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Integrated metatranscriptomic and metagenomic analyses of stratified microbial assemblages in the open ocean
Shi, Yanmei, Tyson, Gene W, Eppley, John M, DeLong, Edward F
Published in The ISME Journal (01.06.2011)
Published in The ISME Journal (01.06.2011)
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Background-Suppressed High-Throughput Mid-Infrared Photothermal Microscopy via Pupil Engineering
Zong, Haonan, Yurdakul, Celalettin, Bai, Yeran, Zhang, Meng, Ünlü, M. Selim, Cheng, Ji-Xin
Published in ACS photonics (17.11.2021)
Published in ACS photonics (17.11.2021)
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Membrane Proteome-Wide Response to the Antifungal Drug Clotrimazole in Candida glabrata: Role of the Transcription Factor CgPdr1 and the Drug:H+ Antiporters CgTpo1_1 and CgTpo1_2
Pais, Pedro, Costa, Catarina, Pires, Carla, Shimizu, Kiminori, Chibana, Hiroji, Teixeira, Miguel C.
Published in Molecular & cellular proteomics (01.01.2016)
Published in Molecular & cellular proteomics (01.01.2016)
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Identification of crucial drought-tolerant genes of barley through comparative transcriptomic analysis and yeast-based stress assay
He, Xiaoyan, Su, Congjun, Zhang, Xinyi, Shi, Zhaoxia, Wang, Yanjie, Peng, Huandi, Fang, Shuying, Chen, Xinyu, Yin, Huayan, Zeng, Jianbin, Mu, Ping
Published in Frontiers in genetics (09.12.2024)
Published in Frontiers in genetics (09.12.2024)
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Shared and distinct brain activation patterns of acupoints HT7, ST36, and KI4: a task-based fMRI study
Hu, Liyu, Zhang, Jinhuan, Wu, Xiaoxiong, Huang, Xingxian, Li, Xinbei, Liu, Xingchen, Lyu, Hanqing, Yang, Nan, Xu, Jinping, Yu, Haibo
Published in Frontiers in neurology (26.06.2025)
Published in Frontiers in neurology (26.06.2025)
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Another Reason for Using Caffeine in Dermocosmetics: Sunscreen Adjuvant
Rosado, Catarina, Tokunaga, Viviane Kaori, Sauce, Rafael, de Oliveira, Camila Areias, Sarruf, Fernanda Daud, Parise-Filho, Roberto, Maurício, Elisabete, de Almeida, Tânia Santos, Velasco, Maria Valéria Robles, Baby, André Rolim
Published in Frontiers in physiology (03.05.2019)
Published in Frontiers in physiology (03.05.2019)
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Intrinsic Disorder in the Human Tear Proteome
Taylor Gonzalez, David J., Djulbegovic, Mak, Antonietti, Michael, Cordova, Matthew, Dayhoff, Guy W., Mattes, Robby, Galor, Anat, Uversky, Vladimir N., Karp, Carol L.
Published in Investigative ophthalmology & visual science (01.08.2023)
Published in Investigative ophthalmology & visual science (01.08.2023)
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A new peptide (Ruviprase) purified from the venom of Daboia russelii russelii shows potent anticoagulant activity via non-enzymatic inhibition of thrombin and factor Xa
Thakur, Rupamoni, Kumar, Ashok, Bose, Biplab, Panda, Dulal, Saikia, Debashree, Chattopadhyay, Pronobesh, Mukherjee, Ashis K.
Published in Biochimie (01.10.2014)
Published in Biochimie (01.10.2014)
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Single SNP- and pathway-based genome-wide association studies for beak deformity in chickens using high-density 600K SNP arrays
Bai, Hao, Sun, Yanyan, Liu, Nian, Xue, Fuguang, Li, Yunlei, Xu, Songshan, Ye, Jianhua, Zhang, Lei, Chen, Yu, Chen, Jilan
Published in BMC genomics (28.06.2018)
Published in BMC genomics (28.06.2018)
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Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout
Vávra, Jiří, Pavelcová, Kateřina, Mašínová, Jana, Hasíková, Lenka, Bubeníková, Eliška, Urbanová, Aneta, Mančíková, Andrea, Stibůrková, Blanka
Published in Disease markers (2024)
Published in Disease markers (2024)
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SHP2's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction
Priolo, Manuela, Palermo, Valentina, Aiello, Francesca, Ciolfi, Andrea, Pannone, Luca, Muto, Valentina, Motta, Marialetizia, Mancini, Cecilia, Radio, Francesca Clementina, Niceta, Marcello, Leoni, Chiara, Pintomalli, Letizia, Carrozzo, Rosalba, Rajola, Giuseppe, Mammì, Corrado, Zampino, Giuseppe, Martinelli, Simone, Dallapiccola, Bruno, Pichierri, Pietro, Tartaglia, Marco
Published in Clinical genetics (01.07.2022)
Published in Clinical genetics (01.07.2022)
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The Esophageal Organoid System Reveals Functional Interplay Between Notch and Cytokines in Reactive Epithelial Changes
Kasagi, Yuta, Chandramouleeswaran, Prasanna M., Whelan, Kelly A., Tanaka, Koji, Giroux, Veronique, Sharma, Medha, Wang, Joshua, Benitez, Alain J., DeMarshall, Maureen, Tobias, John W., Hamilton, Kathryn E., Falk, Gary W., Spergel, Jonathan M., Klein-Szanto, Andres J., Rustgi, Anil K., Muir, Amanda B., Nakagawa, Hiroshi
Published in Cellular and molecular gastroenterology and hepatology (01.01.2018)
Published in Cellular and molecular gastroenterology and hepatology (01.01.2018)
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Molecular and functional characterisation of hepatic slam CD229 and ITS implication in the development of hepatocellular carcinoma
Bouhlal, H, Nyga, R, Cartier, F, Ossart, C, Lamotte, L, Chatelain, D, Marolleau, J P, Lassoued, K, Bouhlal, H
Published in Gut (01.04.2011)
Published in Gut (01.04.2011)
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Biallelic variants in CTU2 cause DREAM‐PL syndrome and impair thiolation of tRNA wobble U34
Shaheen, Ranad, Mark, Paul, Prevost, Christopher T., AlKindi, Adila, Alhag, Ahmad, Estwani, Fatima, Al‐Sheddi, Tarfa, Alobeid, Eman, Alenazi, Mona M., Ewida, Nour, Ibrahim, Niema, Hashem, Mais, Abdulwahab, Firdous, Bryant, Emily M., Spinelli, Egidio, Millichap, John, Barnett, Sarah S., Kearney, Hutton M., Accogli, Andrea, Scala, Marcello, Capra, Valeria, Nigro, Vincenzo, Fu, Dragony, Alkuraya, Fowzan S.
Published in Human mutation (01.11.2019)
Published in Human mutation (01.11.2019)
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Molecular and phenotypic distinctions of macrophages in tolerant and susceptible to hypoxia rats
Dzhalilova, Dzhuliia, Kosyreva, Anna, Lokhonina, Anastasiya, Tsvetkov, Ivan, Vishnyakova, Polina, Makarova, Olga, Fatkhudinov, Timur
Published in PeerJ (San Francisco, CA) (10.10.2023)
Published in PeerJ (San Francisco, CA) (10.10.2023)
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Modulation of FLT3 signal transduction through cytoplasmic cysteine residues indicates the potential for redox regulation
Böhmer, Annette, Barz, Saskia, Schwab, Katjana, Kolbe, Ulrike, Gabel, Anke, Kirkpatrick, Joanna, Ohlenschläger, Oliver, Görlach, Matthias, Böhmer, Frank-D.
Published in Redox biology (01.01.2020)
Published in Redox biology (01.01.2020)
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Novel genotype–phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing loss
Lee, Sang‐Yeon, Han, Jin Hee, Carandang, Marge, Kim, Min Young, Kim, Bonggi, Yi, Nayoung, Kim, Jinho, Kim, Bong Jik, Oh, Doo‐Yi, Koo, Ja‐Won, Lee, Jun Ho, Oh, Seung‐Ha, Choi, Byung Yoon
Published in Human mutation (01.11.2020)
Published in Human mutation (01.11.2020)
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