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Dorothy Trump

Showing results (11-20 of 27) with videos related to

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Plos One|June 12, 2010
Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndromeJunhong Gui, Tao Wang, Richard P O Jones, et al.
Journal of Medical Genetics|December 19, 2006
X-linked retinoschisis: an updateStephen K Sikkink, Susmito Biswas, Neil R A Parry, et al.
Developmental Medicine and Child Neurology|November 21, 2012
Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based studyShruti Garg, Annukka Lehtonen, Susan M Huson, et al.
Human Molecular Genetics|November 6, 2002
Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisisTao Wang, Caroline T Waters, Alex M K Rothman, et al.
Human Molecular Genetics|May 21, 2005
Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat proteinElizabeth O'Connor, Birgit Eisenhaber, Jane Dalley, et al.
Developmental Medicine and Child Neurology|June 22, 2018
Cognition in children with neurofibromatosis type 1: data from a population-based studyAnnukka Lehtonen, Shruti Garg, Stephen A Roberts, et al.
Cellular Signalling|September 8, 2007
Notch3 activation modulates cell growth behaviour and cross-talk to Wnt/TCF signalling pathwayTao Wang, Cathy M Holt, Chiheng Xu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 12, 2007
Allelic variation of the FRMD7 gene in congenital idiopathic nystagmusJames E Self, Fatima Shawkat, Crispin T Malpas, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
Newly recognized recessive syndrome characterized by dysmorphic features, hypogonadotropic hypogonadism, severe microcephaly, and sensorineural hearing loss maps to 3p21.3Emma M Jenkinson, Helen Kingston, Jill Urquhart, et al.
The Journal of Biological Chemistry|July 3, 2009
Differential regulation of elastic fiber formation by fibulin-4 and -5Rawshan Choudhury, Amanda McGovern, Caroline Ridley, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Plos One|June 12, 2010
Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndromeJunhong Gui, Tao Wang, Richard P O Jones, et al.
Journal of Medical Genetics|December 19, 2006
X-linked retinoschisis: an updateStephen K Sikkink, Susmito Biswas, Neil R A Parry, et al.
Developmental Medicine and Child Neurology|November 21, 2012
Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based studyShruti Garg, Annukka Lehtonen, Susan M Huson, et al.
Human Molecular Genetics|November 6, 2002
Intracellular retention of mutant retinoschisin is the pathological mechanism underlying X-linked retinoschisisTao Wang, Caroline T Waters, Alex M K Rothman, et al.
Human Molecular Genetics|May 21, 2005
Species specific membrane anchoring of nyctalopin, a small leucine-rich repeat proteinElizabeth O'Connor, Birgit Eisenhaber, Jane Dalley, et al.
Developmental Medicine and Child Neurology|June 22, 2018
Cognition in children with neurofibromatosis type 1: data from a population-based studyAnnukka Lehtonen, Shruti Garg, Stephen A Roberts, et al.
Cellular Signalling|September 8, 2007
Notch3 activation modulates cell growth behaviour and cross-talk to Wnt/TCF signalling pathwayTao Wang, Cathy M Holt, Chiheng Xu, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 12, 2007
Allelic variation of the FRMD7 gene in congenital idiopathic nystagmusJames E Self, Fatima Shawkat, Crispin T Malpas, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
Newly recognized recessive syndrome characterized by dysmorphic features, hypogonadotropic hypogonadism, severe microcephaly, and sensorineural hearing loss maps to 3p21.3Emma M Jenkinson, Helen Kingston, Jill Urquhart, et al.
The Journal of Biological Chemistry|July 3, 2009
Differential regulation of elastic fiber formation by fibulin-4 and -5Rawshan Choudhury, Amanda McGovern, Caroline Ridley, et al.
Pageof 3