Microcephalin is a new novel prognostic indicator in breast cancer associated with BRCA1 inactivation.
about
The overexpression of MCPH1 inhibits cell growth through regulating cell cycle-related proteins and activating cytochrome c-caspase 3 signaling in cervical cancerCiliogenesis and the DNA damage response: a stressful relationshipA meta-analysis of multiple matched copy number and transcriptomics data sets for inferring gene regulatory relationships.MCPH1: a window into brain development and evolution.Deregulation of microcephalin and ASPM expression are correlated with epithelial ovarian cancer progression.Primary microcephaly gene MCPH1 shows a novel molecular biomarker of human renal carcinoma and is regulated by miR-27a.Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma.Phosphorylation of the BRCA1 C terminus (BRCT) repeat inhibitor of hTERT (BRIT1) protein coordinates TopBP1 protein recruitment and amplifies ataxia telangiectasia-mutated and Rad3-related (ATR) SignalingA high-throughput assay to identify modifiers of premature chromosome condensation.ASPM and microcephalin expression in epithelial ovarian cancer correlates with tumour grade and survivalMcph1/Brit1 deficiency promotes genomic instability and tumor formation in a mouse modelTargeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.Immunoprofile from tissue microarrays to stratify familial breast cancer patientsBRIT1 regulates p53 stability and functions as a tumor suppressor in breast cancer.The DNA damage response molecule MCPH1 in brain development and beyond.Overexpression of MCPH1 inhibits uncontrolled cell growth by promoting cell apoptosis and arresting the cell cycle in S and G2/M phase in lung cancer cellsFrequent alterations of MCPH1 and ATM are associated with primary breast carcinoma: clinical and prognostic implications.Expression of proteins involved in DNA damage response in familial and sporadic breast cancer patients.Expression of DNA Damage Response Proteins and Associations with Clinicopathologic Characteristics in Chinese Familial Breast Cancer Patients with Mutations
P2860
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P2860
Microcephalin is a new novel prognostic indicator in breast cancer associated with BRCA1 inactivation.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en-gb
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@nl
type
label
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en-gb
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@nl
prefLabel
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en-gb
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@nl
P2093
P2860
P50
P1476
Microcephalin is a new novel p ...... iated with BRCA1 inactivation.
@en
P2093
Clare Walker
Julie Richardson
Rawiah Alisary
Sandra M Bell
P2860
P2888
P304
P356
10.1007/S10549-010-1019-4
P407
P577
2010-07-15T00:00:00Z
P5875
P6179
1048546004