(Q52826546)

English

Direct assignment of orosomucoid to human chromosome 9 and alpha 2HS-glycoprotein to chromosome 3 using human fetal liver x rat hepatoma hybrids.

scientific article published in January 1985

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Statements

scholarly article

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

Direct assignment of orosomucoid to human chromosome 9 and alpha 2HS-glycoprotein to chromosome 3 using human fetal liver x rat hepatoma hybrids. (English)

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

0 references

hepatocellular carcinoma

1 reference

based on heuristic

inferred from title

author name string

D W Cox

1

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

U Francke

2

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

publication date

1 January 1985

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

70

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

2

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

109-115

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

describes a project that uses

0 references

https://scigraph.springernature.com/pub.10.1007/bf00273067

0 references

Inheritance of human α1-acid glycoprotein (orosomucoid) variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the mitochondrial aconitase gene (ACONM) to human chromosome 22

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation and characterization of variants of mouse hepatoma cells with defects in hepato-specific gene expression. I. Albumin synthesis variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human serum albumin phenotype activation in mouse hepatoma--human leukocyte cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New variants of alpha 1-antitrypsin: comparison of Pi typing techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of ABO, AK1and ACONSin families with abnormalities of chromosome 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of human alpha 1-antitrypsin gene in rat hepatoma x human fetal liver cell hybrids depends on presence of human chromosome 14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum protein synthesis by somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

delta-Aminolevulinatedehydrase: synteny with ABO-AK1-ORM (and assignment to chromosome 9).

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human transferrin: cDNA characterization and chromosomal localization

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the structural gene for the third component of human complement to chromosome 19.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electroimmuno assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of serum protein production in hepatocyte hybridomas: immortalization and expression of normal hepatocyte genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secretion of? 1-antitrypsin by an established human hepatoma cell line and by human/mouse hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for the assignment of the loci AK1, AK3and ACONsto chromosome 9 in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for linkage between the loci for transferrin and ceruloplasmin in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein and lipoprotein concentrations in familial apolipoprotein C-II deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3859464

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273067

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

1 reference

Europe PubMed Central

8 May 2018

http://europepmc.org/abstract/MED/3859464

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