低タンパク栄養失調症
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- any of a large group of nitrogenous organic compounds that are essential constituents of living cells; consist of polymers of amino acids; essential in the diet of animals for growth and for repair of tissues; can be obtained from meat and eggs and milk and legumes; "a diet high in protein"
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
- 蛋白(たんばく)質
UpToDate Contents
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English Journal
- Clinicopathologic Comparison of Lynch Syndrome-associated and "Lynch-like" Endometrial Carcinomas Identified on Universal Screening Using Mismatch Repair Protein Immunohistochemistry.
- Mills AM1, Sloan EA, Thomas M, Modesitt SC, Stoler MH, Atkins KA, Moskaluk CA.
- The American journal of surgical pathology.Am J Surg Pathol.2016 Feb;40(2):155-65. doi: 10.1097/PAS.0000000000000544.
- Expanded testing for Lynch syndrome (LS) is increasingly recommended for patients with endometrial carcinomas, and immunohistochemistry (IHC) for tumor loss of mismatch-repair (MMR) protein expression is the most common primary screen. This has led to the recognition of MMR-IHC-deficient cases witho
- PMID 26523542
- Large scale analysis of the mutational landscape in β-glucuronidase: A major player of mucopolysaccharidosis type VII.
- Khan FI1, Shahbaaz M1, Bisetty K1, Waheed A2, Sly WS2, Ahmad F3, Hassan MI4.
- Gene.Gene.2016 Jan 15;576(1 Pt 1):36-44. doi: 10.1016/j.gene.2015.09.062. Epub 2015 Sep 28.
- The lysosomal storage disorders are a group of 50 unique inherited diseases characterized by unseemly lipid storage in lysosomes. These malfunctions arise due to genetic mutations that result in deficiency or reduced activities of the lysosomal enzymes, which are responsible for catabolism of biolog
- PMID 26415878
- Poly(ADP-ribosyl)ation of Methyl CpG Binding Domain Protein 2 Regulates Chromatin Structure.
- Becker A1, Zhang P1, Allmann L1, Meilinger D2, Bertulat B1, Eck D1, Hofstaetter M3, Bartolomei G4, Hottiger M4, Schreiber V5, Leonhardt H2, Cardoso MC6.
- The Journal of biological chemistry.J Biol Chem.2016 Jan 15. pii: jbc.M115.698357. [Epub ahead of print]
- The epigenetic information encoded in the genomic DNA methylation pattern is translated by methyl-cytosine binding proteins like MeCP2 into chromatin topology and structure and gene activity states. We have previously shown that MeCP2 level increases during differentiation and causes large-scale chr
- PMID 26772194
Japanese Journal
- Successive MRI Findings of Reversible Cerebral White Matter Lesions in a Patient with Cystathionine β-Synthase Deficiency
Related Links
- The congenital (β-protein deficiency syndrome (congenital beta-protein deficiency syndrome) - β-hyperlipoproteinemia synonyms: Bassen-Kornzweig syndrome, spine-cell anemia, prickle cell anemia, steatorrhea Is by Bassen and ...
- In the diagnosis of protein malnutrition, the first steps are determination of the approximate dietary supply of protein from a quantitative and qualitative standpoint and recognition of the pathologic conditions which are prone to lead to ...
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- 英
- kwashiorkor
- 同
- 低タンパク栄養失調症 protein malnutrition, protein deficiency syndrome
- 関
- マラスムス
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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