26 relations: Achondroplasia, Alternative splicing, Amino acid, Antibody, Basic fibroblast growth factor, Bladder cancer, Chromosome 4, Cluster of differentiation, Craniosynostosis, Exon, FGF1, FGF9, Fibroblast growth factor, Fibroblast growth factor receptor, Gene, Hydrophobe, Hypochondroplasia, Ligand (biochemistry), Osteochondrodysplasia, Protein, Protein–protein interaction, Seborrheic keratosis, Severe achondroplasia with developmental delay and acanthosis nigricans, Thanatophoric dysplasia, Transitional cell carcinoma, Tyrosine kinase.
Achondroplasia
Achondroplasia is a genetic disorder that results in dwarfism.
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Alternative splicing
Alternative splicing, or differential splicing, is a regulated process during gene expression that results in a single gene coding for multiple proteins.
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Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
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Antibody
An antibody (Ab), also known as an immunoglobulin (Ig), is a large, Y-shaped protein produced mainly by plasma cells that is used by the immune system to neutralize pathogens such as pathogenic bacteria and viruses.
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Basic fibroblast growth factor
FGF2, also known as basic fibroblast growth factor (bFGF) and FGF-β, is a growth factor and signaling protein encoded by the FGF2 gene.
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Bladder cancer
Bladder cancer is any of several types of cancer arising from the tissues of the urinary bladder.
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Chromosome 4
Chromosome 4 is one of the 23 pairs of chromosomes in humans.
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Cluster of differentiation
The cluster of differentiation (also known as cluster of designation or classification determinant and often abbreviated as CD) is a protocol used for the identification and investigation of cell surface molecules providing targets for immunophenotyping of cells.
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Craniosynostosis
Craniosynostosis (from cranio, cranium; + syn, together; + ostosis relating to bone) is a condition in which one or more of the fibrous sutures in an infant (very young) skull prematurely fuses by turning into bone (ossification), thereby changing the growth pattern of the skull.
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Exon
An exon is any part of a gene that will encode a part of the final mature RNA produced by that gene after introns have been removed by RNA splicing.
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FGF1
FGF1, also known as acidic fibroblast growth factor (aFGF), is a growth factor and signaling protein encoded by the FGF1 gene.
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FGF9
Glia-activating factor is a protein that in humans is encoded by the FGF9 gene.
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Fibroblast growth factor
The fibroblast growth factors are a family of cell signalling proteins that are involved in a wide variety of processes, most notably as crucial elements for normal development.
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Fibroblast growth factor receptor
The fibroblast growth factor receptors are, as their name implies, receptors that bind to members of the fibroblast growth factor family of proteins.
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Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
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Hydrophobe
In chemistry, hydrophobicity is the physical property of a molecule (known as a hydrophobe) that is seemingly repelled from a mass of water.
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Hypochondroplasia
Hypochondroplasia (HCH) is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene (FGFR3) that results in a disproportionately short stature, micromeliaupdate 2013 and a head that appears large in comparison with the underdeveloped portions of the body.
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Ligand (biochemistry)
In biochemistry and pharmacology, a ligand is a substance that forms a complex with a biomolecule to serve a biological purpose.
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Osteochondrodysplasia
Osteochondrodysplasia or skeletal dysplasia is a general term for a disorder of the development (dysplasia) of bone ("osteo") and cartilage ("chondro").
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Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
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Protein–protein interaction
Protein–protein interactions (PPIs) are the physical contacts of high specificity established between two or more protein molecules as a result of biochemical events steered by electrostatic forces including the hydrophobic effect.
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Seborrheic keratosis
A seborrheic keratosis, also known as seborrheic verruca, basal cell papilloma, or a senile wart,Freedberg, et al.
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Severe achondroplasia with developmental delay and acanthosis nigricans
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN), is a very rare genetic disorder.
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Thanatophoric dysplasia
Thanatophoric dysplasia (thanatophoric dwarfism) is a severe skeletal disorder characterized by a disproportionately small ribcage, extremely short limbs and folds of extra skin on the arms and legs.
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Transitional cell carcinoma
Transitional cell carcinoma, also urothelial carcinoma, is a type of cancer that typically occurs in the urinary system.
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Tyrosine kinase
A tyrosine kinase is an enzyme that can transfer a phosphate group from ATP to a protein in a cell.
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Redirects here:
CD333, Cd333, Cek2, FGFR3, FGFR3 (gene), FGFR3 Inhibitor, Fibroblast growth factor receptor-3, JTK4, Jtk4.
References
[1] https://en.wikipedia.org/wiki/Fibroblast_growth_factor_receptor_3