(Q41208228)

English

Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele

scientific article

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scholarly article

1 reference

Europe PubMed Central

28 September 2017

Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele (English)

1 reference

Europe PubMed Central

28 September 2017

hereditary elliptocytosis

1 reference

based on heuristic

inferred from title

author name string

D Guetarni

1

1 reference

Europe PubMed Central

28 September 2017

A F Roux

2

1 reference

Europe PubMed Central

28 September 2017

N Alloisio

3

1 reference

Europe PubMed Central

28 September 2017

F Morlé

4

1 reference

Europe PubMed Central

28 September 2017

M T Ducluzeau

5

1 reference

Europe PubMed Central

28 September 2017

B G Forget

6

1 reference

Europe PubMed Central

28 September 2017

P Colonna

7

1 reference

Europe PubMed Central

28 September 2017

J Delaunay

8

1 reference

Europe PubMed Central

28 September 2017

J Godet

9

1 reference

Europe PubMed Central

28 September 2017

publication date

1 October 1990

1 reference

Europe PubMed Central

28 September 2017

1 reference

Europe PubMed Central

28 September 2017

85

1 reference

Europe PubMed Central

28 September 2017

6

1 reference

Europe PubMed Central

28 September 2017

627-630

1 reference

Europe PubMed Central

28 September 2017

https://scigraph.springernature.com/pub.10.1007/bf00193587

0 references

Cloning of a portion of the chromosomal gene for human erythrocyte alpha-spectrin by using a synthetic gene fragment

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A structural model of human erythrocyte spectrin. Alignment of chemical and functional domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sp alpha I/65: a new variant of the alpha subunit of spectrin in hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The red cell skeleton and its genetic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sp alpha I/65 hereditary elliptocytosis in North Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary elliptocytosis and related disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three RFLPs are detected by an alpha spectrin genomic clone

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2227954

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00193587

1 reference

Europe PubMed Central

28 September 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

28 September 2017

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