Calvin A Mok
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Explore the profile of Calvin A Mok including associated specialties, affiliations and a list of published articles.
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5
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83
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Recent Articles
1.
Mok C, Au V, Thompson O, Edgley M, Gevirtzman L, Yochem J, et al.
Genetics
. 2017 Aug;
207(2):447-463.
PMID: 28827289
Mutants remain a powerful means for dissecting gene function in model organisms such as Massively parallel sequencing has simplified the detection of variants after mutagenesis but determining precisely which change...
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Mok C, Healey M, Shekhar T, Leroux M, Heon E, Zhen M
PLoS Genet
. 2011 Oct;
7(10):e1002335.
PMID: 22022287
Ciliopathies are pleiotropic and genetically heterogeneous disorders caused by defective development and function of the primary cilium. Bardet-Biedl syndrome (BBS) proteins localize to the base of cilia and undergo intraflagellar...
4.
Bin J, Madhavan J, Ferrini W, Mok C, Billingsley G, Heon E
Hum Mutat
. 2009 Apr;
30(7):E737-46.
PMID: 19402160
Bardet Biedl syndrome is a genetically heterogeneous ciliopathy with fourteen genes currently identified. To date, mutations in BBS7 and TTC8 (BBS8) were reported in 4.2% and 2.8% of BBS families...
5.
Li C, Inglis P, Leitch C, Efimenko E, Zaghloul N, Mok C, et al.
PLoS Genet
. 2008 Mar;
4(3):e1000044.
PMID: 18369462
MIP-T3 is a human protein found previously to associate with microtubules and the kinesin-interacting neuronal protein DISC1 (Disrupted-in-Schizophrenia 1), but whose cellular function(s) remains unknown. Here we demonstrate that the...