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# proj.
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# Ann.
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| @dpavot |
29538454 |
Here, we identify tumor-associated calcium signal transducer 2 (TACSTD2), one of the most downregulated genes in primary HCC tissue, as a host factor that interacts with CLDN1 and OCLN and regulates t |
227 Bytes |
2020-02-26 |
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29666464 |
We report a case with novel AARS2 gene mutations with developed striking cerebellar atrophy and leukoencephalopathy, which helps to further understand the clinical and genetic heterogeneity of AARS2-L |
201 Bytes |
2020-02-26 |
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| @dpavot |
29950560 |
Here we show, using whole-exome and cancer gene panel sequencing of 79 aGCTs from two independent cohorts, that truncating mutation of the histone lysine methyltransferase gene KMT2D (also known as ML |
407 Bytes |
2020-02-26 |
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| @dpavot |
29956815 |
In the present study, we found that the Kankl gene was significantly downregulated in human lung cancer and lung cancer cells. |
126 Bytes |
2020-02-26 |
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| @dpavot |
29992558 |
Only a few genes, including SMARCA4, SMO, ZNF44 and CHD2, were recurrently and specifically mutated in the SS group, confirming the low recurrence of common mutations in this tumor. |
181 Bytes |
2020-02-26 |
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| @dpavot |
30030762 |
Furthermore, a high level of FEZF1 in patients with glioma acted as an independent biomarker to predict reduced survival (P = 0.026). |
133 Bytes |
2020-02-26 |
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| @dpavot |
30128822 |
Promoters of several genes from the KEGG HER2+ breast cancer pathway and 11 signaling pathways linked to 6 hallmarks of cancer contain the NRF1 motif. |
150 Bytes |
2020-02-26 |
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30361777 |
Malfunctioning of nucleoporins is well known in human malignancies, such as gene fusions of NUP214 and NUP98 in hematological neoplasms and overexpression of NUP88 in a variety of human cancers. |
194 Bytes |
2020-02-26 |
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| @dpavot |
30486759 |
The VDR gene FokI CT/TT genotype was associated with an increased papillary thyroid cancer risk (CT vs CC: odds ratio = 1.71, 95% confidence interval = 1.15-2.76, p = 0.028; TT vs CC: odds ratio = 2.4 |
411 Bytes |
2020-02-26 |
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| @dpavot |
30535804 |
Although a digenic inheritance pattern of hearing impairment has been reported for heterozygous missense variants of ATP2B2 and CDH23, our findings indicate a monogenic cause of hearing impairment in |
247 Bytes |
2020-02-26 |
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