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Joseph Gleeson
Concepts (994)
Back to Profile
Concepts are derived automatically from a person's publications.
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Categories
Timeline
Details
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
1-Alkyl-2-acetylglycerophosphocholine Esterase
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
3T3 Cells
4-Hydroxyphenylpyruvate Dioxygenase
5-Methylcytosine
Abnormalities, Multiple
Acetylation
Acetylcholinesterase
Acidosis, Lactic
Acquired Immunodeficiency Syndrome
Actin-Related Protein 2-3 Complex
Actins
Active Transport, Cell Nucleus
Acute Disease
Acyltransferases
Adaptor Protein Complex 4
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenosine Deaminase
Adenosine Diphosphate Ribose
Adenosine Triphosphatases
Adenosine Triphosphate
Adolescent
ADP-Ribosylation Factors
Adult
Age of Onset
Aged
Agenesis of Corpus Callosum
Aging
Aicardi Syndrome
Alcohols
Alleles
alpha Catenin
alpha-Mannosidase
Alzheimer Disease
Amidohydrolases
Amines
Amino Acid Metabolism, Inborn Errors
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Amino Acids, Branched-Chain
Amino Acyl-tRNA Synthetases
Aminopeptidases
Aminophylline
AMP Deaminase
Aneuploidy
Animals
Animals, Genetically Modified
Animals, Newborn
Antibodies, Viral
Antibody Specificity
Anticodon
Anticonvulsants
Antigens
Antigens, Neoplasm
Antipsychotic Agents
Anus, Imperforate
Aortic Valve
Apolipoprotein C-III
Apoptosis
Apraxias
Arabs
Arachidonic Acid
Arginine
Arrhythmias, Cardiac
Arthrogryposis
Aspartate-Ammonia Ligase
Aspartate-tRNA Ligase
Aspartic Acid
Asthma
Astrocytes
Ataxia
ATP-Binding Cassette Transporters
Atrophy
Aurora Kinase A
Aurora Kinases
Autism Spectrum Disorder
Autistic Disorder
Autoantigens
Autophagy
Axons
Bacterial Toxins
Bardet-Biedl Syndrome
Basal Ganglia
Base Sequence
Basement Membrane
Basic Helix-Loop-Helix Transcription Factors
Behavior, Animal
beta Catenin
Binding Sites
Biological Evolution
Biological Transport
Biomarkers
Biopolymers
Bipolar Disorder
Blindness
Blood-Brain Barrier
Blotting, Northern
Blotting, Western
Body Patterning
Bone and Bones
Bone Diseases, Developmental
Bone Diseases, Metabolic
Brain
Brain Chemistry
Brain Diseases
Brain Stem
Breast Neoplasms
Butadienes
CADASIL
Cadherins
Caenorhabditis elegans
Calbindin 2
Calcium-Binding Proteins
Calcium-Calmodulin-Dependent Protein Kinases
California
Calpain
Capillaries
Carboxypeptidases
Carrier Proteins
Case-Control Studies
Catalytic Domain
Cataract
Causality
CD59 Antigens
Cell Adhesion Molecules
Cell Adhesion Molecules, Neuronal
Cell Aggregation
Cell Count
Cell Cycle
Cell Cycle Checkpoints
Cell Cycle Proteins
Cell Death
Cell Differentiation
Cell Division
Cell Line
Cell Line, Tumor
Cell Lineage
Cell Membrane
Cell Movement
Cell Nucleus
Cell Polarity
Cell Proliferation
Cell Shape
Cell Size
Cell Survival
Cells
Cells, Cultured
Central Nervous System
Central Nervous System Diseases
Centrioles
Centromere
Centrosome
Cerebellar Ataxia
Cerebellar Diseases
Cerebellar Vermis
Cerebellum
Cerebral Cortex
Cerebral Palsy
Cerebral Ventricles
Channelopathies
Chelating Agents
Chemotaxis
Child
Child Development Disorders, Pervasive
Child, Preschool
Chloride-Bicarbonate Antiporters
Chondroitin Sulfates
Choristoma
Chromatin
Chromatin Assembly and Disassembly
Chromatin Immunoprecipitation
Chromosomal Proteins, Non-Histone
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Fragility
Chromosome Mapping
Chromosome Pairing
Chromosome Segregation
Chromosome Walking
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 9
Cilia
Ciliary Motility Disorders
Ciliopathies
Class I Phosphatidylinositol 3-Kinases
Classical Lissencephalies and Subcortical Band Heterotopias
Cleavage And Polyadenylation Specificity Factor
Clinical Trials as Topic
Clone Cells
Cloning, Molecular
Cluster Analysis
Cobblestone Lissencephaly
Codon
Codon, Nonsense
Coenzymes
Cogan Syndrome
Cognition
Cognitive Dysfunction
Cohort Studies
Colchicine
Cold Temperature
Collagen Type VI
Coloboma
Combined Modality Therapy
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Congenital Abnormalities
Congenital Disorders of Glycosylation
Consanguinity
Conserved Sequence
Contig Mapping
Contracture
Corpus Callosum
COS Cells
Craniofacial Abnormalities
CRISPR-Cas Systems
Cross Reactions
Cross-Sectional Studies
Cues
Cullin Proteins
Culture Media, Serum-Free
Cyclic Nucleotide Phosphodiesterases, Type 6
Cyclin-Dependent Kinase 5
Cyclin-Dependent Kinases
Cyclosporine
Cysts
Cytochalasin D
Cytochrome P-450 Enzyme System
Cytochrome P450 Family 2
Cytokinesis
Cytoplasm
Cytosine
Cytoskeletal Proteins
Cytoskeleton
Dandy-Walker Syndrome
Databases, Genetic
Databases, Nucleic Acid
DEAD-box RNA Helicases
Death Domain Receptor Signaling Adaptor Proteins
Delusions
Dendrites
Dendritic Spines
Dengue
Dengue Virus
Dermatan Sulfate
Developmental Disabilities
Diabetes Mellitus, Type 1
Diabetic Ketoacidosis
Diagnosis, Differential
Diagnostic Imaging
Diencephalon
Diet
DiGeorge Syndrome
Dihydrolipoyllysine-Residue Acetyltransferase
Dioxygenases
Disability Evaluation
Disease
Disease Models, Animal
Disease Progression
DNA
DNA Breaks, Single-Stranded
DNA Copy Number Variations
DNA Damage
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Repair
DNA Replication
DNA, Complementary
DNA, Intergenic
DNA-Binding Proteins
DNA-Cytosine Methylases
Dominance, Cerebral
Dosage Compensation, Genetic
Dose-Response Relationship, Drug
Double-Blind Method
Down Syndrome
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Drug Delivery Systems
Drug Resistant Epilepsy
Dwarfism
Dyneins
Dyskinesias
Dyslexia
Dystonia
Dystroglycans
Ectodermal Dysplasia
Eczema
Eflornithine
Egypt
Electroencephalography
Electronic Health Records
Electrophoresis, Polyacrylamide Gel
Electroporation
Ellis-Van Creveld Syndrome
Embryo, Mammalian
Embryonic and Fetal Development
Embryonic Development
Embryonic Stem Cells
Encephalitis
Encephalocele
Endocytosis
Endonucleases
Endopeptidases
Endoplasmic Reticulum
Endoplasmic Reticulum Stress
Endoribonucleases
Endosomal Sorting Complexes Required for Transport
Enhancer Elements, Genetic
Enzyme Activation
Ependymoglial Cells
Epilepsies, Myoclonic
Epilepsies, Partial
Epilepsy
Epilepsy, Generalized
Epiphyses
ErbB Receptors
Evoked Potentials, Motor
Evoked Potentials, Somatosensory
Evolution, Molecular
Excitatory Postsynaptic Potentials
Exercise
Exome
Exons
Exonucleases
Extracellular Matrix
Extracellular Matrix Proteins
Eye Abnormalities
Eye Diseases
Eye Diseases, Hereditary
Facies
Failure to Thrive
Family
Family Health
Fatty Acid Desaturases
Fatty Acid-Binding Proteins
Fatty Acids
Fatty Acids, Omega-3
Female
Fetal Development
Fetal Diseases
Fetal Growth Retardation
Fetus
Fibroblasts
Fingolimod Hydrochloride
Fluorescent Antibody Technique
Fluorescent Antibody Technique, Indirect
Folic Acid
Folic Acid Deficiency
Follow-Up Studies
Forkhead Transcription Factors
Founder Effect
Fragile X Syndrome
Frameshift Mutation
Friends
Frontal Lobe
GABA Plasma Membrane Transport Proteins
GABAergic Neurons
Gain of Function Mutation
gamma-Aminobutyric Acid
Gastrulation
Gene Components
Gene Deletion
Gene Dosage
Gene Duplication
Gene Editing
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Knock-In Techniques
Gene Knockout Techniques
Gene Ontology
Gene Order
Gene Regulatory Networks
Gene Targeting
Genes
Genes, Developmental
Genes, Dominant
Genes, Lethal
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetics, Medical
Genetics, Population
Genome
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Globus Pallidus
Glucuronosyltransferase
Glutamic Acid
Glutamine
Glutathione Transferase
Glycogen
Glycogen Synthase Kinase 3
Glycogen Synthase Kinase 3 beta
Glycoproteins
Glycoside Hydrolases
Glycosylation
Glycosylphosphatidylinositols
Golgi Apparatus
GPI-Linked Proteins
Green Fluorescent Proteins
Growth and Development
Growth Disorders
GTP Phosphohydrolases
GTPase-Activating Proteins
GTP-Binding Protein beta Subunits
GTP-Binding Proteins
Guanine Nucleotide Exchange Factors
Guanosine Triphosphate
Guillain-Barre Syndrome
Haplotypes
Hearing Loss
Hearing Loss, Conductive
Hearing Loss, Sensorineural
Heart
Heart Defects, Congenital
Heart Rate
Hedgehog Proteins
HEK293 Cells
HeLa Cells
Hemimegalencephaly
Hemiterpenes
Heparan Sulfate Proteoglycans
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Motor Neuropathy
Heredodegenerative Disorders, Nervous System
Hernia, Hiatal
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histidine
Histone Deacetylases
Histones
History, 19th Century
History, 20th Century
Homeodomain Proteins
Homeostasis
Homosexuality
Homozygote
Hospitalization
Human Migration
Human Umbilical Vein Endothelial Cells
Humans
Hybrid Cells
Hydrocephalus
Hydrolysis
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Hypothyroidism
Ichthyosis
Image Processing, Computer-Assisted
Immunity
Immunoblotting
Immunohistochemistry
Immunoprecipitation
In Situ Hybridization
In Situ Hybridization, Fluorescence
In Vitro Techniques
Induced Pluripotent Stem Cells
Infant
Infant Death
Infant Mortality
Infant, Newborn
Infant, Newborn, Diseases
Inflammation
Infusions, Intravenous
Injections, Spinal
Inosine
Inosine Triphosphate
Intellectual Disability
Intensive Care Units
Interferon Type I
Interferon-Induced Helicase, IFIH1
Interferons
Interneurons
Intracellular Membranes
Intracellular Signaling Peptides and Proteins
Introns
Ion Channels
Iran
Italy
Jews
Kartagener Syndrome
Karyotyping
Katanin
Ki-67 Antigen
Kidney
Kidney Diseases
Kidney Diseases, Cystic
Kinetochores
Kruppel-Like Transcription Factors
Laminin
Language Development Disorders
Large Neutral Amino Acid-Transporter 1
Lateral Ventricles
Leber Congenital Amaurosis
Leukoencephalopathies
Lidocaine
Likelihood Functions
Lipid Metabolism
Lipids
Lipoma
Lissencephaly
Lithium
Liver
Liver Cirrhosis
Liver Diseases
Locomotion
Lod Score
Longitudinal Studies
Loss of Function Mutation
Loss of Heterozygosity
Luminescent Proteins
Lymphocytes
Lysine-tRNA Ligase
Lysophospholipids
Lysosomal Storage Diseases
Lysosomes
Macromolecular Substances
Magnetic Resonance Imaging
Malates
Male
Malformations of Cortical Development
Malformations of Cortical Development, Group I
Malformations of Cortical Development, Group II
Mammals
Megalencephaly
Membrane Glycoproteins
Membrane Proteins
Membranes, Artificial
Meningoencephalitis
Meningomyelocele
Mental Disorders
Mesencephalon
Metabolism, Inborn Errors
Metabolome
Metal Metabolism, Inborn Errors
Metalloproteins
Methionine
Methylation
Methyl-CpG-Binding Protein 2
Methyltransferases
Mice
Mice, 129 Strain
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Inbred ICR
Mice, Inbred Strains
Mice, Knockout
Mice, Mutant Strains
Mice, Neurologic Mutants
Mice, Transgenic
Microcephaly
Microfilament Proteins
Microglia
MicroRNAs
Microsatellite Repeats
Microscopy, Confocal
Microscopy, Electron, Transmission
Microscopy, Fluorescence
Microscopy, Fluorescence, Multiphoton
Microtubule Proteins
Microtubule-Associated Proteins
Microtubules
Middle Aged
Middle East
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Mitosis
Mitral Valve
Mixed Function Oxygenases
Models, Biological
Models, Genetic
Models, Molecular
Models, Neurological
Molar
Molecular Sequence Data
Molecular Targeted Therapy
Molybdoferredoxin
Monoacylglycerol Lipases
Morphogenesis
Mosaicism
Motor Neuron Disease
Motor Neurons
Movement Disorders
MRE11 Homologue Protein
Multifactorial Inheritance
Multigene Family
Muscle Hypotonia
Muscle Weakness
Muscular Atrophy, Spinal
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Musculoskeletal Abnormalities
Mutagenesis
Mutagenesis, Site-Directed
Mutant Proteins
Mutation
Mutation Rate
Mutation, Missense
Myasthenic Syndromes, Congenital
Myelin Proteolipid Protein
Myoclonic Cerebellar Dyssynergia
N-Acetylgalactosaminyltransferases
Natural Language Processing
NAV1.1 Voltage-Gated Sodium Channel
NAV1.2 Voltage-Gated Sodium Channel
Neocortex
Neoplasm Proteins
Neovascularization, Physiologic
Nephrosis
Nephrotic Syndrome
Nerve Fibers
Nerve Fibers, Myelinated
Nerve Net
Nerve Tissue Proteins
Nervous System
Nervous System Diseases
Nervous System Malformations
Netrins
Neural Inhibition
Neural Pathways
Neural Stem Cells
Neural Tube Defects
Neurites
Neurocutaneous Syndromes
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurogenesis
Neuroglia
Neurologic Examination
Neurons
Neuropathology
Neuropeptides
Neurotransmitter Agents
Nevus
Nevus, Sebaceous of Jadassohn
Niemann-Pick Disease, Type C
Nitrogen
Nose
Nuclear Family
Nuclear Pore Complex Proteins
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Conformation
Nucleotides
Obesity
Ocular Motility Disorders
Olfactory Bulb
Oligodendroglia
Oligonucleotides, Antisense
Olivopontocerebellar Atrophies
Oncogene Proteins
Opsins
Optic Atrophies, Hereditary
Optic Lobe, Nonmammalian
Organ Culture Techniques
Organ Specificity
Organ Transplantation
Organogenesis
Organoids
Orofaciodigital Syndromes
Osteochondrodysplasias
Oxidative Phosphorylation
Oxidative Stress
p21-Activated Kinases
Pakistan
Pancreatic Diseases
Paraparesis, Spastic
Parietal Lobe
Paternal Inheritance
Pattern Recognition, Automated
Pedigree
Pelger-Huet Anomaly
Penetrance
Pentamidine
Pentanes
Peptide Synthases
Peptides
Peptidylprolyl Isomerase
Pericytes
Peripheral Nerves
Peripheral Nervous System
Peroxisomal Disorders
Personality
Phagosomes
Pharmacogenetics
Phenotype
Phosphatidylinositol 3-Kinases
Phosphatidylinositol 4,5-Diphosphate
Phosphatidylinositol Phosphates
Phosphatidylinositols
Phospholipases
Phosphoprotein Phosphatases
Phosphoproteins
Phosphoric Monoester Hydrolases
Phosphorylation
Phosphothreonine
Phosphotransferases
Photoreceptor Cells
Photoreceptor Cells, Vertebrate
Physical Chromosome Mapping
Phytic Acid
Pigment Epithelium of Eye
Pneumonia, Pneumocystis
Point Mutation
Polycystic Kidney Diseases
Polydactyly
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Pore Forming Cytotoxic Proteins
Precision Medicine
Predictive Value of Tests
Pregnancy
Pregnancy Complications, Infectious
Pregnancy Proteins
Premenstrual Dysphoric Disorder
Premenstrual Syndrome
Prenatal Diagnosis
Prevalence
Primary Cell Culture
Prognosis
Promoter Regions, Genetic
Prosencephalon
Proteasome Endopeptidase Complex
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Disulfide-Isomerases
Protein Domains
Protein Folding
Protein Interaction Domains and Motifs
Protein Isoforms
Protein Kinase C
Protein Prenylation
Protein Processing, Post-Translational
Protein Structure, Secondary
Protein Structure, Tertiary
Protein Transport
Proteins
Protein-Tyrosine Kinases
Proteoglycans
Proteome
Proteomics
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-akt
Proto-Oncogene Proteins c-fos
Proto-Oncogene Proteins p21(ras)
Pseudopodia
Psychiatric Status Rating Scales
Psychomotor Disorders
Psychopharmacology
Psychotherapy, Brief
Psychotic Disorders
PTEN Phosphohydrolase
Pteridines
Purines
Purkinje Cells
Putamen
Pyramidal Cells
Pyramidal Tracts
Pyrophosphatases
Pyrroline Carboxylate Reductases
Pyruvate Dehydrogenase Complex Deficiency Disease
Quadriplegia
rab GTP-Binding Proteins
Radiography
Radionuclide Imaging
rap1 GTP-Binding Proteins
Rare Diseases
Rats
Rats, Long-Evans
Rats, Sprague-Dawley
Real-Time Polymerase Chain Reaction
Receptor Protein-Tyrosine Kinases
Receptor, ErbB-4
Receptor, Notch3
Receptor, Platelet-Derived Growth Factor alpha
Receptor, TIE-2
Receptors, AMPA
Receptors, Autocrine Motility Factor
Receptors, GABA-A
Receptors, GABA-B
Receptors, G-Protein-Coupled
Receptors, LDL
Receptors, Notch
Recombinant Fusion Proteins
Recombinant Proteins
Recombination, Genetic
Recurrence
Reflex, Startle
Regenerative Medicine
Registries
Regulatory Sequences, Nucleic Acid
Renal Insufficiency
Repressor Proteins
Reproducibility of Results
Research Design
Restriction Mapping
Retina
Retinal Degeneration
Retinal Diseases
Retinal Neurons
Retinal Pigment Epithelium
Retinitis Pigmentosa
Retrospective Studies
Retroviridae
Reverse Transcriptase Polymerase Chain Reaction
rho GTP-Binding Proteins
rhoA GTP-Binding Protein
Ribonuclease H
Ribonuclease, Pancreatic
Ribonucleoproteins, Small Nuclear
Ribosomal Protein S6
Rigor Mortis
Risk
Risk Factors
RNA
RNA Helicases
RNA Interference
RNA Processing, Post-Transcriptional
RNA Splice Sites
RNA Splicing
RNA Splicing Factors
RNA, Messenger
RNA, Small Interfering
RNA, Small Nuclear
RNA, Transfer
RNA, Transfer, Amino Acyl
RNA, Untranslated
RNA-Binding Proteins
ROC Curve
S100 Calcium Binding Protein G
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Schizophrenia
Schizophrenic Psychology
Segmental Duplications, Genomic
Seizures
Seizures, Febrile
Selection, Genetic
Semen
Sensitivity and Specificity
Sensory Receptor Cells
Septins
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Tagged Sites
Serine
Serine Endopeptidases
Serine-Type D-Ala-D-Ala Carboxypeptidase
Serum
Severity of Illness Index
Sex Characteristics
Sex Chromosome Aberrations
Siblings
Signal Transduction
Single-Cell Analysis
Skin
SMN Complex Proteins
Sodium Channels
Sodium-Bicarbonate Symporters
Sodium-Calcium Exchanger
Software
Somatostatin
Sorting Nexins
Spasms, Infantile
Spastic Paraplegia, Hereditary
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spermatogonia
Spermatozoa
Sphingomyelin Phosphodiesterase
Spinal Dysraphism
Spindle Apparatus
Spine
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spliceosomes
src Homology Domains
Stem Cells
Steroids
Structure-Activity Relationship
Subcellular Fractions
Sulfite Oxidase
Suppressor Factors, Immunologic
Suppressor of Cytokine Signaling Proteins
Survival Analysis
Symporters
Synapses
Synaptic Transmission
Synaptic Vesicles
Synaptotagmin II
Syndrome
Tandem Repeat Sequences
Telencephalon
Temporal Lobe
Theophylline
Thioredoxins
Time Factors
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Transcription Factors
Transcriptome
Transfection
Translocation, Genetic
Transport Vesicles
Treatment Outcome
Tremor
Tretinoin
Trimethoprim, Sulfamethoxazole Drug Combination
Triplets
Tuberous Sclerosis
Tubulin
Tumor Microenvironment
Tumor Suppressor Proteins
Turkey
Ubiquitin Thiolesterase
Ubiquitinated Proteins
Ubiquitination
Ubiquitin-Protein Ligases
Ultrasonography
Unfolded Protein Response
United Arab Emirates
United States
United States Food and Drug Administration
Up-Regulation
Urogenital Abnormalities
Valine-tRNA Ligase
Valproic Acid
Vascular Malformations
Vasculitis, Central Nervous System
Vesicular Monoamine Transport Proteins
Vesicular Transport Proteins
Viral Nonstructural Proteins
Viral Tropism
Virus Replication
Vision Disorders
Voltage-Gated Sodium Channel beta-1 Subunit
Walker-Warburg Syndrome
Weaning
Whole Genome Sequencing
Wnt Proteins
Wnt Signaling Pathway
X Chromosome
X-ray Repair Cross Complementing Protein 1
Young Adult
Zebrafish
Zebrafish Proteins
Zellweger Syndrome
Zika Virus
Zika Virus Infection
Zinc Finger Protein Gli3
Zygote
Joseph's Networks
Concepts (994)
Derived automatically from this person's publications.
Microcephaly
Cerebellar Diseases
Mosaicism
Kidney Diseases, Cystic
Cilia
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Co-Authors (97)
People in Profiles who have published with this person.
James, Kiely
UCSD
Vong, Keng Ioi
UCSD
Sebat, Jonathan
UCSD
Barton, Scott
UCSD
Chi, Neil
UCSD
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