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David Chandler

Showing results (141-150 of 167) with videos related to

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European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophreniaTod Fullston, Bronte Gabb, David Callen, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|August 30, 2017
Variable cardiac α-actin (Actc1) expression in early adult skeletal muscle correlates with promoter methylationJordan K Boutilier, Rhonda L Taylor, Ramesh Ram, et al.
Rheumatology (Oxford, England)|July 27, 2013
The 2012 BSR and BHPR guideline for the treatment of psoriatic arthritis with biologicsLaura C Coates, William Tillett, David Chandler, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 2, 2009
Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophreniaDavid Chandler, Milan Dragović, Matthew Cooper, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2008
Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypesKirsten Peters, Steven Wiltshire, Anjali K Henders, et al.
Brain : a Journal of Neurology|March 16, 2007
Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutationVioleta Mihaylova, Janina Hantke, Ivanka Sinigerska, et al.
Science Advances|May 15, 2024
Picosecond carrier dynamics in InAs and GaAs revealed by ultrafast electron microscopyChristopher Perez, Scott R Ellis, Francis M Alcorn, et al.
Rheumatology (Oxford, England)|December 1, 2022
The top 10 research priorities in psoriatic arthritis: a James Lind Alliance Priority Setting PartnershipLouise Hailey, Chris Bundy, Helen Burstow, et al.
BMJ (Clinical Research Ed.)|February 17, 2021
Effective engagement and involvement with community stakeholders in the co-production of global health researchDoreen Tembo, Gary Hickey, Cristian Montenegro, et al.
Pageof 17

Showing results (141-150 of 167) with videos related to

Sort By:
Pageof 17
European Journal of Human Genetics : EJHG|June 19, 2009
A mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR)Janina Hantke, David Chandler, Rosalind King, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 9, 2011
Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophreniaTod Fullston, Bronte Gabb, David Callen, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|August 30, 2017
Variable cardiac α-actin (Actc1) expression in early adult skeletal muscle correlates with promoter methylationJordan K Boutilier, Rhonda L Taylor, Ramesh Ram, et al.
Rheumatology (Oxford, England)|July 27, 2013
The 2012 BSR and BHPR guideline for the treatment of psoriatic arthritis with biologicsLaura C Coates, William Tillett, David Chandler, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 2, 2009
Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophreniaDavid Chandler, Milan Dragović, Matthew Cooper, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2008
Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypesKirsten Peters, Steven Wiltshire, Anjali K Henders, et al.
Brain : a Journal of Neurology|March 16, 2007
Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutationVioleta Mihaylova, Janina Hantke, Ivanka Sinigerska, et al.
Science Advances|May 15, 2024
Picosecond carrier dynamics in InAs and GaAs revealed by ultrafast electron microscopyChristopher Perez, Scott R Ellis, Francis M Alcorn, et al.
Rheumatology (Oxford, England)|December 1, 2022
The top 10 research priorities in psoriatic arthritis: a James Lind Alliance Priority Setting PartnershipLouise Hailey, Chris Bundy, Helen Burstow, et al.
BMJ (Clinical Research Ed.)|February 17, 2021
Effective engagement and involvement with community stakeholders in the co-production of global health researchDoreen Tembo, Gary Hickey, Cristian Montenegro, et al.
Pageof 17