未登录.png)
分享.png)
收藏Modeling invasive breast cancer: growth factors propel progression of HER2-positive premalignant lesions (vol 31, pg 3569, 2012)建模浸润性乳腺癌：生长因子推动HER2阳性癌前病变的进展（卷31，页3569，2012）
Pradeep, C. -R; Zeisel, A.; Kostler, W. J.; Lauriola, M.; Jacob-Hirsch, J.; Haibe-Kains, B.; Amariglio, N.; Ben-Chetrit, N.; Emde, A.; Solomonov, I.; Neufeld, G.; Piccart, M.; Sagi, I.; Sotiriou, C.; Rechavi, G.; Domany, E.; Desmedt, C.; Yarden, Y. 分享 收藏 Modeling invasive breast cancer: growth factors propel progression of HER2-positive premalignant lesions (vol 31, pg 3569, 2012)Pradeep, C. -R; Zeisel, A.; Kostler, W. J.; Lauriola, M.; Jacob-Hirsch, J.; Haibe-Kains, B.; Amariglio, N.; Ben-Chetrit, N.; Emde, A.; Solomonov, I.; Neufeld, G.; Piccart, M.; Sagi, I.; Sotiriou, C.; Rechavi, G.; Domany, E.; Desmedt, C.; Yarden, Y. 分享 收藏 Neoadjuvant BRAF-targeted therapy for ameloblastoma of the mandible: an organ preservation approachGrynberg, Shirly; Vered, Marilena; Shapira-Frommer, Ronnie; Asher, Nethanel; Ben-Betzalel, Guy; Stoff, Ronen; Steinberg, Yael; Amariglio, Ninette; Greenberg, Gahl; Barshack, Iris; Toren, Amos; Yahalom, Ran; Schachter, Jacob; Rechavi, Gideon; Hirschhorn, Ariel; Abebe Campino, Gadi 分享 收藏 Dynamic regulation of N6,2′-O-dimethyladenosine (m6Am) in obesityBen-Haim, Moshe Shay; Pinto, Yishay; Moshitch-Moshkovitz, Sharon; Hershkovitz, Vera; Kol, Nitzan; Diamant-Levi, Tammy; Beeri, Michal Schnaider; Amariglio, Ninette; Cohen, Haim Y.; Rechavi, Gideon 分享 收藏 Upfront rational therapy in BRAF V600E mutated pediatric ameloblastoma promotes ad integrum mandibular regenerationHirschhorn, Ariel; Campino, Gadi Abebe; Vered, Marilena; Greenberg, Gahl; Yacobi, Rinat; Yahalom, Ran; Barshack, Iris; Toren, Amos; Amariglio, Ninette; Rechavi, Gideon 分享 收藏 Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsLev, Atar; Lee, Yu Nee; Sun, Guangping; Hallumi, Enas; Simon, Amos J.; Zrihen, Keren S.; Levy, Shiran; Halevi, Tal Beit; Papazian, Maria; Shwartz, Neta; Somekh, Ido; Levy-Mendelovich, Sarina; Wolach, Baruch; Gavrieli, Ronit; Vernitsky, Helly; Barel, Ortal; Javasky, Elisheva; Stauber, Tali; Ma, Chi A.; Zhang, Yuan; Amariglio, Ninette; Rechavi, Gideon; Hendel, Ayal; Yablonski, Deborah; Milner, Joshua D.; Somech, Raz 分享 收藏 分享 收藏 Cerebral and portal vein thrombosis, macrocephaly and atypical absence seizures in Glycosylphosphatidyl inositol deficiency due to a PIGM promoter mutationPode-Shakked, Ben; Heimer, Gali; Vilboux, Thierry; Marek-Yagel, Dina; Ben-Zeev, Bruria; David, Mariska; Ferreira, Carlos R.; Philosoph, Amit Mary; Veber, Alvit; Pode-Shakked, Naomi; Kenet, Gili; Soudack, Michalle; Hoffmann, Chen; Vernitsky, Helly; Safaniev, Marina; Lodzki, Maya; Lahad, Avishay; Shouval, Dror S.; Levinkopf, Dana; Weiss, Batia; Barg, Assaf Arie; Daka, Ayman; Amariglio, Ninette; Malicdan, May Christine V.; Gahl, William A.; Anikster, Yair 分享 收藏 Newly diagnosed multiple myeloma patients carrying monoallelic deletion of the whole locus of immunoglobulin heavy chain gene have a better prognosis compared to those with t(4;14) and t(14;16)Duek, Adrian; Trakhtenbrot, Luba; Amariglio, Ninette; Benyamini, Noam; Zilbershats, Itay; Ganzel, Chezi; Shevetz, Olga; Leiba, Ronit; Rozic, Gabriela; Nagler, Arnon; Leiba, Merav 分享 收藏 Nm-seq maps 2′-O-methylation sites in human mRNA with base precision (vol 14, pg 695, 2017)Dai, Qing; Moshitch-Moshkovitz, Sharon; Han, Dali; Kol, Nitzan; Amariglio, Ninette; Rechavi, Gideon; Dominissini, Dan; He, Chuan 分享 收藏 Somatic NRAS mutation in patient with generalized lymphatic anomalyManevitz-Mendelson, Eugenia; Leichner, Gil S.; Barel, Ortal; Davidi-Avrahami, Inbal; Ziv-Strasser, Limor; Eyal, Eran; Pessach, Itai; Rimon, Uri; Barzilai, Aviv; Hirshberg, Abraham; Chechekes, Keren; Amariglio, Ninette; Rechavi, Gideon; Yaniv, Karina; Greenberger, Shoshana 分享 收藏 Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disordersJacob-Hirsch, Jasmine; Eyal, Eran; Knisbacher, Binyamin A.; Roth, Jonathan; Cesarkas, Karen; Dor, Chen; Farage-Barhom, Sarit; Kunik, Vered; Simon, Amos J.; Gal, Moran; Yalon, Michal; Moshitch-Moshkovitz, Sharon; Tearle, Rick; Constantini, Shlomi; Levanon, Erez Y.; Amariglio, Ninette; Rechavi, Gideon 分享 收藏 RNA editing by ADAR1 leads to context-dependent transcriptome-wide changes in RNA secondary structureSolomon, Oz; Di Segni, Ayelet; Cesarkas, Karen; Porath, Hagit T.; Marcu-Malina, Victoria; Mizrahi, Orel; Stern-Ginossar, Noam; Kol, Nitzan; Farage-Barhom, Sarit; Glick-Saar, Efrat; Lerenthal, Yaniv; Levanon, Erez Y.; Amariglio, Ninette; Unger, Ron; Goldstein, Itamar; Eyal, Eran; Rechavi, Gidi 分享 收藏 Breaking the Ceiling of Human Maximal Life spanBen-Haim, Moshe Shay; Kanfi, Yariv; Mitchell, Sarah J.; Maoz, Noam; Vaughan, Kelli L.; Amariglio, Ninette; Lerrer, Batia; de Cabo, Rafael; Rechavi, Gideon; Cohen, Haim Y. 分享 收藏 分享 收藏 Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathyBarel, Ortal; Malicdan, May Christine V.; Ben-Zeev, Bruria; Kandel, Judith; Pri-Chen, Hadass; Stephen, Joshi; Castro, Ines G.; Metz, Jeremy; Atawa, Osama; Moshkovitz, Sharon; Ganelin, Eti; Barshack, Iris; Polak-Charcon, Sylvie; Nass, Dvora; Marek-Yagel, Dina; Amariglio, Ninette; Shalva, Nechama; Vilboux, Thierry; Ferreira, Carlos; Pode-Shakked, Ben; Heimer, Gali; Hoffmann, Chen; Yardeni, Tal; Nissenkorn, Andreea; Avivi, Camila; Eyal, Eran; Kol, Nitzan; Saar, Efrat Glick; Wallace, Douglas C.; Gahl, William A.; Rechavi, Gideon; Schrader, Michael; Eckmann, David M.; Anikster, Yair 分享 收藏 G23D: Online tool for mapping and visualization of genomic variants on 3D protein structuresSolomon, Oz; Kunik, Vered; Simon, Amos; Kol, Nitzan; Barel, Ortal; Lev, Atar; Amariglio, Ninette; Somech, Raz; Rechavi, Gidi; Eyal, Eran 分享 收藏 ADAR1 deletion induces NFB and interferon signaling dependent liver inflammation and fibrosisBen-Shoshan, Shirley Oren; Kagan, Polina; Sultan, Maya; Barabash, Zohar; Dor, Chen; Jacob-Hirsch, Jasmine; Harmelin, Alon; Pappo, Orit; Marcu-Malina, Victoria; Ben-Ari, Ziv; Amariglio, Ninette; Rechavi, Gideon; Goldstein, Itamar; Safran, Michal 分享 收藏 Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defectsSimon, Amos J.; Lev, Atar; Zhang, Yong; Weiss, Batia; Rylova, Anna; Eyal, Eran; Kol, Nitzan; Barel, Ortal; Cesarkas, Keren; Soudack, Michalle; Greenberg-Kushnir, Noa; Rhodes, Michele; Wiest, David L.; Schiby, Ginette; Barshack, Iris; Katz, Shulamit; Pras, Elon; Poran, Hana; Reznik-Wolf, Haike; Ribakovsky, Elena; Simon, Carlos; Hazou, Wadi; Sidi, Yechezkel; Lahad, Avishay; Katzir, Hagar; Sagie, Shira; Aqeilan, Haifa A.; Glousker, Galina; Amariglio, Ninette; Tzfati, Yehuda; Selig, Sara; Rechavi, Gideon; Somech, Raz 分享 收藏 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
