Related references
Note: Only part of the references are listed.The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1
Zenobia B. Mehta et al.
TRAFFIC (2014)
Expanding Horizons: Ciliary Proteins Reach Beyond Cilia
Shiaulou Yuan et al.
ANNUAL REVIEW OF GENETICS, VOL 47 (2013)
Assembling a primary cilium
Sehyun Kim et al.
CURRENT OPINION IN CELL BIOLOGY (2013)
TRPV1 Channels Are Intrinsically Heat Sensitive and Negatively Regulated by Phosphoinositide Lipids
Erhu Cao et al.
NEURON (2013)
Compensatory Role of Inositol 5-Phosphatase INPP5B to OCRL in Primary Cilia Formation in Oculocerebrorenal Syndrome of Lowe
Na Luo et al.
PLOS ONE (2013)
Regulation of SPARC by Transforming Growth Factor β2 in Human Trabecular Meshwork
Min Hyung Kang et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2013)
Suppression of intestinal calcium entry channel TRPV6 by OCRL, a lipid phosphatase associated with Lowe syndrome and Dent disease
Guojin Wu et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2012)
TRPV4 Is a Regulator of Adipose Oxidative Metabolism, Inflammation, and Energy Homeostasis
Li Ye et al.
CELL (2012)
The Lowe syndrome protein OCRL1 is involved in primary cilia assembly
Brian G. Coon et al.
HUMAN MOLECULAR GENETICS (2012)
OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome
Na Luo et al.
HUMAN MOLECULAR GENETICS (2012)
Can't get there from here: cilia and hydrocephalus
Bethany N. Sotak et al.
NATURE MEDICINE (2012)
Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model
Calvin S. Carter et al.
NATURE MEDICINE (2012)
Ophthalmic drug discovery: novel targets and mechanisms for retinal diseases and glaucoma
Kang Zhang et al.
NATURE REVIEWS DRUG DISCOVERY (2012)
Etanercept, a Widely Used Inhibitor of Tumor Necrosis Factor-α (TNF-α), Prevents Retinal Ganglion Cell Loss in a Rat Model of Glaucoma
Miin Roh et al.
PLOS ONE (2012)
Cilia at the Node of Mouse Embryos Sense Fluid Flow for Left-Right Determination via Pkd2
Satoko Yoshiba et al.
SCIENCE (2012)
PI4P and PI(4,5)P2 Are Essential But Independent Lipid Determinants of Membrane Identity
Gerald R. V. Hammond et al.
SCIENCE (2012)
Elementary Ca2+ Signals Through Endothelial TRPV4 Channels Regulate Vascular Function
Swapnil K. Sonkusare et al.
SCIENCE (2012)
OCRL1 Modulates Cilia Length in Renal Epithelial Cells
Youssef Rbaibi et al.
TRAFFIC (2012)
Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRL
Michelle Pirruccello et al.
TRENDS IN BIOCHEMICAL SCIENCES (2012)
Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma
Janey L. Wiggs et al.
PLOS GENETICS (2012)
Advances in Glaucoma Treatment and Management: Outflow Drugs
Paul L. Kaufman et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2012)
Scrutinizing ciliopathies by unraveling ciliary interaction networks
Jeroen van Reeuwijk et al.
HUMAN MOLECULAR GENETICS (2011)
Ciliogenesis: building the cell's antenna
Hiroaki Ishikawa et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2011)
Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes
Qihong Zhang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
A systems-biology approach to understanding the ciliopathy disorders
Ji Eun Lee et al.
GENOME MEDICINE (2011)
eNOS, a Pressure-Dependent Regulator of Intraocular Pressure
W. Daniel Stamer et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
Interaction of retinitis pigmentosa GTPase regulator (RPGR) with RAB8A GTPase: implications for cilia dysfunction and photoreceptor degeneration
Carlos A. Murga-Zamalloa et al.
HUMAN MOLECULAR GENETICS (2010)
Mechanosensitive transient receptor potential vanilloid type 1 channels contribute to vascular remodeling of rat fistula veins
Yih-Sharng Chen et al.
JOURNAL OF VASCULAR SURGERY (2010)
Mechanisms of Disease: Primary Open-Angle Glaucoma.
Young H. Kwon et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
TRPP2 and TRPV4 form a polymodal sensory channel complex
Michael Koetttgen et al.
JOURNAL OF CELL BIOLOGY (2008)
Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanism
Amanda M. D. Malone et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
Maxence V. Nachury et al.
CELL (2007)
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
UM Smith et al.
NATURE GENETICS (2006)
Polycystin-1, STAT6, and pathway that transduces P100 function in a ciliary mechanosensation and is activated in polycystic kidney disease
SH Low et al.
DEVELOPMENTAL CELL (2006)
Development of the primate area of high acuity, 3: Temporal relationships between pit formation, retinal elongation and cone packing
AD Springer et al.
VISUAL NEUROSCIENCE (2005)
Mammalian TRPV4 (VR-OAC) directs behavioral responses to osmotic and mechanical stimuli in Caenorhabditis elegans
W Liedtke et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
SM Nauli et al.
NATURE GENETICS (2003)
Share Paper
