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English
Of mice and men: the mice were right
scientific article published on March 1995
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
editorial
0 references
title
Of mice and men: the mice were right
(English)
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
author name string
Bennett V
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
language of work or name
English
0 references
publication date
1 March 1995
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
volume
95
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
page(s)
921-922
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
cites work
The spectrin-based membrane skeleton and micron-scale organization of the plasma membrane
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
Spectrin deficient inherited hemolytic anemias in the mouse: Characterization by spectrin synthesis and mRNA activity in reticulocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
Ankyrin and the hemolytic anemia mutation, nb, map to mouse chromosome 8: presence of the nb allele is associated with a truncated erythrocyte ankyrin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
26 September 2017
Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
15 June 2018
Marked reduction of spectrinin hereditary spherocytosis in the common house mouse
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
15 June 2018
Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=441420
retrieved
19 August 2018
Deficient red-cell spectrin in severe, recessively inherited spherocytosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7883989
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI117797
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
PMCID
441420
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
PubMed ID
7883989
1 reference
stated in
Europe PubMed Central
PMCID
441420
retrieved
25 September 2017
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