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R Fitzpatrick

Showing results (421-430 of 555) with videos related to

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Genome Research|June 23, 2019
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutationsJoanna Kaplanis, Nadia Akawi, Giuseppe Gallone, et al.
The Bone & Joint Journal|March 30, 2013
Five-year results of a randomised controlled trial comparing mobile and fixed bearings in total knee replacementS Breeman, M K Campbell, H Dakin, et al.
Journal of Medical Genetics|October 22, 2009
Disruption of ST5 is associated with mental retardation and multiple congenital anomaliesIna Göhring, Andreas Tagariello, Sabine Endele, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 1, 1995
RP 73870, a gastrin/cholecystokinin-B receptor antagonist with potent anti-ulcer activity in the ratC E Pendley, L R Fitzpatrick, A J Capolino, et al.
Mucosal Immunology|March 6, 2009
MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel diseaseS Banerjee, B Oneda, L M Yap, et al.
Osteoarthritis and Cartilage|May 13, 2019
Impact of a national enhanced recovery after surgery programme on patient outcomes of primary total knee replacement: an interrupted time series analysis from "The National Joint Registry of England, Wales, Northern Ireland and the Isle of Man"C Garriga, J Murphy, J Leal, et al.
American Journal of Medical Genetics. Part A|October 3, 2008
Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughtersAdele Schneider, Tanya M Bardakjian, Jie Zhou, et al.
Journal of Virology|January 1, 1991
Expression of bovine herpesvirus 1 glycoprotein gIV by recombinant baculovirus and analysis of its immunogenic propertiesS van Drunen Littel-van den Hurk, M D Parker, D R Fitzpatrick, et al.
Molecular Genetics & Genomic Medicine|July 22, 2016
Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disabilityWayne W K Lam, John J Millichap, Dinesh C Soares, et al.
Pageof 56

Showing results (421-430 of 555) with videos related to

Sort By:
Pageof 56
Genome Research|June 23, 2019
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutationsJoanna Kaplanis, Nadia Akawi, Giuseppe Gallone, et al.
The Bone & Joint Journal|March 30, 2013
Five-year results of a randomised controlled trial comparing mobile and fixed bearings in total knee replacementS Breeman, M K Campbell, H Dakin, et al.
Journal of Medical Genetics|October 22, 2009
Disruption of ST5 is associated with mental retardation and multiple congenital anomaliesIna Göhring, Andreas Tagariello, Sabine Endele, et al.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 1, 1995
RP 73870, a gastrin/cholecystokinin-B receptor antagonist with potent anti-ulcer activity in the ratC E Pendley, L R Fitzpatrick, A J Capolino, et al.
Mucosal Immunology|March 6, 2009
MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel diseaseS Banerjee, B Oneda, L M Yap, et al.
Osteoarthritis and Cartilage|May 13, 2019
Impact of a national enhanced recovery after surgery programme on patient outcomes of primary total knee replacement: an interrupted time series analysis from "The National Joint Registry of England, Wales, Northern Ireland and the Isle of Man"C Garriga, J Murphy, J Leal, et al.
American Journal of Medical Genetics. Part A|October 3, 2008
Familial recurrence of SOX2 anophthalmia syndrome: phenotypically normal mother with two affected daughtersAdele Schneider, Tanya M Bardakjian, Jie Zhou, et al.
Journal of Virology|January 1, 1991
Expression of bovine herpesvirus 1 glycoprotein gIV by recombinant baculovirus and analysis of its immunogenic propertiesS van Drunen Littel-van den Hurk, M D Parker, D R Fitzpatrick, et al.
Molecular Genetics & Genomic Medicine|July 22, 2016
Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disabilityWayne W K Lam, John J Millichap, Dinesh C Soares, et al.
Pageof 56