Mullins RF - Search Results

1

Stem cells as tools for studying the genetics of inherited retinal degenerations.

Wiley LA, Burnight ER, Mullins RF, Stone EM, Tucker BA. Wiley LA, et al. Among authors: mullins rf. Cold Spring Harb Perspect Med. 2014 Dec 11;5(5):a017160. doi: 10.1101/cshperspect.a017160. Cold Spring Harb Perspect Med. 2014. PMID: 25502747 Free PMC article. Review.

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

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

4

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

5

Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly.

Mykytyn K, Mullins RF, Andrews M, Chiang AP, Swiderski RE, Yang B, Braun T, Casavant T, Stone EM, Sheffield VC. Mykytyn K, et al. Among authors: mullins rf. Proc Natl Acad Sci U S A. 2004 Jun 8;101(23):8664-9. doi: 10.1073/pnas.0402354101. Epub 2004 Jun 1. Proc Natl Acad Sci U S A. 2004. PMID: 15173597 Free PMC article.

6

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.

7

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

8

Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlation.

Mullins RF, Oh KT, Heffron E, Hageman GS, Stone EM. Mullins RF, et al. Arch Ophthalmol. 2005 Nov;123(11):1588-94. doi: 10.1001/archopht.123.11.1588. Arch Ophthalmol. 2005. PMID: 16286623

9

Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse.

Pinto LH, Vitaterna MH, Shimomura K, Siepka SM, McDearmon EL, Fenner D, Lumayag SL, Omura C, Andrews AW, Baker M, Invergo BM, Olvera MA, Heffron E, Mullins RF, Sheffield VC, Stone EM, Takahashi JS. Pinto LH, et al. Among authors: mullins rf. Vis Neurosci. 2005 Sep-Oct;22(5):619-29. doi: 10.1017/S0952523805225117. Vis Neurosci. 2005. PMID: 16332273

10

Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function.

Yen HJ, Tayeh MK, Mullins RF, Stone EM, Sheffield VC, Slusarski DC. Yen HJ, et al. Among authors: mullins rf. Hum Mol Genet. 2006 Mar 1;15(5):667-77. doi: 10.1093/hmg/ddi468. Epub 2006 Jan 6. Hum Mol Genet. 2006. PMID: 16399798

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