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Protein Science : a Publication of the Protein Society
|
September 25, 2004
Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
Timothy A Hinsley, Pamela Cunliffe, Hannah J Tipney, et al.
The Journal of Hand Surgery
|
June 22, 2010
Genome-wide high-resolution screening in Dupuytren's disease reveals common regions of DNA copy number alterations
Barbara B Shih, May Tassabehji, James S Watson, et al.
Perception
|
August 11, 2009
Inefficient search of large-scale space in Williams syndrome: further insights on the role of LIMK1 deletion in deficits of spatial cognition
Alastair D Smith, Iain D Gilchrist, Bruce Hood, et al.
European Journal of Human Genetics : EJHG
|
April 22, 2004
Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome
Hannah J Tipney, Timothy A Hinsley, Andrew Brass, et al.
Plos One
|
September 17, 2010
Claudin 13, a member of the claudin family regulated in mouse stress induced erythropoiesis
Pamela D Thompson, Hannah Tipney, Andy Brass, et al.
Plos One
|
November 3, 2012
A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome
Melanie A Porter, Carol Dobson-Stone, John B J Kwok, et al.
Journal of Neurodevelopmental Disorders
|
July 25, 2014
Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients
Hannah Broadbent, Emily K Farran, Esther Chin, et al.
Behavioural Brain Research
|
June 2, 2012
Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome
Tomasz Schneider, Zara Skitt, Yiwen Liu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 16, 2013
Rapamycin inhibits smooth muscle cell proliferation and obstructive arteriopathy attributable to elastin deficiency
Wei Li, Qingle Li, Lingfeng Qin, et al.
Frontiers in Psychology
|
June 5, 2012
Social cognition in williams syndrome: genotype/phenotype insights from partial deletion patients
Annette Karmiloff-Smith, Hannah Broadbent, Emily K Farran, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Protein Science : a Publication of the Protein Society
|
September 25, 2004
Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
Timothy A Hinsley, Pamela Cunliffe, Hannah J Tipney, et al.
The Journal of Hand Surgery
|
June 22, 2010
Genome-wide high-resolution screening in Dupuytren's disease reveals common regions of DNA copy number alterations
Barbara B Shih, May Tassabehji, James S Watson, et al.
Perception
|
August 11, 2009
Inefficient search of large-scale space in Williams syndrome: further insights on the role of LIMK1 deletion in deficits of spatial cognition
Alastair D Smith, Iain D Gilchrist, Bruce Hood, et al.
European Journal of Human Genetics : EJHG
|
April 22, 2004
Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome
Hannah J Tipney, Timothy A Hinsley, Andrew Brass, et al.
Plos One
|
September 17, 2010
Claudin 13, a member of the claudin family regulated in mouse stress induced erythropoiesis
Pamela D Thompson, Hannah Tipney, Andy Brass, et al.
Plos One
|
November 3, 2012
A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome
Melanie A Porter, Carol Dobson-Stone, John B J Kwok, et al.
Journal of Neurodevelopmental Disorders
|
July 25, 2014
Genetic contributions to visuospatial cognition in Williams syndrome: insights from two contrasting partial deletion patients
Hannah Broadbent, Emily K Farran, Esther Chin, et al.
Behavioural Brain Research
|
June 2, 2012
Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome
Tomasz Schneider, Zara Skitt, Yiwen Liu, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
March 16, 2013
Rapamycin inhibits smooth muscle cell proliferation and obstructive arteriopathy attributable to elastin deficiency
Wei Li, Qingle Li, Lingfeng Qin, et al.
Frontiers in Psychology
|
June 5, 2012
Social cognition in williams syndrome: genotype/phenotype insights from partial deletion patients
Annette Karmiloff-Smith, Hannah Broadbent, Emily K Farran, et al.
Page
of 4