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A Corbett

Showing results (511-520 of 576) with videos related to

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Stem Cells Translational Medicine|April 3, 2015
Inhibition of an NAD⁺ salvage pathway provides efficient and selective toxicity to human pluripotent stem cellsErin M Kropp, Bryndon J Oleson, Katarzyna A Broniowska, et al.
NPJ Genomic Medicine|January 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Diabetes Care|September 24, 2008
Improving Diabetes Care in Practice: findings from the TRANSLATE trialKevin A Peterson, David M Radosevich, Patrick J O'Connor, et al.
Human Molecular Genetics|October 19, 2018
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylationWujood Khayat, Anna Hackett, Marie Shaw, et al.
Neurology|April 12, 2012
Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophyM P Menezes, L B Waddell, F J Evesson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Exon expression and alternatively spliced genes in Tourette SyndromeYingfang Tian, Isaac H Liao, Xinhua Zhan, et al.
Experimental Neurology|March 18, 2009
Anti-melanin antibodies are increased in sera in Parkinson's diseaseK L Double, D B Rowe, F M Carew-Jones, et al.
NPJ Genomic Medicine|November 9, 2019
Targeted resequencing identifies genes with recurrent variation in cerebral palsyC L van Eyk, M A Corbett, M S B Frank, et al.
Molecular Cancer Therapeutics|June 18, 2014
Selective activity of the histone deacetylase inhibitor AR-42 against leukemia stem cells: a novel potential strategy in acute myelogenous leukemiaMonica L Guzman, Neng Yang, Krishan K Sharma, et al.
Neurology. Genetics|January 31, 2022
Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and EpilepsyMark F Bennett, Michael S Hildebrand, Sayaka Kayumi, et al.
Pageof 58

Showing results (511-520 of 576) with videos related to

Sort By:
Pageof 58
Stem Cells Translational Medicine|April 3, 2015
Inhibition of an NAD⁺ salvage pathway provides efficient and selective toxicity to human pluripotent stem cellsErin M Kropp, Bryndon J Oleson, Katarzyna A Broniowska, et al.
NPJ Genomic Medicine|January 29, 2022
Oligonucleotide correction of an intronic TIMMDC1 variant in cells of patients with severe neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Diabetes Care|September 24, 2008
Improving Diabetes Care in Practice: findings from the TRANSLATE trialKevin A Peterson, David M Radosevich, Patrick J O'Connor, et al.
Human Molecular Genetics|October 19, 2018
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylationWujood Khayat, Anna Hackett, Marie Shaw, et al.
Neurology|April 12, 2012
Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophyM P Menezes, L B Waddell, F J Evesson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Exon expression and alternatively spliced genes in Tourette SyndromeYingfang Tian, Isaac H Liao, Xinhua Zhan, et al.
Experimental Neurology|March 18, 2009
Anti-melanin antibodies are increased in sera in Parkinson's diseaseK L Double, D B Rowe, F M Carew-Jones, et al.
NPJ Genomic Medicine|November 9, 2019
Targeted resequencing identifies genes with recurrent variation in cerebral palsyC L van Eyk, M A Corbett, M S B Frank, et al.
Molecular Cancer Therapeutics|June 18, 2014
Selective activity of the histone deacetylase inhibitor AR-42 against leukemia stem cells: a novel potential strategy in acute myelogenous leukemiaMonica L Guzman, Neng Yang, Krishan K Sharma, et al.
Neurology. Genetics|January 31, 2022
Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and EpilepsyMark F Bennett, Michael S Hildebrand, Sayaka Kayumi, et al.
Pageof 58