Related references
Note: Only part of the references are listed.Alopecia-mental retardation syndrome: Molecular genetics of a rare neuro-dermal disorder
Muhammad Muzammal et al.
ANNALS OF HUMAN GENETICS (2021)
Qki activates Srebp2-mediated cholesterol biosynthesis for maintenance of eye lens transparency
Seula Shin et al.
NATURE COMMUNICATIONS (2021)
The E3 Ligase PIAS1 Regulates p53 Sumoylation to Control Stress-Induced Apoptosis of Lens Epithelial Cells Through the Proapoptotic Regulator Bax
Qian Nie et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)
Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
Yoichi Wada et al.
PLOS GENETICS (2020)
Prohibitin 2 deficiency impairs cardiac fatty acid oxidation and causes heart failure
Dechao Wu et al.
CELL DEATH & DISEASE (2020)
In vivo detecting mouse persistent hyperplastic primary vitreous by Spectralis Optical Coherence Tomography
Qing Lian et al.
EXPERIMENTAL EYE RESEARCH (2019)
Endogenous sterol intermediates of the mevalonate pathway regulate HMGCR degradation and SREBP-2 processing[S]
Liang Chen et al.
JOURNAL OF LIPID RESEARCH (2019)
Protective Effects of Lanosterol Synthase Up-Regulation in UV-B-Induced Oxidative Stress
Hui Hua et al.
FRONTIERS IN PHARMACOLOGY (2019)
A novel mutation of PANK4 causes autosomal dominant congenital posterior cataract
Min Sun et al.
HUMAN MUTATION (2019)
Lanosterol Synthase Pathway Alleviates Lens Opacity in Age-Related Cortical Cataract
Xinyue Shen et al.
JOURNAL OF OPHTHALMOLOGY (2018)
Crk proteins transduce FGF signaling to promote lens fiber cell elongation
Tamica N. Collins et al.
ELIFE (2018)
Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
Maria-Teresa Romano et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
RNA sequencing-based transcriptomic profiles of embryonic lens development for cataract gene discovery
Deepti Anand et al.
HUMAN GENETICS (2018)
Congenital cataract with LSS gene mutations: a new case report
Xiaodan Chen et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2017)
Signaling and Gene Regulatory Networks in Mammalian Lens Development
Ales Cvekl et al.
TRENDS IN GENETICS (2017)
Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis
Olga Messina-Baas et al.
MOLECULAR SYNDROMOLOGY (2017)
Prox1 and fibroblast growth factor receptors form a novel regulatory loop controlling lens fiber differentiation and gene expression
Dylan S. Audette et al.
DEVELOPMENT (2016)
Chromatin remodeling enzyme Snf2h regulates embryonic lens differentiation and denucleation
Shuying He et al.
DEVELOPMENT (2016)
Lanosterol reverses protein aggregation in cataracts
Ling Zhao et al.
NATURE (2015)
Transcriptome Profiling of Developing Murine Lens Through RNA Sequencing
Shahid Y. Khan et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2015)
Nuclear removal during terminal lens fiber cell differentiation requires CDK1 activity: appropriating mitosis-related nuclear disassembly
Blake R. Chaffee et al.
DEVELOPMENT (2014)
HSF4 regulates DLAD expression and promotes lens de-nucleation
Xiukun Cui et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
Deletion of Autophagy-related 5 (Atg5) and Pik3c3 Genes in the Lens Causes Cataract Independent of Programmed Organelle Degradation
Hideaki Morishita et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Cx43, ZO-1, alpha-catenin and beta-catenin in cataractous lens epithelial cells
Anshul I. Arora et al.
JOURNAL OF BIOSCIENCES (2012)
Chromatin remodeling enzyme Brg1 is required for mouse lens fiber cell terminal differentiation and its denucleation
Shuying He et al.
EPIGENETICS & CHROMATIN (2010)
The Tumor Suppressor Merlin Is Required for Cell Cycle Exit, Terminal Differentiation, and Cell Polarity in the Developing Murine Lens
Luke A. Wiley et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Pax6 is essential for lens fiber cell differentiation
Ohad Shaham et al.
DEVELOPMENT (2009)
A cell polarity protein aPKCλ is required for eye lens formation and growth
Yuki Sugiyama et al.
DEVELOPMENTAL BIOLOGY (2009)
Congenital cataracts and their molecular genetics
J. Fielding Hejtmancik
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2008)
Lanosterol synthase mutations cause cholesterol deficiency-associated cataracts in the Shumiya cataract rat
M Mori et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
Lord of the rings -: the mechanism for oxidosqualene:lanosterol cyclase becomes crystal clear
MW Huff et al.
TRENDS IN PHARMACOLOGICAL SCIENCES (2005)
Mafs, Prox1, and Pax6 can regulate chicken βB1-crystallin gene expression
WW Cui et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Insight into steroid scaffold formation from the structure of human oxidosqualene cyclase
R Thoma et al.
NATURE (2004)
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract
L Bu et al.
NATURE GENETICS (2002)
Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye
R Ashery-Padan et al.
GENES & DEVELOPMENT (2000)
Spatiotemporal distribution of zonulae adherens and associated actin bundles in both epithelium and fiber cells during chicken lens development
WK Lo et al.
EXPERIMENTAL EYE RESEARCH (2000)