(Q28586870)

31 January 2017

title

A glucose-6-phosphate dehydrogenase (G6PD) splice site consensus sequence mutation associated with G6PD enzyme deficiency (English)

1 reference

Glucose-6-phosphate dehydrogenase X-linked

31 January 2017

0 references

1 reference

GOA release 2020-03-11

author name string

S. Sanders

1

1 reference

31 January 2017

D. P. Smith

2

1 reference

31 January 2017

G. A. Thomas

3

1 reference

31 January 2017

E. D. Williams

4

1 reference

31 January 2017

language of work or name

English

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publication date

4 March 1997

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31 January 2017

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31 January 2017

volume

374

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31 January 2017

issue

1

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31 January 2017

page(s)

79–87

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Hematologically important mutations: glucose-6-phosphate dehydrogenase

31 January 2017

cites work

1 reference

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Deficiency in red blood cells

7 January 2021

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X-ray-induced mutations in mice

7 January 2021

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Linear dose-response relationship of erythrocyte enzyme-activity mutations in offspring of ethylnitrosourea-treated mice

7 January 2021

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The demonstration of tissue clonality by X-linked enzyme histochemistry

7 January 2021

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Demonstration of somatic mutation and colonic crypt clonality by X-linked enzyme histochemistry

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The clonal organization of the squamous epithelium of the tongue

7 January 2021

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X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus

7 January 2021

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Temporal and molecular characteristics of mutations induced by ethylnitrosourea in germ cells isolated from seminiferous tubules and in spermatozoa of lacZ transgenic mice

7 January 2021

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Molecular analysis of four ENU induced triosephosphate isomerase null mutants in Mus musculus.

7 January 2021

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Characterization of mutations induced by ethylnitrosourea in seminiferous tubule germ cells of transgenic B6C3F1 mice

7 January 2021

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A review of the genotoxicity of 1-ethyl-1-nitrosourea

7 January 2021

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Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome.

7 January 2021

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A single-base change at a splice site in a beta 0-thalassemic gene causes abnormal RNA splicing.

7 January 2021

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Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

7 January 2021

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Construction of a novel database containing aberrant splicing mutations of mammalian genes

7 January 2021

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Hematologically important mutations: red cell pyruvate kinase

7 January 2021

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Hematologically important mutations: X-linked chronic granulomatous disease

7 January 2021

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A catalogue of splice junction sequences

7 January 2021

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Elimination of mRNA splicing by a point mutation outside the conserved GU at 5' splice sites

7 January 2021

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Sequence requirements for splicing of higher eukaryotic nuclear pre-mRNA

7 January 2021

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The role of nucleotide sequences in splice site selection in eukaryotic pre-messenger RNA

7 January 2021

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7 January 2021

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inferred from DOI database lookup

7 January 2021

based on heuristic

A role for exon sequences and splice-site proximity in splice-site selection

1 reference

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A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNA

7 January 2021

1 reference

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The U1 small nuclear ribonucleoprotein/5' splice site interaction affects U2AF65 binding to the downstream 3' splice site

7 January 2021

1 reference

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Unusual splice sites revealed by mutagenic inactivation of an authentic splice site of the rabbit β-globin gene

7 January 2021

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Stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences

7 January 2021

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Biochemical Mechanisms of Constitutive and Regulated Pre-mRNA Splicing

7 January 2021

1 reference

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Preferential excision of the 5' proximal intron from mRNA precursors with two introns as mediated by the cap structure

7 January 2021

1 reference

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Splicing of messenger RNA precursors

7 January 2021

1 reference

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Signals for the selection of a splice site in pre-mRNA. Computer analysis of splice junction sequences and like sequences

7 January 2021

1 reference

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10.1016/S0027-5107(96)00222-9

7 January 2021

Identifiers

DOI

0 references

1 reference