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S Ramsden

Showing results (21-30 of 32) with videos related to

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European Journal of Medical Genetics|June 3, 2006
Detection of a deletion of exons 8-16 of the UBE3A gene in familial Angelman syndrome using a semi-quantitative dosage PCR based assayL Boyes, A J Wallace, M Krajewska-Walasek, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 1, 1993
Influence of birth weight on adult bone mineral densityH M Hamed, D W Purdie, C S Ramsden, et al.
Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology|November 18, 2005
Seasonal cycle in vitamin A1/A2-based visual pigment composition during the life history of coho salmon (Oncorhynchus kisutch)S E Temple, E M Plate, S Ramsden, et al.
Aquatic Toxicology (Amsterdam, Netherlands)|November 27, 2012
Subtle alterations in swimming speed distributions of rainbow trout exposed to titanium dioxide nanoparticles are associated with gill rather than brain injuryDavid Boyle, Genan A Al-Bairuty, Christopher S Ramsden, et al.
BMJ (Clinical Research Ed.)|April 18, 1992
Psychiatric morbidity and substance abuse among residents of a cold weather shelterA Reed, S Ramsden, J Marshall, et al.
Journal of Fish Biology|October 5, 2011
Effects of manufactured nanomaterials on fishes: a target organ and body systems physiology approachR D Handy, G Al-Bairuty, A Al-Jubory, et al.
Neuropsychologia|March 10, 2012
Structural correlates for lexical efficiency and number of languages in non-native speakers of EnglishA Grogan, O Parker Jones, N Ali, et al.
Journal of Medical Genetics|August 1, 1997
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome familiesH L Gilbert, J L Buxton, C T Chan, et al.
European Journal of Medical Genetics|May 4, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanismsA Redwood, S Douzgou, S Waller, et al.
Molecular Vision|June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophyZ Saihan, Z Li, J Rice, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
European Journal of Medical Genetics|June 3, 2006
Detection of a deletion of exons 8-16 of the UBE3A gene in familial Angelman syndrome using a semi-quantitative dosage PCR based assayL Boyes, A J Wallace, M Krajewska-Walasek, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 1, 1993
Influence of birth weight on adult bone mineral densityH M Hamed, D W Purdie, C S Ramsden, et al.
Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology|November 18, 2005
Seasonal cycle in vitamin A1/A2-based visual pigment composition during the life history of coho salmon (Oncorhynchus kisutch)S E Temple, E M Plate, S Ramsden, et al.
Aquatic Toxicology (Amsterdam, Netherlands)|November 27, 2012
Subtle alterations in swimming speed distributions of rainbow trout exposed to titanium dioxide nanoparticles are associated with gill rather than brain injuryDavid Boyle, Genan A Al-Bairuty, Christopher S Ramsden, et al.
BMJ (Clinical Research Ed.)|April 18, 1992
Psychiatric morbidity and substance abuse among residents of a cold weather shelterA Reed, S Ramsden, J Marshall, et al.
Journal of Fish Biology|October 5, 2011
Effects of manufactured nanomaterials on fishes: a target organ and body systems physiology approachR D Handy, G Al-Bairuty, A Al-Jubory, et al.
Neuropsychologia|March 10, 2012
Structural correlates for lexical efficiency and number of languages in non-native speakers of EnglishA Grogan, O Parker Jones, N Ali, et al.
Journal of Medical Genetics|August 1, 1997
Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome familiesH L Gilbert, J L Buxton, C T Chan, et al.
European Journal of Medical Genetics|May 4, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanismsA Redwood, S Douzgou, S Waller, et al.
Molecular Vision|June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophyZ Saihan, Z Li, J Rice, et al.
Pageof 4