Publications by authors named "Gayle Collin"

Claim this Profile
A
A biometric survey of known and prospective murine models of posterior microphthalmia-nanophthalmia.
Navdeep Gogna, Jai Pinkney, Lisa Stone, Mhd Mustafa Khorzom, Fuxin Zhao, Gayle B Collin

Exp Eye Res· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Current Views on Chr10q26 Contribution to Age-Related Macular Degeneration.
Navdeep Gogna, Lillian F Hyde, Gayle B Collin, Lisa Stone, Jurgen K Naggert

Adv Exp Med Biol· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chromophore supply modulates cone function and survival in retinitis pigmentosa mouse models.
Yunlu Xue, Xiaomei Sun, Sean K Wang, Gayle B Collin, Vladimir J Kefalov

Proc Natl Acad Sci U S A· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A mouse model of cone photoreceptor function loss with degeneration due to a mutation in .
Anna S E N Naggert, Gayle B Collin, Jieping Wang, Mark P Krebs, Bo Chang

Front Mol Neurosci· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice.
Lillian F Hyde, Yang Kong, Lihong Zhao, Sriganesh Ramachandra Rao, Jieping Wang, Gayle B Collin

Int J Mol Sci· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model.
Sonia M Weatherly, Gayle B Collin, Jeremy R Charette, Lisa Stone, Nattaya Damkham

PLoS Genet· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Splicing Mutation in Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction.
Gayle B Collin, Lanying Shi, Minzhong Yu, Nurten Akturk, Jeremy R Charette

Int J Mol Sci· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Interaction between and Mutations Affect Retinal Disease Phenotypes.
Navdeep Gogna, Sonia Weatherly, Fuxin Zhao, Gayle B Collin, Jai Pinkney

Int J Mol Sci· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.
Gayle B Collin, Navdeep Gogna, Bo Chang, Nattaya Damkham, Jai Pinkney

Cells· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spectral-domain optical coherence tomography findings in Alström syndrome.
Gad Dotan, Vikas Khetan, Jan D Marshall, Elizabeth Affel, Denise Armiger-George, Gayle B Collin

Ophthalmic Genet· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mouse models of human ocular disease for translational research.
Mark P Krebs, Gayle B Collin, Wanda L Hicks, Minzhong Yu, Jeremy R Charette

PLoS One· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease.
Scott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, Lan Ying Shi, Steve D M Brown, Gayle B Collin

Am J Pathol· July 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pituitary morphovolumetric changes in Alström syndrome.
Valentina Citton, Pietro Maffei, Jan D Marshall, Alessandro Baglione, Gayle B Collin

J Neuroradiol· June 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity.
Nicole T M Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, Wanda Hicks, Minzhong Yu, Gayle B Collin

Nat Genet· February 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GLUT4 defects in adipose tissue are early signs of metabolic alterations in Alms1GT/GT, a mouse model for obesity and insulin resistance.
Francesca Favaretto, Gabriella Milan, Gayle B Collin, Jan D Marshall, Fabio Stasi

PLoS One· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.
Gayle B Collin, Dirk Hubmacher, Jeremy R Charette, Wanda L Hicks, Lisa Stone

Hum Mol Genet· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Alström Syndrome: Mutation Spectrum of ALMS1.
Jan D Marshall, Jean Muller, Gayle B Collin, Gabriella Milan, Stephen F Kingsmore

Hum Mutat· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAs.
Ramani Soundararajan, Jungyeon Won, Timothy M Stearns, Jeremy R Charette, Wanda L Hicks, Gayle B Collin

PLoS One· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia.
Dennis M Maddox, Gayle B Collin, Akihiro Ikeda, C Herbert Pratt, Sakae Ikeda

Invest Ophthalmol Vis Sci· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall

J Hum Genet· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall

J Hum Genet· January 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in Alström protein impair terminal differentiation of cardiomyocytes.
Lincoln T Shenje, Peter Andersen, Marc K Halushka, Cecillia Lui, Laviel Fernandez, Gayle B Collin

Nat Commun· March 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Extreme clinical variability of dilated cardiomyopathy in two siblings with Alström syndrome.
Jamal Mahamid, Avraham Lorber, Yoseph Horovitz, Stavit A Shalev, Gayle B Collin

Pediatr Cardiol· February 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Differences in the clinical spectrum of two adolescent male patients with Alström syndrome.
Vladimir Kuburović, Jan D Marshall, Gayle B Collin, Keith Nykamp, Nina Kuburović

Clin Dysmorphol· January 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway.
Gayle B Collin, Jan D Marshall, Benjamin L King, Gabriella Milan, Pietro Maffei

PLoS One· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis