Littérature scientifique sur le sujet « YAE1 »
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Articles de revues sur le sujet "YAE1"
Merlin, Christophe, Gregory Gardiner, Sylvain Durand et Millicent Masters. « The Escherichia coli metD Locus Encodes an ABC Transporter Which Includes Abc (MetN), YaeE (MetI), and YaeC (MetQ) ». Journal of Bacteriology 184, no 19 (1 octobre 2002) : 5513–17. http://dx.doi.org/10.1128/jb.184.19.5513-5517.2002.
Texte intégralPrusty, Nihar Ranjan, Francesca Camponeschi, Simone Ciofi-Baffoni et Lucia Banci. « The human YAE1-ORAOV1 complex of the cytosolic iron-sulfur protein assembly machinery binds a [4Fe-4S] cluster ». Inorganica Chimica Acta 518 (avril 2021) : 120252. http://dx.doi.org/10.1016/j.ica.2021.120252.
Texte intégralWiatrowski, Heather A., et Marian Carlson. « Yap1 Accumulates in the Nucleus in Response to Carbon Stress in Saccharomyces cerevisiae ». Eukaryotic Cell 2, no 1 (février 2003) : 19–26. http://dx.doi.org/10.1128/ec.2.1.19-26.2003.
Texte intégralBen, Chi, Xiaojing Wu, Atsushi Takahashi-Kanemitsu, Christopher Takaya Knight, Takeru Hayashi et Masanori Hatakeyama. « Alternative splicing reverses the cell-intrinsic and cell-extrinsic pro-oncogenic potentials of YAP1 ». Journal of Biological Chemistry 295, no 41 (6 août 2020) : 13965–80. http://dx.doi.org/10.1074/jbc.ra120.013820.
Texte intégralGál, József, Attila Szvetnik, Róbert Schnell et Miklós Kálmán. « The metDd-Methionine Transporter Locus of Escherichia coli Is an ABC Transporter Gene Cluster ». Journal of Bacteriology 184, no 17 (1 septembre 2002) : 4930–32. http://dx.doi.org/10.1128/jb.184.17.4930-4932.2002.
Texte intégralKawauchi, Daisuke, Kristian Pajtler, Yiju Wei, Konstantin Okonechnikov, Patricia Silva, David Jones, Mikio Hoshino, Stefan Pfister, Marcel Kool et Wei Li. « TB-06 MOLECULAR MECHANISM OF BRAIN TUMOUR FORMATION DRIVEN BY SUPRATENTORIAL EPENDYMOMA-SPECIFIC YAP1 FUSION GENES ». Neuro-Oncology Advances 1, Supplement_2 (décembre 2019) : ii11. http://dx.doi.org/10.1093/noajnl/vdz039.048.
Texte intégralKim, Yong Sook, Mira Kim, Dong Im Cho, Soo Yeon Lim, Ju Hee Jun, Mi Ra Kim, Bo Gyeong Kang et al. « PSME4 Degrades Acetylated YAP1 in the Nucleus of Mesenchymal Stem Cells ». Pharmaceutics 14, no 8 (9 août 2022) : 1659. http://dx.doi.org/10.3390/pharmaceutics14081659.
Texte intégralHartley, A. D., M. P. Ward et S. Garrett. « The Yak1 protein kinase of Saccharomyces cerevisiae moderates thermotolerance and inhibits growth by an Sch9 protein kinase-independent mechanism. » Genetics 136, no 2 (1 février 1994) : 465–74. http://dx.doi.org/10.1093/genetics/136.2.465.
Texte intégralZeng, Cheng, Pei-Li Wu, Zhao-Tong Dong, Xin Li, Ying-Fang Zhou et Qing Xue. « YAP1 inhibits ovarian endometriosis stromal cell invasion through ESR2 ». Reproduction 160, no 3 (septembre 2020) : 481–90. http://dx.doi.org/10.1530/rep-19-0565.
Texte intégralSzulzewsky, Frank, Pia Hoellerbauer, Hua-Jun Wu, P. J. Cimino, Franziska Michor, Patrick Paddison, Valeri Vasioukhin et Eric Holland. « GENE-04. THE ONCOGENIC FUNCTIONS OF YAP1-GENE FUSIONS CAN BE INHIBITED BY DISRUPTION OF YAP1-TEAD INTERACTION ». Neuro-Oncology 21, Supplement_6 (novembre 2019) : vi98. http://dx.doi.org/10.1093/neuonc/noz175.406.
Texte intégralThèses sur le sujet "YAE1"
Shah, Nupur R. « Functional studies of YAP1 in cancer and embryonic development ». Thesis, University of Aberdeen, 2018. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=238733.
Texte intégralSchlegelmilch, Karin [Verfasser]. « YAP1 and the Hippo Signaling Pathway Regulate Progenitor Proliferation / Karin Schlegelmilch ». Berlin : Freie Universität Berlin, 2013. http://d-nb.info/1042186170/34.
Texte intégral金原, 和江. « 膜結合型プロテアーゼYaeLの機能解析 ». 京都大学 (Kyoto University), 2003. http://hdl.handle.net/2433/148589.
Texte intégralCaetano, Soraia Cristina Marques. « O Yap1 no stress causado pelo excesso de cobalto em S. cerevisiae ». Master's thesis, Universidade de Aveiro, 2011. http://hdl.handle.net/10773/8214.
Texte intégralA capacidade dos organismos em alterar os seus padrões de expressão de genes em resposta a perturbações do meio ambiente é essencial para a sua viabilidade. Neste trabalho, utilizando Saccharomyces cerevisiae como organismo eucariota modelo, foi estudada a relevância do factor de transcrição da família Yap, o Yap1, na desintoxicação do excesso de cobalto. Os resultados obtidos neste trabalho demonstram que, após a incubação das células com cobalto, o factor de transcrição Yap1 é acumulado no núcleo, através de um mecanismo independente de Orp1/Gpx3. Verificámos que o cobalto tem a capacidade de ligar-se directamente ao Yap1, sugerindo que, à semelhança do que acontece com outros metais, seja este o mecanismo de retenção nuclear após o stress. Confirmámos que uma vez no núcleo, o Yap1 medeia a indução de genes envolvidos na regulação do stress oxidativo em levedura (tais como GPX2, SOD1, TRR1 e TRX2) e constatámos que a presença de cobalto aumenta os níveis de carbonilação das proteínas, sendo esse aumento mais acentuado na ausência de Yap1. Verificámos ainda que os níveis de cobalto estão levemente diminuídos no mutante yap1 ao contrário do ferro que está em concentrações mais elevadas neste mutante relativamente à estirpe selvagem, quer na presença como na ausência de cobalto. Este facto leva-nos a propor que o cobalto altere a homeostase do ferro e que em consequência, conjuntamente com a diminuição das defesas anti-oxidantes, gere stress oxidativo. Foi descrito que a glutationa (GSH) é importante na homeostase do ferro e o excesso de cobalto leva ao aumento dos níveis de ferro intracelulares. Verificámos não só que a expressão de GSH1 está diminuída aos 30 minutos de tratamento do mutante yap1 com cobalto mas também que a adição de GSH faz recuperar os fenótipos de crescimento na presença deste metal. Finalmente apresentámos um modelo de acção do factor Yap1 no stress provocado pelo cobalto.
The ability of organisms to reprogram gene expression in response to changes in the environment is essential for their viability. In this work, using Saccharomyces cerevisiae as a eukaryotic model organism, we studied the relevance of the transcription factor, Yap1, in the detoxification of cobalt excess. The results here reported show that after incubation of cells with cobalt, Yap1 accumulates in the nucleus, through a mechanism independent of the peroxidase Orp1/Gpx3. We found that cobalt has the ability to directly bind to Yap1, suggesting that this is the mechanism for its nuclear retention after cobalt treatment. We confirmed that, once in the nucleus, Yap1 mediates the induction of genes involved in the regulation of oxidative stress in yeast (such as GPX2, SOD1, TRX2 and TRR1). Moreover, we found that the presence of cobalt increases the levels of protein carbonylation, being the damage more pronounced in the absence of Yap1. It was also found that cobalt levels are slightly decreased in the yap1 mutant. In contrast, the iron concentration is higher in this mutant than in the wild type, in the presence and absence of cobalt. This led us to propose that the cobalt alters iron homeostasis and iin consequence generate oxidative stress. It was reported that glutathione (GSH) is important in the homeostasis of iron. As the excess of cobalt leads to increased levels of intracellular iron, we found not only that in the yap1 mutant GSH1 expression is decreased after 30 minutes of treatment with cobalt but also, the addition of GSH can recover the growth phenotypes in the presence of this metal. . Finally we present a working model of the transcription factor Yap1 in stress caused by cobalt.
Sha, Wei. « Microarray data analysis methods and their applications to gene expression data analysis for Saccharomyces cerevisiae under oxidative stress ». Diss., Virginia Tech, 2006. http://hdl.handle.net/10919/27840.
Texte intégralPh. D.
Fechtner, Tim [Verfasser]. « Charakterisierung der neuen, potentiellen Adhäsine Yaa1, Yaa2 und Yaa3 von Chlamydia pneumoniae / Tim Fechtner ». Düsseldorf : Universitäts- und Landesbibliothek der Heinrich-Heine-Universität Düsseldorf, 2013. http://d-nb.info/1036261921/34.
Texte intégralHegerfeldt, Yael [Verfasser], et Peter [Akademischer Betreuer] Friedl. « Kollektive Invasion in Melanomexplantaten : Bedeutung von Zell-Matrix-Interaktionen / Yael Hegerfeldt. Betreuer : Peter Friedl ». Würzburg : Universitätsbibliothek der Universität Würzburg, 2012. http://d-nb.info/1028326785/34.
Texte intégralMolina-Castro, Silvia. « Study of the Hippo/YAP1 signaling pathway in gastric carcinogenesis induced by Helicobacter pylori ». Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0623/document.
Texte intégralGastric cancer (GC) is a multifactorial disease, most frequently associated to chronic infection with CagA-positive Helicobacter pylori strains. Epithelial-to-mesenchymal transition (EMT) is reversible process in which polarized epithelial cells acquire a mesenchymal phenotype. EMT is at the origin of cancer stem cells (CSC). In GC, CSCs express CD44 and high aldehyde-dehydrogenase (ALDH) activity. Infection with H. pylori of human gastric cancer cell lines (hGECs) in vitro induces the emergence of a population of CD44+ cells with CSC-properties through an EMT process in a CagA-dependent manner. The Hippo pathway is composed by the kinases MST and LATS, and their phosphorylation targets,YAP1 and TAZ. Upon phosphorylation by LATS, YAP1 and TAZ are inhibited. Active YAP1 and TAZ bind to TEAD transcription factors to promote the expression of genes that regulate cell growth and apoptosis.The first aim of this work was to investigate whether H. pylori affects the activation state of the Hippo pathway, and its effect on the EMT process and the CSCs. Second, we intended to characterize the role of YAP1/TEAD in gastric CSC properties in vitro and the consequences of its pharmacological inhibition on tumor growth in vivo.To study the Hippo pathway regulation during infection, LATS2, YAP1 and CD44 were evaluated in gastric mucosae of non-infected or H. pylori-infected patients. They were upregulated in infected mucosae and were associated to pathology. Hippo pathway regulation by H. pylori infection has biphasic kinetics and is CagA-dependent. Early in infection, H. pylori transiently triggered YAP1 expression and co-transcriptional activity, along with LATS2. This period of Hippo pathway inactivity is followed by a progressive activation, sustained by LATS2 accumulation and inhibitory YAP1Ser127-phosphorylation. LATS2 siRNA-mediated repression accelerated the acquisition of the EMT-phenotype upon infection, the up-regulation of EMT-markers ZEB1 and Snail1, and the decrease of the epithelial miR-200. H. pylori-induced CD44 upregulation, invasion and sphere-forming capacity were further enhanced upon LATS2 knockdown, suggesting that LATS2 restricts the EMT and CSC-like phenotype in hGECs upon H. pylori infection. Inhibition of either LATS2 or YAP1 reduced the expression of both proteins, revealing a positive feedback loop. In tissue sections of GC, LATS2 and YAP1 were heterogeneous and co-expressed. The positive correlation between LATS2 and YAP1 was confirmed in the 38 hGECs of the CCLE. The expression of CTGF and CYR61 was also strongly correlated to LATS2, suggesting that LATS2 could also be a YAP1/TEAD target gene.hGECs of the CCLE. The expression of CTGF and CYR61 was also strongly correlated to LATS2, suggesting that LATS2 could also be a YAP1/TEAD target gene.Verteporfin (VP) disrupts the YAP1/TEAD interaction inhibiting its transcriptional activity. In vitro, using hGECs and cells from patient derived primary tumor xenogratfs (PDXs), we showed that treatment with VP decreased cell growth, expression of YAP1/TAZ/TEAD target genes, TEAD-luciferase reporter activity and sphere-forming capacity. The activity of VP was tested in vivo, by peritumoral injection in a model of subcutaneous graft of hGECs (MKN45 and MKN74) and PDX (GC10) in NGS mice. Tumor growth was followed and a decrease was observed. Tumor weight measurement, IHC analysis (CD44, ALDH and Ki67), and CSCs were decreased in treated tumors. These results show the CSC-inhibitory activity of VP both in vitro and in vivo.We showed for the first time that the LATS2/YAP1/TEAD axis is early activated during the carcinogenesis process induced by chronic H. pylori infection and controls the subsequent EMT and CSC-like features. Targeting the Hippo pathway efficiently prevented tumor growth in a PDX model, highlighting the potential of its inhibition to be implemented in gastric cancer therapy
Stegmeier, Johannes Friedrich. « Study of Omp85 family proteins YaeT and YtfM and multidrug export machineries in Escherichia coli ». Doctoral thesis, [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980586682.
Texte intégralGuzzo, Cristiane Rodrigues. « Estudo estrutural e funcional das proteínas PilZ e YaeQ do fitopatógeno Xanthomonas axonopodis pv citri ». Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-26042010-134457/.
Texte intégralThe aim of the project was to perform structural and functional studies of different Xanthomonas axonopodis pv citri (Xac) proteins including the hypothetical proteins YaeQ and SufE; RpfC, RpfF and RpfG involved in the quorum sensing and PilZ, FimX and PilB that play roles in type IV pilus (T4P) biogenesis. Several experimental techniques were employed including cloning, expression and purification of recombinant proteins, thermal denaturation, protein crystallography, X-ray diffraction, NMR, two-hybrid assays, Western- and Far-Western Blotting assays, site direct mutagenesis, and the production of Xac knockouts strains. The most important results include the determination of the three-dimensional crystal structures of PilZ and YaeQ using the MAD technique. In both cases, the structures reveled new protein topologies. The comparison of the YaeQ structure with others deposited in public databases revealed that YaeQ proteins represent a new variation within the PD-(D/E)XK magnesium dependent endonucleases superfamily. Functional assays suggest that YaeQ may be envolved in DNA repair in Xac. The PilZ three-dimensional structure revealed an unexpected structural variation within the PilZ domain superfamily and showed why PilZ orthologs are not able to bind the important bacterial second messenger, c-diGMP. We assigned the PilZ main chain by NMR and used this information to demonstrate that the PilZ secondary structure in solution is consistent with the PilZ crystal structure. We identified two proteins that interact with PilZ: PilB and FimX. As with PilZ, both PilB and FimX are involved in T4P biogenesis. PilZ binds specifically to the EAL domain of FimX and the conserved residues located in the PilZ unstructured C-terminal region contribute to binding with PilB but not with FimX. Site direct mutagenesis studies showed that PilZ residue Y22 is necessary for its capability to interact with both PilB and FimX. Although PilZ does not bind c-diGMP, her partner, FimX, does. We present evidence that PilZ can bind simultaneously to FimX and PilB, forming a ternary complex that is independent of c-diGMP. These results allow us to propose possible mechanisms by which PilZ and FimX control T4P biogenesis. Other results obtained during this period include the resolution of the crystal structure of the SufE protein from Xac using the molecular replacement technique. We show that SufE induces a 10-fold increase in the cysteine desulfurase activity of SufS, similar to that observed for the SufE-SufS complex from E. coli. Several proteins involved in quorum sensing and c-di-GMP signaling were cloned, expressed and submitted to crystallization trials. Crystals of the HPT (histidine phophotransferase) domain) of the RpfC sensor histidine kinase were obtained
Livres sur le sujet "YAE1"
Cócora : La historia de Yael. Panamá, República de Panamá : Puello's Books, 2015.
Trouver le texte intégraleditor, Yoneda Yūsuke 1936, dir. Yae no zanka. Tōkyō : Chūō Kōron Bijutsu Shuppan, 2018.
Trouver le texte intégralYura, Yayoi. Niijima Yae to Ishin : Aizu ni saita yae no sakura. Tōkyō : Bungeisha, 2013.
Trouver le texte intégralYae, Kurō. Yae Kurō no denshō. Sapporo-shi : Hokkaidō Kyōiku Iinkai, 1993.
Trouver le texte intégralAsano, Yae. Asano Yae yusai, 1955-nen-1982-nen = : Yae Asano paintings, 1955-1982. Nagoya : Sakura Gallery, 1985.
Trouver le texte intégralYael and the party of the year. New York : Simon & Schuster, 2018.
Trouver le texte intégralThe Geneva option : A Yael Azoulay novel. New York, NY : HarperCollins Publishers, 2013.
Trouver le texte intégralDōsōkai, Dōshisha. Niijima Yae : Hansamu na joketsu no shōgai = The life history of Yae Neesima. Kyōto-shi : Tankōsha, 2012.
Trouver le texte intégralTah zamā ṭolah shāʻirī yae ! Peṣhawar : Dānish Khparandūyah Ṭolanah, 2013.
Trouver le texte intégralYae-san, onorini narimasu ka. Kyōto-shi : Shibunkaku Shuppan, 2012.
Trouver le texte intégralChapitres de livres sur le sujet "YAE1"
Leavy, Patricia, et Victoria Scotti. « Yael ». Dans Low-Fat Love Stories, 105–10. Rotterdam : SensePublishers, 2017. http://dx.doi.org/10.1007/978-94-6300-818-1_14.
Texte intégralMolos, Dimitrios. « Tamir, Yael ». Dans Encyclopedia of Global Justice, 1057–58. Dordrecht : Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-1-4020-9160-5_131.
Texte intégralWilmer, S. E. « Yael Ronen ». Dans Dramaturgies of Interweaving, 176–96. London : Routledge, 2021. http://dx.doi.org/10.4324/9781003187233-17.
Texte intégralKoch, Roberta Maria. « Wie innovative Start-ups zu Kapital kommen ». Dans Die Wirtschaft im Wandel, 59–63. Wiesbaden : Springer Fachmedien Wiesbaden, 2021. http://dx.doi.org/10.1007/978-3-658-31735-5_10.
Texte intégralAssis, Elie. « “THE HAND OF A WOMAN” : DEBORAH AND YAEL (JUDGES 4) ». Dans Perspectives on Hebrew Scriptures II, 363–70. Piscataway, NJ, USA : Gorgias Press, 2007. http://dx.doi.org/10.31826/9781463212834-025.
Texte intégralSudol, Marius, Irwin H. Gelman et Jianmin Zhang. « YAP1 Uses Its Modular Protein Domains and Conserved Sequence Motifs to Orchestrate Diverse Repertoires of Signaling ». Dans The Hippo Signaling Pathway and Cancer, 53–70. New York, NY : Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-6220-0_4.
Texte intégralHutchison, Yvette. « Women Playwrights in Post-Apartheid South Africa : Yael Farber, Lara Foot-Newton, and the Call for Ubuntu ». Dans Contemporary Women Playwrights, 148–63. London : Macmillan Education UK, 2013. http://dx.doi.org/10.1007/978-1-137-27080-1_10.
Texte intégral« YAP1 ». Dans Encyclopedia of Genetics, Genomics, Proteomics and Informatics, 2123. Dordrecht : Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_18310.
Texte intégralGarrett, S. « Yak1 ». Dans The Protein Kinase FactsBook, 254–55. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012324719-3/50076-5.
Texte intégral« 54 Yael ». Dans Jews in East Norse Literature, 1109–10. De Gruyter, 2022. http://dx.doi.org/10.1515/9783110775747-066.
Texte intégralActes de conférences sur le sujet "YAE1"
Bölöni, Ladislau, et Damla Turgut. « YAES ». Dans the 8th ACM international symposium. New York, New York, USA : ACM Press, 2005. http://dx.doi.org/10.1145/1089444.1089473.
Texte intégralDouze, Matthijs, et Hervé Jégou. « The Yael Library ». Dans MM '14 : 2014 ACM Multimedia Conference. New York, NY, USA : ACM, 2014. http://dx.doi.org/10.1145/2647868.2654892.
Texte intégralBotelho Paz, Giovanni Scataglia, et Solange Wagner Locatelli. « METACOGNITIVE INCIDENTS MANIFESTED BY STUDENTS OF YOUTH AND ADULT EDUCATION IN AN INVESTIGATIVE ACTIVITY ». Dans 3rd International Baltic Symposium on Science and Technology Education (BalticSTE2019). Scientia Socialis Ltd., 2019. http://dx.doi.org/10.33225/balticste/2019.158.
Texte intégralCalvet, Loreley, Odette Dos Santos, Véronique Jean-Baptiste, Emmanuel Spanakis, Yvette Ruffin, Isabelle Sanchez, Jessica Mestadier et al. « Abstract 4858 : Oncogenic HIPPO-YAP1:in vivotarget validation of YAP1 in malignant mesothelioma ». Dans Proceedings : AACR Annual Meeting 2020 ; April 27-28, 2020 and June 22-24, 2020 ; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-4858.
Texte intégralZhu, Ming, Ruiqing Peng, Xin Liang, Zhengdao Lan, Meng Tang, Pingping Hou, Jian H. Song et al. « Yap1 Hydroxylation Suppress Prostate Cancer Metastasis ». Dans Leading Edge of Cancer Research Symposium. The University of Texas at MD Anderson Cancer Center, 2022. http://dx.doi.org/10.52519/00102.
Texte intégral« Session YA1 : Signal Processing 3 ». Dans 2005 IEEE Instrumentationand Measurement Technology Conference Proceedings. IEEE, 2005. http://dx.doi.org/10.1109/imtc.2005.1604434.
Texte intégralMarino, Gloria, Shuai Ye, Koreana Pak, Jennifer Shah, Jason Godfrey, Susan Chor, Shaun Egolf et T. S. Karin Eisinger-Mathason. « Abstract 3531 : YAP1-mediated circadian oscillation in sarcoma ». Dans Proceedings : AACR Annual Meeting 2017 ; April 1-5, 2017 ; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3531.
Texte intégralMarino, Gloria, Shaun Egolf, Shuai Ye, Koreana Pak, Jenn Shah, Adrian Rivera-Reyes, Susan Chor et T. S. Karin Eisinger-Mathason. « Abstract B21 : YAP1-mediated circadian oscillation in sarcoma ». Dans Abstracts : Advances in Sarcomas : From Basic Science to Clinical Translation ; May 16-19, 2017 ; Philadelphia, PA. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1557-3265.sarcomas17-b21.
Texte intégralLiu, Ying, Gabrielle Ciotti et T. S. Karin Eisinger-Mathason. « Abstract A02 : YAP1 opposes differentiation in mesenchymal tumors ». Dans Abstracts : AACR Special Conference on the Hippo Pathway : Signaling, Cancer, and Beyond ; May 8-11, 2019 ; San Diego, CA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1557-3125.hippo19-a02.
Texte intégralBiagioni, Francesca, Ottavio Croci, Elisa Donato, Silvia Sberna, Serena De Fazio, Arianna Sabò, Bruno Amati et Stefano Campaner. « Abstract B37 : Genomic view of YAP1 dependent transcription ». Dans Abstracts : AACR Special Conference on the Hippo Pathway : Signaling, Cancer, and Beyond ; May 8-11, 2019 ; San Diego, CA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1557-3125.hippo19-b37.
Texte intégralRapports d'organisations sur le sujet "YAE1"
Camargo, Fernando, et Betty Diamond. Yap1 as a New Therapeutic Target in Neurofibromatosis Type 2. Fort Belvoir, VA : Defense Technical Information Center, septembre 2013. http://dx.doi.org/10.21236/ada606101.
Texte intégralCamargo, Fernando. Yap1 as a New Therapeutic Target in Neurofibromatosis Type 2. Fort Belvoir, VA : Defense Technical Information Center, mai 2014. http://dx.doi.org/10.21236/ada611708.
Texte intégralIs infant empathy linked with later externalizing problems ? ACAMH, novembre 2020. http://dx.doi.org/10.13056/acamh.13959.
Texte intégral