Concepts (149)
Concepts are derived automatically from a person's publications.
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
- Activins
- Adaptor Proteins, Signal Transducing
- Adenosine Triphosphate
- Adolescent
- Adult
- Africa, Northern
- Alleles
- Amino Acid Sequence
- Amino Acid Substitution
- Animals
- Apoptosis Regulatory Proteins
- Base Sequence
- Blastocyst
- Bone Morphogenetic Protein 4
- Cadherin Related Proteins
- Cadherins
- Calcium Channels, L-Type
- Carrier Proteins
- Cataract
- Cell Differentiation
- Cell Line
- Cells
- Cells, Cultured
- Child
- Child, Preschool
- Chromosome Disorders
- Chromosome Mapping
- Chromosome Segregation
- Cilia
- Ciliopathies
- Cochlea
- Codon, Nonsense
- Collagen Type XI
- Computational Biology
- Consanguinity
- COS Cells
- DEAD-box RNA Helicases
- Deafness
- Disease Models, Animal
- DNA Fragmentation
- DNA Methylation
- DNA Mutational Analysis
- Ear, Inner
- Embryo Culture Techniques
- Embryo Transfer
- Embryonic Development
- Embryonic Stem Cells
- Endothelium
- Epigenesis, Genetic
- Exome
- Family
- Family Health
- Female
- Fertilization in Vitro
- Fibroblast Growth Factor 2
- Fingers
- Gene Expression
- Gene Frequency
- Genes, Dominant
- Genes, Recessive
- Genes, Reporter
- Genetic Association Studies
- Genetic Diseases, Inborn
- Genetic Linkage
- Genetic Loci
- Genetic Markers
- Genetic Predisposition to Disease
- Genetic Variation
- Genomic Imprinting
- Genotype
- Germ Cells
- Hair Cells, Auditory
- Hair Cells, Auditory, Inner
- Hearing Loss
| - Hearing Loss, Sensorineural
- Heart Diseases
- HEK293 Cells
- Heterozygote
- High-Throughput Nucleotide Sequencing
- Histone Demethylases
- HLA-G Antigens
- Homozygote
- Human Embryonic Stem Cells
- Humans
- Hungary
- Intellectual Disability
- Intracellular Signaling Peptides and Proteins
- LIM-Homeodomain Proteins
- Male
- Maternal Inheritance
- Mechanotransduction, Cellular
- Mediterranean Region
- Membrane Glycoproteins
- Membrane Proteins
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Microfilament Proteins
- Microtubule-Associated Proteins
- Middle Aged
- Models, Molecular
- Molecular Sequence Data
- Multifactorial Inheritance
- Mutation
- Mutation, Missense
- Myosin Heavy Chains
- Myosin Type III
- Nerve Tissue Proteins
- Neurodevelopmental Disorders
- Nuclear Proteins
- Nucleotide Mapping
- Oligonucleotide Array Sequence Analysis
- Oocytes
- Ophthalmoscopy
- Organic Cation Transport Proteins
- Pakistan
- Pedigree
- Phenotype
- Placenta
- Polydactyly
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Polymorphism, Single Nucleotide
- Pregnancy
- Pregnancy Outcome
- Prognosis
- Protein Structure, Tertiary
- Proteins
- Rats
- Rats, Sprague-Dawley
- Retinitis Pigmentosa
- RNA Splice Sites
- RNA Splicing Factors
- Roma
- Sequence Alignment
- Sequence Analysis, DNA
- Sequence Homology, Amino Acid
- Sinoatrial Node
- Superovulation
- Symporters
- Toes
- Transcription Factors
- Transcriptome
- Transforming Growth Factor beta
- Trophoblasts
- Usher Syndromes
- Young Adult
- Zebrafish
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Concepts
(149)
Derived automatically from this person's publications.
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Co-Authors
(11)
People in Profiles who have published with this person.
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(60)
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