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Ian M Carr

Showing results (81-90 of 96) with videos related to

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British Journal of Cancer|July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy responseNoha Gwili, Stacey J Jones, Waleed Al Amri, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)James A Poulter, Alice E Davidson, Manir Ali, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics|November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality DefectsSerge Bonnefoy, Christopher M Watson, Kristin D Kernohan, et al.
Human Molecular Genetics|November 10, 2011
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defectsKamron Khan, Clare V Logan, Martin McKibbin, et al.
Nature Genetics|November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics|September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatusChristine P Diggle, Daniel J Moore, Girish Mali, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
British Journal of Cancer|July 13, 2021
Transcriptome profiles of stem-like cells from primary breast cancers allow identification of ITGA7 as a predictive marker of chemotherapy responseNoha Gwili, Stacey J Jones, Waleed Al Amri, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR)James A Poulter, Alice E Davidson, Manir Ali, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
American Journal of Human Genetics|February 10, 2009
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfectaDavid A Parry, Alan J Mighell, Walid El-Sayed, et al.
American Journal of Human Genetics|November 3, 2018
Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality DefectsSerge Bonnefoy, Christopher M Watson, Kristin D Kernohan, et al.
Human Molecular Genetics|November 10, 2011
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defectsKamron Khan, Clare V Logan, Martin McKibbin, et al.
Nature Genetics|November 22, 2011
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Clare V Logan, Barbara Lucke, Caroline Pottinger, et al.
Plos Genetics|September 19, 2014
HEATR2 plays a conserved role in assembly of the ciliary motile apparatusChristine P Diggle, Daniel J Moore, Girish Mali, et al.
American Journal of Human Genetics|August 21, 2012
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfectaDavid A Parry, Steven J Brookes, Clare V Logan, et al.
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Pageof 10