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1401por Wei, Caihong, Wang, Huihua, Liu, Gang, Wu, Mingming, Cao, Jiaxve, Liu, Zhen, Liu, Ruizao, Zhao, Fuping, Zhang, Li, Lu, Jian, Liu, Chousheng, Du, Lixin“…One region was in OAR2 including three genes (NPR2, SPAG8 and HINT2) the influence growth traits. …”
Publicado 2015
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1402por Upadhyay, Dinesh Kumar, Ibrahim, Mohamed Izham Mohamed, Mishra, Pranaya, Alurkar, Vijay M., Ansari, Mukhtar“…Direct healthcare costs (direct medical and non-medical costs) from patients perspective was estimated by ‘bottom up’ approach to identify their out-of-pocket expenses (1USD = NPR 73.38) before and after intervention at the baseline, 3, 6, 9 and 12 months follow-ups. …”
Publicado 2016
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1403por Li, Tiemei, Cheng, Xin, Wang, Yuting, Yin, Xiao, Li, Zhiqian, Liu, Ruiqi, Liu, Guotian, Wang, Yuejin, Xu, Yan“…However, VvGLYI-like1 was highly expressed 48 h after inoculation, similar to VvPR1 and VvNPR1 which are involved in the defence response. …”
Publicado 2019
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1404por Zhang, Rong, Gehlen, Jan, Kawalia, Amit, Melissari, Maria-Theodora, Dakal, Tikam Chand, Menon, Athira M., Höfele, Julia, Riedhammer, Korbinian, Waffenschmidt, Lea, Fabian, Julia, Breuer, Katinka, Kalanithy, Jeshurun, Hilger, Alina Christine, Sharma, Amit, Hölscher, Alice, Boemers, Thomas M., Pauly, Markus, Leutner, Andreas, Fuchs, Jörg, Seitz, Guido, Ludwikowski, Barbara M., Gomez, Barbara, Hubertus, Jochen, Heydweiller, Andreas, Kurz, Ralf, Leonhardt, Johannes, Kosch, Ferdinand, Holland-Cunz, Stefan, Münsterer, Oliver, Ure, Beno, Schmiedeke, Eberhard, Neser, Jörg, Degenhardt, Petra, Märzheuser, Stefanie, Kleine, Katharina, Schäfer, Mattias, Spychalski, Nicole, Deffaa, Oliver J., Gosemann, Jan-Hendrik, Lacher, Martin, Heilmann-Heimbach, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Ludwig, Michael, Grote, Phillip, Schumacher, Johannes, Thiele, Holger, Reutter, Heiko“…RESULTS: In total we prioritized 14 novel de novo variants in 14 different genes (APOL2, EEF1D, CHD7, FANCB, GGT6, KIAA0556, NFX1, NPR2, PIGC, SLC5A2, TANC2, TRPS1, UBA3, and ZFHX3) and eight rare de novo variants in eight additional genes (CELSR1, CLP1, GPR133, HPS3, MTA3, PLEC, STAB1, and PPIP5K2). …”
Publicado 2020
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1405por Chen, Qiming, Dong, Chaohua, Sun, Xiaohong, Zhang, Yugang, Dai, Hongyi, Bai, Suhua“…Other tested genes, including NbNPR1, NbPR1a, NbERF1, and NbLOX1, did not exhibit significant changes after A. alternata infection in OE plants compared to EV or WT plants. …”
Publicado 2020
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1406“…The enhanced cell cycle activity observed in combined treatment of ANP/BNP and dominant-negative FOXO (DN-FOXO), which can bind FOXO recognition sites on DNA but cannot activate transcription, was primarily mediated through natriuretic peptide receptor 3 (Npr3). In mice, simultaneous application of ANP and DN-FOXO in postnatal hearts reactivated cell cycle in cardiomyocytes, resulting in reduced scar formation after experimental myocardial infarction. …”
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1407por Xu, Xin, Lu, Yida, Wu, Youliang, Wang, Mingliang, Wang, Xiaodong, Wang, Huizhen, Chen, Bo, Li, Yongxiang“…Subsequently, a seven-IRGs signature (LCN12, CCL21, RNASE2, CGB5, NRG4, AGTR1 and NPR3) was identified to be significantly associated with the overall survival (OS) of male GC patients. …”
Publicado 2021
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1408“…Some of these genes encoded calcium-dependent protein kinases (CDPKs), chitin elicitor receptor kinases (CERKs), LRR receptor serine/threonine protein kinases (LRR-LRKs), NPR family proteins in the salicylic acid synthesis pathway, and MAPKs which were potato late blight response proteins. …”
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1409por Chen, Meiping, Miao, Hui, Liang, Hanting, Ke, Xiaoan, Yang, Hongbo, Gong, Fengying, Wang, Linjie, Duan, Lian, Chen, Shi, Pan, Hui, Zhu, Huijuan“…Other frequent mutations associated with skeletal development include FGFR3, ACAN, NPR2, COMP, and FBN1 in 12.2%, 0.9%, 0.8%, 0.4%, and 0.4%, respectively, resulting in significantly different degrees of short stature. …”
Publicado 2022
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1410por Saville, Naomi M., Shrestha, Bhim P., Style, Sarah, Harris-Fry, Helen, Beard, B. James, Sengupta, Aman, Jha, Sonali, Rai, Anjana, Paudel, Vikas, Pulkki-Brannstrom, Anni-Maria, Copas, Andrew, Skordis-Worrall, Jolene, Bhandari, Bishnu, Neupane, Rishi, Morrison, Joanna, Gram, Lu, Sah, Raghbendra, Basnet, Machhindra, Harthan, Jayne, Manandhar, Dharma S., Osrin, David, Costello, Anthony“…Women receive up to 7 monthly transfers per pregnancy: cash is NPR 750 (~US$7) and food is 10 kg of fortified sweetened wheat-soya Super Cereal per month. …”
Publicado 2016
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1411“…Lymphovascular invasion and a node positive rate (NPR) ≥ 0.8 were associated with a poor prognosis (P = 0.01 and P = 0.048, respectively). …”
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1412por Habra, Mouhammed Amir, Stephen, Bettzy, Campbell, Matthew, Hess, Kenneth, Tapia, Coya, Xu, Mingxuan, Rodon Ahnert, Jordi, Jimenez, Camilo, Lee, Jeffrey E., Perrier, Nancy D., Boraddus, Russell R., Pant, Shubham, Subbiah, Vivek, Hong, David S., Zarifa, Abdulrazzak, Fu, Siqing, Karp, Daniel D., Meric-Bernstam, Funda, Naing, Aung“…The primary endpoint was non-progression rate (NPR) at 27 weeks. Other endpoints included adverse events, tumor responses measured independently by objective radiologic criteria, and select immunological markers. …”
Publicado 2019
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1413
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1414“…Moreover, expression of four methylated genes (PLCXD3 (Phosphatidylinositol-Specific Phospholipase C, X Domain Containing 3), BAIAP2L2 (BAR/IMD Domain Containing Adaptor Protein 2 Like 2), NPR3 (Natriuretic Peptide Receptor 3), SNX10 (Sorting Nexin 10)) can influence patients’ prognosis. …”
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1415por Toni, Ledjona, Plachy, Lukas, Dusatkova, Petra, Elblova, Lenka, Amaratunga, Shenali Anne, Kolouskova, Stanislava, Obermannova, Barbora, Snajderova, Marta, Sumnik, Zdenek, Pruhova, Stepanka, Lebl, Jan“…We confirmed (likely) pathogenic gene variants affecting pituitary development and/or the GH-IGF-1 axis in 10/73 (14%) patients (PTCH1, HGMA2 [in two], OTX2, LHX4, GHSR, STAT3, IGFALS, IGF1R [in two]), abnormal components of cartilaginous matrix in 17/73 (23%) (ACAN [in two], FLNB [in three], FBLN5, COL11A1[in four], COL1A2, COL2A1[in five], MATN3), impaired paracrine regulation of chondrocytes in 4/73 (6%) (NPR2 [in three], FGFR3), SHOX gene defects in 12/73 (16%), gene variants affecting other components of intracellular regulation and signaling in 9/73 (12%) (CDC42, KMT2A, KMT2D, NSD1, SRCAP, PRG4, PTPN11, SON, LMNA), Silver-Russell syndrome (11p15 [in seven] or UPD7) in 11/73 (15%), and miscellaneous single-gene or chromosomal conditions (TRPS1, TRHR, RAI1, chromosomal microdeletions and/or translocations) in an additional ten (14%) children. …”
Publicado 2021
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1416“…Finally, we generated 4 genes (aprE, nprE, wprA, and bamHIR) mutant strain, LB1ba02△4. …”
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1417“…In addition, the PpCAD1_OE gametophore inhibited the Botrytis cinerea assault mainly by enhanced phenylpropanoids in the cell wall instead of influencing transcripts of defense genes pathogenesis-related 10 (PR10) and nonexpresser of PR genes 1 (NPR1). Likewise, ectopic expression of PpCAD1 in Arabidopsis led to a significant increase in lignin content, exhibiting chunky roots, robust seedlings, advanced flowering, and efficient resistance against pathogens. …”
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1418“…METHODS: Information on developmental disorders was from the Norwegian Patient Register (NPR) and information on immigrant background, parental country of origin, parental education, and household income from Statistics Norway. …”
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1419por Chen, Shasha, Jin, Qinchun, Hou, Shiqiang, Li, Mingfei, Zhang, Yuan, Guan, Lihua, Pan, Wenzhi, Ge, Junbo, Zhou, Daxin“…The whole-exome sequencing (WES) was performed in 20 BAV patients and identified 40 different heterozygous missense mutations in 36 genes (MIB2, FAAH, S100A1, RGS16, MAP3K19, NEB, TTN, TNS1, CAND2, CCK, KALRN, ATP10D, SLIT3, ROS1, FABP7, NUP205, IL11RA, NPR2, COL5A1, CUBN, JMJD1C, ANXA7, TRIM8, LGR4, TPCN2, APOA5, GPR84, LRP1, NCOR2, AKAP11, ESRRB, NGB, AKAP13, WWOX, KCNJ12, ARHGEF1). …”
Publicado 2022
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1420por de Polli Cellin, Laurana, Menezes De Andrade, Nathalia Liberatoscioli, Rezende, Raíssa Carneiro, Rezende, Raíssa, Souza, Vinicius, Branco Dantas, Naiara Castelo, Quedas, Elisangela, de Assis Funari, Mariana Ferreira, Vasques, Gabriela, Da Cunha Scalco, Renata, Malaquias, Alexsandra C, Jorge, Alexander“…Fifteen patients have variants of uncertain significance (VUS) in genes already associated with growth disorder: IHH (3x), FGFR3 (2x), NPR2 (2x), LZTR1 (2x), MMP13, COL11A1, COL11A2, EXT2, IGF1R, and WNT5. …”
Publicado 2023
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