コレステロールエステル転送蛋白欠損症
WordNet
- of the period coinciding with the Christian era; preferred by some writers who are not Christians; "in 200 CE" (同)C.E., Common Era
PrepTutorEJDIC
- 〈U〉〈C〉(…の)(量・額などの)不足,欠乏《+『of』(『in』)+『名』》 / 〈C〉不足分,不足量,不足額 / 〈C〉(精神・肉体などの)欠陥
UpToDate Contents
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English Journal
- Lipid and Apoprotein Composition of HDL in Partial or Complete CETP Deficiency.
- Niesor EJ, von der Mark E, Calabresi L, Averna M, Cefalu AB, Tarugi P, Nilsson P, Dernick G.SourcePharmaceuticals Division, F. Hoffmann-La Roche Ltd., Metabolic DBA, Bldg. 70/411 Grenzacherstrasse 124, CH-4070 Basel, Switzerland. eric_j.niesor@roche.com.
- Current vascular pharmacology.Curr Vasc Pharmacol.2012 Jul 1;10(4):422-31.
- Hyperalphalipoproteinemia, as observed in patients who are either homozygous or heterozygous for cholesteryl ester transfer protein (CETP) deficiency, has been shown to be associated with striking changes in apolipoprotein size distribution, namely, of high-density lipoprotein (HDL) and HDL-like par
- PMID 22339301
- Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of growth hormone deficient (GHD) adults before and after GH replacement therapy.
- Barbosa EJ, Glad C, Nilsson AG, Filipsson Nyström H, Götherström G, Svensson PA, Vinotti I, Bengtsson BA, Nilsson S, Boguszewski CL, Johannsson G.SourceE Barbosa, Sahlgrenska Academy, Univresity of Gothenburg, Department of Endocrinology, Gothenburg, S-41345, Sweden.
- European journal of endocrinology / European Federation of Endocrine Societies.Eur J Endocrinol.2012 Jun 19. [Epub ahead of print]
- OBJECTIVE: Growth hormone deficiency (GHD) in adults is associated with an altered serum lipid profile that responds to GH replacement therapy (GHRT). This study evaluated the influence of polymorphisms in genes related to lipid metabolism on serum lipid profile before and after 1 year of GHRT in ad
- PMID 22715478
Japanese Journal
- Novel mutations of cholesteryl ester transfer protein (CETP) gene in Japanese hyperalphalipoproteinemic subjects
- Ohtani Rumiko,Inazu Akihiro,Noji Yoshihiro,Wakasugi Takanobu,Miwa Kenji,Tada Hayato,Kawashiri Masa-aki,Noguchi Tohru,Nohara Atsushi,Kobayashi Junji,Koizumi Junji,Yamagishi Masakazu,Mabuchi Hiroshi
- Clinica Chimica Acta 413(5-6), 537-543, 2012-03-22
- … Background: The half of hyperalphalipoproteinemia (HALP) in Japan is caused by CETP gene mutations. … 1G>A), some rare CETP mutations are found in Japanese HALP subjects. … Methods: CETP gene analysis of genomic DNA from subjects was performed by restriction fragment length polymorphism (RFLP) and sequencing analysis. …
- NAID 120004026116
- Two Adjacent Mutations on Chromosome 16 Discovered in a Patient Presenting with Generalized Convulsions after Influenza A Virus Infection
- Iwasaki Yorihiro,Takahashi Makio,Nozu Kandai,Matsumoto Sadayuki,Koshiyama Hiroyuki
- Internal Medicine 50(19), 2179-2183, 2011
- … He was diagnosed with Gitelmans syndrome and cholesteryl ester transfer protein deficiency by identifying homozygous mutations of causative genes, SLC12A3 and CETP, respectively. …
- NAID 130001087924
Related Links
- These findings support the contention that HDL functionality is maintained in heterozygous CETP deficiency despite modifications in lipid and protein composition. The NOS3 T allele strongly interacts with CETP B1 allele to ...
- CETP deficiency symptoms, causes, diagnosis, and treatment information for CETP deficiency (Cholesteryl ester transfer protein deficiency) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments ...
★リンクテーブル★
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- 不足、欠乏、欠失、欠如、欠損、不十分。栄養不足、栄養素欠乏、欠乏症。(遺伝子)(染色体内の)遺伝子欠失
- 欠けているもの、不足している物。不足分。不完全なもの、欠点のあるもの
- 関
- absence, agenesis, dearth, defect, defective, deficient, deficit, delete, deletion, deletional, depletion, deprivation, deprive, lack, miss, missing, morphological defect, paucity, scarce, scarcity, starve
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コレステロールエステル転送蛋白 cholesterol ester transfer protein