WordNet

bruise, cut, or injure the skin or the surface of; "The boy skinned his knee when he fell" (同)scrape
a persons skin regarded as their life; "he tried to save his skin"
a bag serving as a container for liquids; it is made from the hide of an animal
an outer surface (usually thin); "the skin of an airplane"
a natural protective body covering and site of the sense of touch; "your skin is the largest organ of your body" (同)tegument, cutis
strip the skin off; "pare apples" (同)peel, pare
an impairment of health or a condition of abnormal functioning
pertaining to or referring to origin; "genetic history reconstructs the origins of a literary work"
of or relating to the science of genetics; "genetic research" (同)genetical
move along on skis; "We love to ski the Rockies"; "My children dont ski"
narrow wood or metal or plastic runners used in pairs for gliding over snow
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid, pathologic, pathological

PrepTutorEJDIC

〈U〉〈C〉(人・動物の)『皮膚』,肌 / 〈C〉〈U〉(動物からはいだ)『皮』,『毛皮』;皮製品,皮袋 / 〈C〉(果物・野菜の)皮 / 〈U〉〈C〉(液体の表面にできる)薄い膜,上皮 / 〈C〉(枠組み・表面などを覆う)外皮,外被,外板 / 〈動物・果物など〉‘の'皮をはぐ(むく) / 〈手・脚など〉‘を'擦りむく / 《話》(金などを)〈人〉‘から'巻き上げる《+『名』〈人〉+『of』+『名』》 / 〈傷口などが〉皮で覆われる《+『over』》
(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
『スキー』 / 『スキーで滑走する』 / …‘を'スキーで滑る / スキーの,スキー用の
病気にかかった / 病的な,不健全な(morbid)

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1. 線状IgA水疱性皮膚症 linear iga bullous dermatosis
2. 結節性硬化症：遺伝学、臨床的特徴、および診断 tuberous sclerosis complex genetics clinical features and diagnosis
3. プリオンの生物学および遺伝学 biology and genetics of prions
4. 不整脈原性右室心筋症の遺伝学および病因 genetics and pathogenesis of arrhythmogenic right ventricular cardiomyopathy
5. 小頭症に対する臨床遺伝学的アプローチ a clinical genetics approach to microcephaly

Fine mapping under linkage peaks for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil.

Weirather JL1, Duggal P2, Nascimento EL3, Monteiro GR4, Martins DR5, Lacerda HG6, Fakiola M7, Blackwell JM8, Jeronimo SM9, Wilson ME10.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.Infect Genet Evol.2016 Sep;43:1-5. doi: 10.1016/j.meegid.2016.05.005. Epub 2016 May 4.
Infection with the protozoan Leishmania infantum can lead to asymptomatic infection and protective immunity, or to the progressive and potentially fatal disease visceral leishmaniasis (VL). Published studies show host genetic background determines in part whether infected individuals will develop a
PMID 27155051

A recessive syndrome of intellectual disability, moderate overgrowth, and renal dysplasia predisposing to Wilms tumor is caused by a mutation in FIBP gene.

Akawi N1, Ben-Salem S1, Lahti L2, Partanen J2, Ali BR2, Al-Gazali L3.
American journal of medical genetics. Part A.Am J Med Genet A.2016 Aug;170(8):2111-8. doi: 10.1002/ajmg.a.37741. Epub 2016 May 17.
Clinical classification of overgrowth syndromes represents a challenge since a wide spectrum of disorders result in marked overgrowth. Therefore, there is a continuous effort to identify the genetic basis of these disorders that will eventually facilitate their molecular classification. Here, we hav
PMID 27183861

Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.

Rothwell S1, Cooper RG2, Lundberg IE3, Miller FW4, Gregersen PK5, Bowes J1, Vencovsky J6, Danko K7, Limaye V8, Selva-O'Callaghan A9, Hanna MG10, Machado PM10, Pachman LM11, Reed AM12, Rider LG4, Cobb J13, Platt H14, Molberg Ø15, Benveniste O16, Mathiesen P17, Radstake T18, Doria A19, De Bleecker J20, De Paepe B20, Maurer B21, Ollier WE14, Padyukov L3, O'Hanlon TP4, Lee A5, Amos CI22, Gieger C23, Meitinger T24, Winkelmann J25, Wedderburn LR26, Chinoy H27, Lamb JA14; Myositis Genetics Consortium.
Annals of the rheumatic diseases.Ann Rheum Dis.2016 Aug;75(8):1558-66. doi: 10.1136/annrheumdis-2015-208119. Epub 2015 Sep 11.
OBJECTIVES: The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of rare autoimmune diseases characterised by muscle weakness and extramuscular manifestations such as skin rashes and interstitial lung disease. We genotyped 2566 IIM cases of Caucasian descent using the Immunochip;
PMID 26362759