화학공학소재연구정보센터
검색결과 : 9건
No. Article
1 Electrochemical synthesis of flower like Mn-Co mixed metal oxides as electrode material for supercapacitor application
Kadam SL, Mane SM, Tirmali PM, Kulkarni SB
Current Applied Physics, 18(4), 397, 2018
2 Hybrid microwave sintering and shifting of Tc in lead-free ferroelectric composition x(Ba0.7Ca0.3TiO3)-(1-x)(BaZr0.2Ti0.8O3)
Mane SM, Tirmali PM, Kulkarni SB
Materials Chemistry and Physics, 213, 482, 2018
3 Molecular and cellular reorganization of neural circuits in the human lineage
Sousa AMM, Zhu Y, Raghanti MA, Kitchen RR, Onorati M, Tebbenkamp ATN, Stutz B, Meyer KA, Li MF, Kawasawa YI, Liu FC, Perez RG, Mele M, Carvalho T, Skarica M, Gulden FO, Pletikos M, Shibata A, Stephenson AR, Edler MK, Ely JJ, Elsworth JD, Horvath TL, Hof PR, Hyde TM, Kleinman JE, Weinberger DR, Reimers M, Lifton RP, Mane SM, Noonan JP, State MW, Lein ES, Knowles JA, Marques-Bonet T, Sherwood CC, Gerstein MB, Sestan N
Science, 358(6366), 1027, 2017
4 Enhanced specific capacitance and supercapacitive properties of polyaniline-iron oxide (PANI-Fe2O3) composite electrode material
Padwal PM, Kadam SL, Mane SM, Kulkarni SB
Journal of Materials Science, 51(23), 10499, 2016
5 Synthesis and characterization of PANI/MnO2 bi-layered electrode and its electrochemical supercapacitor properties
Kharade PM, Chavan SG, Salunkhe DJ, Joshi PB, Mane SM, Kulkarni SB
Materials Research Bulletin, 52, 37, 2014
6 The contribution of de novo coding mutations to autism spectrum disorder
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei LP, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang ZH, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma BC, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M
Nature, 515(7526), 216, 2014
7 De novo mutations in histone-modifying genes in congenital heart disease
Zaidi S, Choi M, Wakimoto H, Ma LJ, Jiang JM, Overton JD, Romano-Adesman A, Bjornson RD, Breitbart RE, Brown KK, Carriero NJ, Cheung YH, Deanfield J, DePalma S, Fakhro KA, Glessner J, Hakonarson H, Italia MJ, Kaltman JR, Kaski J, Kim R, Kline JK, Lee T, Leipzig J, Lopez A, Mane SM, Mitchell LE, Newburger JW, Parfenov M, Pe'er I, Porter G, Roberts AE, Sachidanandam R, Sanders SJ, Seiden HS, State MW, Subramanian S, Tikhonova IR, Wang W, Warburton D, White PS, Williams IA, Zhao HY, Seidman JG, Brueckner M, Chung WK, Gelb BD, Goldmuntz E, Seidman CE, Lifton RP
Nature, 498(7453), 220, 2013
8 Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Valimaki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, Tucci JR, Stockigt JR, Keppler-Noreuil KM, Porter CC, Anand SK, Whiteford ML, Davis ID, Dewar SB, Bettinelli A, Fadrowski JJ, Belsha CW, Hunley TE, Nelson RD, Trachtman H, Cole TRP, Pinsk M, Bockenhauer D, Shenoy M, Vaidyanathan P, Foreman JW, Rasoulpour M, Thameem F, Al-Shahrouri HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP
Nature, 482(7383), 98, 2012
9 De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Gunel M, Roeder K, Geschwind DH, Devlin B, State MW
Nature, 485(7397), 237, 2012