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/vufind/Search/Results?lookfor=%22Ribonuclease+HII%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22Ribonuclease+HII%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
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PubPharm (212)
1
RNASEH2C c.194G>A is a Chinese-specific founder mutation in three unrelated patients with Aicardi-Goutières syndrome 3
enthalten in:
Clinical genetics
| 2023
von
Wang, Q.
|
Han, Y.
|
Zhou, X.
| +4
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2
Altered DNA methylation and gene expression predict disease severity in patients with Aicardi-Goutières syndrome
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2023
von
Garau, J.
|
Charras, A.
|
Varesio, C.
| +8
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3
CRISPR/Cas9-mediated targeted knock-in of large constructs using nocodazole and RNase HII
enthalten in:
Scientific reports
| 2023
von
Eghbalsaied, S.
|
Kues, W.
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4
Ribonuclease H2 Subunit A Preserves Genomic Integrity and Promotes Prostate Cancer Progression
enthalten in:
Cancer research communications
| 2022
von
Kimura, N.
|
Takayama, K.
|
Yamada, Y.
| +3
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5
Depletion of RNASEH2 Activity Leads to Accumulation of DNA Double-strand Breaks and Reduced Cellular Survivability in T Cell Leukemia
enthalten in:
Journal of molecular biology
| 2022
von
Ghosh, D.
|
Kumari, S.
|
Raghavan, S.
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6
Decrease in RNase HII and Accumulation of lncRNAs/DNA Hybrids : A Causal Implication in Psoriasis?
enthalten in:
Biomolecules
| 2022
von
Mehmetbeyoglu, E.
|
Kianmehr, L.
|
Borlu, M.
| +5
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7
RB1 loss overrides PARP inhibitor sensitivity driven by RNASEH2B loss in prostate cancer
enthalten in:
Science advances
| 2022
von
Miao, C.
|
Tsujino, T.
|
Takai, T.
| +10
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8
Hypoxia-induced RNASEH2A limits activation of cGAS-STING signaling in HCC and predicts poor prognosis
enthalten in:
Tumori
| 2022
von
Zhao, F.
|
Liu, A.
|
Gong, X.
| +7
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9
Long noncoding RNA LINC01287 promotes proliferation and inhibits apoptosis of lung adenocarcinoma cells via the miR-3529-5p/RNASEH2A axis under the competitive endogenous RNA pattern
enthalten in:
Environmental toxicology
| 2021
von
Zhang, J.
|
Ma, D.
|
Kang, H.
| +2
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10
Atypical phenotype? The answer's in the genotype : AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency
enthalten in:
Rheumatology (Oxford, England)
| 2021
von
Boulanger, C.
|
Chatzis, O.
|
Nolf, D.
| +4
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212
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Nucleic acids research
10
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7
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Thema
212
EC 3.1.26.-
212
ribonuclease HII
209
EC 3.1.26.4
209
Ribonuclease H
206
Journal Article
137
Research Support, Non-U.S. Gov't
50
9007-49-2
50
DNA
42
EC 3.1.-
39
Research Support, N.I.H., Extramural
34
Ribonucleotides
29
ribonuclease HI
24
63231-63-0
24
RNA
21
Research Support, N.I.H., Intramural
20
EC 2.7.7.7
18
Exodeoxyribonucleases
15
EC 2.7.7.-
14
Bacterial Proteins
13
Archaeal Proteins
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Erscheinungszeitraum
180
2000-
8
1900-1999
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Englisch
2
Spanisch
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