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Sandrine Pereira Selected Research

Complementation Group D Xeroderma Pigmentosum

1/2020Some mutations in the xeroderma pigmentosum D gene may lead to moderate but significant radiosensitivity associated with a delayed radiation-induced ATM nuclear localization.

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Sandrine Pereira Research Topics

Disease

4Neoplasms (Cancer)
12/2022 - 11/2008
2Ataxia Telangiectasia (Louis Bar Syndrome)
04/2023 - 01/2023
2Progeria (Hutchinson Gilford Syndrome)
07/2008 - 07/2008
2Premature Aging
07/2008 - 07/2008
2Benign Neonatal Epilepsy (Benign Familial Neonatal Convulsions)
04/2004 - 02/2002
1Squamous Cell Carcinoma of Head and Neck
04/2023
1Alzheimer Disease (Alzheimer's Disease)
01/2023
1Complementation Group D Xeroderma Pigmentosum
01/2020
1Chromosome Breakage
01/2020
1Huntington Disease (Huntington's Disease)
06/2014
1Brain Neoplasms (Brain Tumor)
11/2008
1Lipodystrophy
07/2008
1Alopecia (Baldness)
07/2008
1Temporal Lobe Epilepsy
03/2006
1Seizures (Absence Seizure)
04/2004
1familial Infantile convulsions and paroxysmal choreoathetosis
02/2002

Drug/Important Bio-Agent (IBA)

3Proteins (Proteins, Gene)FDA Link
04/2023 - 07/2008
3DNA (Deoxyribonucleic Acid)IBA
01/2023 - 06/2014
21,2- di- (4- sulfamidophenyl)- 4- butylpyrazolidine- 3,5- dione (DSB)IBA
01/2023 - 01/2020
2Hydroxymethylglutaryl-CoA Reductase Inhibitors (HMG-CoA Reductase Inhibitors)IBA
06/2014 - 07/2008
1Biomarkers (Surrogate Marker)IBA
04/2023
1Ataxia Telangiectasia Mutated ProteinsIBA
01/2023
1ChromatinIBA
01/2020
1Huntingtin ProteinIBA
06/2014
1Diphosphonates (Bisphosphonates)IBA
06/2014
1Lamin Type A (Lamin A)IBA
11/2008
1prelamin AIBA
07/2008
1LaminsIBA
07/2008
1Metalloproteases (Metalloproteinases)IBA
07/2008
1Complement System Proteins (Complement)IBA
03/2006
1KCNQ2 Potassium ChannelIBA
04/2004
1Sodium-Glucose Transport ProteinsIBA
02/2002

Therapy/Procedure

4Radiotherapy
04/2023 - 03/2016
1Drug Therapy (Chemotherapy)
05/2021