المؤلفون: Amom Ruhikanta Meetei, Michael M. Seidman, Kebola Wahengbam, Arun Pradhan, Manikandan Paramasivam, Abdullah Mahmood Ali, Thiyam Ramsing Singh

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28e4184fae5977477d041c5a7b84ac3f
https://doi.org/10.1158/0008-5472.c.6504926.v1

المؤلفون: Amom Ruhikanta Meetei, Michael M. Seidman, Kebola Wahengbam, Arun Pradhan, Manikandan Paramasivam, Abdullah Mahmood Ali, Thiyam Ramsing Singh

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a1ccd220c7484cb50505b640ac59b1
https://doi.org/10.1158/0008-5472.22397852.v1

المؤلفون: Amom Ruhikanta Meetei, Michael M. Seidman, Kebola Wahengbam, Arun Pradhan, Manikandan Paramasivam, Abdullah Mahmood Ali, Thiyam Ramsing Singh

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf64ceaeba909bfeec8f719f2265517
https://doi.org/10.1158/0008-5472.22397849

المؤلفون: Abdullah Mahmood Ali, Amom Ruhikanta Meetei, Arun Pradhan, Kebola Wahengbam, Thiyam Ramsing Singh

المصدر: Journal of Biological Chemistry. 288:33500-33508

مصطلحات موضوعية: Genome instability, congenital, hereditary, and neonatal diseases and abnormalities, RecQ helicase, Mutation, Missense, Cell Cycle Proteins, Spindle Apparatus, Protein Serine-Threonine Kinases, DNA and Chromosomes, Biology, Biochemistry, RecQ-Mediated Genome Instability Protein 2, RMI1, Chromosomal Instability, Serine, medicine, Humans, Bloom syndrome, Phosphorylation, Molecular Biology, Mitosis, RecQ Helicases, Nuclear Proteins, nutritional and metabolic diseases, Cell Biology, Protein-Tyrosine Kinases, medicine.disease, Molecular biology, Spindle apparatus, Cell biology, DNA-Binding Proteins, Spindle checkpoint, HEK293 Cells, Amino Acid Substitution, DNA Topoisomerases, Type I, Multiprotein Complexes, M Phase Cell Cycle Checkpoints, Carrier Proteins, HeLa Cells

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d5c30d1b0a82e0c46c264e8a0fae73e
https://doi.org/10.1074/jbc.m113.470823

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

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4c0f17dffe3a5197e5d84acbfceecd1

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-2009-02-207811

مصطلحات 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