Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular level (Q35810128)

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scientific article published on February 1988

Language	Label	Description	Also known as
English	Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular level	scientific article published on February 1988

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scholarly article

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5 October 2019

Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular level (English)

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5 October 2019

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1

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5 October 2019

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Gregg RE

2

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5 October 2019

Law SW

3

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5 October 2019

Monge JC

4

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5 October 2019

Grant SM

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5 October 2019

Higuchi K

6

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5 October 2019

Triche TJ

7

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5 October 2019

Jefferson J

8

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5 October 2019

Brewer HB Jr

9

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5 October 2019

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1 February 1988

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5 October 2019

Journal of Clinical Investigation

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5 October 2019

81

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5 October 2019

2

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5 October 2019

590-595

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5 October 2019

Nonsense and frameshift mutations in beta 0-thalassemia detected in cloned beta-globin genes

1 reference

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RNA processing errors in patients with beta-thalassemia

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beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site

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cDNA cloning of human apoA-I: amino acid sequence of preproapoA-I

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ATA box transcription mutation in beta-thalassemia

1 reference

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Hybridization of nucleic acids immobilized on solid supports

1 reference

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Nucleotide sequence and the encoded amino acids of human apolipoprotein A-I mRNA

1 reference

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Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC

1 reference

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11 July 2018

The mutation and polymorphism of the human beta-globin gene and its surrounding DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329607

11 July 2018

Analysis of the apolipoprotein B gene and messenger ribonucleic acid in abetalipoproteinemia

1 reference

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11 July 2018

Isolation of a cDNA clone encoding the amino-terminal region of human apolipoprotein B.

1 reference

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Human liver apolipoprotein B-100 cDNA: complete nucleic acid and derived amino acid sequence

1 reference

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The human apolipoprotein A-II gene: complete nucleic acid sequence and genomic organization

1 reference

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Structure of the human apolipoprotein B gene

1 reference

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

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11 July 2018

The genetic relationship of abetalipoproteinemia and hypobetalipoproteinemia: a report of the occurence of both diseases within the same family

1 reference

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Alpha-thalassaemia caused by a polyadenylation signal mutation.

1 reference

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1 reference

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1 reference

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Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes)

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DEMYELINATING CENTRAL NERVOUS SYSTEM DISEASE, MACULAR ATROPHY AND ACANTHOCYTOSIS (BASSEN-KORNZWEIG SYNDROME)

1 reference

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Absorption and metabolism of vitamin D3 in man

1 reference

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Plasma apolipoprotein A-1 absence associated with a marked reduction of high density lipoproteins and premature coronary artery disease

1 reference

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

1 reference

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Identifiers

10.1172/JCI113357

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2828430%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

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1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2828430%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

PubMed publication ID

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Europe PubMed Central

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5 October 2019

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