Deschênes SM - Search Results

1

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease.

Scherer SS, Bone LJ, Deschênes SM, Abel A, Balice-Gordon RJ, Fischbeck KH. Scherer SS, et al. Among authors: deschenes sm. Novartis Found Symp. 1999;219:175-85; discussion 185-7. doi: 10.1002/9780470515587.ch11. Novartis Found Symp. 1999. PMID: 10207904 Review.

2

Connexin32 is a myelin-related protein in the PNS and CNS.

Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL. Scherer SS, et al. Among authors: deschenes sm. J Neurosci. 1995 Dec;15(12):8281-94. doi: 10.1523/JNEUROSCI.15-12-08281.1995. J Neurosci. 1995. PMID: 8613761 Free PMC article.

3

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Fischbeck KH, Deschênes SM, Bone LJ, Scherer SS. Fischbeck KH, et al. Among authors: deschenes sm. Cold Spring Harb Symp Quant Biol. 1996;61:673-7. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246493 Review. No abstract available.

4

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS. Bone LJ, et al. Among authors: deschenes sm. Neurobiol Dis. 1997;4(3-4):221-30. doi: 10.1006/nbdi.1997.0152. Neurobiol Dis. 1997. PMID: 9361298 Free article. Review.

5

Altered trafficking of mutant connexin32.

Deschênes SM, Walcott JL, Wexler TL, Scherer SS, Fischbeck KH. Deschênes SM, et al. J Neurosci. 1997 Dec 1;17(23):9077-84. doi: 10.1523/JNEUROSCI.17-23-09077.1997. J Neurosci. 1997. PMID: 9364054 Free PMC article.

6

Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins.

VanSlyke JK, Deschenes SM, Musil LS. VanSlyke JK, et al. Among authors: deschenes sm. Mol Biol Cell. 2000 Jun;11(6):1933-46. doi: 10.1091/mbc.11.6.1933. Mol Biol Cell. 2000. PMID: 10848620 Free PMC article.

7

Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.

Deschênes SM, Puck JM, Dutra AS, Somberg RL, Felsburg PJ, Henthorn PS. Deschênes SM, et al. Genomics. 1994 Sep 1;23(1):62-8. doi: 10.1006/geno.1994.1459. Genomics. 1994. PMID: 7829103 Free article.

8

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

Puck JM, Deschênes SM, Porter JC, Dutra AS, Brown CJ, Willard HF, Henthorn PS. Puck JM, et al. Among authors: deschenes sm. Hum Mol Genet. 1993 Aug;2(8):1099-104. doi: 10.1093/hmg/2.8.1099. Hum Mol Genet. 1993. PMID: 8401490

9

Mammalian DNA mismatch repair.

Buermeyer AB, Deschênes SM, Baker SM, Liskay RM. Buermeyer AB, et al. Among authors: deschenes sm. Annu Rev Genet. 1999;33:533-64. doi: 10.1146/annurev.genet.33.1.533. Annu Rev Genet. 1999. PMID: 10690417 Review.

10

Mutations affecting a putative MutLalpha endonuclease motif impact multiple mismatch repair functions.

Erdeniz N, Nguyen M, Deschênes SM, Liskay RM. Erdeniz N, et al. Among authors: deschenes sm. DNA Repair (Amst). 2007 Oct 1;6(10):1463-70. doi: 10.1016/j.dnarep.2007.04.013. Epub 2007 Jun 12. DNA Repair (Amst). 2007. PMID: 17567544 Free PMC article.

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