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  2. Apoptosis - Wikipedia

    en.wikipedia.org/wiki/Apoptosis

    Apoptosis (from Ancient Greek: ἀπόπτωσις, romanized: apóptōsis, lit. 'falling off') is a form of programmed cell death that occurs in multicellular organisms and in some eukaryotic, single-celled microorganisms such as yeast. [1] Biochemical events lead to characteristic cell changes and death. [2]

  3. Apoptosome - Wikipedia

    en.wikipedia.org/wiki/Apoptosome

    [1] [2] Following the NBD is a small helical domain (HD1), a second linker and a conserved winged helix domain (WHD). [2] The NOD region comprises NBD, HD1 and WHD, creating an ATPase domain that is part of the AAA+ family of ATPases. [1] [2] There is a super helical domain (HD2) present in the junction between the NOD and the WD-40 repeats. [1]

  4. APAF1 - Wikipedia

    en.wikipedia.org/wiki/APAF1

    Apoptotic protease activating factor 1, also known as APAF1, is a ... This gene encodes a cytoplasmic protein that forms one of the central hubs in the apoptosis ...

  5. Fas receptor - Wikipedia

    en.wikipedia.org/wiki/Fas_receptor

    The Fas receptor, also known as Fas, FasR, apoptosis antigen 1 (APO-1 or APT), cluster of differentiation 95 (CD95) or tumor necrosis factor receptor superfamily member 6 (TNFRSF6), is a protein that in humans is encoded by the FAS gene. [5] [6] Fas was first identified using a monoclonal antibody generated by immunizing mice with the FS-7 cell ...

  6. Mitochondrial outer membrane permeabilization - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_outer...

    Mitochondrial outer membrane permeabilization (MOMP), also known as the mitochondrial outer membrane permeability, is one of two ways apoptosis (a type of programmed cell death) can be activated. [1] It is part of the intrinsic pathway of apoptosis, also known as the mitochondrial pathway. MOMP is known as the point of no return in apoptosis.

  7. Carcinogenesis - Wikipedia

    en.wikipedia.org/wiki/Carcinogenesis

    The central role of DNA damage and epigenetic defects in DNA repair genes in carcinogenesis. DNA damage is considered to be the primary cause of cancer. [17] More than 60,000 new naturally-occurring instances of DNA damage arise, on average, per human cell, per day, due to endogenous cellular processes (see article DNA damage (naturally occurring)).

  8. Apoptotic DNA fragmentation - Wikipedia

    en.wikipedia.org/wiki/Apoptotic_DNA_fragmentation

    The apoptotic DNA fragmentation is being used as a marker of apoptosis and for identification of apoptotic cells either via the DNA laddering assay, [2] the TUNEL assay, [3] [4] or the by detection of cells with fractional DNA content ("sub G 1 cells") on DNA content frequency histograms e.g. as in the Nicoletti assay. [5] [6]

  9. Inhibitor of apoptosis - Wikipedia

    en.wikipedia.org/wiki/Inhibitor_of_apoptosis

    Regarding the activation of caspases, there exists a gene called ced-9 in C. elegans that protects against cell death that is a part of the Bcl-2 family. ced-9 encodes a protein that is structurally similar to Bcl-2 that binds to another protein ced-4, a homolog of APAF-1 in humans, and prevents it from activating caspase ced-3, which is necessary for killing of the cell. [4]