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Stephen R Williams

Showing results (71-80 of 145) with videos related to

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American Journal of Medical Genetics. Part A|March 9, 2019
Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributorTrang N Le, Stephen R Williams, Joseph T Alaimo, et al.
Neuroimage|June 16, 2022
Neurochemical profiles of the anterior temporal lobe predict response of repetitive transcranial magnetic stimulation on semantic processingJeYoung Jung, Stephen R Williams, Faezeh Sanaei Nezhad, et al.
Neuron|August 13, 2013
Potassium channels control the interaction between active dendritic integration compartments in layer 5 cortical pyramidal neuronsMark T Harnett, Ning-Long Xu, Jeffrey C Magee, et al.
The Journal of Chemical Physics|December 9, 2009
On violations of Le Chatelier's principle for a temperature change in small systems observed for short timesPouria Dasmeh, Debra J Searles, Davood Ajloo, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 10, 2006
Dynamical signatures of freezing: stable fluids, metastable fluids, and crystalsStephen R Williams, Peter McGlynn, Gary Bryant, et al.
Magnetic Resonance in Medicine|November 1, 2016
Quantification of glutathione in the human brain by MR spectroscopy at 3 Tesla: Comparison of PRESS and MEGA-PRESSFaezeh Sanaei Nezhad, Adriana Anton, Laura M Parkes, et al.
Iscience|June 16, 2022
Phototransduction in a marine sponge provides insights into the origin of animal visionEunice Wong, Victor Anggono, Stephen R Williams, et al.
Human Molecular Genetics|July 29, 2010
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndromeBrooke Burns, Kristie Schmidt, Stephen R Williams, et al.
American Journal of Human Genetics|May 15, 2012
Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicityStephen R Williams, Deborah Zies, Sureni V Mullegama, et al.
Journal of Medical Genetics|September 16, 2009
Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delayStephen R Williams, Santhosh Girirajan, David Tegay, et al.
Pageof 15

Showing results (71-80 of 145) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics. Part A|March 9, 2019
Genotype and phenotype correlation in 103 individuals with 2q37 deletion syndrome reveals incomplete penetrance and supports HDAC4 as the primary genetic contributorTrang N Le, Stephen R Williams, Joseph T Alaimo, et al.
Neuroimage|June 16, 2022
Neurochemical profiles of the anterior temporal lobe predict response of repetitive transcranial magnetic stimulation on semantic processingJeYoung Jung, Stephen R Williams, Faezeh Sanaei Nezhad, et al.
Neuron|August 13, 2013
Potassium channels control the interaction between active dendritic integration compartments in layer 5 cortical pyramidal neuronsMark T Harnett, Ning-Long Xu, Jeffrey C Magee, et al.
The Journal of Chemical Physics|December 9, 2009
On violations of Le Chatelier's principle for a temperature change in small systems observed for short timesPouria Dasmeh, Debra J Searles, Davood Ajloo, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 10, 2006
Dynamical signatures of freezing: stable fluids, metastable fluids, and crystalsStephen R Williams, Peter McGlynn, Gary Bryant, et al.
Magnetic Resonance in Medicine|November 1, 2016
Quantification of glutathione in the human brain by MR spectroscopy at 3 Tesla: Comparison of PRESS and MEGA-PRESSFaezeh Sanaei Nezhad, Adriana Anton, Laura M Parkes, et al.
Iscience|June 16, 2022
Phototransduction in a marine sponge provides insights into the origin of animal visionEunice Wong, Victor Anggono, Stephen R Williams, et al.
Human Molecular Genetics|July 29, 2010
Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndromeBrooke Burns, Kristie Schmidt, Stephen R Williams, et al.
American Journal of Human Genetics|May 15, 2012
Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicityStephen R Williams, Deborah Zies, Sureni V Mullegama, et al.
Journal of Medical Genetics|September 16, 2009
Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delayStephen R Williams, Santhosh Girirajan, David Tegay, et al.
Pageof 15