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Items: 6

1.

MIP-MAP: High-Throughput Mapping of Caenorhabditis elegans Temperature-Sensitive Mutants via Molecular Inversion Probes.

Mok CA, Au V, Thompson OA, Edgley ML, Gevirtzman L, Yochem J, Lowry J, Memar N, Wallenfang MR, Rasoloson D, Bowerman B, Schnabel R, Seydoux G, Moerman DG, Waterston RH.

Genetics. 2017 Oct;207(2):447-463. doi: 10.1534/genetics.117.300179. Epub 2017 Aug 21.

2.

Caenorhabditis elegans as a model organism for ciliopathies and related forms of photoreceptor degeneration.

Mok CA, Héon E.

Adv Exp Med Biol. 2012;723:533-8. doi: 10.1007/978-1-4614-0631-0_67. Review. No abstract available.

PMID:
22183374
3.

Mutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegans.

Mok CA, Healey MP, Shekhar T, Leroux MR, Héon E, Zhen M.

PLoS Genet. 2011 Oct;7(10):e1002335. doi: 10.1371/journal.pgen.1002335. Epub 2011 Oct 13.

4.

Ciliary dysfunction and obesity.

Mok CA, Héon E, Zhen M.

Clin Genet. 2010 Jan;77(1):18-27. doi: 10.1111/j.1399-0004.2009.01305.x. Epub 2009 Nov 20.

PMID:
19968672
5.

BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population.

Bin J, Madhavan J, Ferrini W, Mok CA, Billingsley G, Héon E.

Hum Mutat. 2009 Jul;30(7):E737-46. doi: 10.1002/humu.21040.

PMID:
19402160
6.

An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes.

Li C, Inglis PN, Leitch CC, Efimenko E, Zaghloul NA, Mok CA, Davis EE, Bialas NJ, Healey MP, Héon E, Zhen M, Swoboda P, Katsanis N, Leroux MR.

PLoS Genet. 2008 Mar 28;4(3):e1000044. doi: 10.1371/journal.pgen.1000044.

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