldberg YP, Nicholson DW, Rasper DM, Kalchman MA, Koide HB, Graham RK, Bromm M, Kazemi-Esfarjani P, Thornberry NA, Vaillancourt JP, Hayden MR. Goldberg YP, et al. Among authors: kalchman ma. Nat Genet. 1996 Aug;13(4):442-9. doi: 10.1038/ng0896-442. Nat Genet. 1996. PMID: 8696339

4

Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzyme.

Kalchman MA, Graham RK, Xia G, Koide HB, Hodgson JG, Graham KC, Goldberg YP, Gietz RD, Pickart CM, Hayden MR. Kalchman MA, et al. J Biol Chem. 1996 Aug 9;271(32):19385-94. doi: 10.1074/jbc.271.32.19385. J Biol Chem. 1996. PMID: 8702625 Free article.

5

Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript.

Goldberg YP, Kalchman MA, Metzler M, Nasir J, Zeisler J, Graham R, Koide HB, O'Kusky J, Sharp AH, Ross CA, Jirik F, Hayden MR. Goldberg YP, et al. Among authors: kalchman ma. Hum Mol Genet. 1996 Feb;5(2):177-85. doi: 10.1093/hmg/5.2.177. Hum Mol Genet. 1996. PMID: 8824873

6

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression.

Lin B, Rommens JM, Graham RK, Kalchman M, MacDonald H, Nasir J, Delaney A, Goldberg YP, Hayden MR. Lin B, et al. Among authors: kalchman m. Hum Mol Genet. 1993 Oct;2(10):1541-5. doi: 10.1093/hmg/2.10.1541. Hum Mol Genet. 1993. PMID: 7903579

7

Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms.

Lin B, Nasir J, Kalchman MA, McDonald H, Zeisler J, Goldberg YP, Hayden MR. Lin B, et al. Among authors: kalchman ma. Genomics. 1995 Feb 10;25(3):707-15. doi: 10.1016/0888-7543(95)80014-d. Genomics. 1995. PMID: 7759106

8

Forskolin and dopamine D1 receptor activation increase huntingtin's association with endosomes in immortalized neuronal cells of striatal origin.

Kim M, Velier J, Chase K, Laforet G, Kalchman MA, Hayden MR, Won L, Heller A, Aronin N, Difiglia M. Kim M, et al. Among authors: kalchman ma. Neuroscience. 1999;89(4):1159-67. doi: 10.1016/s0306-4522(98)00400-x. Neuroscience. 1999. PMID: 10362304

9

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.

Andrew SE, Goldberg YP, Kremer B, Telenius H, Theilmann J, Adam S, Starr E, Squitieri F, Lin B, Kalchman MA, et al. Andrew SE, et al. Among authors: kalchman ma. Nat Genet. 1993 Aug;4(4):398-403. doi: 10.1038/ng0893-398. Nat Genet. 1993. PMID: 8401589

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