WordNet

(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
the 13th letter of the Roman alphabet (同)m
informal term for information; "give me the gen on your new line of computers"

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1. LDLコレステロール代謝の遺伝性疾患 inherited disorders of ldl cholesterol metabolism
2. 遺伝性運動失調の概要 overview of the hereditary ataxias
3. 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
4. フリードライヒ失調症 friedreich ataxia
5. 神経有棘赤血球症 neuroacanthocytosis

Liver fat accumulation may be dissociated from adiposity gain in ovariectomized rats.

Côté I, Yasari S, Pighon A, Barsalani R, Rabasa-Lhoret R, Prud'homme D, Lavoie JM.SourceDepartment of Kinesiology, Université de Montréal , Montréal, Québec.
Climacteric : the journal of the International Menopause Society.Climacteric.2012 Jan 23. [Epub ahead of print]
Objective The purpose of the present study was to establish a model of rats prone and resistant to intra-abdominal fat accumulation in response to ovariectomy (Ovx-P and Ovx-R) and to determine its relationship with molecular biomarkers. Design Two experiments were conducted in which female rats w
PMID 22268446

ApoA-IV modulates the secretory trafficking of apoB and the size of triglyceride-rich lipoproteins.

Weinberg RB, Gallagher JW, Fabritius MA, Shelness GS.SourceWake Forest School of Medicine, United States.
Journal of lipid research.J Lipid Res.2012 Jan 18. [Epub ahead of print]
Although the evidence linking apoA-IV expression and triglyceride (TG)-rich lipoprotein assembly and secretion is compelling, the intracellular mechanisms by which apoA-IV could modulate these processes remain poorly understood. We therefore examined the functional impact of apoA-IV expression on en
PMID 22257482

The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians

Two Siblings of Lewis Rats with a Congenital Homozygous Mutation ofGene Encoding the Large Subunit of Liver-Specific Microsomal TriglycerideTransfer Protein (MTP), Resulting in Pure Red Cell Aplasia and OneSibling with the Heterozygous Genetic Mutation of the Liver MTP Gene

Tadako NAKATSUJI
Acta medica et biologica 48(4), 127-133, 2000-12
… A homozygous sequence mutation of microsomal triglyceride transfer protein (MTP) was studied in three Lewis rat siblings. … Two of the three siblings had a homozygous sequence mutation in the exon-1 of the large subunit gene of liver-specific MTP and one of the three siblings had a heterozygous mutation of the large subunit gene. …
NAID 110004461717

ミクロソームトリグリセリド輸送タンパク質遺伝子 : 1 件
ミクロソームトリグリセリド輸送タンパク遺伝子 : nothing

リンク元	「ミクロソームトリグリセリド輸送タンパク質遺伝子」
関連記事	「MTP」「MT」「M」