WordNet
- be a contributing factor; "make things factor into a companys profitability"
- any of the numbers (or symbols) that form a product when multiplied together
- an independent variable in statistics
- anything that contributes causally to a result; "a number of factors determined the outcome"
- consider as relevant when making a decision; "You must factor in the recent developments" (同)factor in, factor out
- resolve into factors; "a quantum computer can factor the number 15" (同)factor in, factor out
- an event known to have happened or something known to have existed; "your fears have no basis in fact"; "how much of the story is fact and how much fiction is hard to tell"
- a concept whose truth can be proved; "scientific hypotheses are not facts"
- a piece of information about circumstances that exist or events that have occurred; "first you must collect all the facts of the case"
- a statement or assertion of verified information about something that is the case or has happened; "he supported his argument with an impressive array of facts"
- the 9th letter of the Roman alphabet (同)i
PrepTutorEJDIC
- (…の)『要因』,(…を生み出す)要素《+『in』+『名』(do『ing』)》 / 囲数,約数 / 代理人,《おもに英》仲買人 / =factorize
- 〈C〉『事実』,実際にある(あった)事 / 〈U〉真相,真実(truth) / 《the~》(法律用語で)犯行
- 〈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
- 『私は』私が
- iodineの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/05/29 16:29:30」(JST)
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- 1. 補体系の遺伝性疾患 inherited disorders of the complement system
- 2. フィブリノゲンの異常 disorders of fibrinogen
- 3. 第ⅩＩ因子欠乏症 factor xi deficiency
- 4. 稀な（劣性遺伝性）凝固異常 rare recessively inherited coagulation disorders
- 5. Pathogenesis and biomarkers of cardiovascular disease in HIV-infected patients
English Journal
- Yes or no for secondary prophylaxis in afibrinogenemia?
- Simurda T1, Stanciakova L, Stasko J, Dobrotova M, Kubisz P.
- Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.Blood Coagul Fibrinolysis.2015 Dec;26(8):978-80. doi: 10.1097/MBC.0000000000000392.
- PMID 26484644
- Asphyxia by Drowning Induces Massive Bleeding Due To Hyperfibrinolytic Disseminated Intravascular Coagulation.
- Schwameis M1, Schober A, Schörgenhofer C, Sperr WR, Schöchl H, Janata-Schwatczek K, Kürkciyan EI, Sterz F, Jilma B.
- Critical care medicine.Crit Care Med.2015 Nov;43(11):2394-402. doi: 10.1097/CCM.0000000000001273.
- OBJECTIVE: To date, no study has systematically investigated the impact of drowning-induced asphyxia on hemostasis. Our objective was to test the hypothesis that asphyxia induces bleeding by hyperfibrinolytic disseminated intravascular coagulation.DESIGN: Observational study.SETTING: A 2,100-bed ter
- PMID 26327200
- Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?
- Stanciakova L1, Simurda T1, Stasko J1, Snahnicanova Z2, Loderer D2, Lasabova Z2, Kubisz P1.
- Seminars in thrombosis and hemostasis.Semin Thromb Hemost.2015 Nov;41(8):901-2. doi: 10.1055/s-0035-1564802. Epub 2015 Oct 20.
- PMID 26485721
Japanese Journal
- A novel in-frame deletion in the leucine zipper domain of C/EBPε leads to neutrophil-specific granule deficiency
- Wada Taizo,Akagi Tadayuki,Muraoka Masahiro,Toma Tomoko,Kaji Kenzo,Agematsu Kazunaga,Koeffler Phillip,Yokota Takashi,Yachie Akihiro
- Journal of Immunology 195(1), 80-86, 2015-07-01
- … Neutrophil-specific granule deficiency (SGD) is a rare autosomal recessive primary immunodeficiency characterized by neutrophil dysfunction, bilobed neutrophil nuclei and lack of neutrophil-specific granules. … Defects in a myeloid-specific transcription factor, CCAAT/enhancer binding protein-ε (C/EBPε), have been identified in two cases in which homozygous frameshift mutations led to loss of the leucine zipper domain. …
- NAID 120005647665
- A case of sagittal splitting ramus osteotomy and genioplasty in a patient with congenital factor VII deficiency
- Rokutanda Satoshi,Yoshida Masashi,Kuroe Kazuto,Yanamoto Souichi,Yamada Shin-ichi,Kawano Toshihiro,Naruse Tomofumi,Obama Kosuke,Umeda Masahiro
- Acta medica Nagasakiensia 60(1), 21-24, 2015-07
- … Blood coagulation factor VII is involved in the extrinsic clotting system, and congenital defects or deficiencies affecting blood coagulation factor VII are rare. … We report the case of a patient who was diagnosed with factor VII deficiency based on a preoperative examination and then underwent factor VII replacement therapy and orthognathic surgery, together with a brief discussion of the literature.The patient was a 25-year-old woman. …
- NAID 120005627332
- Chronological urodynamic evaluation of changing bladder and urethral functions after robot-assisted radical prostatectomy
- Kadono Yoshifumi,Ueno Satoru,Iwamoto Daiki,Takezawa Yuta,Nohara Takahiro,Izumi Kouji,Mizokami Atsushi,Namiki Mikio
- Urology 85(6), 1441-1447, 2015-06-01
- … Intrinsic sphincter deficiency (ISD) evaluated by the ALPP test was observed in 53 patients immediately after RARP, although no patient showed ISD before RARP. … Urethral sphincter dysfunction is considered the main factor for urinary incontinence after RARP. …
- NAID 120005647652
Related Links
- factor X deficiency An autosomal-recessive condition caused by a mutation on chromosome 13q34, resulting in decreased factor X production. Clinical findings • Infancy—Severe umbilical cord stump bleeding, prolonged bleeding ...
- factor /fac·tor/ (fak´ter) an agent or element that contributes to the production of a result. accelerator factor coagulation f. V. angiogenesis factor a ... Most patients with congenital factor XI deficiency do not have any significant ...
Related Pictures
★リンクテーブル★
| リンク元 | 「I因子欠損症」「第I因子欠乏症」「第I因子欠損症」 |
| 関連記事 | 「deficiency」「I」「fact」「factor」「Id」 |
「I因子欠損症」
「第I因子欠乏症」
「第I因子欠損症」
「deficiency」
- n.
- 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
「I」
「fact」
- n.
「factor」
- n.