(Q28289182)

2

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T Fukushige

3

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N Shaheen

4

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H Terazono

5

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T Saheki

Intron sequences involved in lariat formation during pre-mRNA splicing.

6

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language of work or name

English

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publication date

October 1995

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published in

Human Genetics

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volume

96

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issue

4

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page(s)

454-63

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cites work

1 reference

12 December 2020

A search for the primary abnormality in adult-onset type II citrullinemia.

1 reference

12 December 2020

Sequence for human argininosuccinate synthetase cDNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis

1 reference

12 December 2020

Splicing of messenger RNA precursors

1 reference

12 December 2020

Mutations in argininosuccinate synthetase mRNA of Japanese patients, causing classical citrullinemia

1 reference

12 December 2020

Alpha-galactosidase A gene rearrangements causing Fabry disease. Identification of short direct repeats at breakpoints in an Alu-rich gene

1 reference

12 December 2020

Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia

1 reference

12 December 2020

Modification of enzymatically amplified DNA for the detection of point mutations.

1 reference

12 December 2020

Molecular Structure of the Human Argininosuccinate Synthetase Gene: Occurrence of Alternative mRNA Splicing

1 reference

12 December 2020

β Thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site

1 reference

12 December 2020

Molecular analysis of argininosuccinate synthetase deficiency in human fibroblasts

1 reference

12 December 2020

Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease

1 reference

12 December 2020

Mutant human adenosine deaminase alleles and their expression by transfection into fibroblasts

1 reference

12 December 2020

Additional mutations in argininosuccinate synthetase causing citrullinemia

1 reference

12 December 2020

Clinical application of enzyme immunoassay in the analysis of citrullinemia

1 reference

12 December 2020

Dispersion of argininosuccinate synthetase-like human genes to multiple autosomes and the X chromosome

1 reference

12 December 2020

Simultaneous detection of mutant gene and transgene in ornithine carbamoyl-transferase-deficient spf-ash mice with rat OCT gene

1 reference

12 December 2020

Somatic cell genetic evidence for the presence of a gene for citrullinemia on human chromosome 9

1 reference

12 December 2020

Qualitative and quantitative abnormalities of argininosuccinate synthetase in citrullinemia

1 reference

12 December 2020

The human argininosuccinate synthetase locus and citrullinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular structures of human argininosuccinate synthetase pseudogenes. Evolutionary and mechanistic implications

1 reference

12 December 2020

Analysis of a splice acceptor site mutation which produces multiple splicing abnormalities in the human argininosuccinate synthetase locus

1 reference

12 December 2020

Structure of an abnormal messenger RNA for argininosuccinate synthetase in citrullinemia

1 reference

12 December 2020

Methods for analysis of multiple cystic fibrosis mutations

1 reference

12 December 2020

Amplification of human argininosuccinate synthetase pseudogenes

1 reference

12 December 2020

Analysis of deletions at the human argininosuccinate synthetase locus

1 reference

12 December 2020

Abnormal mRNA for argininosuccinate synthetase in citrullinaemia

1 reference

12 December 2020

A case of citrullinemia with abnormal messenger RNA for argininosuccinate synthetase

1 reference

12 December 2020

Multilocus linkage analysis with the human argininosuccinate synthetase gene

1 reference

12 December 2020

Specific and stable intron-factor interactions are established early during in vitro pre-mRNA splicing.

1 reference

12 December 2020

Molecular basis of enzyme abnormalities in urea cycle disorders. With special reference to citrullinemia and argininosuccinic aciduria

1 reference

12 December 2020

Speculations on RNA splicing

1 reference

12 December 2020

An intron mutation in the human alpha 1(I) collagen gene alters the efficiency of pre-mRNA splicing and is associated with osteogenesis imperfecta type II.

1 reference

12 December 2020

Role of the 3' splice site consensus sequence in mammalian pre-mRNA splicing.

1 reference

12 December 2020

Hereditary disorders of the urea cycle in man: biochemical and molecular approaches.

1 reference

12 December 2020