(Q24317036)

GOA release 2020-03-11

AMP deaminase activity

1 reference

GOA release 2020-03-11

author name string

D K Mahnke-Zizelman

1

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F van den Bergh

2

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M T Bausch-Jurken

3

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R Eddy

4

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S Sait

5

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T B Shows

6

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R L Sabina

Biochimica et Biophysica Acta

7

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language of work or name

English

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publication date

14 August 1996

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published in

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volume

1308

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issue

2

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page(s)

122-32

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Characterization of the human AMPD3 gene reveals that 5' exon useage is subject to transcriptional control by three tandem promoters and alternative splicing

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AMP deaminase isozymes in human tissues

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The mouse Rxrb gene encoding RXR beta: genomic organization and two mRNA isoforms generated by alternative splicing of transcripts initiated from CpG island promoters

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Ampd-2 maps to distal mouse chromosome 3 in linkage with Ampd-1

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Characterization of human AMP deaminase 2 (AMPD2) gene expression reveals alternative transcripts encoding variable N-terminal extensions of isoform L

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Human immune interferon gene is located on chromosome 12

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Molecular basis for human erythrocyte AMP deaminase deficiency: screening for the major point mutation and identification of other mutations

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A novel pathway for alternative splicing: identification of an RNA intermediate that generates an alternative 5' splice donor site not present in the primary transcript of AMPD1.

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Functionally distinct elements are required for expression of the AMPD1 gene in myocytes

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A nuclease-hypersensitive element of the human c-myc promoter interacts with a transcription initiation factor.

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Expression of three stage-specific transcripts of AMP deaminase during myogenesis

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Organization and expression of eucaryotic split genes coding for proteins

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Alternative splicing: a mechanism for phenotypic rescue of a common inherited defect

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Immunolocalization of AMP-deaminase isozymes in human skeletal muscle and cultured muscle cells: concentration of isoform M at the neuromuscular junction

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Molecular analysis of the myoadenylate deaminase deficiencies

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