Citation Impact
Citing Papers
Angiotensin II causes hypertension and cardiac hypertrophy through its receptors in the kidney
2006 StandoutNobel
Modulating Sphingolipid Biosynthetic Pathway Rescues Photoreceptor Degeneration
2003 Science
Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression
2014 StandoutNobel
Electron tomography : methods for three-dimensional visualization of structures in the cell
2010 StandoutNobel
β-Arrestin-2 Mediates Anti-apoptotic Signaling through Regulation of BAD Phosphorylation
2009 StandoutNobel
No health without mental health
2007 Standout
Ets-1 is a critical regulator of Ang II-mediated vascular inflammation and remodeling
2005
Mutation of CERKL, a Novel Human Ceramide Kinase Gene, Causes Autosomal Recessive Retinitis Pigmentosa (RP26)
2004
The Retinal Pigment Epithelium in Visual Function
2005 Standout
Dissection of a QTL Hotspot on Mouse Distal Chromosome 1 that Modulates Neurobehavioral Phenotypes and Gene Expression
2008
Temporal changes in gene expression in the skin of patients treated with isotretinoin provide insight into its mechanism of action
2009
Post-transcriptional gene regulation by mRNA modifications
2016 Standout
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Principles of nanoparticle design for overcoming biological barriers to drug delivery
2015 Standout
TGFβ signalling in context
2012 Standout
Kinesin-1-Mediated Capsid Disassembly and Disruption of the Nuclear Pore Complex Promote Virus Infection
2011
The functions of the nuclear envelope in mediating the molecular crosstalk between the nucleus and the cytoplasm
2011
Intellectual disability and its relationship to autism spectrum disorders
2009 Standout
The Small Molecule NS11021 Is a Potent and Specific Activator of Ca2+-Activated Big-Conductance K+ Channels
2007
Nuclear pore complex composition: a new regulator of tissue-specific and developmental functions
2012
Retinitis Pigmentosa: Genes and Disease Mechanisms
2011 Standout
Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia
2007 StandoutNobel
Atherosclerosis: current pathogenesis and therapeutic options
2011 Standout
Molecular basis of ancestral vertebrate electroreception
2017 StandoutNatureNobel
Novel ENU-induced eye mutations in the mouse: models for human eye disease
2002
Modeling the human Na<sub>v</sub>1.5 sodium channel: structural and mechanistic insights of ion permeation and drug blockade
2017 StandoutNobel
Breakpoint characterization of a novel ∼59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance
2008
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
Association of a Functional Deficit of the BK Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation
2006
Retinitis pigmentosa
2006 Standout
Nuclear Pore Complex
2011
Hydrogen sulfide increases calcium-activated potassium (BK) channel activity of rat pituitary tumor cells
2009
From molecule to malady
2006 Nature
Leber congenital amaurosis: Genes, proteins and disease mechanisms
2008 Standout
PTEN hamartoma tumor syndromes
2008 Standout
Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
2010 Standout
Genetics and cardiac channelopathies
2010
Alternative, Nonapoptotic Programmed Cell Death
2004
Toward transcriptional therapies for the failing heart: chemical screens to modulate genes
2005
Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs
2009
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome
2003
The many roles of histone deacetylases in development and physiology: implications for disease and therapy
2008 Standout
Prescribing Personalized Nutrition for Cardiovascular Health: Are We Ready?
2014 Standout
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay
2008
Transcription factors: from enhancer binding to developmental control
2012 Standout
Multiple Hits during Early Embryonic Development: Digenic Diseases and Holoprosencephaly
2002
The MEF2D transcription factor mediates stress-dependent cardiac remodeling in mice
2008
Inflammation in Atherosclerosis
2009 Standout
Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome: Table 1
2004
A Temporal Map of Transcription Factor Activity: Mef2 Directly Regulates Target Genes at All Stages of Muscle Development
2006
Vitamin A metabolism in the retinal pigment epithelium: genes, mutations, and diseases
2003
Transient Receptor Potential Cation Channels in Disease
2007 Standout
Common Genetic Vulnerability to Depressive Symptoms and Coronary Artery Disease: A Review and Development of Candidate Genes Related to Inflammation and Serotonin
2006
The Transcription Factor Mef2 Links the Drosophila Core Clock to Fas2, Neuronal Morphology, and Circadian Behavior
2013 StandoutNobel
Genetics of myocardial infarction: a progress report
2010
Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports
2010
Identification of Cyclobutane Pyrimidine Dimer-Responsive Genes Using UVB-Irradiated Human Keratinocytes Transfected with In Vitro-Synthesized Photolyase mRNA
2015 StandoutNobel
Control of mammalian gene expression by selective mRNA export
2015
Integrating cell-signalling pathways with NF-κB and IKK function
2006 Standout
Modeling neurodevelopmental disorder-associated humanAGO1mutations inCaenorhabditis elegansArgonautealg-1
2024 StandoutNobel
Tumor Necrosis Factor Alpha-Mediated Reduction of KLF2 Is Due to Inhibition of MEF2 by NF-κB and Histone Deacetylases
2005
Physiological Implications of Hydrogen Sulfide: A Whiff Exploration That Blossomed
2012 Standout
Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosa.
2008
Arterial Stiffness and Cardiovascular Events
2010 Standout
Velvet, a Dominant Egfr Mutation That Causes Wavy Hair and Defective Eyelid Development in Mice
2004 StandoutNobel
Heat shock proteins: Biological functions, pathological roles, and therapeutic opportunities
2022
Key transcriptional regulators of the vasoprotective effects of shear stress
2009
Specific Nucleoporin Requirement for Smad Nuclear Translocation
2010
Seven-Transmembrane Receptor Signaling Through β-Arrestin
2005 StandoutNobel
Apoptosis, Pyroptosis, and Necrosis: Mechanistic Description of Dead and Dying Eukaryotic Cells
2005 Standout
Genome-Wide Association Study of Coronary Artery Disease
2010
Multifaceted roles of β-arrestins in the regulation of seven-membrane-spanning receptor trafficking and signalling
2003 StandoutNobel
Kruppel-Like Factor 2 as a Novel Mediator of Statin Effects in Endothelial Cells
2005
Endothelial Cell Dysfunction and the Pathobiology of Atherosclerosis
2016 Standout
Biomarkers of Cardiovascular Disease
2006
Finding and interpreting genetic variations that are important to ophthalmologists.
2003
E3 ubiquitin ligase Mindbomb 1 facilitates nuclear delivery of adenovirus genomes
2020 StandoutNobel
Effects of Disturbed Flow on Vascular Endothelium: Pathophysiological Basis and Clinical Perspectives
2011 Standout
Genes and mutations causing retinitis pigmentosa
2013 Standout
Computational design of a red fluorophore ligase for site-specific protein labeling in living cells
2014 StandoutNobel
Role of Renal Angiotensin II Type 1 Receptors in the Genesis of Hypertension
2007 StandoutNobel
Works of Lejin Wang being referenced
Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease
2003 Science
Novel deletion in the pre‐mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family
2003
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder
2005
Update on the molecular genetics of retinitis pigmentosa
2001
Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa
2001
Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death
2008