No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles (Q28766214)

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scientific article (publication date: February 1991)

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Language	Label	Description	Also known as
English	No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles	scientific article (publication date: February 1991)

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instance of

scholarly article

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title

No severe bottleneck during human evolution: evidence from two apolipoprotein C-II deficiency alleles (English)

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main subject

familial apolipoprotein C-II deficiency

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based on heuristic

inferred from title

author name string

W J Xiong

series ordinal

1

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W H Li

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2

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I Posner

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3

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T Yamamura

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4

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A Yamamoto

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5

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A M Gotto

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6

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L Chan

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7

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language of work or name

English

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publication date

February 1991

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published in

American Journal of Human Genetics

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volume

48

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issue

2

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page(s)

383-9

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cites work

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Evolutionary Rate at the Molecular Level

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16 March 2017

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16 March 2017

Apolipoprotein CIISt. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease

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16 March 2017

Structure of apolipoprotein C-IIToronto, a nonfunctional human apolipoprotein

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16 March 2017

A deletion mutation in the ApoC-II gene (ApoC-II Nijmegen) of a patient with a deficiency of apolipoprotein C-II

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16 March 2017

The molecular clock runs more slowly in man than in apes and monkeys

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16 March 2017

Mitochondrial DNA and human evolution

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16 March 2017

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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16 March 2017

The structure of the human apolipoprotein C-II gene. Electron microscopic analysis of RNA:DNA hybrids, complete nucleotide sequence, and identification of 5' homologous sequences among apolipoprotein genes

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16 March 2017

DNA sequencing with chain-terminating inhibitors

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16 March 2017

Genetic and fossil evidence for the origin of modern humans

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3 June 2018

Nucleotide sequences of chimpanzee MHC class I alleles: evidence for trans-species mode of evolution

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3 June 2018

Familial type I hyperlipoproteinemia caused by apolipoprotein C-II deficiency

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3 June 2018

Radioimmunoassay of human apolipoprotein CII. A study in normal and hypertriglyceridemic subjects

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MHC polymorphism pre-dating speciation

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27 November 2018

An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-II

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12 December 2020

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Population size and protein variation in man

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Probability of identical monomorphism in related species

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Apolipoprotein CII in type I hyperlipoproteinemia. A study in three cases

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12 December 2020

based on heuristic

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How small was the bottleneck?

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reference URL

https://pubmed.ncbi.nlm.nih.gov/1990844

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

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12 December 2020

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Genetic structure of human populations II. Differentiation of blood group gene frequencies among isolated populations

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1683008

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PubMed publication ID

1990844

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