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Authors: Naoyuki Tanimoto
Journal Article
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2
Human Molecular Genetics, Volume 26, Issue 2, 15 January 2017, Page 466, https://doi.org/10.1093/hmg/ddw424
Published: 10 March 2017
Journal Article
Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia
Human Molecular Genetics, Volume 25, Issue 6, 15 March 2016, Pages 1165–1175, https://doi.org/10.1093/hmg/ddv639
Published: 05 January 2016
Journal Article
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice Get access
Human Molecular Genetics, Volume 23, Issue 14, 15 July 2014, Pages 3759–3771, https://doi.org/10.1093/hmg/ddu089
Published: 23 February 2014
Journal Article
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 Get access
Human Molecular Genetics, Volume 23, Issue 6, 15 March 2014, Pages 1538–1550, https://doi.org/10.1093/hmg/ddt541
Published: 26 October 2013
Journal Article
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death
Human Molecular Genetics, Volume 21, Issue 24, 15 December 2012, Page 5395, https://doi.org/10.1093/hmg/dds404
Published: 12 October 2012
Journal Article
Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene Get access
Human Molecular Genetics, Volume 22, Issue 1, 1 January 2013, Pages 35–50, https://doi.org/10.1093/hmg/dds398
Published: 21 September 2012
Journal Article
Gene therapy restores vision and delays degeneration in the CNGB1−/− mouse model of retinitis pigmentosa Get access
Human Molecular Genetics, Volume 21, Issue 20, 15 October 2012, Pages 4486–4496, https://doi.org/10.1093/hmg/dds290
Published: 16 July 2012
Journal Article
A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa Get access
Human Molecular Genetics, Volume 20, Issue 5, 1 March 2011, Pages 941–947, https://doi.org/10.1093/hmg/ddq539
Published: 10 December 2010
Journal Article
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death Get access
Human Molecular Genetics, Volume 18, Issue 7, 1 April 2009, Pages 1266–1275, https://doi.org/10.1093/hmg/ddp026
Published: 15 January 2009
Journal Article
R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal Get access
Human Molecular Genetics, Volume 17, Issue 2, 15 January 2008, Pages 281–292, https://doi.org/10.1093/hmg/ddm304
Published: 12 October 2007
Journal Article
Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapse Get access
Human Molecular Genetics, Volume 15, Issue 8, 15 April 2006, Pages 1291–1302, https://doi.org/10.1093/hmg/ddl047
Published: 06 March 2006
