Items where Author is "Kim, J"

Article

Dueck, H and Khaladkar, M and Kim, TK and Spaethling, JM and Francis, C and Suresh, S and Fisher, SA and Seale, P and Beck, SG and Bartfai, T and Kuhn, B and Eberwine, J and Kim, J (2015) Deep sequencing reveals cell-type-specific patterns of single-cell transcriptome variation. Genome Biology, 16 (1). ISSN 1474-7596

Tourette, C and Farina, F and Vazquez-Manrique, RP and Orfila, AM and Voisin, J and Hernandez, S and Offner, N and Parker, JA and Menet, S and Kim, J and Lyu, J and Choi, SH and Cormier, K and Edgerly, CK and Bordiuk, OL and Smith, K and Louise, A and Halford, M and Stacker, S and Vert, JP and Ferrante, RJ and Lu, W and Neri, C (2014) The Wnt Receptor Ryk Reduces Neuronal and Cell Survival Capacity by Repressing FOXO Activity During the Early Phases of Mutant Huntingtin Pathogenicity. PLoS Biology, 12 (6). ISSN 1544-9173

Kim, J and Stirling, KJ and Cooper, ME and Ascoli, M and Momany, AM and McDonald, EL and Ryckman, KK and Rhea, L and Schaa, KL and Cosentino, V and Gadow, E and Saleme, C and Shi, M and Hallman, M and Plunkett, J and Teramo, KA and Muglia, LJ and Feenstra, B and Geller, F and Boyd, HA and Melbye, M and Marazita, ML and Dagle, JM and Murray, JC (2013) Sequence variants in oxytocin pathway genes and preterm birth: A candidate gene association study. BMC Medical Genetics, 14 (1).

Pope, WH and Jacobs-Sera, D and Russel, DA and Peebles, CL and Al-Atrache, Z and Alcoser, TA and Alexander, LM and Alfano, MB and Alford, ST and Amy, NE and Anderson, MD and Anderson, AG and Ang, AAS and Manuel, A and Barber, AJ and Barker, LP and Barrett, JM and Barshop, WD and Bauerle, CM and Bayles, IM and Belfield, KL and Best, AA and Agustin, B and Bowman, CA and Boyer, CA and Bradley, KW and Bradley, VA and Broadway, LN and Budwal, K and Busby, KN and Campbell, IW and Campbell, AM and Carey, A and Caruso, SM and Chew, RD and Cockburn, CL and Cohen, LB and Corajod, JM and Cresawn, SG and Davis, KR and Deng, L and Denver, DR and Dixon, BR and Ekram, S and Elgin, SCR and Engelsen, AE and English, BEV and Erb, ML and Estrada, C and Filliger, LZ and Findley, AM and Forbes, L and Forsyth, MH and Fox, TM and Fritz, MJ and Garcia, R and George, ZD and Georges, AE and Gissendanner, CR and Goff, S and Goldstein, R and Gordon, KC and Green, RD and Guerra, SL and Guiney-Olsen, KR and Guiza, BG and Haghighat, L and Hagopian, GV and Harmon, CJ and Harmson, JS and Hartzog, GA and Harvey, SE and He, S and He, KJ and Healy, KE and Higinbotham, ER and Hildebrandt, EN and Ho, JH and Hogan, GM and Hohenstein, VG and Holz, NA and Huang, VJ and Hufford, EL and Hynes, PM and Jackson, AS and Jansen, EC and Jarvik, J and Jasinto, PG and Jordan, TC and Kasza, T and Katelyn, MA and Kelsey, JS and Kerrigan, LA and Khaw, D and Kim, J and Knutter, JZ and Ko, CC and Larkin, GV and Laroche, JR and Latif, A (2011) Expanding the diversity of mycobacteriophages: Insights into genome architecture and evolution. PLoS ONE, 6 (1).

Bucan, M and Abrahams, BS and Wang, K and Glessner, JT and Herman, EI and Sonnenblick, LI and Alvarez Retuerto, AI and Imielinski, M and Hadley, D and Bradfield, JP and Kim, C and Gidaya, NB and Lindquist, I and Hutman, T and Sigman, M and Kustanovich, V and Lajonchere, CM and Singleton, A and Kim, J and Wassink, TH and McMahon, WM and Owley, T and Sweeney, JA and Coon, H and Nurnberger, JI and Li, M and Cantor, RM and Minshew, NJ and Sutcliffe, JS and Cook, EH and Dawson, G and Buxbaum, JD and Grant, SFA and Schellenberg, GD and Geschwind, DH and Hakonarson, H (2009) Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genetics, 5 (6). ISSN 1553-7390