Xiaolei Xu

Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin.

Pseudophosphorylated prolactin (S179D PRL) inhibits growth and promotes beta-casein gene expression in the rat mammary gland.

Maternal prolactin composition can permanently affect epidermal gammadeltaT cell function in the offspring.

Opposite effects of unmodified prolactin and a molecular mimic of phosphorylated prolactin on morphology and the expression of prostate specific genes in the normal rat prostate.

Different biological effects of unmodified prolactin and a molecular mimic of phosphorylated prolactin involve different signaling pathways.

Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin.

C terminus of RGS-GAIP-interacting protein conveys neuropilin-1-mediated signaling during angiogenesis.

Depletion of zebrafish titin reduces cardiac contractility by disrupting the assembly of Z-discs and A-bands.

Depletion of Med10 enhances Wnt and suppresses Nodal signaling during zebrafish embryogenesis.

Neuropilin-1 modulates p53/caspases axis to promote endothelial cell survival.

Wnt3a regulates the development of cardiac neural crest cells by modulating expression of cysteine-rich intestinal protein 2 in rhombomere 6.

Depletion of zebrafish essential and regulatory myosin light chains reduces cardiac function through distinct mechanisms.

[Effect of higher iron in diet on iron levels and hepcidin mRNA expression levels in rats].

Distinct functions of Wnt/beta-catenin signaling in KV development and cardiac asymmetry.

Transient and transgenic analysis of the zebrafish ventricular myosin heavy chain (vmhc) promoter: an inhibitory mechanism of ventricle-specific gene expression.

Myofibrillogenesis in the developing zebrafish heart: A functional study of tnnt2.

Cardiac hypertrophy involves both myocyte hypertrophy and hyperplasia in anemic zebrafish.

Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly.

[Effect of iron deficiency on vitamin A metabolism in rats].

Iron-catalyzed, microwave-promoted, one-pot synthesis of 9-substituted xanthenes by a cascade benzylation-cyclization process.

In vivo protein trapping produces a functional expression codex of the vertebrate proteome.

Haploinsufficiency of target of rapamycin attenuates cardiomyopathies in adult zebrafish.

Functions of the Wnt/β-catenin pathway in an anemia-induced zebrafish model of cardiomyopathy are location dependent.

TOR-autophagy signaling in adult zebrafish models of cardiomyopathy.

Wnt/β-catenin signaling directly regulates Foxj1 expression and ciliogenesis in zebrafish Kupffer's vesicle.

Quantifying cardiac functions in embryonic and adult zebrafish.

Target of rapamcyin (TOR)-based therapeutics for cardiomyopathy: Insights from zebrafish genetics.

Cardiac transcriptome and dilated cardiomyopathy genes in zebrafish.

Exon- and contraction-dependent functions of titin in sarcomere assembly.

Oxidative Stress-Induced Afterdepolarizations and Protein Kinase C Signaling.

Systematic identification and characterization of cardiac long intergenic noncoding RNAs in zebrafish.

Real-Time Monitoring and Analysis of Zebrafish Electrocardiogram with Anomaly Detection.

α-Actinin2 is required for the lateral alignment of Z discs and ventricular chamber enlargement during zebrafish cardiogenesis.

Target of rapamycin (TOR)-based therapy for cardiomyopathy: evidence from zebrafish and human studies.

Guidelines for the use and interpretation of assays for monitoring autophagy.

Trapping cardiac recessive mutants via expression-based insertional mutagenesis screening.

New and TALENted genome engineering toolbox.

Anti-remodeling effects of rapamycin in experimental heart failure: dose response and interaction with angiotensin receptor blockade.

Cessation of contraction induces cardiomyocyte remodeling during zebrafish cardiogenesis.

Cardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patients.

Understanding cardiac sarcomere assembly with zebrafish genetics.

Both ciliary and non-ciliary functions of Foxj1a confer Wnt/β-catenin signaling in zebrafish left-right patterning.

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).

Cardiac Light-Sheet Fluorescent Microscopy for Multi-Scale and Rapid Imaging of Architecture and Function.

De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.

Effects of ventricular conduction block patterns on mortality in hospitalized patients with dilated cardiomyopathy: a single-center cohort study.

A modifier screen identifies as a cardiomyopathy susceptibility gene.

Autophagy activators suppress cystogenesis in an autosomal dominant polycystic kidney disease model.

Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy.

Automated Segmentation of Light-Sheet Fluorescent Imaging to Characterize Experimental Doxorubicin-Induced Cardiac Injury and Repair.

Modeling -Associated Dilated Cardiomyopathy in Adult Zebrafish.

Phenotyping cardiomyopathy in adult zebrafish.

A Langendorff-like system to quantify cardiac pump function in adult zebrafish.

Displacement analysis of myocardial mechanical deformation (DIAMOND) reveals segmental susceptibility to doxorubicin-induced injury and regeneration.

Phenotyping an adult zebrafish lamp2 cardiomyopathy model identifies mTOR inhibition as a candidate therapy.

Haploinsufficiency of mechanistic target of rapamycin ameliorates cardiomyopathy in adult zebrafish.

Retinoid X receptor alpha is a spatiotemporally predominant therapeutic target for anthracycline-induced cardiotoxicity.

Aging-associated sinus arrest and sick sinus syndrome in adult zebrafish.

A feasibility study for noninvasive measurement of shear wave speed in live zebrafish.

Building the vertebrate codex using the gene breaking protein trap library.

Knockout of SORBS2 Protein Disrupts the Structural Integrity of Intercalated Disc and Manifests Features of Arrhythmogenic Cardiomyopathy.

Acquisition, Processing and Analysis of Electrocardiogram in Awake Zebrafish.

Continuous Electrocardiogram Monitoring in Zebrafish with Prolonged Mild Anesthesia.

Modeling Inherited Cardiomyopathies in Adult Zebrafish for Precision Medicine.

Haploinsufficiency Ameliorates Renal Cysts and Cilia Abnormality in Adult Zebrafish Mutants.

Induction of Wnt signaling antagonists and p21-activated kinase enhances cardiomyocyte proliferation during zebrafish heart regeneration.

TFEB Overexpression, Not mTOR Inhibition, Ameliorates RagC Cardiomyopathy.

Deep learning-based framework for cardiac function assessment in embryonic zebrafish from heart beating videos.

Disruption of Gene Function Increases the Risk of Doxorubicin-Induced Cardiomyopathy and Heart Failure.

-Based Autophagy Activation Reverses Doxorubicin-Induced Cardiotoxicity.

A Swimming-based Assay to Determine the Exercise Capacity of Adult Zebrafish Cardiomyopathy Models.

Changes in ion channel expression and function associated with cardiac arrhythmogenic remodeling by Sorbs2.

A novel wireless ECG system for prolonged monitoring of multiple zebrafish for heart disease and drug screening studies.

Inhibition of mTOR or MAPK ameliorates vmhcl/myh7 cardiomyopathy in zebrafish.

Corrigendum to 'Induction of Wnt signaling antagonists and p21-activated kinase enhances cardiomyocyte proliferation during zebrafish heart regeneration'.

Vascular Injury in the Zebrafish Tail Modulates Blood Flow and Peak Wall Shear Stress to Restore Embryonic Circular Network.

Application of an F0-based genetic assay in adult zebrafish to identify modifier genes of an inherited cardiomyopathy.

A Primer Genetic Toolkit for Exploring Mitochondrial Biology and Disease Using Zebrafish.

Genetic Susceptibility and Mechanisms Underlying the Pathogenesis of Anthracycline-Associated Cardiotoxicity.

A missense mutation in the proprotein convertase gene furinb causes hepatic cystogenesis during liver development in zebrafish.

A phenotype-based forward genetic screen identifies as a sick sinus syndrome gene.

Genetic therapy in a mitochondrial disease model suggests a critical role for liver dysfunction in mortality.

Radiation therapy induces immunosenescence mediated by p90RSK.

Transcriptome studies of inherited dilated cardiomyopathies.

Using Zebrafish Animal Model to Study the Genetic Underpinning and Mechanism of Arrhythmogenic Cardiomyopathy.

Molecular mechanisms of anthracycline induced cardiotoxicity: Zebrafish come into play.

Kidney transcriptome and cystic kidney disease genes in zebrafish.

Premature senescence and cardiovascular disease following cancer treatments: mechanistic insights.

Zbtb16 increases susceptibility of atrial fibrillation in type 2 diabetic mice via Txnip-Trx2 signaling.

Allelic heterogeneity of TTNtv cardiomyopathy can be modeled in adult zebrafish.