WordNet
- United States geneticist who (with Crick in 1953) helped discover the helical structure of DNA (born in 1928) (同)James Watson, James Dewey Watson
- United States psychologist considered the founder of behavioristic psychology (1878-1958) (同)John Broadus Watson
- United States telephone engineer who assisted Alexander Graham Bell in his experiments (1854-1934) (同)Thomas Augustus Watson
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (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
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/01/13 08:21:47」(JST)
wiki en
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 神経線維腫症I型（NF1）：病因、臨床的特徴、および診断 neurofibromatosis type 1 nf1 pathogenesis clinical features and diagnosis
- 2. 間歇的血液透析の透析量への残存腎機能の組入れ incorporating residual kidney function into the dosing of intermittent hemodialysis
- 3. 持続的腹膜透析における溶質クリアランスの測定：Kt/Vとクレアチニンクリアランス measurement of solute clearance in continuous peritoneal dialysis kt v and creatinine clearance
- 4. 強イオンおよび酸塩基障害の解析（スチュワート法） strong ions and the analysis of acid base disturbances stewart approach
- 5. 遺伝コプロポルフィリン症 hereditary coproporphyria
English Journal
- Base-Pairing Energies of Proton-Bound Dimers and Proton Affinities of 1-Methyl-5-Halocytosines: Implications for the Effects of Halogenation on the Stability of the DNA i-Motif.
- Yang B1, Wu RR, Rodgers MT.
- Journal of the American Society for Mass Spectrometry.J Am Soc Mass Spectrom.2015 Sep;26(9):1469-82. doi: 10.1007/s13361-015-1174-2. Epub 2015 Jul 7.
- (CCG)n•(CGG)n trinucleotide repeats have been found to be associated with fragile X syndrome, the most widespread inherited cause of mental retardation in humans. The (CCG)n•(CGG)n repeats adopt i-motif conformations that are preferentially stabilized by base-pairing interactions of noncanonical
- PMID 26148525
- Optic pathway glioma in children: does visual deficit correlate with radiology in focal exophytic lesions?
- Aquilina K1, Daniels DJ, Spoudeas H, Phipps K, Gan HW, Boop FA.
- Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery.Childs Nerv Syst.2015 Aug 16. [Epub ahead of print]
- PURPOSE: Unlike pilocytic astrocytomas in other parts of the brain, optic pathway gliomas (OPG) are usually diffuse lesions involving the anterior optic pathways and hypothalamus. Their infiltrative nature often precludes complete surgical resection. We sought to determine whether careful magnetic r
- PMID 26277358
Japanese Journal
- ヒトRecQヘリカーゼWRNとBLMの結晶構造解析
- 2015-05-01
- NAID 120005841621
- Structural mechanisms of human RecQ helicases WRN and BLM
- 2014-10-29
- NAID 120005841619
- ヒトRecQヘリカーゼWRNとBLMの結晶構造解析
- 日本結晶学会誌 56(2), 133-138, 2014
- NAID 130004552886
Related Links
- Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary ... Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.
- 12 Feb 2013 ... Watson syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Related Pictures
★リンクテーブル★
| リンク元 | 「neurofibromatosis type 1」「type 1 neurofibromatosis」「ワトソン症候群」「Watson症候群」 |
| 関連記事 | 「syndrome」 |
「neurofibromatosis type 1」
- 関
- neurofibromatosis 1、neurofibromatosis I、neurofibromatosis type I、type 1 neurofibromatosis、type I neurofibromatosis、von Recklinghausen disease、von Recklinghausen's disease、Watson syndrome
「type 1 neurofibromatosis」
- 関
- neurofibromatosis 1、neurofibromatosis I、neurofibromatosis type 1、neurofibromatosis type I、type I neurofibromatosis、von Recklinghausen disease、von Recklinghausen's disease、Watson syndrome
「ワトソン症候群」
「Watson症候群」
「syndrome」
- n.