-
1
-
-
0029054796
-
Plasma lipid transfer proteins
-
Tall A. Plasma lipid transfer proteins. Annu Rev Biochem. 1995;64:235-257.
-
(1995)
Annu Rev Biochem
, vol.64
, pp. 235-257
-
-
Tall, A.1
-
2
-
-
0022346576
-
Deficiency of serum cholesleryl-ester transfer activity in patients with familial hyperalphalipoproteinemia
-
Koizumi J, Mabuchi H, Yoshimura A, Michishita I, Takeda M, Itoh H, Sakai Y, Sakai T, Ueda K, Takeda R. Deficiency of serum cholesleryl-ester transfer activity in patients with familial hyperalphalipoproteinemia. Atherosclerosis. 1985;58:175-186.
-
(1985)
Atherosclerosis
, vol.58
, pp. 175-186
-
-
Koizumi, J.1
Mabuchi, H.2
Yoshimura, A.3
Michishita, I.4
Takeda, M.5
Itoh, H.6
Sakai, Y.7
Sakai, T.8
Ueda, K.9
Takeda, R.10
-
3
-
-
0022346924
-
Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia
-
Kurasawa T, Yokoyama S, Miyake Y, Yamamura T, Yamamoto A. Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia. J Biochem. 1985;98:1499-1508.
-
(1985)
J Biochem
, vol.98
, pp. 1499-1508
-
-
Kurasawa, T.1
Yokoyama, S.2
Miyake, Y.3
Yamamura, T.4
Yamamoto, A.5
-
4
-
-
0024415898
-
Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
-
Brown ML, Inazu A, Hesler CB, Agellon LB, Mann C, Whitlock ME, Marcel YL, Milne RW, Koizumi J, Mabuchi H, Takeda R, Tall AR. Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins. Nature. 1989;342:448-451.
-
(1989)
Nature
, vol.342
, pp. 448-451
-
-
Brown, M.L.1
Inazu, A.2
Hesler, C.B.3
Agellon, L.B.4
Mann, C.5
Whitlock, M.E.6
Marcel, Y.L.7
Milne, R.W.8
Koizumi, J.9
Mabuchi, H.10
Takeda, R.11
Tall, A.R.12
-
5
-
-
0025091421
-
Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygous for the intron 14 splicing defect
-
Yamashita S, Hui DY, Sprecher DL, Matsuzawa Y, Sakai N, Tarui S, Kaplan D, Wetterau JR, Harmony JAK. Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygous for the intron 14 splicing defect. Biochem Biophys Res Commun. 1990;170:1346-1351.
-
(1990)
Biochem Biophys Res Commun
, vol.170
, pp. 1346-1351
-
-
Yamashita, S.1
Hui, D.Y.2
Sprecher, D.L.3
Matsuzawa, Y.4
Sakai, N.5
Tarui, S.6
Kaplan, D.7
Wetterau, J.R.8
Harmony, J.A.K.9
-
6
-
-
0025104275
-
Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation
-
Inazu A, Brown ML, Hesler CB, Agellon LB, Koizumi J, Takata K, Maruhama Y, Mabuchi H, Tall AR. Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation. N Engl J Med. 1990;323:1234-1238.
-
(1990)
N Engl J Med
, vol.323
, pp. 1234-1238
-
-
Inazu, A.1
Brown, M.L.2
Hesler, C.B.3
Agellon, L.B.4
Koizumi, J.5
Takata, K.6
Maruhama, Y.7
Mabuchi, H.8
Tall, A.R.9
-
7
-
-
0028135441
-
Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol
-
Inazu A, Jiang XC, Haraki T, Yagi K, Kamon N, Koizumi J, Mabuchi H, Takeda R, Takata K, Moriyama Y, Doi M, Tall A. Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol. J Clin Invest. 1994;94:1872-1882.
-
(1994)
J Clin Invest
, vol.94
, pp. 1872-1882
-
-
Inazu, A.1
Jiang, X.C.2
Haraki, T.3
Yagi, K.4
Kamon, N.5
Koizumi, J.6
Mabuchi, H.7
Takeda, R.8
Takata, K.9
Moriyama, Y.10
Doi, M.11
Tall, A.12
-
8
-
-
0027481233
-
Detection of a point mutation in cholesteryl ester transfer protein gene by polymerase chain reaction-mediated site-directed mutagenesis
-
Matsunaga A, Araki K, Moriyama K, Handa K, Arakawa F, Nishi K, Sasaki J, Arakawa K. Detection of a point mutation in cholesteryl ester transfer protein gene by polymerase chain reaction-mediated site-directed mutagenesis. Biochim Biophys Acta. 1993;1166:131-134.
-
(1993)
Biochim Biophys Acta
, vol.1166
, pp. 131-134
-
-
Matsunaga, A.1
Araki, K.2
Moriyama, K.3
Handa, K.4
Arakawa, F.5
Nishi, K.6
Sasaki, J.7
Arakawa, K.8
-
9
-
-
0027516284
-
Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by intron 14 splicing defect in hyperalphalipoproteinemia
-
Inazu A, Koizumi J, Haraki T, Yagi K, Wakasugi T, Takegoshi T, Mabuchi H, Takeda R. Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by intron 14 splicing defect in hyperalphalipoproteinemia. Hum Genet. 1993;91:13-16.
-
(1993)
Hum Genet
, vol.91
, pp. 13-16
-
-
Inazu, A.1
Koizumi, J.2
Haraki, T.3
Yagi, K.4
Wakasugi, T.5
Takegoshi, T.6
Mabuchi, H.7
Takeda, R.8
-
10
-
-
0027205174
-
Frequency of intron 14 splicing defect of cholesteryl ester transfer protein gene in the Japanese general population: Relation between the mutation and hyperalphalipoproteinemia
-
Hirano K, Yamashita S, Funahashi T, Sakai N, Menju M, Ishigami M, Hiraoka H, Kameda-Takemura K, Tokunaga K, Hoshino T, Kumasaka K, Kawano K, Matsuzawa Y. Frequency of intron 14 splicing defect of cholesteryl ester transfer protein gene in the Japanese general population: relation between the mutation and hyperalphalipoproteinemia. Atherosclerosis. 1993;100:85-90.
-
(1993)
Atherosclerosis
, vol.100
, pp. 85-90
-
-
Hirano, K.1
Yamashita, S.2
Funahashi, T.3
Sakai, N.4
Menju, M.5
Ishigami, M.6
Hiraoka, H.7
Kameda-Takemura, K.8
Tokunaga, K.9
Hoshino, T.10
Kumasaka, K.11
Kawano, K.12
Matsuzawa, Y.13
-
11
-
-
0020620321
-
Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes
-
Treisman R, Orkin SH, Maniatis T. Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes. Nature. 1983;302:591-596.
-
(1983)
Nature
, vol.302
, pp. 591-596
-
-
Treisman, R.1
Orkin, S.H.2
Maniatis, T.3
-
12
-
-
0026316732
-
Occurrence of multiple aberrantly spliced mRNAs upon a donor splice site mutation that causes familial lipoprotein lipase deficiency
-
Gotoda T, Yamada N, Murase T, Inaba T, Ishibashi S, Shimano H, Koga S, Yazaki Y, Furuichi Y, Takaku F. Occurrence of multiple aberrantly spliced mRNAs upon a donor splice site mutation that causes familial lipoprotein lipase deficiency. J Biol Chem. 1991;266:24757-24762.
-
(1991)
J Biol Chem
, vol.266
, pp. 24757-24762
-
-
Gotoda, T.1
Yamada, N.2
Murase, T.3
Inaba, T.4
Ishibashi, S.5
Shimano, H.6
Koga, S.7
Yazaki, Y.8
Furuichi, Y.9
Takaku, F.10
-
13
-
-
0023260886
-
GT to at transition at a splice donor site causes skipping of the preceding exon in phenylketonuria
-
Marvit J, DiLella AG, Brayton K, Ledley FD, Robson KJH, Woo SLC. GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria. Nucleic Acids Res. 1987;15:5613-5628.
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 5613-5628
-
-
Marvit, J.1
DiLella, A.G.2
Brayton, K.3
Ledley, F.D.4
Robson, K.J.H.5
Woo, S.L.C.6
-
14
-
-
0024326187
-
A point mutation G→A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria
-
Grandchamp B, Picat C, deRooij F, Beaumont C, Wilson P, Deybach JC, Nordmann Y. A point mutation G→A in exon 12 of the porphobilinogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Res. 1989;17:6637-6649.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 6637-6649
-
-
Grandchamp, B.1
Picat, C.2
DeRooij, F.3
Beaumont, C.4
Wilson, P.5
Deybach, J.C.6
Nordmann, Y.7
-
15
-
-
0025339711
-
Identical G+1 to A mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome, IV: An explanation for exon skipping with some mutations and not others
-
Kuivaniemi H, Kontusaari S, Tromp G, Zhao M, Sabol C, Prockop DJ. Identical G+1 to A mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome, IV: an explanation for exon skipping with some mutations and not others. J Biol Chem. 1990;265:12067-12074.
-
(1990)
J Biol Chem
, vol.265
, pp. 12067-12074
-
-
Kuivaniemi, H.1
Kontusaari, S.2
Tromp, G.3
Zhao, M.4
Sabol, C.5
Prockop, D.J.6
-
16
-
-
0023251539
-
Cloning and sequencing of human cholesteryl ester transfer protein cDNA
-
Drayna D, Jarnagin AS, McLean J, Henzel W, Kohr W, Fielding C, Lawn R. Cloning and sequencing of human cholesteryl ester transfer protein cDNA. Nature. 1987;327:632-634.
-
(1987)
Nature
, vol.327
, pp. 632-634
-
-
Drayna, D.1
Jarnagin, A.S.2
McLean, J.3
Henzel, W.4
Kohr, W.5
Fielding, C.6
Lawn, R.7
-
17
-
-
0025105228
-
Organization of the human cholesteryl ester transfer protein gene
-
Agellon LB, Quinet EM, Gillette TG, Drayna DT, Brown ML, Tall AR. Organization of the human cholesteryl ester transfer protein gene. Biochemistry. 1990;29:1372-1376.
-
(1990)
Biochemistry
, vol.29
, pp. 1372-1376
-
-
Agellon, L.B.1
Quinet, E.M.2
Gillette, T.G.3
Drayna, D.T.4
Brown, M.L.5
Tall, A.R.6
-
18
-
-
0026344120
-
Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency
-
Gotoda T, Yamada N, Kawamura M, Kozaki K, Mori N, Ishibashi S, Shimano H, Takaku F, Yazaki Y, Furuichi Y, Murase T. Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency. J Clin Invest. 1991;88:1856-1864.
-
(1991)
J Clin Invest
, vol.88
, pp. 1856-1864
-
-
Gotoda, T.1
Yamada, N.2
Kawamura, M.3
Kozaki, K.4
Mori, N.5
Ishibashi, S.6
Shimano, H.7
Takaku, F.8
Yazaki, Y.9
Furuichi, Y.10
Murase, T.11
-
19
-
-
0026633396
-
Simultaneous and quantitative isolation of nuclear and cytoplasmic RNA from eukaryotic cells
-
Memet S, Besançon F, Bourgeade MF. Simultaneous and quantitative isolation of nuclear and cytoplasmic RNA from eukaryotic cells. Trends Genet. 1992;8:190.
-
(1992)
Trends Genet
, vol.8
, pp. 190
-
-
Memet, S.1
Besançon, F.2
Bourgeade, M.F.3
-
20
-
-
0027499050
-
Apolipoprotein E enhances lipid exchange between lipoproteins mediated by cholesteryl ester transfer protein
-
Kinoshita M, Arai H, Fukasawa M, Watanabe T, Tsukamoto K, Hashimoto Y, Inoue K, Kurokawa K, Teramoto T. Apolipoprotein E enhances lipid exchange between lipoproteins mediated by cholesteryl ester transfer protein. J Lipid Res. 1993;34:261-268.
-
(1993)
J Lipid Res
, vol.34
, pp. 261-268
-
-
Kinoshita, M.1
Arai, H.2
Fukasawa, M.3
Watanabe, T.4
Tsukamoto, K.5
Hashimoto, Y.6
Inoue, K.7
Kurokawa, K.8
Teramoto, T.9
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