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Human Molecular Genetics|September 6, 2008
CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary ciliumJoon Kim, Suguna Rani Krishnaswami, Joseph G GleesonDevelopmental Biology|November 6, 2012
Negative regulation of Shh levels by Kras and Fgfr2 during hair follicle developmentAnandaroop Mukhopadhyay, Suguna Rani Krishnaswami, Christopher Cowing-Zitron, et al.Disease Models & Mechanisms|March 29, 2018
<i>Mek1</i><sup>Y130C</sup> mice recapitulate aspects of human cardio-facio-cutaneous syndromeRifdat Aoidi, Nicolas Houde, Kim Landry-Truchon, et al.Nature Genetics|May 10, 2006
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndromeEnza Maria Valente, Jennifer L Silhavy, Francesco Brancati, et al.Nature Protocols|February 19, 2016
Using single nuclei for RNA-seq to capture the transcriptome of postmortem neuronsSuguna Rani Krishnaswami, Rashel V Grindberg, Mark Novotny, et al.Pageof 1