WordNet
- 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
- (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. 全身疾患と関連した遺伝性ニューロパチー hereditary neuropathies associated with generalized disorders
- 2. ペリツェウス・メルツバッハー病 pelizaeus merzbacher disease
- 3. 小児における常染色体劣性多発性嚢胞腎 autosomal recessive polycystic kidney disease in children
- 4. 原発性免疫不全症に対する遺伝子治療 gene therapy for primary immunodeficiency
- 5. アルツハイマー病の遺伝学 genetics of alzheimer disease
English Journal
- The effects of APOE on the functional architecture of the resting brain.
- Trachtenberg AJ, Filippini N, Ebmeier KP, Smith SM, Karpe F, Mackay CE.SourceFunctional Magnetic Resonance Imaging of the Brain (FMRIB) Centre, University of Oxford, Department of Clinical Neurology, John Radcliffe Hospital, Headington, Oxford, OX3 9DU, United Kingdom.
- NeuroImage.Neuroimage.2012 Jan 2;59(1):565-72. Epub 2011 Aug 7.
- There is a well-established association between APOE genotype and the risk of developing Alzheimer's disease (AD). Relative to individuals with the common ε3/ε3 genotype, carriers of the ε4 allele are at increased risk of developing AD, while carriers of the ε2 allele appear to be protected agai
- PMID 21851856
- Toll-Like Receptor Transcriptome in the HPV-Positive Cervical Cancer Microenvironment.
- Decarlo CA, Rosa B, Jackson R, Niccoli S, Escott NG, Zehbe I.SourceProbe Development and Biomarker Exploration Thunder Bay Regional Research Institute, Thunder Bay, ON, Canada P7B 6V4.
- Clinical & developmental immunology.Clin Dev Immunol.2012;2012:785825. Epub 2011 Oct 13.
- The human papillomavirus (HPV) directly infects cervical keratinocytes and interferes with TLR signalling. To shed light on the effect of HPV on upstream receptors, we evaluated TLRs 1-9 gene expression in HPV-negative normal and HPV-positive pre-malignant and malignant ex vivo cervical tissue. Quan
- PMID 22013487
Japanese Journal
- Genetic Background Strongly Modifies the Severity of Symptoms of Hirschsprung Disease, but not Hearing Loss in Rats Carrying Ednrb^[sl] Mutations
- Dang Ruihua,Torigoe Daisuke,Suzuki Sari,Kikkawa Yoshiaki,Moritoh Kanako,Sasaki Nobuya,Agui Takashi
- PLoS One 6(9), e24086, 2011-09-07
- … Hirschsprung disease (HSCR) is thought to result as a consequence of multiple gene interactions that modulate the ability of enteric neural crest cells to populate the developing gut. … However, it remains unknown whether the single complete deletion of important HSCR-associated genes is sufficient to result in HSCR disease. …
- NAID 120003370691
- Familial Parkinson disease mutations influence α-Synuclein assembly
- Ono Kenjiro,Ikeda Tokuhei,Takasaki Jun-ichi,Yamada Masahito
- Neurobiology of Disease
- … Lewy bodies composed of aggregates of α-Synuclein (αS) in the brain are the main histopathological features of Lewy body diseases (LBD) such as Parkinson's disease and dementia with Lewy bodies. … Mutations such as E46K, A30P and A53T in the αS gene cause autosomal dominant LBD in a number of kindreds. …
- NAID 120003308572
Related Links
- Information about several medically important genes and related diseases. Illustrates the use of bioinformatics in their study.
Related Pictures
★リンクテーブル★
| リンク元 | 「疾患遺伝子」「責任遺伝子」「疾患原因遺伝子」 |
| 拡張検索 | 「Wilson disease gene」 |
| 関連記事 | 「disease」 |
「疾患遺伝子」
- 英
- disease gene
- 関
- 疾患原因遺伝子、責任遺伝子
「責任遺伝子」
- 英
- disease gene
- 関
- 疾患遺伝子、疾患原因遺伝子
「疾患原因遺伝子」
- 英
- disease gene
- 関
- 疾患遺伝子、責任遺伝子
「Wilson disease gene」
「disease」
- n.
- 疾患：illnessより厳密な概念。「ある臓器に明確な障害が確認され、それによって症状が出ているとはっきり説明できる場合」 (PSY.9)
- 特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9)
- something that is very wrong with people's attitudes, way of life or with society.
- 注意