Wensel TG - Search Results

1

Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration.

Shroyer NF, Lewis RA, Yatsenko AN, Wensel TG, Lupski JR. Shroyer NF, et al. Among authors: wensel tg. Hum Mol Genet. 2001 Nov 1;10(23):2671-8. doi: 10.1093/hmg/10.23.2671. Hum Mol Genet. 2001. PMID: 11726554

2

ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies.

Wiszniewski W, Zaremba CM, Yatsenko AN, Jamrich M, Wensel TG, Lewis RA, Lupski JR. Wiszniewski W, et al. Among authors: wensel tg. Hum Mol Genet. 2005 Oct 1;14(19):2769-78. doi: 10.1093/hmg/ddi310. Epub 2005 Aug 15. Hum Mol Genet. 2005. PMID: 16103129

3

Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.

Khajavi M, Shiga K, Wiszniewski W, He F, Shaw CA, Yan J, Wensel TG, Snipes GJ, Lupski JR. Khajavi M, et al. Among authors: wensel tg. Am J Hum Genet. 2007 Sep;81(3):438-53. doi: 10.1086/519926. Epub 2007 Aug 3. Am J Hum Genet. 2007. PMID: 17701891 Free PMC article.

4

The nature of dominant mutations of rhodopsin and implications for gene therapy.

Wilson JH, Wensel TG. Wilson JH, et al. Among authors: wensel tg. Mol Neurobiol. 2003 Oct;28(2):149-58. doi: 10.1385/MN:28:2:149. Mol Neurobiol. 2003. PMID: 14576453 Review.

5

Rhodopsin gene expression determines rod outer segment size and rod cell resistance to a dominant-negative neurodegeneration mutant.

Price BA, Sandoval IM, Chan F, Nichols R, Roman-Sanchez R, Wensel TG, Wilson JH. Price BA, et al. Among authors: wensel tg. PLoS One. 2012;7(11):e49889. doi: 10.1371/journal.pone.0049889. Epub 2012 Nov 21. PLoS One. 2012. PMID: 23185477 Free PMC article.

6

Blocking transcription of the human rhodopsin gene by triplex-mediated DNA photocrosslinking.

Intody Z, Perkins BD, Wilson JH, Wensel TG. Intody Z, et al. Among authors: wensel tg. Nucleic Acids Res. 2000 Nov 1;28(21):4283-90. doi: 10.1093/nar/28.21.4283. Nucleic Acids Res. 2000. PMID: 11058128 Free PMC article.

7

Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration.

Gross AK, Decker G, Chan F, Sandoval IM, Wilson JH, Wensel TG. Gross AK, et al. Among authors: wensel tg. Vision Res. 2006 Dec;46(27):4510-8. doi: 10.1016/j.visres.2006.07.012. Epub 2006 Sep 18. Vision Res. 2006. PMID: 16979686 Free article.

8

Subcellular localization of mutant P23H rhodopsin in an RFP fusion knock-in mouse model of retinitis pigmentosa.

Robichaux MA, Nguyen V, Chan F, Kailasam L, He F, Wilson JH, Wensel TG. Robichaux MA, et al. Among authors: wensel tg. Dis Model Mech. 2022 May 1;15(5):dmm049336. doi: 10.1242/dmm.049336. Epub 2022 May 6. Dis Model Mech. 2022. PMID: 35275162 Free PMC article.

9

Triplex targets in the human rhodopsin gene.

Perkins BD, Wilson JH, Wensel TG, Vasquez KM. Perkins BD, et al. Among authors: wensel tg. Biochemistry. 1998 Aug 11;37(32):11315-22. doi: 10.1021/bi980525s. Biochemistry. 1998. PMID: 9698379

10

Activation of RGS9-1GTPase acceleration by its membrane anchor, R9AP.

Hu G, Zhang Z, Wensel TG. Hu G, et al. Among authors: wensel tg. J Biol Chem. 2003 Apr 18;278(16):14550-4. doi: 10.1074/jbc.M212046200. Epub 2003 Jan 30. J Biol Chem. 2003. PMID: 12560335 Free article.

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