(Q35815997)

English

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

scientific article published in October 1989

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

Sahr KE

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Tobe T

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Scarpa A

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Laughinghouse K

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Marchesi SL

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Agre P

6

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Linnenbach AJ

7

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Marchesi VT

8

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Forget BG

9

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 October 1989

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

84

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

1243-1252

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

A catalogue of splice junction sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

The structure and evolution of the human beta-globin gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Identification of functional domains of human erythrocyte spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Erythrocyte spectrin is comprised of many homologous triple helical segments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Efficient isolation of genes by using antibody probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Stabilizing infrastructure of cell membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Sp alpha I/65 hereditary elliptocytosis in North Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

The membrane skeleton of human erythrocytes and its implications for more complex cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

[Hereditary elliptocytosis in West Africa: frequency and repartition of spectrin variants]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Ovalbumin gene: evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

Human beta-globin messenger RNA. III. Nucleotide sequences derived from complementary DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=329784

24 September 2018

[Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

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/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular heterogeneity of hereditary pyropoikilocytosis: identification of a second variant of the spectrin alpha-subunit

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of human erythrocyte spectrin. II. The sequence of the alpha-I domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal spectrin in hereditary elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2794061

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI114291

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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