Disease: Laterality defects dominant
- <em>MICAL1</em> Monooxygenase in Autosomal Dominant Lateral Temporal Epilepsy: Role in Cytoskeletal Regulation and Relation to Cancer
- A <em>Eucalyptus</em> Pht1 Family Gene EgPT8 Is Essential for Arbuscule Elongation of <em>Rhizophagus irregularis</em>
- A comprehensive study of skeletal muscle imaging in FHL1-related reducing body myopathy
- A facile strategy for the growth of high-quality tungsten disulfide crystals mediated by oxygen-deficient oxide precursors
- A gain-of-function mutation in BnaIAA13 disrupts vascular tissue and lateral root development in Brassica napus
- A nationwide survey of facial onset sensory and motor neuronopathy in Japan
- A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review
- A Novel Intronic <em>KMT2D</em> Variant as a Cause of Kabuki Syndrome: A Case Report
- A novel Lgi1 mutation causes white matter abnormalities and impairs motor coordination in mice
- A patient with 18p11.32-p11.21 deletion have monaural deafness caused by an inadequate haplodose of THOC1: A case report
- A patient-derived mutation of epilepsy-linked LGI1 increases seizure susceptibility through regulating K<sub>v</sub>1.1
- Aberrant dynein function promotes TDP-43 aggregation and upregulation of p62 in male mice harboring transgenic human TDP-43
- Abnormalities of hemispheric specialization in drug-naive and drug-receiving self-limited epilepsy with centrotemporal spikes
- Adult-onset dominant muscular dystrophy in Greek families caused by Annexin A11
- Amyotrophic lateral sclerosis associated with a pathological expansion in the <em>ATXN7</em> gene
- Amyotrophic lateral sclerosis associated with a pathological expansion in the ATXN7 gene
- An anatomical study of persistent trigeminal artery detected by computed tomography angiography and magnetic resonance angiography: proposal for a modified classification and a novel basilar artery grading system
- Anatomical differences of the vertebrobasilar artery between normal subjects and patients with cerebral infarction
- Annexin A11 mutations are associated with nuclear envelope dysfunction in vivo and in human tissue
- Anterior tibial artery injury is not the contraindication of medial plantar flap: digital subtraction angiography evidence and clinical application
- Arterial supply to the scrotum: A cadaveric angiographic study
- Assembling carbon nitride quantum dots into hollow fusiformis and loading CoP for photocatalytic hydrogen evolution
- Association between malformation type, location and functional deficits in lymphatic malformations of the head and neck in children
- Association of Vertebral Artery Hypoplasia and Vertebrobasilar Cerebrovascular Accident
- Associations between subregional thalamic volume and brain pathology in autosomal dominant Alzheimer's disease
- Atomic-Scale Insights into the Lateral and Vertical Epitaxial Growth in Two-Dimensional Pd(2)Se(3)-MoS(2) Heterostructures
- Atomic-Scale Insights into the Lateral and Vertical Epitaxial Growth in Two-Dimensional Pd<sub>2</sub>Se<sub>3</sub>-MoS<sub>2</sub> Heterostructures
- Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalus
- Capillary Flow Dynamics in Composite Rectangular Microchannels with Rough Walls
- Case report and literature review: Novel compound heterozygous <em>FIG4</em> variants causing both of peripheral and central nervous system defects
- Case report and literature review: Novel compound heterozygous FIG4 variants causing both of peripheral and central nervous system defects
- Case report: Diagnosis of a patient with Sifrim-Hitz-Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency
- Cephalometric Evaluation of Children with Short Stature of Genetic Etiology: A Review
- Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration
- Cleidocranial dysplasia associated with dentigerous cyst-review of literature and case report of two siblings
- Clinical application of expanded internal mammary artery perforator flap combined with vascular supercharge in reconstruction of faciocervical scar
- Clinicopathological associations of hemispheric dominance in primary progressive apraxia of speech
- Comparison of ultrasound with electrodiagnosis of scapular winging: A prospective case control study
- Controlled formation of three-dimensional cavities during lateral epitaxial growth
- Craniosynostosis of the Metopic Suture in a Patient With CADASIL/Lehman Syndrome
- Darier Disease Presenting with Recurrent Kaposi Varicelliform Eruption in a 10-year-old Boy with Seborrheic Dermatitis
- Diastolic myocardial mechanics and their relation to ventricular filling pressures and postoperative course in functionally single ventricles
- Effect of combining eight weeks of neuromuscular training with dual cognitive tasks on landing mechanics in futsal players with knee ligament dominance defect: a randomized controlled trial
- Enhanced Electron Delocalization Induced by Ferromagnetic Sulfur doped C 3 N 4 Triggers Selective H 2 O 2 Production
- Enhanced Electron Delocalization Induced by Ferromagnetic Sulfur doped C<sub>3</sub>N<sub>4</sub> Triggers Selective H<sub>2</sub>O<sub>2</sub> Production
- Epidemiological characteristics and distribution of congenital thumb duplication in south China: An analysis of 2,300 thumbs in 2,108 children
- Epilepsy-causing Reelin mutations result in impaired secretion and intracellular degradation of mutant proteins
- Expansion of the mutation spectrum and phenotype of <em>USP7</em>-related neurodevelopmental disorder
- Far-red light inhibits lateral bud growth mainly through enhancing apical dominance independently of strigolactone synthesis in tomato
- FDA-approved PDE4 inhibitors reduce the dominant toxicity of ALS-FTD-associated CHCHD10 (S59L)
- Fused in sarcoma regulates DNA replication timing and kinetics
- Genetic testing in the management of inherited cardiac disorders: two cases of Filamin-C arrhythmogenic left ventricular cardiomyopathy
- Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control
- Genotoxic Damage During Brain Development Presages Prototypical Neurodegenerative Disease
- Horseshoe Kidney
- Horseshoe Kidney
- Huntington's Disease: A Report of an Interesting Case and Literature Review
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- Is the Acetabular Cup Orientation Different in Robot-Assisted and Conventional Total Hip Arthroplasty With Right-Handed Surgeons Using an Anterolateral Approach?
- Is the Anterolateral Thigh Flap the Solution for Orthopedic Trauma Complication Reconstructions?: A Case Series
- Lateral semicircular canal dilatation in a patient with congenital hearing loss due to alpha-tectorin mutation: microanatomical considerations
- Lateral semicircular canal dilatation in a patient with congenital hearing loss due to α-tectorin mutation: microanatomical considerations
- Letter to the Editor: Depression As The First Symptom Of Frontal Lobe Grade 2 Malignant Glioma
- Long-Term Results of the Murawski Unilateral Cleft Lip Repair
- Lower extremity postaxial polydactyly: Current literature status and future avenues
- Magnetic resonance imaging of extraocular rectus muscles abnormalities in acute acquired concomitant esotropia
- Magnetic Resonance Imaging of Internal Derangements and Other Knee Pathologies in Adult Nigerians
- MICAL1 Monooxygenase in Autosomal Dominant Lateral Temporal Epilepsy: Role in Cytoskeletal Regulation and Relation to Cancer
- Micrococcus luteus LS570 promotes root branching in Arabidopsis via decreasing apical dominance of the primary root and an enhanced auxin response
- Modulating Golgi Stress Signaling Ameliorates Cell Morphological Phenotypes Induced by CHMP2B with Frontotemporal Dementia-Associated p.Asp148Tyr
- MRI Evaluation of the Relationship Between Abnormalities in Vision-Related Brain Networks and Quality of Life in Patients with Migraine without Aura
- Nail-based reconstruction strategies for Wassel-Flatt type IVh thumb polydactyly with a floating ulnar digit: A preliminary report with 63 thumbs
- Nanometer-Resolved Operando Photo-Response of Faceted BiVO<sub>4</sub> Semiconductor Nanoparticles
- Oral Cleft Related-Genes may be Involved in Root Curvature of Maxillary Lateral Incisors
- Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur-Chung neurodevelopmental syndrome
- Pediatric thoracic outlet syndrome: a systematic review and meta-analysis
- Prevalence of zygomatic air cell defects in a North American population
- Proteostasis Deregulation in Neurodegeneration and Its Link with Stress Granules: Focus on the Scaffold and Ribosomal Protein RACK1
- Pseudarthrosis of distal radial growth plate treated with Blount clip: A case report
- Pulmonary Embolism in Autosomal Dominant Polycystic Kidney Patient Induced by Inferior Vena Cava Mechanical Compression
- Quantitative proteomics unveils known and previously unrecognized alterations in neuropathic nerves
- RNA Is a Double-Edged Sword in ALS Pathogenesis
- Role of Surface Features on the Initial Dissolution of CH<sub>3</sub>NH<sub>3</sub>PbI<sub>3</sub> Perovskite in Liquid Water: An Ab Initio Molecular Dynamics Study
- Siblings with profound connective tissue disease: First report of biallelic TGFBR1-related Loeys-Dietz syndrome
- Simultaneous Association of Variations in the Origin and Diameter of the Left Vertebral Artery in a Patient with a C1 Lateral Mass Tumor
- Staged unifocalization revisited
- The accessory vascularization of the tensor fasciae latae muscle: towards a new classification?
- The hereditary spastic paraplegias
- The pectoralis major musculo-mammary transposition flap to close a radical mastectomy defect: the breast switch
- The Relationship Between Coronary Dominance and Positive Results in Myocardial Perfusion Imaging
- The role of internal defects on anisotropic tensile failure of L-PBF AlSi10Mg alloys
- Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunction
- Type I Dentin Dysplasia: The Literature Review and Case Report of a Family Affected by Misrecognition and Late Diagnosis
- Unusual Defect-Related Room-Temperature Emission from WS(2) Monolayers Synthesized through a Potassium-Based Precursor
- Unusual Defect-Related Room-Temperature Emission from WS<sub>2</sub> Monolayers Synthesized through a Potassium-Based Precursor
- Update on the pathogenesis and genetics of Paget's disease of bone
- Visual Cortical Plasticity: Molecular Mechanisms as Revealed by Induction Paradigms in Rodents
- Waardenburg Syndrome
- Waardenburg Syndrome
- Whi3 mnemon association with endoplasmic reticulum membranes confines the memory of deceptive courtship to the yeast mother cell