(Q48081492)

8 February 2018

title

Molecular cloning of mouse erythrocyte protein 4.2: a membrane protein with strong homology with the transglutaminase supergene family. (English)

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8 February 2018

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A C Rybicki

1

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8 February 2018

R S Schwartz

series ordinal

2

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8 February 2018

J J Qiu

series ordinal

3

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8 February 2018

J G Gilman

series ordinal

4

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8 February 2018

publication date

1 July 1994

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8 February 2018

number of pages

8

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inferred from page(s)

published in

Mammalian Genome

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8 February 2018

volume

5

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8 February 2018

issue

7

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8 February 2018

page(s)

438-445

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8 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00357005

exact match

0 references

cites work

Isolation and characterization of band 3, the predominant polypeptide of the human erythrocyte membrane

1 reference

12 December 2020

Amino acid sequence of the a subunit of human factor XIII

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12 December 2020

Lysosomal dysfunctions associated with mutations at mouse pigment genes

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12 December 2020

A simple method for displaying the hydropathic character of a protein

1 reference

12 December 2020

Molecular cloning of human protein 4.2: a major component of the erythrocyte membrane

1 reference

12 December 2020

Human erythrocyte protein 4.2, a high copy number membrane protein, is N-myristylated

1 reference

12 December 2020

Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII

1 reference

12 December 2020

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

12 December 2020

Human erythrocyte protein 4.2: isoform expression, differential splicing, and chromosomal assignment

1 reference

12 December 2020

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)

1 reference

12 December 2020

The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

1 reference

12 December 2020

Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2

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12 December 2020

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings

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12 December 2020

Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins

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12 December 2020

A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis

1 reference

12 December 2020

A simple method for predicting the secondary structure of globular proteins: implications and accuracy

1 reference

12 December 2020

Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane

1 reference

12 December 2020

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

12 December 2020

Demonstration of immunoreactive forms of erythrocyte protein 4.2 in nonerythroid cells and tissues

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12 December 2020

Primary structure of blood coagulation factor XIIIa (fibrinoligase, transglutaminase) from human placenta

1 reference

12 December 2020

Authentic beta-globin mRNA sequences in homozygous betaO-thalassemia

1 reference

12 December 2020

Structural domain mapping and phosphorylation of human erythrocyte pallidin (band 4.2)

1 reference

12 December 2020

Associations of human erythrocyte band 4.2. Binding to ankyrin and to the cytoplasmic domain of band 3

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00357005

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8 February 2018

PubMed ID

7919657

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8 February 2018