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A Quinlan

Showing results (101-110 of 268) with videos related to

Pageof 27
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Ophthalmic Genetics|July 3, 2024
A novel frameshift variant in <i>BCOR</i> causes congenital nuclear cataractVanita Berry, Manav B Ponnekanti, Nikolas Pontikos, et al.
The British Journal of Radiology|February 2, 2016
Radiation protection of the eye lens in medical workers--basis and impact of the ICRP recommendationsStephen Gr Barnard, Elizabeth A Ainsbury, Roy A Quinlan, et al.
Molecular Biology of the Cell|December 12, 2002
Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma proteinEwa Markiewicz, Thomas Dechat, Roland Foisner, et al.
Development (Cambridge, England)|January 1, 1995
Neuroectodermal fate of epiblast cells in the distal region of the mouse egg cylinder: implication for body plan organization during early embryogenesisG A Quinlan, E A Williams, S S Tan, et al.
Current Eye Research|September 1, 1992
The 53kDa polypeptide component of the bovine fibre cell cytoskeleton is derived from the 115kDa beaded filament protein: evidence for a fibre cell specific intermediate filament proteinR A Quinlan, J M Carter, A M Hutcheson, et al.
Experimental Cell Research|July 3, 2003
Nuclear speckle localisation of the small heat shock protein alpha B-crystallin and its inhibition by the R120G cardiomyopathy-linked mutationPaul van den IJssel, Robert Wheelock, Alan Prescott, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 27, 2013
Changes in the quaternary structure and function of MjHSP16.5 attributable to deletion of the IXI motif and introduction of the substitution, R107G, in the α-crystallin domainRoy A Quinlan, Yan Zhang, Andrew Lansbury, et al.
Ophthalmic Genetics|November 8, 2021
Pathogenic variants in the <i>CYP21A2</i> gene cause isolated autosomal dominant congenital posterior polar cataractsVanita Berry, Nikolas Pontikos, Alex Ionides, et al.
Nucleic Acids Research|January 5, 2001
Antagonistic action of Six3 and Prox1 at the gamma-crystallin promoterJ Lengler, E Krausz, S Tomarev, et al.
The Journal of Physiology|April 14, 2011
Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosisK A Quinlan, J E Schuster, R Fu, et al.
Pageof 27

Showing results (101-110 of 268) with videos related to

Sort By:
Pageof 27
Ophthalmic Genetics|July 3, 2024
A novel frameshift variant in <i>BCOR</i> causes congenital nuclear cataractVanita Berry, Manav B Ponnekanti, Nikolas Pontikos, et al.
The British Journal of Radiology|February 2, 2016
Radiation protection of the eye lens in medical workers--basis and impact of the ICRP recommendationsStephen Gr Barnard, Elizabeth A Ainsbury, Roy A Quinlan, et al.
Molecular Biology of the Cell|December 12, 2002
Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma proteinEwa Markiewicz, Thomas Dechat, Roland Foisner, et al.
Development (Cambridge, England)|January 1, 1995
Neuroectodermal fate of epiblast cells in the distal region of the mouse egg cylinder: implication for body plan organization during early embryogenesisG A Quinlan, E A Williams, S S Tan, et al.
Current Eye Research|September 1, 1992
The 53kDa polypeptide component of the bovine fibre cell cytoskeleton is derived from the 115kDa beaded filament protein: evidence for a fibre cell specific intermediate filament proteinR A Quinlan, J M Carter, A M Hutcheson, et al.
Experimental Cell Research|July 3, 2003
Nuclear speckle localisation of the small heat shock protein alpha B-crystallin and its inhibition by the R120G cardiomyopathy-linked mutationPaul van den IJssel, Robert Wheelock, Alan Prescott, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|March 27, 2013
Changes in the quaternary structure and function of MjHSP16.5 attributable to deletion of the IXI motif and introduction of the substitution, R107G, in the α-crystallin domainRoy A Quinlan, Yan Zhang, Andrew Lansbury, et al.
Ophthalmic Genetics|November 8, 2021
Pathogenic variants in the <i>CYP21A2</i> gene cause isolated autosomal dominant congenital posterior polar cataractsVanita Berry, Nikolas Pontikos, Alex Ionides, et al.
Nucleic Acids Research|January 5, 2001
Antagonistic action of Six3 and Prox1 at the gamma-crystallin promoterJ Lengler, E Krausz, S Tomarev, et al.
The Journal of Physiology|April 14, 2011
Altered postnatal maturation of electrical properties in spinal motoneurons in a mouse model of amyotrophic lateral sclerosisK A Quinlan, J E Schuster, R Fu, et al.
Pageof 27