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Sequence of Age-Associated Changes to the Mouse Neuromuscular Junction and the Protective Effects of Voluntary Exercise.
Published in:
PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067970
By:
- Cheng, Anson;
- Morsch, Marco;
- Murata, Yui;
- Ghazanfari, Nazanin;
- Reddel, Stephen W.;
- Phillips, William D.
Publication type:
Article
Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 20, p. 5789, doi. 10.1093/hmg/ddv298
By:
- Greenlees, Rebecca;
- Mihelec, Marija;
- Yousoof, Saira;
- Speidel, Daniel;
- Wu, Selwin K.;
- Rinkwitz, Silke;
- Prokudin, Ivan;
- Perveen, Rahat;
- Cheng, Anson;
- Ma, Alan;
- Nash, Benjamin;
- Gillespie, Rachel;
- Loebel, David A. F.;
- Clayton-Smith, Jill;
- Lloyd, I. Christopher;
- Grigg, John R.;
- Tam, Patrick P. L.;
- Yap, Alpha S.;
- Becker, Thomas S.;
- Black, Graeme C. M.
Publication type:
Article
Selective disruption of Drp1-independent mitophagy and mitolysosome trafficking by an Alzheimer's disease relevant tau modification in a novel Caenorhabditis elegans model.
Published in:
Genetics, 2022, v. 222, n. 1, p. 1, doi. 10.1093/genetics/iyac104
By:
- Guha, Sanjib;
- Cheng, Anson;
- Carroll, Trae;
- King, Dennisha;
- Koren, Shon A.;
- Swords, Sierra;
- Nehrke, Keith;
- Johnson, Gail V. W.
Publication type:
Article
Genome sequencing in congenital cataracts improves diagnostic yield.
Published in:
Human Mutation, 2021, v. 42, n. 9, p. 1173, doi. 10.1002/humu.24240
By:
- Ma, Alan;
- Grigg, John R.;
- Flaherty, Maree;
- Smith, James;
- Minoche, Andre E.;
- Cowley, Mark J.;
- Nash, Benjamin M.;
- Ho, Gladys;
- Gayagay, Thet;
- Lai, Tiffany;
- Farnsworth, Elizabeth;
- Hackett, Emma L.;
- Slater, Katrina;
- Wong, Karen;
- Holman, Katherine J.;
- Jenkins, Gemma;
- Cheng, Anson;
- Martin, Frank;
- Brown, Natasha J.;
- Leighton, Sarah E.
Publication type:
Article
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Published in:
Human Mutation, 2016, v. 37, n. 4, p. 371, doi. 10.1002/humu.22948
By:
- Ma, Alan S.;
- Grigg, John R.;
- Ho, Gladys;
- Prokudin, Ivan;
- Farnsworth, Elizabeth;
- Holman, Katherine;
- Cheng, Anson;
- Billson, Frank A.;
- Martin, Frank;
- Fraser, Clare;
- Mowat, David;
- Smith, James;
- Christodoulou, John;
- Flaherty, Maree;
- Bennetts, Bruce;
- Jamieson, Robyn V.
Publication type:
Article
Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells.
Published in:
Stem Cells International, 2021, p. 1, doi. 10.1155/2021/4536382
By:
- Nash, Benjamin M.;
- Loi, To Ha;
- Fernando, Milan;
- Sabri, Amin;
- Robinson, James;
- Cheng, Anson;
- Eamegdool, Steven S.;
- Farnsworth, Elizabeth;
- Bennetts, Bruce;
- Grigg, John R.;
- Chung, Seo-Kyung;
- Gonzalez-Cordero, Anai;
- Jamieson, Robyn V.
Publication type:
Article

Found: 6

Sequence of Age-Associated Changes to the Mouse Neuromuscular Junction and the Protective Effects of Voluntary Exercise.

Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.

Selective disruption of Drp1-independent mitophagy and mitolysosome trafficking by an Alzheimer's disease relevant tau modification in a novel Caenorhabditis elegans model.

Genome sequencing in congenital cataracts improves diagnostic yield.

Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.

Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells.