(Q30986717)

28 June 2017

Oxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders (English)

1 reference

28 June 2017

M Hayashi

1

1 reference

28 June 2017

M Itoh

2

1 reference

28 June 2017

S Araki

3

1 reference

28 June 2017

S Kumada

4

1 reference

28 June 2017

K Shioda

5

1 reference

28 June 2017

K Tamagawa

6

1 reference

28 June 2017

T Mizutani

7

1 reference

28 June 2017

Y Morimatsu

8

1 reference

28 June 2017

M Minagawa

9

1 reference

28 June 2017

M Oda

10

1 reference

28 June 2017

1 April 2001

1 reference

Journal of Neuropathology & Experimental Neurology

28 June 2017

1 reference

28 June 2017

60

1 reference

28 June 2017

4

1 reference

28 June 2017

350-356

1 reference

Neurodegeneration in hereditary nucleotide repair disorders

28 June 2017

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Cerebellar neurodegeneration in human hereditary DNA repair disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Immunohistochemical study of advanced glycation end products in aging and Alzheimer's disease brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Nitration and inactivation of manganese superoxide dismutase in chronic rejection of human renal allografts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

N (epsilon)-(carboxymethyl)lysine protein adduct is a major immunological epitope in proteins modified with advanced glycation end products of the Maillard reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Grumose or foamy spheroid bodies involving astrocytes in the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Hereditary ceruloplasmin deficiency increases advanced glycation end products in the brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Ultrastructure of nonenzymatically glycated mesangial matrix in diabetic nephropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Defects in antioxidant defense and calcium transport in the epidermis of xeroderma pigmentosum patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Localization of neuronal and glial glutamate transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Distribution of glutamate transporter subtypes during human brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F60.4.350

21 January 2018

Identifiers

DOI

10.1093/JNEN/60.4.350

1 reference

28 June 2017

1 reference