A citation-based method for searching scientific literature

Jillian N Pearring, Pasano Bojang, Yin Shen, Chieko Koike, Takahisa Furukawa, Scott Nawy, Ronald G Gregg. J Neurosci 2011
Times Cited: 64

C M Pusch, C Zeitz, O Brandau, K Pesch, H Achatz, S Feil, C Scharfe, J Maurer, F K Jacobi, A Pinckers, S Andreasson, A Hardcastle, B Wissinger, W Berger, A Meindl. Nat Genet 2000
Times Cited: 186

List of shared articles

Times cited

Properties and functions of TRPM1 channels in the dendritic tips of retinal ON-bipolar cells.
Franziska M Schneider, Florian Mohr, Marc Behrendt, Johannes Oberwinkler. Eur J Cell Biol 2015

Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindness.
Andreas Schatz, Carina Kelbsch, Christina Zeitz, Susanne Kohl, Eberhart Zrenner, Florian Gekeler, Helmut Wilhelm, Barbara Wilhelm, Gabriel Willmann. Graefes Arch Clin Exp Ophthalmol 2019

The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.
Kirill A Martemyanov, Alapakkam P Sampath. Annu Rev Vis Sci 2017

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.
Rueben G Das, Doreen Becker, Vidhya Jagannathan, Orly Goldstein, Evelyn Santana, Kendall Carlin, Raghavi Sudharsan, Tosso Leeb, Yuji Nishizawa, Mineo Kondo,[...]. Sci Rep 2019

Molecular mechanisms underlying selective synapse formation of vertebrate retinal photoreceptor cells.
Takahisa Furukawa, Akiko Ueno, Yoshihiro Omori. Cell Mol Life Sci 2020

Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Christina Zeitz, Samuel G Jacobson, Christian P Hamel, Kinga Bujakowska, Marion Neuillé, Elise Orhan, Xavier Zanlonghi, Marie-Elise Lancelot, Christelle Michiels, Sharon B Schwartz,[...]. Am J Hum Genet 2013

Oligomeric state of purified transient receptor potential melastatin-1 (TRPM1), a protein essential for dim light vision.
Melina A Agosto, Zhixian Zhang, Feng He, Ivan A Anastassov, Sara J Wright, Jennifer McGehee, Theodore G Wensel. J Biol Chem 2014

Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.
Jan Klooster, Maria M van Genderen, Minzhong Yu, Ralph J Florijn, Frans C C Riemslag, Arthur A B Bergen, Ronald G Gregg, Neal S Peachey, Maarten Kamermans. Invest Ophthalmol Vis Sci 2013

Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
Marion Neuillé, Said El Shamieh, Elise Orhan, Christelle Michiels, Aline Antonio, Marie-Elise Lancelot, Christel Condroyer, Kinga Bujakowska, Olivier Poch, José-Alain Sahel,[...]. PLoS One 2014

Mouse b-wave mutants.
Machelle T Pardue, Neal S Peachey. Doc Ophthalmol 2014

Differential epitope masking reveals synapse-specific complexes of TRPM1.
Melina A Agosto, Ivan A Anastassov, Theodore G Wensel. Vis Neurosci 2018

Two Novel NYX Gene Mutations in the Chinese Families with X-linked Congenital Stationary Night Blindness.
Shuzhen Dai, Ming Ying, Kai Wang, Liming Wang, Ruifang Han, Peng Hao, Ningdong Li. Sci Rep 2015

Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.
Sivasankar Malaichamy, Parveen Sen, Ramya Sachidanandam, Tharigopala Arokiasamy, Marie Elise Lancelot, Isabelle Audo, Christina Zeitz, Nagasamy Soumittra. Mol Vis 2014

Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
Elise Orhan, Laurent Prézeau, Said El Shamieh, Kinga M Bujakowska, Christelle Michiels, Yvrick Zagar, Claire Vol, Shomi S Bhattacharya, José-Alain Sahel, Florian Sennlaub,[...]. Invest Ophthalmol Vis Sci 2013

Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
Virginie Dinet, Giuseppe D Ciccotosto, Kimberley Delaunay, Céline Borras, Isabelle Ranchon-Cole, Corinne Kostic, Michèle Savoldelli, Mohamed El Sanharawi, Laurent Jonet, Caroline Pirou,[...]. Mol Brain 2016

The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies.
Samantha R De Silva, Gavin Arno, Anthony G Robson, Ana Fakin, Nikolas Pontikos, Moin D Mohamed, Alan C Bird, Anthony T Moore, Michel Michaelides, Andrew R Webster,[...]. Prog Retin Eye Res 2021

A novel missense mutation in the NYX gene associated with high myopia.
Shea Ping Yip, Choi Chu Li, Wai Chi Yiu, Wing Hong Hung, Wai Wa Lam, Man Chi Lai, Po Wah Ng, Wai Yan Fung, Patrick H W Chu, Bo Jiang,[...]. Ophthalmic Physiol Opt 2013

Leucine Rich Repeat Proteins: Sequences, Mutations, Structures and Diseases.
Norio Matsushima, Shintaro Takatsuka, Hiroki Miyashita, Robert H Kretsinger. Protein Pept Lett 2019

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Neal S Peachey, Thomas A Ray, Ralph Florijn, Lucy B Rowe, Trijntje Sjoerdsma, Susana Contreras-Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P Michael Iuvone,[...]. Am J Hum Genet 2012

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Neal S Peachey, Jillian N Pearring, Pasano Bojang, Matthew E Hirschtritt, Gwen Sturgill-Short, Thomas A Ray, Takahisa Furukawa, Chieko Koike, Andrew F X Goldberg, Yin Shen,[...]. J Neurophysiol 2012

Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans.
Norio Matsushima, Hiroki Miyashita, Robert H Kretsinger. J Cell Commun Signal 2021

Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.
Virginia Miraldi Utz, Wanda Pfeifer, Susannah Q Longmuir, Richard John Olson, Kai Wang, Arlene V Drack. JAMA Ophthalmol 2018

Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1.
Nazarul Hasan, Gobinda Pangeni, Catherine A Cobb, Thomas A Ray, Emily R Nettesheim, Kristina J Ertel, Daniel M Lipinski, Maureen A McCall, Ronald G Gregg. Cell Rep 2019

A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.
Elise Orhan, Marion Neuillé, Miguel de Sousa Dias, Thomas Pugliese, Christelle Michiels, Christel Condroyer, Aline Antonio, José-Alain Sahel, Isabelle Audo, Christina Zeitz. Int J Mol Sci 2021

Small Leucine-Rich Proteoglycans (SLRPs) in the Retina.
Shermaine W Y Low, Thomas B Connor, Iris S Kassem, Deborah M Costakos, Shyam S Chaurasia. Int J Mol Sci 2021

Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation.
J Jason McAnany, Kenneth R Alexander, Nalin M Kumar, Hongyu Ying, Anastasios Anastasakis, Gerald A Fishman. Ophthalmic Genet 2013