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Annals of the New York Academy of Sciences|June 8, 2000
Molecular mechanism of metabolic syndrome X: contribution of adipocytokines adipocyte-derived bioactive substancesY Matsuzawa, T Funahashi, T Nakamura
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 1, 1996
Plasma leptin levels and body fat distributionM Takahashi, T Funahashi, I Shimomura, et al.
Human Genetics|June 1, 1988
Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemiaT Funahashi, Y Miyake, A Yamamoto, et al.
The American Journal of Cardiology|July 25, 1988
Selective reduction of cholesterol in HDL2 fraction by probucol in familial hypercholesterolemia and hyperHDL2 cholesterolemia with abnormal cholesteryl ester transferY Matsuzawa, S Yamashita, T Funahashi, et al.
European Journal of Biochemistry|September 15, 1995
A single point mutation in the splice donor site of the low-density-lipoprotein-receptor gene produces intron read-through, exon-skipped and cryptic-site-utilized transcriptsT Maruyama, Y Miyake, S Tajima, et al.
Biochimica Et Biophysica Acta|August 19, 1992
Stimulation of the activity and mRNA level of hepatic triacylglycerol lipase by triiodothyronine in HepG2 cellsS Nozaki, I Shimomura, T Funahashi, et al.
The American Journal of Cardiology|June 27, 1986
Effects of probucol on xanthomata regression in familial hypercholesterolemiaA Yamamoto, Y Matsuzawa, S Yokoyama, et al.
Metabolism: Clinical and Experimental|August 26, 1998
Effect of visceral fat accumulation on uric acid metabolism in male obese subjects: visceral fat obesity is linked more closely to overproduction of uric acid than subcutaneous fat obesityF Matsuura, S Yamashita, T Nakamura, et al.
Atherosclerosis|March 1, 1988
Characterization of low-density lipoproteins from patients with recessive X-linked ichthyosisT Nakamura, Y Matsuzawa, M Okano, et al.
Human Mutation|April 13, 1999
A novel point mutation in a splice acceptor site of intron 1 of the human low density lipoprotein receptor gene which causes severe hypercholesterolemia: an unexpected absence of exon skipping. Mutations in brief no. 139. OnlineT Maruyama, Y Miyake, T Yamamura, et al.
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