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1
المؤلفون: Arun Pradhan, Kebola Wahengbam, Chang-hu Du, Abdullah Mahmood Ali, Thiyam Ramsingh Singh, Qishen Pang, Arleen D. Auerbach, Amom Ruhikanta Meetei, Elke Grassman, Jie Li
المصدر: Blood. 119:3285-3294
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, DNA Repair, Ubiquitin binding, Hematopoiesis and Stem Cells, DNA damage, DNA repair, Immunology, Biology, Biochemistry, Ubiquitin, Fanconi anemia, hemic and lymphatic diseases, medicine, Humans, Protein Interaction Domains and Motifs, Cells, Cultured, Fanconi Anemia Complementation Group A Protein, Protein Stability, nutritional and metabolic diseases, Zinc Fingers, Cell Biology, Hematology, DNA Repair Pathway, medicine.disease, Chromatin, Fanconi Anemia Complementation Group Proteins, FANCA, Fanconi Anemia, biology.protein, DNA Damage, Protein Binding, Signal Transduction
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75577c61d6e7da497125036d7ef69dc7
https://doi.org/10.1182/blood-2011-10-385963 -
2
المؤلفون: Amom Ruhikanta Meetei, Andrew J. Pierce, Xiaofeng Zheng, Dorina Saro, Patrick Sung, Yong Xiong, Chang hu Du, Aristidis Sachpatzidis, Thiyam Ramsing Singh, Kebola Wahengbam, Michael W. Killen, Abdullah Mahmood Ali
المصدر: Molecular Cell. 37(6):879-886
مصطلحات موضوعية: DNA Replication, congenital, hereditary, and neonatal diseases and abnormalities, Fanconi anemia, complementation group C, DNA damage, DNA repair, Biology, Article, Genomic Instability, Evolution, Molecular, Fanconi anemia, hemic and lymphatic diseases, FANCD2, medicine, Humans, FANCM, Replication protein A, Molecular Biology, DNA Helicases, nutritional and metabolic diseases, Cell Biology, Chromatin Assembly and Disassembly, medicine.disease, Molecular biology, Chromatin, Fanconi Anemia, Protein Multimerization, Signal Transduction
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المؤلفون: Paul R. Andreassen, Qiang Fan, Amom Ruhikanta Meetei, Valeria Busygina, Patrick Sung, Chang hu Du, Thiyam Ramsing Singh, Abdullah Mahmood Ali, Steven Raynard
المصدر: Genes & Development. 22:2856-2868
مصطلحات موضوعية: Genome instability, congenital, hereditary, and neonatal diseases and abnormalities, DNA repair, nutritional and metabolic diseases, Helicase, Biology, medicine.disease, Molecular biology, RMI1, Genetics, medicine, biology.protein, Holliday junction, Bloom syndrome, Chromosome breakage, Homologous recombination, Developmental Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7f09f1714abdba730bd13b5f0bf695da
https://doi.org/10.1101/gad.1725108 -
4
المؤلفون: Sheba Agarwal, Paul R. Andreassen, Thiyam Ramsing Singh, Elke Grassman, Michael Jansen, Qiang Fan, Hans Joenje, Abdullah Mahmood Ali, Barbara C. Godthelp, Martin A. Rooimans, Amom Ruhikanta Meetei, Kebola Wahengbam, David A. Williams, Chang-hu Du, Sietske T. Bakker, Jurgen Steltenpool, Johan P. de Winter
المساهمون: Internal medicine, Human genetics, Pediatric surgery, CCA - Oncogenesis
المصدر: Blood, 114(1), 174-180. American Society of Hematology
Singh, T R, Bakker, S D, Agarwal, S, Jansen, M H A, Grassman, E, Godthelp, B C, Ali, A M, Du, C, Rooimans, M A, Fan, Q, Wahengbam, K, Steltenpool, J, Andreassen, P R, Williams, D J, Joenje, H, de Winter, J P & Meetei, AR 2009, ' Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M ', Blood, vol. 114, no. 1, pp. 174-180 . https://doi.org/10.1182/blood-2009-02-207811مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Ultraviolet Rays, medicine.drug_class, Immunology, Mutant, Drug Resistance, Gene Expression, Biology, Transfection, medicine.disease_cause, Radiation Tolerance, Biochemistry, Red Cells, Iron, and Erythropoiesis, Fanconi anemia, Cell Line, Tumor, hemic and lymphatic diseases, FANCD2, medicine, Humans, FANCM, Adenosine Triphosphatases, Mutation, Fanconi Anemia Complementation Group A Protein, Fanconi Anemia Complementation Group D2 Protein, DNA Helicases, Ubiquitination, nutritional and metabolic diseases, Cell Biology, Hematology, medicine.disease, Molecular biology, Recombinant Proteins, FANCA, Complementation, Cross-Linking Reagents, Fanconi Anemia, Camptothecin, Topoisomerase inhibitor
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::795792d2cc400278055d9fda2000a301
https://research.vumc.nl/en/publications/1c5e8386-2198-4c1a-afa6-1e2547adb54b -
5
المؤلفون: Chang-hu, Du, Zhuang, Wu, Jun, Xu
المصدر: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases. 29(9)
مصطلحات موضوعية: Mice, Inbred BALB C, Lung Neoplasms, Mice, Nude, Transfection, Combined Modality Therapy, Recombinant Proteins, Adenoviridae, Mice, Doxorubicin, Drug Resistance, Neoplasm, Cell Line, Tumor, Carcinoma, Squamous Cell, Animals, Tumor Suppressor Protein p53, Neoplasm Transplantation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::5f596f29ed76325accc373844248d9a8
https://pubmed.ncbi.nlm.nih.gov/17129471 -
6
المؤلفون: Chang-hu, Du, Jun, Xu, Nan-shan, Zhong
المصدر: Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 26(10)
مصطلحات موضوعية: Models, Molecular, Lung Neoplasms, Base Sequence, Molecular Sequence Data, Humans, Point Mutation, Amino Acid Sequence, Tumor Suppressor Protein p53, Codon, Protein Structure, Tertiary
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::78c5e7710ee8a38291150ec051708861
https://pubmed.ncbi.nlm.nih.gov/17062352 -
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المؤلفون: Chang-hu, Du, Jun, Xu, Nan-shan, Zhong
المصدر: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases. 28(3)
مصطلحات موضوعية: Lung Neoplasms, Phenotype, Drug Resistance, Neoplasm, 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide, Tumor Cells, Cultured, Humans, Point Mutation, Apoptosis, Genes, p53, Transfection
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::46e67dcea9672aa4ea828d2bd32cf948
https://pubmed.ncbi.nlm.nih.gov/15854413 -
8
المصدر: Blood. 110:837-837
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, DNA damage, Kinase, Immunology, nutritional and metabolic diseases, Cell Biology, Hematology, Cell cycle, Biology, medicine.disease, Biochemistry, Cell biology, Fanconi anemia, hemic and lymphatic diseases, FANCD2, Cancer research, medicine, Monoubiquitination, Phosphorylation, FANCM
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8081199ef918dbbd395ed06427e412ed
https://doi.org/10.1182/blood.v110.11.837.837
