Hearing Dysfunction in Xpa-Deficient Mice.

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Hearing Dysfunction in Xpa-Deficient Mice.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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name

Hearing Dysfunction in Xpa-Deficient Mice.

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Hearing Dysfunction in Xpa-Deficient Mice.

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type

Item

label

Hearing Dysfunction in Xpa-Deficient Mice.

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Hearing Dysfunction in Xpa-Deficient Mice.

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Hearing Dysfunction in Xpa-Deficient Mice.

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Hearing Dysfunction in Xpa-Deficient Mice.

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P1476

Hearing Dysfunction in Xpa-Deficient Mice.

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P2093

Chikako Nishigori

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Daisuke Yamashita

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Eiji Nakano

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Go Inokuchi

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Hitomi Shinomiya

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Ken-Ichi Nibu

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Shingo Hasegawa

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Takeshi Fujita

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P2860

DNA repair diseases: What do they tell us about cancer and aging?

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A high-fat diet delays age-related hearing loss progression in C57BL/6J mice

Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration

The photocarcinogenesis of antibiotic lomefloxacin and UVA radiation is enhanced in xeroderma pigmentosum group A gene-deficient mice.

Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population.

Cisplatin induces cytoplasmic to nuclear translocation of nucleotide excision repair factors among spiral ganglion neurons.

Neurological symptoms and natural course of xeroderma pigmentosum.

The 8,5'-cyclopurine-2'-deoxynucleosides: candidate neurodegenerative DNA lesions in xeroderma pigmentosum, and unique probes of transcription and nucleotide excision repair.

Neuroimaging features of xeroderma pigmentosum group A.

P304

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scholarly article

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10.3389/FNAGI.2017.00019

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P478

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Naoki Otsuki

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2017-02-10T00:00:00Z

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28239347

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5301083

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