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Payam Soltanzadeh
Concepts (124)
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Concepts are derived automatically from a person's publications.
Cloud
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.
3' Untranslated Regions
Adolescent
Adult
Age of Onset
Aged
Agrin
Alternative Splicing
Amino Acid Sequence
Amino Acid Substitution
Animals
Antibodies, Monoclonal
Autoantibodies
Autoimmune Diseases
Back
Biomarkers
Biopsy
Bone Marrow
Brain
Buttocks
Calpain
Cardiomyopathy, Dilated
Cell Membrane
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Chromosomes, Human, Pair 9
Codon, Nonsense
Cohort Studies
Computer Simulation
Consanguinity
Deglutition Disorders
Dermatomyositis
Diagnosis, Differential
Diagnostic Techniques and Procedures
Distal Myopathies
DNA Mutational Analysis
Double-Blind Method
Dysarthria
Dystonia
Dystrophin
Exons
Female
Femur
Follow-Up Studies
Gain of Function Mutation
Gait Disorders, Neurologic
Genetic Predisposition to Disease
Haplotypes
Heart
Heart Function Tests
HEK293 Cells
Hepatolenticular Degeneration
Heterozygote
High-Throughput Nucleotide Sequencing
Homozygote
Humans
Hydroxymethylglutaryl CoA Reductases
Immunoconjugates
In Vitro Techniques
Iran
Islam
Jews
LDL-Receptor Related Proteins
Lymphoma, T-Cell
Magnetic Resonance Imaging
Male
Mental Disorders
Mice
Middle Aged
Molecular Dynamics Simulation
Molecular Sequence Data
Multienzyme Complexes
Muscle Proteins
Muscle Weakness
Muscle, Skeletal
Muscular Diseases
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Duchenne
Mutation
Mutation, Missense
Myasthenia Gravis
Myasthenic Syndromes, Congenital
Myelin P0 Protein
Myopathies, Structural, Congenital
Myositis
Myositis, Inclusion Body
Myotonic Dystrophy
Myotonin-Protein Kinase
Nervous System Diseases
Neural Conduction
Neurofibroma
Neurologic Examination
Neuromuscular Junction
Nevus, Pigmented
Oligonucleotides
Open Reading Frames
Pedigree
Phenotype
POEMS Syndrome
Polymorphism, Single Nucleotide
Positron Emission Tomography Computed Tomography
Protein Conformation
Protein Stability
Protein Subunits
Receptor Protein-Tyrosine Kinases
Receptors, Cholinergic
Receptors, Growth Factor
Receptors, Transferrin
Retrospective Studies
RNA Splicing
RNA, Messenger
Sequence Analysis, DNA
Sequence Homology
Sialorrhea
Signal Transduction
Skin Neoplasms
Spina Bifida Occulta
Spinal Nerve Roots
Synaptic Transmission
Treatment Outcome
Tremor
Vascular Neoplasms
X Chromosome Inactivation
Young Adult
Payam's Networks
Concepts (124)
Derived automatically from this person's publications.
Myotonic Dystrophy
Receptors, Cholinergic
Dystrophin
Myasthenia Gravis
Muscular Dystrophy, Duchenne
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Co-Authors (8)
People in Profiles who have published with this person.
Chhetri, Dinesh
UCLA
Savjani, Ricky
UCLA
Khanlou, Negar
UCLA
Chin, Robert
UCLA
Wiedau, Martina
UCLA
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_
Similar People (60)
People who share similar concepts with this person.
Mcdonald, Craig
UC Davis
Mahadevan, Manish
UCSF
Shelton, G Diane
UCSD
Richman, David
UC Davis
Spencer, Melissa
UCLA
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_
Same Department
Halabi, Anasheh
Ho, Michael
Mathews, Paul
Nwaobi-Petersen, Sinifunanya
Williamson, Eric
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