WordNet
- impatience with annoyances; "his intolerance of interruptions"
- unwillingness to recognize and respect differences in opinions or beliefs
- a simple sugar found in lactose (同)brain sugar
PrepTutorEJDIC
- 〈U〉(宗教・意見・習慣の相違について)偏狭で認めないこと / 〈U〉(寒暑・痛みなどに)耐えられないこと;〈C〉過敏症
- ガラクトース(乳糖から得られる六炭糖)
UpToDate Contents
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- 1. 乳児および小児における低血糖症の原因 causes of hypoglycemia in infants and children
- 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. 吸収不良の治療の概要 overview of the treatment of malabsorption
- 4. グリコーゲン代謝のその他の障害：GLUT2欠損症およびアルドラーゼA欠損症 other disorders of glycogen metabolism glut2 deficiency and aldolase a deficiency
- 5. Overview of the causes of chronic diarrhea in children in resource-rich countries
English Journal
- Misfolding of galactose 1-phosphate uridylyltransferase can result in type I galactosemia.
- McCorvie TJ, Gleason TJ, Fridovich-Keil JL, Timson DJ.SourceSchool of Biological Sciences, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, UK.
- Biochimica et biophysica acta.Biochim Biophys Acta.2013 Aug;1832(8):1279-93. doi: 10.1016/j.bbadis.2013.04.004. Epub 2013 Apr 11.
- Type I galactosemia is a genetic disorder that is caused by the impairment of galactose-1-phosphate uridylyltransferase (GALT; EC 2.7.7.12). Although a large number of mutations have been detected through genetic screening of the human GALT (hGALT) locus, for many it is not known how they cause thei
- PMID 23583749
- In silico prediction of the effects of mutations in the human UDP-galactose 4'-epimerase gene: towards a predictive framework for type III galactosemia.
- McCorvie TJ, Timson DJ.SourceSchool of Biological Sciences, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, UK.
- Gene.Gene.2013 Jul 25;524(2):95-104. doi: 10.1016/j.gene.2013.04.061. Epub 2013 May 1.
- The enzyme UDP-galactose 4'-epimerase (GALE) catalyses the reversible epimerisation of both UDP-galactose and UDP-N-acetyl-galactosamine. Deficiency of the human enzyme (hGALE) is associated with type III galactosemia. The majority of known mutations in hGALE are missense and private thus making cli
- PMID 23644136
- Modifiers of ovarian function in girls and women with classic galactosemia.
- Spencer JB, Badik JR, Ryan EL, Gleason TJ, Broadaway KA, Epstein MP, Fridovich-Keil JL.SourceDivision of Reproductive Endocrinology and Infertility, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
- The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2013 Jul;98(7):E1257-65. doi: 10.1210/jc.2013-1374. Epub 2013 May 20.
- CONTEXT: Classic galactosemia is a potentially lethal genetic disorder resulting from profound impairment of galactose-1P uridylyltransferase (GALT). More than 80% of girls and women with classic galactosemia experience primary or premature ovarian insufficiency despite neonatal diagnosis and rigoro
- PMID 23690308
Japanese Journal
- Effect of Lactase Preparations in Asymptomatic Individuals with Lactase Deficiency - Gastric Digestion of Lactose and Breath Hydrogen Analysis -
- Nagoya journal of medical science 65(1/2), 21-28, 2002-05
- NAID 110000023225
- Galactose intolerance and the risk of cataract
- Brit J Ophthalmol 66, 438-441, 1982
- NAID 30029620422
- Ｈｂ中の単糖類の存在様式からみたＧｌｙｃｏｓｙｌａｔｅｄ Ｈｂ分画測定の臨床的評価
- 糖尿病 25(5), 545-555, 1982
- NAID 130004337025
Related Links
- Glucose-galactose malabsorption is a condition in which the cells lining the intestine cannot take in the sugars glucose and ... Glucose and galactose are called simple sugars, or monosaccharides. ... Lactose intolerance · Sucrose intolerance.
- The malabsorption and secondary intolerance of glucose and galactose is due to a genetic abnormality on chromosome 22 regulating a sugar transporter protein ( SGLT1) and leading to a decreased ability to absorb the sugars across the ...
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