(Q24336646)

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Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins

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Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins (English)

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cholesteryl ester transfer protein

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GOA release 2020-03-11

cholesterol homeostasis

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GOA release 2020-03-11

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based on heuristic

inferred from title

protein deficiency

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author name string

M L Brown

1

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A Inazu

2

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C B Hesler

3

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L B Agellon

4

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C Mann

5

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M E Whitlock

6

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Y L Marcel

7

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R W Milne

8

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J Koizumi

9

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H Mabuchi

10

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language of work or name

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publication date

23 November 1989

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342

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6248

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448-51

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Splicing of messenger RNA precursors

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Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia

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Expression of apolipoprotein B epitopes in lipoproteins. Relationship to conformation and function

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Cloning and sequencing of human cholesteryl ester transfer protein cDNA

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Dideoxy sequencing method using denatured plasmid templates

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A catalogue of splice junction sequences

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Pre-mRNA splicing

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Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNA

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Spliceosome assembly involves the binding and release of U4 small nuclear ribonucleoprotein

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Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

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A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia

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Unusual splice sites revealed by mutagenic inactivation of an authentic splice site of the rabbit β-globin gene

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DNA methylation and the frequency of CpG in animal DNA.

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Molecular basis of base substitution hotspots in Escherichia coli

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Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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DNA typing from single hairs

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53 Determination of fragment order through partial digests and multiple enzyme digests

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