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24 relations: Acro–dermato–ungual–lacrimal–tooth syndrome, Adenocarcinoma, Alpha-methylacyl-CoA racemase, Cell (biology), Cleft lip and cleft palate, Ectrodactyly, Ectrodactyly–ectodermal dysplasia–cleft syndrome, Epithelium, Gene, Hay–Wells syndrome, HNRPAB, Immunostaining, Limb–mammary syndrome, Malignancy, Mesenchyme, MiR-203, P53, P73, Prostate, Prostate cancer, Protein, Protein–protein interaction, Rapp–Hodgkin syndrome, Transcription factor.
Acro–dermato–ungual–lacrimal–tooth syndrome
Acro–dermato–ungual–lacrimal–tooth (ADULT) syndrome is a rare genetic disease.
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Adenocarcinoma
Adenocarcinoma (plural adenocarcinomas or adenocarcinomata) is a type of cancerous tumor that can occur in several parts of the body.
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Alpha-methylacyl-CoA racemase
In enzymology, an alpha-methylacyl-CoA racemase, also known as AMACR, is an enzyme that catalyzes the following chemical reaction: In mammalian cells, the enzyme is responsible for converting (2R)-methylacyl-CoA esters to their (2S)-methylacyl-CoA epimers and known substrates, including coenzyme A esters of pristanic acid (mostly derived from phytanic acid, a 3-methyl branched-chain fatty acid that is abundant in the diet) and bile acids derived from cholesterol.
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Cell (biology)
The cell (from Latin cella, meaning "small room") is the basic structural, functional, and biological unit of all known living organisms.
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Cleft lip and cleft palate
Cleft lip and cleft palate, also known as orofacial cleft, is a group of conditions that includes cleft lip (CL), cleft palate (CP), and both together (CLP).
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Ectrodactyly
Ectrodactyly, split hand, cleft hand, derived from the Greek ektroma (abortion) and daktylos (finger) involves the deficiency or absence of one or more central digits of the hand or foot and is also known as split hand/split foot malformation (SHFM).
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Ectrodactyly–ectodermal dysplasia–cleft syndrome
Ectrodactyly–ectodermal dysplasia–cleft syndrome, or EEC, and also referred to as EEC syndrome (also known as "Split hand–split foot–ectodermal dysplasia–cleft syndrome"Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill..) is a rare form of ectodermal dysplasia, an autosomal dominant disorder inherited as an genetic trait.
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Epithelium
Epithelium is one of the four basic types of animal tissue, along with connective tissue, muscle tissue and nervous tissue.
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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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Hay–Wells syndrome
Hay–Wells syndrome (also known as AEC syndrome; see Naming) is one of at least 150 known types of ectodermal dysplasia.
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HNRPAB
Heterogeneous nuclear ribonucleoprotein A/B, also known as HNRPAB, is a protein which in humans is encoded by the HNRPAB gene.
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Immunostaining
In biochemistry, immunostaining is any use of an antibody-based method to detect a specific protein in a sample.
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Limb–mammary syndrome
Limb–mammary syndrome is a cutaneous condition characterized by p63 mutations.
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Malignancy
Malignancy is the tendency of a medical condition to become progressively worse.
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Mesenchyme
Mesenchyme, in vertebrate embryology, is a type of connective tissue found mostly during the development of the embryo.
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MiR-203
In molecular biology miR-203 is a short non-coding RNA molecule.
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P53
Tumor protein p53, also known as p53, cellular tumor antigen p53 (UniProt name), phosphoprotein p53, tumor suppressor p53, antigen NY-CO-13, or transformation-related protein 53 (TRP53), is any isoform of a protein encoded by homologous genes in various organisms, such as TP53 (humans) and Trp53 (mice).
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P73
p73 is a protein related to the p53 tumor protein.
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Prostate
The prostate (from Ancient Greek προστάτης, prostates, literally "one who stands before", "protector", "guardian") is a compound tubuloalveolar exocrine gland of the male reproductive system in most mammals.
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Prostate cancer
Prostate cancer is the development of cancer in the prostate, a gland in the male reproductive system.
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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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Rapp–Hodgkin syndrome
Rapp–Hodgkin syndrome was formerly thought to be a unique autosomal dominant disorder due to a P63 gene mutation.
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Transcription factor
In molecular biology, a transcription factor (TF) (or sequence-specific DNA-binding factor) is a protein that controls the rate of transcription of genetic information from DNA to messenger RNA, by binding to a specific DNA sequence.
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Redirects here:
EEC3, Eec3, P73H, P73L, P73h, P73l, SHFM4, Shfm4, TP63 (gene), TP73L, Tp63, Tumor protein p73-like.
References
[1] https://en.wikipedia.org/wiki/TP63
