β-galactosidase gene

β-ガラクトシダーゼ遺伝子

WordNet

1. (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
2. informal term for information; "give me the gen on your new line of computers"

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1. 遺伝子

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• 1. BおよびTリンパ球の正常な発生 normal b and t lymphocyte development
• 2. 乳糖不耐症：臨床症状、診断、およびマネージメント lactose intolerance clinical manifestations diagnosis and management
• 3. 遺伝学およびゲノミクスのためのツール：研究用に育種された遺伝子改変マウス tools for genetics and genomics specially bred and genetically engineered mice
• 4. アンギノーサス群レンサ球菌（扁桃レンサ球菌）による感染症 infections due to the streptococcus anginosus streptococcus milleri group
• 5. ムコ多糖症：臨床的特徴および診断 mucopolysaccharidoses clinical features and diagnosis

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

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リンク元	「β-ガラクトシダーゼ遺伝子」

「β-ガラクトシダーゼ遺伝子」

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英

β-galactosidase gene

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