Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors. - Wikidata - awgldk - TriplyDB

Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.

Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.

http://www.wikidata.org/entity/Q38495093

about

A BEN-domain-containing protein associates with heterochromatin and represses transcription Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites Molecular basis for expression of common and rare fragile sites Common fragile sites: genomic hotspots of DNA damage and carcinogenesis BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution Variability in the incidence of miRNAs and genes in fragile sites and the role of repeats and CpG islands in the distribution of genetic material.Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites.Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?Laser ionization mass spectrometry in oral squamous cell carcinoma.Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes.Schizophrenia, cancer and obstetric complications in an evolutionary perspective-an empirically based hypothesis A Synthetic Lethal Screen Identifies DNA Repair Pathways that Sensitize Cancer Cells to Combined ATR Inhibition and Cisplatin Treatments.Is mammalian chromosomal evolution driven by regions of genome fragility?Chromosomal instability in oral cancer cells.Replication stress induces tumor-like microdeletions in FHIT/FRA3B DNA polymerases and cancer.Critical pathways in cellular senescence and immortalization revealed by gene expression profiling.The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome.Translesion DNA synthesis in the context of cancer research.Molecular characterization of common fragile sites as a strategy to discover cancer susceptibility genes.Genome position and gene amplification Oncogene-induced replication stress preferentially targets common fragile sites in preneoplastic lesions. A genome-wide study.Characterization of chromosomal translocation breakpoint sequences in solid tumours: "an in silico analysis".Genomic vulnerability to LINE-1 hypomethylation is a potential determinant of the clinicogenetic features of multiple myeloma.Significant Role of Segmental Duplications and SIDD Sites in Chromosomal Translocations of Hematological Malignancies: A Multi-parametric Bioinformatic Analysis.

P2860

Q24337843-CF758E55-0ED5-4EA9-94B1-1E763F76473C Q24536351-75CA5163-214C-4D10-8815-6C2D59A41EFC Q24622097-9EA22BF3-8A0F-4936-A615-86C2C6B3E091 Q24653358-D7C2A54F-5473-4148-96CB-23089FFF4145 Q26825040-BDECA76C-6F9C-4443-B540-53E995C77412 Q28508100-FC7DA1BE-662E-4037-B64E-B22D32CED2F7 Q28754427-4CC7AF67-91A4-43CE-A5C1-260F7046FC5A Q33612207-50B7FEE6-53CC-4BA4-8CA5-315250AF90C8 Q33960440-156F9763-A07E-4B19-BA3C-CE7522013B01 Q34212683-F3B9171F-D9FD-4775-A225-DCAE9AB92ADD Q34515728-BFA1D42E-BD47-44CF-8B7D-58C3E4F21433 Q35013394-936EE3B6-EE7A-424E-8D49-506E5356E600 Q35056705-08AA0A80-903B-49D3-9659-32B61D534EF0 Q35144224-6584E1B8-0265-4730-9DC7-F1B0B8A641DD Q35627868-CDAF9183-F491-48FE-9509-FD7C6A03FBA1 Q35629768-6FD8F462-FC23-469F-A1B1-F4D903C60C92 Q36019105-9E7F2498-AC0F-41B7-84B3-25AC5B96D150 Q36423451-0F67C13C-26D7-48B8-9171-2F8A77DA7213 Q37084895-D391FFF9-2069-4B32-BE4C-19457B75E686 Q37246647-970CEB5B-D1ED-4CE6-A461-862C9018B2DA Q37273647-94D33153-EA76-4BBC-9E0C-DE0C702477F8 Q37952001-35F5F9A1-ADA9-4D2D-861A-A3FE26E9647A Q38250822-945F970E-2D03-43A5-8D9E-7FD9C635135D Q38606305-DA8E0968-E32C-48F5-9760-CB601F0354F5 Q40034793-7849205F-174F-4A97-9570-958EF6800210 Q40343514-F3BFF98A-37A8-4AA1-925A-6BBFB0724DA9 Q40914883-C06DDA4E-4206-41F6-9BB0-BDD96632C87B Q52796956-B1A2973A-8310-47B0-9791-FD74A63CA825

P2860

Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.

http://www.wikidata.org/entity/Q38495093

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年論文

@yue

2002年論文

@zh-hant

2002年論文

@zh-hk

2002年論文

@zh-mo

2002年論文

@zh-tw

2002年论文

@wuu

2002年论文

@zh

2002年论文

@zh-cn

name

Cloning and characterization o ...... ently deleted in human tumors.

@en

type

label

Cloning and characterization o ...... ently deleted in human tumors.

@en

prefLabel

Cloning and characterization o ...... ently deleted in human tumors.

@en

P1433

Q38495093-0E78FA45-EEAD-4E5F-8F43-E1B25EFA9F2B

P1476

Q38495093-3418A2B4-14AC-4716-9C3C-914F444DDA61

P2093

Q38495093-04904E28-9F2F-4241-8E98-6AF49D5EF53B

Q38495093-0F15706E-BAA6-43BF-8145-E77027776B75

Q38495093-23B0A093-A016-4889-8009-E9529D7C103C

Q38495093-C1850CC8-B6FC-4ABB-9340-E5A2F6EB5A55

Q38495093-CEC3853D-7FCF-444D-9C79-02945779E7E1

Q38495093-E7EEEB1C-F678-4DEC-B4A5-011EDEAF8AE3

P2860

Q38495093-0EDF453E-8181-4E98-88DC-B03FF2A91AA9

Q38495093-11CA4AC7-E38A-445E-88E4-668A140DEBCE

Q38495093-1EB66AED-3987-4430-B367-1D02B5889F86

Q38495093-1FFA169C-3F6E-42D1-9F5F-960FB2A81B3A

Q38495093-28141F2F-BB9F-4EFF-B9D9-376560E3BD96

Q38495093-3FA676A0-1C19-40EC-9C0A-2C5C79E352EA

Q38495093-4636F8DD-B892-4072-8A00-71D0F22DD1E3

Q38495093-4BAC4B41-67E0-4347-B571-79596A987190

Q38495093-508FCB96-2DA7-46E9-B0CF-7665588BDB84

Q38495093-5C7EE052-8656-475A-B867-6A65F375F653

P2888

Q38495093-AA81ACCD-DA35-44EF-BF73-8864C98E4BB1

P304

Q38495093-E2F2C85F-974E-4325-868C-8445D5395830

P31

Q38495093-D6B4EA64-22A3-4B94-B043-961C0FDE9638

P356

Q38495093-84C06715-6E17-486B-A545-ED1CB094F34E

P407

Q38495093-C2182429-610D-4132-881B-CD81DD846363

P433

Q38495093-0DF3945A-92A3-4661-9570-C9D7E11AA890

P478

Q38495093-6C5E72AD-41F9-4D4E-92A7-00F71C29C169

P50

Q38495093-3D503F5E-C972-49AC-B23B-604541012BD9

Q38495093-5771342E-584F-487E-8379-7774D711E325

P577

Q38495093-ED80B6B0-199D-4146-A803-FDA6B898E6C3

P5875

Q38495093-89550BC3-0A33-462F-8F4E-AD36296D7D3D

P6179

Q38495093-F5D53F59-5987-49E9-9E96-A7E37028048E

P698

Q38495093-6C2FB773-88CF-4859-85F1-F6EF5ACAE63A

P356

P1433

P1476

Cloning and characterization o ...... ently deleted in human tumors.

@en

P2093

Chiara Magnanini

http://www.w3.org/2001/XMLSchema#string

Cristina Morelli

http://www.w3.org/2001/XMLSchema#string

David I Smith

http://www.w3.org/2001/XMLSchema#string

Efthimia Karayianni

http://www.w3.org/2001/XMLSchema#string

Erik Thorland

http://www.w3.org/2001/XMLSchema#string

Giuseppe Barbanti-Brodano

http://www.w3.org/2001/XMLSchema#string

P2860

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

A human homolog of the Saccharomyces cerevisiae REV3 gene, which encodes the catalytic subunit of DNA polymerase zeta

The human homologue of the Drosophila tailless gene (TLX): characterization and mapping to a region of common deletion in human lymphoid leukemia on chromosome 6q21

Characterization of the human TESTIN gene localized in the FRA7G region at 7q31.2

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites

Transcriptional map of chromosome region 6q16-->q21.

Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia.

Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability.

P2888

P304

7266-7276

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/SJ.ONC.1205573

http://www.w3.org/2001/XMLSchema#string

P407

P433

47

http://www.w3.org/2001/XMLSchema#string

P478

21

http://www.w3.org/2001/XMLSchema#string

P50

Massimo Negrini

P577

2002-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

11088598

http://www.w3.org/2001/XMLSchema#string

P6179

1016592737

http://www.w3.org/2001/XMLSchema#string

P698

12370818

http://www.w3.org/2001/XMLSchema#string