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Ophthalmic Genetics
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July 3, 2024
A novel frameshift variant in <i>BCOR</i> causes congenital nuclear cataract
Vanita 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 recommendations
Stephen 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 protein
Ewa 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 embryogenesis
G 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 protein
R 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 mutation
Paul 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 domain
Roy 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 cataracts
Vanita Berry, Nikolas Pontikos, Alex Ionides, et al.
Nucleic Acids Research
|
January 5, 2001
Antagonistic action of Six3 and Prox1 at the gamma-crystallin promoter
J 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 sclerosis
K A Quinlan, J E Schuster, R Fu, et al.
Page
of 27
Search research articles
Search
Showing results (101-110 of 268) with videos related to
Sort By:
Page
of 27
Ophthalmic Genetics
|
July 3, 2024
A novel frameshift variant in <i>BCOR</i> causes congenital nuclear cataract
Vanita 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 recommendations
Stephen 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 protein
Ewa 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 embryogenesis
G 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 protein
R 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 mutation
Paul 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 domain
Roy 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 cataracts
Vanita Berry, Nikolas Pontikos, Alex Ionides, et al.
Nucleic Acids Research
|
January 5, 2001
Antagonistic action of Six3 and Prox1 at the gamma-crystallin promoter
J 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 sclerosis
K A Quinlan, J E Schuster, R Fu, et al.
Page
of 27