β-ガラクトシダーゼ遺伝子
WordNet
- (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
- informal term for information; "give me the gen on your new line of computers"
PrepTutorEJDIC
- 遺伝子
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Japanese Journal
- New insights into the molecular basis of lactase non-persistence/persistence: a brief review
- Kuchay Raja Amir Hassan
- Drug Discoveries & Therapeutics, 2020
- … This hydrolysis is catalyzed by the enzyme lactase, a β-galactosidase located in the brush border membrane of small intestinal enterocytes. … Non-persistence or persistence of lactase expression into adult life being a polymorphic trait has been attributed to various single nucleotide polymorphisms in the enhancer region surrounding lactase gene (<i>LCT</i>). …
- NAID 130007802570
- Involvement of ERK1/2 activation in the gene expression of senescence-associated secretory factors in human hepatic stellate cells
- Odagiri Naoshi,Matsubara Tsutomu,Higuchi Moe,Takada Sayuri,Urushima Hayato,Sato-Matsubara Misako,Teranishi Yuga,Yoshizato Katsutoshi,Kawada Norifumi,Ikeda Kazuo
- Molecular and Cellular Biochemistry 455(1-2), 7-19, 2019-05-15
- … In the current study, we characterized senescence-associated β-galactosidase-positive senescent human HSCs (hHSCs) induced by repetitive passaging. … However, transient ERK1/2 activation induced by epidermal growth factor could not mimic the gene profile of the senescent hHSCs. …
- NAID 120006847891
- A new heterozygous compound mutation in the CTSA gene in galactosialidosis
- Nakajima Hideki,Ueno Miki,Adachi Kaori,Nanba Eiji,Narita Aya,Tsukimoto Jun,Itoh Kohji,Kawakami Atushi
- Human Genome Variation (6), 22, 2019-04-26
- … Galactosialidosis is an autosomal recessive lysosomal storage disease caused by the combined deficiency of lysosomal β-galactosidase and neuraminidase due to a defect in the protective protein/cathepsin A. … The patient was diagnosed with galactosialidosis with confirmation of impaired β-galactosidase and neuraminidase function in cultured skin fibroblasts. …
- NAID 120006842037
★リンクテーブル★
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- 英
- β-galactosidase gene
- 関
- レポーター遺伝子