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1
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations
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Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations

Ajore, Ram ; Raiser, David ; McConkey, Marie ; Jöud, Magnus ; Boidol, Bernd ; Mar, Brenton ; Saksena, Gordon ; Weinstock, David M ; Armstrong, Scott ; Ellis, Steven R ; Ebert, Benjamin L ; Nilsson, Björn

EMBO molecular medicine, 2017-04, Vol.9 (4), p.498-507 [Periódico revisado por pares]

England: John Wiley and Sons Inc

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2
Identification of potential diagnostic and prognostic biomarkers for LUAD based on TCGA and GEO databases
Identification of potential diagnostic and prognostic biomarkers for LUAD based on TCGA and GEO databases
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Identification of potential diagnostic and prognostic biomarkers for LUAD based on TCGA and GEO databases

Zheng, Qiangqiang ; Min, Shihui ; Zhou, Qinghua

Bioscience reports, 2021-06, Vol.41 (6) [Periódico revisado por pares]

England: Portland Press Ltd The Biochemical Society

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3
Guiding deployment of resistance in cereals using evolutionary principles
Guiding deployment of resistance in cereals using evolutionary principles
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Guiding deployment of resistance in cereals using evolutionary principles

Burdon, Jeremy J. ; Barrett, Luke G. ; Rebetzke, Greg ; Thrall, Peter H.

Evolutionary applications, 2014-06, Vol.7 (6), p.609-624 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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4
GCH1-regulated miRNAs are potential targets for microglial activation in neuropathic pain
GCH1-regulated miRNAs are potential targets for microglial activation in neuropathic pain
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GCH1-regulated miRNAs are potential targets for microglial activation in neuropathic pain

Jia, Shu ; Chen, Guowu ; Liang, Yanhu ; Liang, Xiao ; Meng, Chunyang

Bioscience reports, 2021-09, Vol.41 (9), p.1 [Periódico revisado por pares]

England: Portland Press Ltd The Biochemical Society

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5
LncIRS1 controls muscle atrophy via sponging miR‐15 family to activate IGF1‐PI3K/AKT pathway
LncIRS1 controls muscle atrophy via sponging miR‐15 family to activate IGF1‐PI3K/AKT pathway
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LncIRS1 controls muscle atrophy via sponging miR‐15 family to activate IGF1‐PI3K/AKT pathway

Li, Zhenhui ; Cai, Bolin ; Abdalla, Bahareldin Ali ; Zhu, Xuenong ; Zheng, Ming ; Han, Peigong ; Nie, Qinghua ; Zhang, Xiquan

Journal of cachexia, sarcopenia and muscle, 2019-04, Vol.10 (2), p.391-410 [Periódico revisado por pares]

Germany: John Wiley & Sons, Inc

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6
Targeted gene silencing in vivo by platelet membrane-coated metal-organic framework nanoparticles
Targeted gene silencing in vivo by platelet membrane-coated metal-organic framework nanoparticles
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Targeted gene silencing in vivo by platelet membrane-coated metal-organic framework nanoparticles

Zhuang, Jia ; Gong, Hua ; Zhou, Jiarong ; Zhang, Qiangzhe ; Gao, Weiwei ; Fang, Ronnie H ; Zhang, Liangfang

Science advances, 2020-03, Vol.6 (13), p.eaaz6108 [Periódico revisado por pares]

United States: American Association for the Advancement of Science

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7
CXCL2/10/12/14 are prognostic biomarkers and correlated with immune infiltration in hepatocellular carcinoma
CXCL2/10/12/14 are prognostic biomarkers and correlated with immune infiltration in hepatocellular carcinoma
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CXCL2/10/12/14 are prognostic biomarkers and correlated with immune infiltration in hepatocellular carcinoma

Lin, Tong ; Zhang, E ; Mai, Pei-Pei ; Zhang, Ying-Zhao ; Chen, Xiang ; Peng, Li-Sheng

Bioscience reports, 2021-06, Vol.41 (6) [Periódico revisado por pares]

England: Portland Press Ltd The Biochemical Society

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8
Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system
Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system
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Enhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery system

Zhang, Yu ; Li, Hui ; Min, Yi-Li ; Sanchez-Ortiz, Efrain ; Huang, Jian ; Mireault, Alex A ; Shelton, John M ; Kim, Jiwoong ; Mammen, Pradeep P A ; Bassel-Duby, Rhonda ; Olson, Eric N

Science advances, 2020-02, Vol.6 (8), p.eaay6812-eaay6812 [Periódico revisado por pares]

United States: American Association for the Advancement of Science

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9
The dark matter of the cancer genome: aberrations in regulatory elements, untranslated regions, splice sites, non‐coding RNA and synonymous mutations
The dark matter of the cancer genome: aberrations in regulatory elements, untranslated regions, splice sites, non‐coding RNA and synonymous mutations
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The dark matter of the cancer genome: aberrations in regulatory elements, untranslated regions, splice sites, non‐coding RNA and synonymous mutations

Diederichs, Sven ; Bartsch, Lorenz ; Berkmann, Julia C ; Fröse, Karin ; Heitmann, Jana ; Hoppe, Caroline ; Iggena, Deetje ; Jazmati, Danny ; Karschnia, Philipp ; Linsenmeier, Miriam ; Maulhardt, Thomas ; Möhrmann, Lino ; Morstein, Johannes ; Paffenholz, Stella V ; Röpenack, Paula ; Rückert, Timo ; Sandig, Ludger ; Schell, Maximilian ; Steinmann, Anna ; Voss, Gjendine ; Wasmuth, Jacqueline ; Weinberger, Maria E ; Wullenkord, Ramona

EMBO molecular medicine, 2016-05, Vol.8 (5), p.442-457 [Periódico revisado por pares]

England: EMBO Press

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10
A rare case of Bardet-Biedl syndrome with BBS12 gene
A rare case of Bardet-Biedl syndrome with BBS12 gene
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A rare case of Bardet-Biedl syndrome with BBS12 gene

Jain, Gunjan ; Kumari, Sarswati ; Jain, Vaibhav

Indian journal of ophthalmology, 2023-10, Vol.3 (4), p.1043 [Periódico revisado por pares]

Medknow Publications and Media Pvt. Ltd

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