WordNet

(baseball) a failure of a defensive player to make an out when normal play would have sufficed (同)misplay
departure from what is ethically acceptable (同)wrongdoing
(computer science) the occurrence of an incorrect result produced by a computer (同)computer error
a misconception resulting from incorrect information (同)erroneous belief
part of a statement that is not correct; "the book was full of errors" (同)mistake
to make a mistake or be incorrect (同)mistake, slip
the organic processes (in a cell or organism) that are necessary for life (同)metabolic_process
an orange-yellow pigment in the bile that forms as a product of hemoglobin; excess amounts in the blood produce the yellow appearance observed in jaundice (同)hematoidin, haematoidin

PrepTutorEJDIC

《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
〈C〉『誤り』,『まちがい』 / 〈U〉思い違い,誤解 / 〈U〉〈C〉過ち,過失 / 〈U〉(計数の)誤差 / 〈C〉(野球で)エラー,失策
(判断・考え方・選択などで)『誤る』,まちがえる;過ちを犯す,罪を犯す《+『in』+『名』(do『ing』)》 / (正道・目的などから)それる,逸脱する《+『from』+『名』》
新陳代謝,物質交代

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Correction of hyperbilirubinemia in gunn rats using clinically relevant low doses of helper-dependent adenoviral vectors.

Dimmock D, Brunetti-Pierri N, Palmer DJ, Beaudet AL, Ng P.SourceDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Human gene therapy.Hum Gene Ther.2011 Apr;22(4):483-8. doi: 10.1089/hum.2010.167. Epub 2011 Feb 16.
Crigler-Najjar syndrome type I is a severe inborn error of bilirubin metabolism caused by a complete deficiency of uridine diphospho-glucuronosyl transferase 1A1 (UGT1A1) and results in life-threatening unconjugated hyperbilirubinemia. Lifelong correction of hyperbilirubinemia by liver-directed gene
PMID 20973621

Kelly DA.SourceLiver Unit, Birmingham Children's Hospital, NHS Trust, Lady Wood Middleway, Birmingham, B 16 8ET, UK.
Indian journal of pediatrics.Indian J Pediatr.1999;66(1 Suppl):S104-9.
Acute liver failure is a rare but potentially fatal disease. Adult definition of fulminant hepatic failure, which includes the development of hepatic necrosis and encephalopathy within 8 weeks of onset of liver disease does not apply to acute liver failure in children particularly if secondary to au
PMID 11132456

柏俣重夫,慶野宏臣,佐藤浩,青野幸子,仙波禮治,青木英子
日本疾患モデル動物研究会記録 1, 28-34, 1985
… A mutant strain of Wistar rats with hereditary acholuric jaundice, now known as"Gunn rat, "was first reported by C. … The trait of jaundice has been characterized as autosomal recessive inheritance and evidenced to be due to a virtually complete deficiency of an enzyme in hepatic bilirubin metabolism, bilirubin : UDP-glucuronyltransferase. …
NAID 130004198954