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  2. Notch 1 - Wikipedia

    en.wikipedia.org/wiki/Notch_1

    4851 18128 Ensembl ENSG00000148400 ENSMUSG00000026923 UniProt P46531 Q01705 RefSeq (mRNA) NM_017617 NM_008714 RefSeq (protein) NP_060087 NP_032740 Location (UCSC) Chr 9: 136.49 – 136.55 Mb Chr 2: 26.35 – 26.41 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Neurogenic locus notch homolog protein 1 (Notch 1) is a protein encoded in humans by the NOTCH1 gene. Notch 1 is a single ...

  3. Notch signaling pathway - Wikipedia

    en.wikipedia.org/wiki/Notch_signaling_pathway

    Notch-mediated juxtacrine signal between adjacent cells Notch signaling steps. The Notch signaling pathway is a highly conserved cell signaling system present in most animals. [1] Mammals possess four different notch receptors, referred to as NOTCH1, NOTCH2, NOTCH3, and NOTCH4. [2] The notch receptor is a single-pass transmembrane receptor protein.

  4. JAG1 - Wikipedia

    en.wikipedia.org/wiki/JAG1

    JAG1 was first identified as a ligand that was able to activate notch receptors when the rat gene Jagged encoding a protein homolog was cloned in 1995. [5] [6] The structure of the JAG1 protein includes a small intracellular component, a transmembrane motif, proceeded by an extracellular region containing a cystine-rich region, 16 EGF-like repeats, a DSL domain, and finally a signal peptide ...

  5. Notch proteins - Wikipedia

    en.wikipedia.org/wiki/Notch_proteins

    Notch proteins are a family of type 1 transmembrane proteins that form a core component of the Notch signaling pathway, which is highly conserved in animals. The Notch extracellular domain mediates interactions with DSL family ligands , allowing it to participate in juxtacrine signaling .

  6. CADASIL - Wikipedia

    en.wikipedia.org/wiki/CADASIL

    CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder and is thought to be caused by mutations of the NOTCH3 gene on chromosome 19. [1] The disease belongs to a family of disorders called the leukodystrophies.

  7. NOTCH3 - Wikipedia

    en.wikipedia.org/wiki/NOTCH3

    4854 18131 Ensembl ENSG00000074181 ENSMUSG00000038146 UniProt Q9UM47 Q61982 RefSeq (mRNA) NM_000435 NM_008716 RefSeq (protein) NP_000426 NP_032742 Location (UCSC) Chr 19: 15.16 – 15.2 Mb Chr 17: 32.34 – 32.39 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Neurogenic locus notch homolog protein 3 (Notch 3) is a protein that in humans is encoded by the NOTCH3 gene. Function This ...

  8. NFL coaching hire winners and losers: Who made out best in ...

    www.aol.com/nfl-coaching-hire-winners-losers...

    The NFL's coaching carousel made for a particularly long ride this go-around. More than four months passed from the time of the first firing of a head coach – the New York Jets dumping Robert ...

  9. HES1 - Wikipedia

    en.wikipedia.org/wiki/HES1

    3280 15205 Ensembl ENSG00000114315 ENSMUSG00000022528 UniProt Q14469 P35428 RefSeq (mRNA) NM_005524 NM_008235 RefSeq (protein) NP_005515 NP_032261 Location (UCSC) Chr 3: 194.14 – 194.14 Mb Chr 16: 29.88 – 29.89 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Transcription factor HES1 (hairy and enhancer of split-1) is a protein that is encoded by the Hes1 gene, and is the ...