(Q72160523)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

platelet storage pool deficiency

24 October 2019

main subject

1 reference

E P O'Brien

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

E K Novak

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

L Zhen

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

K F Manly

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

D Stephenson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

R T Swank

6

1 reference

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24 October 2019

publication date

1 January 1995

1 reference

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24 October 2019

number of pages

6

1 reference

inferred from page(s)

published in

Mammalian Genome

1 reference

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24 October 2019

volume

6

1 reference

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24 October 2019

issue

1

1 reference

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24 October 2019

page(s)

19-24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha

24 October 2019

cites work

1 reference

12 December 2020

Characterization of abnormalities in the visual system of the mutant mouse pearl

1 reference

12 December 2020

Disorders of platelet function

1 reference

12 December 2020

Sandy: a new mouse model for platelet storage pool deficiency

1 reference

12 December 2020

A Macintosh program for storage and analysis of experimental genetic mapping data

1 reference

12 December 2020

Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV

1 reference

12 December 2020

Lysosomal dysfunctions associated with mutations at mouse pigment genes

1 reference

12 December 2020

Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci

1 reference

12 December 2020

Genetic mapping of the integrin alpha 1 gene (Vla1) to mouse chromosome 13

1 reference

12 December 2020

Molecular cloning of microtubule-associated protein 1 (MAP1A) and microtubule-associated protein 5 (MAP1B): identification of distinct genes and their differential expression in developing brain

1 reference

12 December 2020

Molecular cloning of the rat integrin alpha 1-subunit: a receptor for laminin and collagen

1 reference

12 December 2020

Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm

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

Synergistic effect of storage pool deficient platelets and low plasma von Willebrand factor on the severity of the hemorrhagic diathesis in Hermansky-Pudlak syndrome

1 reference

12 December 2020

DNA sequence polymorphism in an androgen-regulated gene is associated with alteration in the encoded RNAs

1 reference

12 December 2020

Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 13

1 reference

12 December 2020

The mouse pale ear pigment mutant as a possible animal model for human platelet storage pool deficiency

1 reference

12 December 2020

Cocoa: a new mouse model for platelet storage pool deficiency

1 reference

12 December 2020

Heterogeneity in storage pool deficiency: studies on granule-bound substances in 18 patients including variants deficient in alpha-granules, platelet factor 4, beta-thromboglobulin, and platelet-derived growth factor

1 reference

12 December 2020

Genomic organization of adrenergic and serotonin receptors in the mouse: Linkage mapping of sequence-related genes provides a method for examining mammalian chromosome evolution

1 reference

12 December 2020

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

1 reference

12 December 2020

Lysosomal mutations increase susceptibility to anaesthetics

1 reference

12 December 2020

Cloning of two additional catecholamine receptors from rat brain

1 reference

12 December 2020

Associations between microtubules and intracellular organelles

1 reference

12 December 2020

A simple, rapid, and sensitive DNA assay procedure

1 reference

12 December 2020

An intronless gene encoding a potential member of the family of receptors coupled to guanine nucleotide regulatory proteins

1 reference

12 December 2020

Mus spretus-specific LINE-1 DNA probes applied to the cloning of the murine pearl locus

1 reference

12 December 2020

Inherited abnormalities in platelet organelles and platelet formation and associated altered expression of low molecular weight guanosine triphosphate-binding proteins in the mouse pigment mutant gunmetal.

1 reference

12 December 2020

Molecular genetics of von Willebrand disease

1 reference

12 December 2020

Mutation rates at a new set of specific loci in the mouse

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00350888

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7719021%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference