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Michael S Nahorski

Showing results (1-10 of 22) with videos related to

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Molecular Pain|October 10, 2018
A third HSAN5 mutation disrupts the nerve growth factor furin cleavage siteSamiha S Shaikh, Michael S Nahorski, C Geoffrey Woods
Trends in Neurosciences|November 10, 2015
New Mendelian Disorders of PainlessnessMichael S Nahorski, Ya-Chun Chen, C Geoffrey Woods
European Journal of Human Genetics : EJHG|July 14, 2018
Before progressing from "exomes" to "genomes"… don't forget splicing variantsSamiha S Shaikh, Michael S Nahorski, Harjeet Rai, et al.
Anticancer Research|November 17, 2012
Gene expression and protein array studies of folliculin-regulated pathwaysAnne Reiman, Xiaohong Lu, Laurence Seabra, et al.
Scientific Reports|February 7, 2018
Clathrin heavy chain 22 contributes to the control of neuropeptide degradation and secretion during neuronal developmentMichael S Nahorski, Georg H H Borner, Samiha S Shaikh, et al.
Molecular Cancer Therapeutics|January 12, 2011
Therapeutic targeting the loss of the birt-hogg-dube suppressor geneXiaohong Lu, Wenbin Wei, Janine Fenton, et al.
Human Mutation|September 28, 2016
A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV)Samiha S Shaikh, Ya-Chun Chen, Sally-Anne Halsall, et al.
Human Molecular Genetics|September 12, 2012
Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesisMichael S Nahorski, Laurence Seabra, Ania Straatman-Iwanowska, et al.
Brain : a Journal of Neurology|February 27, 2016
CCDC88A mutations cause PEHO-like syndrome in humans and mouseMichael S Nahorski, Masato Asai, Emma Wakeling, et al.
Human Mutation|May 4, 2011
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stabilityMichael S Nahorski, Anne Reiman, Derek H K Lim, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Molecular Pain|October 10, 2018
A third HSAN5 mutation disrupts the nerve growth factor furin cleavage siteSamiha S Shaikh, Michael S Nahorski, C Geoffrey Woods
Trends in Neurosciences|November 10, 2015
New Mendelian Disorders of PainlessnessMichael S Nahorski, Ya-Chun Chen, C Geoffrey Woods
European Journal of Human Genetics : EJHG|July 14, 2018
Before progressing from "exomes" to "genomes"… don't forget splicing variantsSamiha S Shaikh, Michael S Nahorski, Harjeet Rai, et al.
Anticancer Research|November 17, 2012
Gene expression and protein array studies of folliculin-regulated pathwaysAnne Reiman, Xiaohong Lu, Laurence Seabra, et al.
Scientific Reports|February 7, 2018
Clathrin heavy chain 22 contributes to the control of neuropeptide degradation and secretion during neuronal developmentMichael S Nahorski, Georg H H Borner, Samiha S Shaikh, et al.
Molecular Cancer Therapeutics|January 12, 2011
Therapeutic targeting the loss of the birt-hogg-dube suppressor geneXiaohong Lu, Wenbin Wei, Janine Fenton, et al.
Human Mutation|September 28, 2016
A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV)Samiha S Shaikh, Ya-Chun Chen, Sally-Anne Halsall, et al.
Human Molecular Genetics|September 12, 2012
Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesisMichael S Nahorski, Laurence Seabra, Ania Straatman-Iwanowska, et al.
Brain : a Journal of Neurology|February 27, 2016
CCDC88A mutations cause PEHO-like syndrome in humans and mouseMichael S Nahorski, Masato Asai, Emma Wakeling, et al.
Human Mutation|May 4, 2011
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stabilityMichael S Nahorski, Anne Reiman, Derek H K Lim, et al.
Pageof 3