(Q24306836)

GOA release 2020-03-11

damaged DNA binding

1 reference

GOA release 2020-03-11

author name string

Yasuteru Sano

1

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Hidetoshi Date

2

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Shuichi Igarashi

3

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Osamu Onodera

4

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Mutsuo Oyake

5

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Toshiaki Takahashi

6

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Shintaro Hayashi

7

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Mitsunori Morimatsu

8

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Hitoshi Takahashi

9

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Takao Makifuchi

10

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Nobuyoshi Fukuhara

11

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Shoji Tsuji

Recessive ataxia with ocular apraxia: review of 22 Portuguese patients

12

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language of work or name

English

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publication date

February 2004

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published in

Annals of Neurology

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volume

55

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issue

2

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page(s)

241-9

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cites work

1 reference

7 January 2021

Cockayne syndrome: Review of 140 cases

1 reference

7 January 2021

Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia

1 reference

7 January 2021

The histidine triad superfamily of nucleotide-binding proteins

1 reference

7 January 2021

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): a new disease.

1 reference

7 January 2021

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family.

1 reference

7 January 2021

XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair

1 reference

7 January 2021

DNA single-strand break repair and spinocerebellar ataxia

1 reference

7 January 2021

Neurodegeneration in hereditary nucleotide repair disorders

1 reference

7 January 2021

Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein

1 reference

7 January 2021

Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast

1 reference

7 January 2021

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

1 reference

7 January 2021

The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin

1 reference

7 January 2021

Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes

1 reference

7 January 2021

Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3'-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage

1 reference

7 January 2021

Molecular characterization of a human DNA kinase

1 reference

7 January 2021

Adenosine monophosphoramidase activity of Hint and Hnt1 supports function of Kin28, Ccl1, and Tfb3

1 reference

7 January 2021

Nucleotide excision repair and human syndromes

1 reference

7 January 2021

A model for the tertiary structure of the 28 residue DNA-binding motif ('zinc finger') common to many eukaryotic transcriptional regulatory proteins

1 reference

7 January 2021

Molecular mechanism of nucleotide excision repair.

1 reference

7 January 2021

Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G

1 reference

7 January 2021

The HIT protein family: a new family of proteins present in prokaryotes, yeast and mammals

1 reference

7 January 2021