Mullins RF - Search Results

1

Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort.

Kuehn MH, Wang K, Roos B, Stone EM, Kwon YH, Alward WL, Mullins RF, Fingert JH. Kuehn MH, et al. Among authors: mullins rf. Mol Vis. 2011 Feb 8;17:430-5. Mol Vis. 2011. PMID: 21321670 Free PMC article.

2

Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor.

Jacobson N, Andrews M, Shepard AR, Nishimura D, Searby C, Fingert JH, Hageman G, Mullins R, Davidson BL, Kwon YH, Alward WL, Stone EM, Clark AF, Sheffield VC. Jacobson N, et al. Hum Mol Genet. 2001 Jan 15;10(2):117-25. doi: 10.1093/hmg/10.2.117. Hum Mol Genet. 2001. PMID: 11152659

3

Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head.

Clark AF, Kawase K, English-Wright S, Lane D, Steely HT, Yamamoto T, Kitazawa Y, Kwon YH, Fingert JH, Swiderski RE, Mullins RF, Hageman GS, Alward WL, Sheffield VC, Stone EM. Clark AF, et al. Among authors: mullins rf. FASEB J. 2001 May;15(7):1251-3. doi: 10.1096/fj.00-0663fje. FASEB J. 2001. PMID: 11344104 No abstract available.

4

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

Alagramam KN, Yuan H, Kuehn MH, Murcia CL, Wayne S, Srisailpathy CR, Lowry RB, Knaus R, Van Laer L, Bernier FP, Schwartz S, Lee C, Morton CC, Mullins RF, Ramesh A, Van Camp G, Hageman GS, Woychik RP, Smith RJ. Alagramam KN, et al. Among authors: mullins rf. Hum Mol Genet. 2001 Aug 1;10(16):1709-18. doi: 10.1093/hmg/10.16.1709. Hum Mol Genet. 2001. PMID: 11487575

5

Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors.

Lotery AJ, Derksen TA, Russell SR, Mullins RF, Sauter S, Affatigato LM, Stone EM, Davidson BL. Lotery AJ, et al. Among authors: mullins rf. Hum Gene Ther. 2002 Apr 10;13(6):689-96. doi: 10.1089/104303402317322258. Hum Gene Ther. 2002. PMID: 11936968

6

Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retina.

Lotery AJ, Yang GS, Mullins RF, Russell SR, Schmidt M, Stone EM, Lindbloom JD, Chiorini JA, Kotin RM, Davidson BL. Lotery AJ, et al. Among authors: mullins rf. Hum Gene Ther. 2003 Nov 20;14(17):1663-71. doi: 10.1089/104303403322542301. Hum Gene Ther. 2003. PMID: 14633408

7

Results from screening over 9000 mutation-bearing mice for defects in the electroretinogram and appearance of the fundus.

Pinto LH, Vitaterna MH, Siepka SM, Shimomura K, Lumayag S, Baker M, Fenner D, Mullins RF, Sheffield VC, Stone EM, Heffron E, Takahashi JS. Pinto LH, et al. Among authors: mullins rf. Vision Res. 2004 Dec;44(28):3335-45. doi: 10.1016/j.visres.2004.07.025. Vision Res. 2004. PMID: 15536001 Free PMC article.

8

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.

Nishimura DY, Fath M, Mullins RF, Searby C, Andrews M, Davis R, Andorf JL, Mykytyn K, Swiderski RE, Yang B, Carmi R, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: mullins rf. Proc Natl Acad Sci U S A. 2004 Nov 23;101(47):16588-93. doi: 10.1073/pnas.0405496101. Epub 2004 Nov 11. Proc Natl Acad Sci U S A. 2004. PMID: 15539463 Free PMC article.

9

Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome.

Fath MA, Mullins RF, Searby C, Nishimura DY, Wei J, Rahmouni K, Davis RE, Tayeh MK, Andrews M, Yang B, Sigmund CD, Stone EM, Sheffield VC. Fath MA, et al. Among authors: mullins rf. Hum Mol Genet. 2005 May 1;14(9):1109-18. doi: 10.1093/hmg/ddi123. Epub 2005 Mar 16. Hum Mol Genet. 2005. PMID: 15772095

10

Glycoconjugates of choroidal neovascular membranes in age-related macular degeneration.

Mullins RF, Grassi MA, Skeie JM. Mullins RF, et al. Mol Vis. 2005 Jul 14;11:509-17. Mol Vis. 2005. PMID: 16052166 Free article.

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