WordNet

Scottish ornithologist in the United States (1766-1813) (同)Alexander Wilson
Scottish physicist who invented the cloud chamber (1869-1959) (同)Charles Thomson Rees Wilson
United States entomologist who has generalized from social insects to other animals including humans (born in 1929) (同)E. O. Wilson, Edward Osborne Wilson
United States literary critic (1895-1972) (同)Edmund Wilson
author of the first novel by an African American that was published in the United States (1808-1870) (同)Harriet Wilson
American Revolutionary leader who was one of the signers of the Declaration of Independence (1742-1798) (同)James Wilson
Canadian geophysicist who was a pioneer in the study of plate tectonics (1908-1993) (同)John Tuzo Wilson
United States physicist honored for his work on cosmic microwave radiation (born in 1918) (同)Robert Woodrow Wilson
English writer of novels and short stories (1913-1991) (同)Sir Angus Wilson, Angus Frank Johnstone Wilson
28th President of the United States; led the United States in World War I and secured the formation of the League of Nations (1856-1924) (同)Woodrow Wilson, Thomas Woodrow Wilson, President Wilson
a peak in the San Juan mountains of Colorado (14,246 feet high) (同)Mount Wilson
an impairment of health or a condition of abnormal functioning
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological
informal term for information; "give me the gen on your new line of computers"

PrepTutorEJDIC

ウィルソン(Thomas Woodrow Wilson;1856‐1924;米国第28代大統領1913‐21)
(体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
女性の話術芸人 =diseur
遺伝子
病気にかかった / 病的な,不健全な(morbid)

UpToDate Contents

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1. ウィルソン病：診断のための検査 wilson disease diagnostic tests
2. 遺伝性運動失調の概要 overview of the hereditary ataxias
3. ウィルソン病：臨床症状、診断、および自然史 wilson disease clinical manifestations diagnosis and natural history
4. ウィルソン病：疫学および病因 wilson disease epidemiology and pathogenesis
5. 舞踏病の概要 overview of chorea

English Journal

Non-coding RNAs in Mammary Gland Development and Disease.

Sandhu GK1, Milevskiy MJ1, Wilson W1, Shewan AM1, Brown MA2.
Advances in experimental medicine and biology.Adv Exp Med Biol.2016;886:121-153.
Non-coding RNAs (ncRNAs) are untranslated RNA molecules that function to regulate the expression of numerous genes and associated biochemical pathways and cellular functions. NcRNAs include small interfering RNAs (siRNAs), microRNAs (miRNAs), PIWI-interacting RNAs (piRNAs), small nucleolar RNAs (sno
PMID 26659490

Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).

Daiger SP1,2, Sullivan LS3, Bowne SJ4, Koboldt DC5, Blanton SH6, Wheaton DK7, Avery CE8, Cadena ED9, Koenekoop RK10, Fulton RS11, Wilson RK12, Weinstock GM13, Lewis RA14, Birch DG15.
Advances in experimental medicine and biology.Adv Exp Med Biol.2016;854:193-200. doi: 10.1007/978-3-319-17121-0_26.
Whole-genome linkage mapping identified a region on chromosome 10q21.3-q22.1 with a maximum LOD score of 3.0 at 0 % recombination in a six-generation family with autosomal dominant retinitis pigmentosa (adRP). All known adRP genes and X-linked RP genes were excluded in the family by a combination
PMID 26427411

Identification of p38 MAPK and JNK as new targets for correction of Wilson disease-causing ATP7B mutants.

Chesi G1, Hegde RN2, Iacobacci S1, Concilli M1, Parashuraman S2, Festa BP1, Polishchuk EV1, Di Tullio G1, Carissimo A1, Montefusco S1, Canetti D3, Monti M3, Amoresano A3, Pucci P3, van de Sluis B4, Lutsenko S5, Luini A2, Polishchuk RS1.
Hepatology (Baltimore, Md.).Hepatology.2015 Dec 13. doi: 10.1002/hep.28398. [Epub ahead of print]
Wilson disease (WD) is an autosomal recessive disorder that is caused by the toxic accumulation of copper (Cu) in the liver. The ATP7B gene, which is mutated in WD, encodes a multi-transmembrane domain ATPase that traffics from the trans-Golgi network (TGN) to the canalicular area of hepatocytes, wh
PMID 26660341

Japanese Journal

Role of p38 Mapk in Development of Acute Hepatic Injury in Long-Evans Cinnamon (LEC) Rats, an Animal Model of Human Wilson's Disease

KADOWAKI Shingo,MEGURO Saori,IMAIZUMI Yoshitaka [他],SAKAI Hiroshi,ENDOH Daiji,HAYASHI Masanobu
Journal of Veterinary Medical Science 75(12), 1551-1556, 2013
… The Long-Evans Cinnamon (LEC) rat, an animal model of human Wilson's disease, spontaneously develops fulminant hepatitis associated with severe jaundice at about 4 months of age. … In this study, we examined the changes in gene expression during progression of acute hepatic injury. …
NAID 130003362258

Identification of a novel Wilson disease gene mutation frequent in Upper Austria : a genetic and clinical study

Hofer Harald,Willheim-Polli Claudia,Knoflach Peter [他],GABRIEL Christian,VOGEL Wolfgang,TRAUNER Michael,MULLER Thomas,FERENCI Peter
Journal of human genetics 57(9), 564-567, 2012-09-01
NAID 10031056841

New mutations in the GLA gene in Brazilian families with Fabry disease

Turaca Lauro Thiago,Pessoa Juliana Gilbert,Motta Fabiana Louise [他],MUNOZ ROJAS Maria Veronica,MULLER Karen Barbosa,LOURENCO Charles Marques,MARQUES Wilson Junior,D'ALMEIDA Vania,MARTINS Ana Maria,PESQUERO Joao Bosco
Journal of human genetics 57(6), 347-351, 2012-06-01
NAID 10030807905