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Cancer Genetics
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1. Editorial Board
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1. Editorial Board
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1. Editorial Board
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1. Editorial Board
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1. Editorial Board
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1. Editorial Board
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1. Editorial Board
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2. Confirmation of damaging effect of MSH2 c.2634+1G>C mutation on splicing, its classification and implications for counseling
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Jelena Rakobradović, Ana Krivokuća, Stevo Jovandić, Vesna Kesić, Mirjana Branković-Magić.
2. 2019 USPS Statement of Ownership form
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2. Down-regulation of STIP1 regulate apoptosis and invasion of glioma cells via TRAP1/AKT signaling pathway
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Hongwei Yin, ZhiTong Deng, Xuetao Li, YanYan Li, ... Youxin Zhou.
2. A comparison of survival analysis methods for cancer gene expression RNA-Sequencing data
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Pichai Raman, Samuel Zimmerman, Komal S. Rathi, Laurence de Torrenté, ... Jessica C. Mar.
2. A familial germline mutation in KIT associated with achalasia, mastocytosis and gastrointestinal stromal tumors shows response to kinase inhibitors
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Alison L. Halpern, Robert J. Torphy, Martin D. McCarter, Cosimo G. Sciotto, ... William A. Robinson.
2. Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusions
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Peter Papenhausen, Carla A. Kelly, Zhenxi Zhang, James Tepperberg, ... Stuart Schwartz.
2. Establishing a human adrenocortical carcinoma (ACC)-specific gene mutation signature
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Chinmay Satish Rahane, Arne Kutzner, Klaus Heese.
3. A complex and cryptic intrachromosomal rearrangement generating the FIP1L1_PDGFRA in adult acute myeloid leukemia
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Nicoletta Coccaro, Luisa Anelli, Paola Orsini, Antonella Zagaria, ... Francesco Albano.
3. Cytogenetic profile of a representative cohort of young adults with de novo acute myéloblastic leukaemia in Morocco
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Nisrine Khoubila, Mounia Bendari, Nezha Hda, Mouna Lamchahab, ... Asmaa Quessar.
3. PD-L1 gene copy number and promoter polymorphisms regulate PD-L1 expression in tumor cells of non-small cell lung cancer patients
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Paweł Krawczyk, Anna Grenda, Kamila Wojas-Krawczyk, Marcin Nicoś, ... Janusz Milanowski.
3. A novel CHEK2 variant identified by next generation sequencing in an Indian family with hereditary breast cancer syndrome
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Pratibha Bhai, Renu Saxena, Samarth Kulshrestha, Ishwar Chander Verma.
3. Mutagenic players in ALL progression and their associated signaling pathways
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Saadiya Zia, Ramla Shahid.
3. Influence of bcr-3 PML-RARα transcript on outcome in Acute Promyelocytic Leukemia patients of Kashmir treated with all-trans retinoic acid and/or arsenic tri-oxide
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Shahid M. Baba, Zafar A. Shah, Arshad A. Pandith, Dil-Afroze, ... Zahoor Ahmad.
3. Novel rearrangements involving the RET gene in papillary thyroid carcinoma
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Julia Isabelle Staubitz, Arno Schad, Erik Springer, Krishnaraj Rajalingam, ... Thomas Johannes Musholt.
4. Potential of epigenetic events in human thyroid cancer
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Abdelkareem A. Ahmed, Mohammed Elmujtba Adam Essa.
4. ANKRD26-RET - A novel gene fusion involving RET in papillary thyroid carcinoma
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Julia Isabelle Staubitz, Thomas Johannes Musholt, Arno Schad, Erik Springer, ... Nils Hartmann.
4. Association of transcriptional levels of folate-mediated one-carbon metabolism-related genes in cancer cell lines with drug treatment response
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Dong-Joon Min, Suleyman Vural, Julia Krushkal.
4. Classic bladder exstrophy and adenocarcinoma of the bladder: Methylome analysis provide no evidence for underlying disease-mechanisms of this association
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Amit Sharma, Holger Fröhlich, Rong Zhang, Anne-Karoline Ebert, ... Heiko Reutter.
4. Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrations
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Zhenya Tang, Guilin Tang, Shimin Hu, Keyur P. Patel, ... L. Jeffrey Medeiros.
4. Down-regulation of miR-9 promotes epithelial mesenchymal transition via regulating anoctamin-1 (ANO1) in CRC cells
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Young Ran Park, Soo Teik Lee, Se Lim Kim, Shi Mao Zhu, ... Sang Wook Kim.
4. MiR-708-5p is inversely associated with EWS/FLI1 Ewing sarcoma but does not represent a prognostic predictor
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Gabriela Molinari Roberto, Gabriela Maciel Vieira, Lara Elis Alberici Delsin, Marcela de Oliveira Silva, ... María Sol Brassesco.
5. Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing
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Chun Hang Au, Dona N. Ho, Beca B.K. Ip, Thomas S.K. Wan, ... Edmond S.K. Ma.
5. Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT2A amplification in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS)
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Ali Sakhdari, Zhenya Tang, Chi Young Ok, Carlos E. Bueso-Ramos, ... Yang O. Huh.
5. Expression deregulation of DNA repair pathway genes in gastric cancer
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Shahzad Yousaf, Asad Ullah Khan, Zertashia Akram, Mahmood Akhtar Kayani, ... Ishrat Mahjabeen.
5. p53 major hotspot variants are associated with poorer prognostic features in hereditary cancer patients
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Cristina Fortuno, Tina Pesaran, Jill Dolinsky, Amal Yussuf, ... Amanda B. Spurdle.
5. Evaluating gene fusions in solid tumors – Clinical experience using an RNA based 53 gene next-generation sequencing panel
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Pavalan Selvam, Kevin Kelly, Andrew N Hesse, Daniel Spitzer, Honey V Reddi.
5. Novel pleiotropic BRCA2 pathogenic variants in Lebanese families
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Riyad El-Khoury, Mirna Hajj, Jinan Khraibani, Emma Audi, ... Chantal Farra.
5. Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)
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Jennelle C. Hodge, David Bosler, Lauren Rubinstein, Navid Sadri, Shashirekha Shetty.
6. A novel BRCA1 germline mutation promotes triple-negative breast cancer cells progression and enhances sensitivity to DNA damage agents
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Kun Xu, Yaqin Shi, Xin Wang, Yajuan Chen, ... Xiaoxiang Guan.
6. Variants in COL6A3 gene influence susceptibility to esophageal cancer in the Chinese population
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Yang Li, Yao Sun, Qinshuai Yang, Jiamin Wu, ... Tianbo Jin.
6. Characterization of a rarely reported STAT5B/RARA gene fusion in a young adult with newly diagnosed acute promyelocytic leukemia with resistance to ATRA therapy
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Jess F. Peterson, Rui R. He, Hassan Nayer, Raymund S. Cuevo, ... Linda B. Baughn.
6. PTPRD copy number variants and Ewing's sarcoma: Strengthening the association and therapeutic implications
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Avi Saskin, Kimberly Seath, Frederique Tihy, Emmanuelle Lemyre, ... Linlea Armstrong.
6. The benefits of a model of interval comprehensive assessments (MICA) in hereditary cancer Syndromes: Hereditary diffuse gastric cancer (HDGC) as an example
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Henry T. Lynch, Rosemary Nustas, Thamer Kassim, Carrie Snyder, ... Osama Diab.
6. A diagnosis of discernment: Identifying a novel ATRX mutation in myelodysplastic syndrome with acquired α-thalassemia
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Jedrzej Wykretowicz, Yeohan Song, Brooke McKnight, Sung Won Choi, ... Rami Khoriaty.
6. Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature
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Tác giả
Jess F. Peterson, Beth A. Pitel, Stephanie A. Smoley, James B. Smadbeck, ... Patricia T. Greipp.
7. Burkitt-like lymphoma in a pediatric patient with familial adenomatous polyposis
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Katie M. Strobel, Jacquelyn N. Crane, Kathryn L. Bradford, Yalda Naeini, ... Vivian Y. Chang.
7. Chronic myelomonocytic leukemia with ETV6-ABL1 rearrangement and SMC1A mutation
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Melissa H. Cessna, Prabakaran Paulraj, Benjamin Hilton, Kianoush Sadre-Bazzaz, ... Reha M. Toydemir.
7. Inherited cancer syndromes in 220 Italian ovarian cancer patients
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I. Carnevali, C. Riva, A.M. Chiaravalli, N. Sahnane, ... M.G. Tibiletti.
7. Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing
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Thomas P. Slavin, Bradford Coffee, Ryan Bernhisel, Jennifer Logan, ... Debora Mancini-DiNardo.
7. Aberrant methylation status of SPG20 promoter in hepatocellular carcinoma: A potential tumor metastasis biomarker
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Tác giả
Lifeng He, Xiaoxiao Fan, Yirun Li, Bin Cui, ... Hui Lin.
7. RBM10 truncation in astroblastoma in a patient with history of mandibular ameloblastoma: A case report
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Tác giả
Nazanin K. Majd, Nicolas R. Metrus, Fernando Santos-Pinheiro, Christopher R. Trevino, ... Marta Penas-Prado.
7. STK11 gene analysis reveals a significant number of splice mutations in Chinese PJS patients
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Yu-Liang Jiang, Zi-Ye Zhao, Bai-Rong Li, Hao Wang, ... Shou-Bin Ning.
8. Dysregulated expression of repetitive DNA in ER+/HER2- breast cancer
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Tác giả
Cihangir Yandım, Gökhan Karakülah.
8. RUNX1 deletion/amplification in therapy-related acute myeloid leukemia: A case report and review of the literature
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Tác giả
David Nguyen, Yuwen Li, Hana Safah, Theresa C. Brown
8. Concurrent chromothripsis events in a case of TP53 depleted acute myeloid leukemia with myelodysplasia-related changes
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Tác giả
D. Tolomeo, A. L'Abbate, A. Lonoce, P. D'Addabbo, ... C.T. Storlazzi.
8. Retrotransposon elements among initial sites of hepatitis B virus integration into human genome in the HepG2-NTCP cell infection model
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Ranjit Chauhan, Yoshimi Shimizu, Koichi Watashi, Takaji Wakita, ... Tomasz I Michalak.
8. PIP4K2A and PIP4K2C transcript levels are associated with cytogenetic risk and survival outcomes in acute myeloid leukemia
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Tác giả
Keli Lima, Juan Luiz Coelho-Silva, Gabriela Sarti Kinker, Diego Antonio Pereira-Martins, ... João Agostinho Machado-Neto.
8. Molecular evaluation of BRAF V600 mutation and its association with clinicopathological characteristics: First findings from Indian malignant melanoma patients
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Firoz Ahmad, Nagashree Avabhrath, Sripriya Natarajan, Jeenal Parikh, ... Bibhu Ranjan Das.
8. Genome-wide isoform-level analysis reveals tumor-specific isoforms for lung adenocarcinoma diagnosis and prognosis
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Hu Zhuhong, Bai Zhenyu, Chen Xiangyuan, Xu Tingzhen, Song Libin.
9. Single nucleotide polymorphism rs10889677 in miRNAs Let-7e and Let-7f binding site of IL23R gene is a strong colorectal cancer determinant: Report and meta-analysis
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Meysam Mosallaei, Miganoosh Simonian, Emran Esmaeilzadeh, Hadi Bagheri, ... Rasoul Salehi.
9. Clinical implications of clonal chromosomal abnormalities in Philadelphia negative cells in CML patients after treated with tyrosine kinase inhibitors
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Tác giả
Hongyu Ni, Xinlai Sun, Yin Xu, Derek Lyle, ... Jie-Gen Jiang.
9. Single-cell cloning of human T-cell lines reveals clonal variation in cell death responses to chemotherapeutics
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Tác giả
Kathleen Hanlon, Alex Thompson, Lorena Pantano, John N. Hutchinson, ... Ben A. Croker.
9. FANCM, RAD1, CHEK1 and TP53I3 act as BRCA-like tumor suppressors and are mutated in hereditary ovarian cancer
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Tác giả
Jaime L. Lopes, Sophia Chaudhry, Guilherme S. Lopes, Nancy K. Levin, Michael A. Tainsky.
9. Prognostic significance of CDC25C in lung adenocarcinoma: An analysis of TCGA data
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Tác giả
Zengfei Xia, Wen Ou-yang, Ting Hu, Ketao Du.
9. Genomic landscape of synchronous tubulovillous adenoma and multiple non-familial colon cancers from a single patient
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Tác giả
Kyung Kim, Su-Hye Choi, Jeeyun Lee, Won-Suk Lee.
10. A new prognostic factor of breast cancer: High carboxyl ester lipase expression related to poor survival
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Tác giả
Yingnan Cui, Yan Jiao, Keren Wang, Miao He, Zhaoying Yang.
10. Telomere length measurement in tumor and non‐tumor cells as a valuable prognostic for tumor progression
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Fatma Mehrez, Karim Bougatef, Elisa Delle Monache, Ivan Arisi, ... Silvia Bongiorni.
10. A unique case of complex variant translocation of t(6;9;22)(p22;q34;q11.2), der(19) in a newly diagnosed patient with chronic myeloid leukemia
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Tác giả
Rafiye Ciftciler, Emine Arzu Saglam, Ayten Inanc, Osman Ozcebe, Ibrahim Celalettin Haznedaroglu.
10. Circulating cell-free DNA integrity as a diagnostic and prognostic marker for breast and prostate cancers
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Benjamin Arko-Boham, Nii Ayite Aryee, Richard Michael Blay, Ewurama Dedea Ampadu Owusu, ... Nii Armah Adu-Aryee.
10. Identification of eight meta-signature miRNAs as potential biomarkers for oropharyngeal cancers
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Tác giả
Bo Li, Hee-moon Kyung.
10. Embryonal rhabdomyosarcoma in a patient with a germline CBL pathogenic variant
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Jianling Ji, Fariba Navid, Mathew C. Hiemenz, Maki Kaneko, ... Jaclyn A. Biegel.
11. Transcriptomics-based screening of molecular signatures associated with patients overall survival and their key regulators in subtypes of breast cancer
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Elaheh Eskandari, Jamshid Motalebzadeh.
11. Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group
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Andrew J. Carroll, Mary Shago, Fady M. Mikhail, Susana C. Raimondi, ... Nyla A. Heerema.
11. Non-invasive genotyping of metastatic colorectal cancer using circulating cell free DNA
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Xuemei Shi, Dzifa Y. Duose, Meenakshi Mehrotra, Michael A. Harmon, ... Rajyalakshmi Luthra.
11. Uptake of genetic testing for germline BRCA1/2 pathogenic variants in a predominantly Hispanic population
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Julia E. McGuinness, Meghna S. Trivedi, Thomas Silverman, Awilda Marte, ... Katherine D. Crew.
11. The clinical and prognostic significance of FIS1, SPI1, PDCD7 and Ang2 expression levels in acute myeloid leukemia
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Tác giả
Reham Abo Elwafa, Marwa Gamaleldin, Omar Ghallab.
11. Untouchable genes in the human genome: Identifying ideal targets for cancer treatment
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Tác giả
Ivan.P. Gorlov, Olga Y. Gorlova, Christopher I. Amos.
12. Progress in quantitative technique of circulating cell free DNA and its role in cancer diagnosis and prognosis
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Tác giả
Jia-Lei Weng, Manar Atyah, Chen-Hao Zhou, Ning Ren
12. Cytogenomic characterization of double minute heterogeneity in therapy related acute myeloid leukemia
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Tác giả
Prasad Koduru, Weina Chen, Barbara Haley, Kevin Ho, ... Kathleen Wilson.
12. Prevalence and founder effect of the BRCA1 p.(Val1833Met) variant in the Greek population, with further evidence for pathogenicity and risk modification
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Myrto Papamentzelopoulou, Paraskevi Apostolou, Florentia Fostira, Constantine Dimitrakakis, ... Irene Konstantopoulou.
12. Outcomes of disease-specific next-generation sequencing gene panel testing in adolescents and young adults with colorectal cancer
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Maureen E. Mork, Andrea Rodriguez, Sarah A. Bannon, Patrick M. Lynch, ... Eduardo Vilar.
12. Maintaining a methods database to optimize solid tumor tissue culture: Review of a 15-year database from a single institution
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Scott C. Smith, Lisa M. Warren, Linda D. Cooley.
13. Somatic mutation panels: Time to clear their names
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Tác giả
Amy M. Trottier, Marcela Cavalcante de Andrade Silva, Zejuan Li, Lucy A. Godley.
13. Corrigendum to “The cancer COMPASS: Navigating the functions of MLL complexes in cancer” [Cancer Genetics 208 (2015) pp. 178–191]
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Tác giả
David J. Ford, Andrew K. Dingwall.
14. Acute lymphoblastic leukemia in a nine-year-old girl with isodicentric chromosome 15 syndrome
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Tác giả
Roberto Antonucci, Nadia Vacca, Elisa Ghisu, Gloria Acquaviva, ... Claudio Fozza.