Kunst CB - Search Results

1

Evolution of the cryptic FMR1 CGG repeat.

Eichler EE, Kunst CB, Lugenbeel KA, Ryder OA, Davison D, Warren ST, Nelson DL. Eichler EE, et al. Among authors: kunst cb. Nat Genet. 1995 Nov;11(3):301-8. doi: 10.1038/ng1195-301. Nat Genet. 1995. PMID: 7581454

2

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ. van den Ouweland AM, et al. Among authors: kunst cb. Hum Mol Genet. 1994 Oct;3(10):1823-7. doi: 10.1093/hmg/3.10.1823. Hum Mol Genet. 1994. PMID: 7849707

3

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Ashley CT, et al. Among authors: kunst cb. Nat Genet. 1993 Jul;4(3):244-51. doi: 10.1038/ng0793-244. Nat Genet. 1993. PMID: 8358432

4

FMR1 in global populations.

Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST. Kunst CB, et al. Am J Hum Genet. 1996 Mar;58(3):513-22. Am J Hum Genet. 1996. PMID: 8644711 Free PMC article.

5

The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.

Kunst CB, Leeflang EP, Iber JC, Arnheim N, Warren ST. Kunst CB, et al. J Med Genet. 1997 Aug;34(8):627-31. doi: 10.1136/jmg.34.8.627. J Med Genet. 1997. PMID: 9279752 Free PMC article.

6

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST. Gunter C, et al. Among authors: kunst cb. Hum Mol Genet. 1998 Nov;7(12):1935-46. doi: 10.1093/hmg/7.12.1935. Hum Mol Genet. 1998. PMID: 9811938

7

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

Kunst CB, Warren ST. Kunst CB, et al. Cell. 1994 Jun 17;77(6):853-61. doi: 10.1016/0092-8674(94)90134-1. Cell. 1994. PMID: 7911740

8

Actin-binding protein (ABP-280) filamin gene (FLN) maps telomeric to the color vision locus (R/GCP) and centromeric to G6PD in Xq28.

Gorlin JB, Henske E, Warren ST, Kunst CB, D'Urso M, Palmieri G, Hartwig JH, Bruns G, Kwiatkowski DJ. Gorlin JB, et al. Among authors: kunst cb. Genomics. 1993 Aug;17(2):496-8. doi: 10.1006/geno.1993.1354. Genomics. 1993. PMID: 8406501

9

Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactions.

Kunst CB, Mezey E, Brownstein MJ, Patterson D. Kunst CB, et al. Nat Genet. 1997 Jan;15(1):91-4. doi: 10.1038/ng0197-91. Nat Genet. 1997. PMID: 8988176

10

Genetic mapping of a mouse modifier gene that can prevent ALS onset.

Kunst CB, Messer L, Gordon J, Haines J, Patterson D. Kunst CB, et al. Genomics. 2000 Dec 1;70(2):181-9. doi: 10.1006/geno.2000.6379. Genomics. 2000. PMID: 11112346

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