Výsledky vyhledávání - Veeraraghavan, Narayanan

Long distance communication in the HDV ribozyme: Insights from molecular dynamics and experiments Autor Veeraraghavan, Narayanan, Bevilacqua, Philip C., Hammes-Schiffer, Sharon

Získat plný text Získat plný text Získat plný text

Mechanistic Strategies in the HDV Ribozyme: Chelated and Diffuse Metal Ion Interactions and Active Site Protonation Autor Veeraraghavan, Narayanan, Ganguly, Abir, Golden, Barbara L., Bevilacqua, Philip C., Hammes-Schiffer, Sharon

Získat plný text Získat plný text Získat plný text

Metal Binding Motif in the Active Site of the HDV Ribozyme Binds Divalent and Monovalent Ions Autor Veeraraghavan, Narayanan, Ganguly, Abir, Chen, Jui-Hui, Bevilacqua, Philip C., Hammes-Schiffer, Sharon, Golden, Barbara L.

Získat plný text Získat plný text Získat plný text

A hybrid computational strategy to address WGS variant analysis in >5000 samples Autor Huang, Zhuoyi, Rustagi, Navin, Veeraraghavan, Narayanan, Carroll, Andrew, Gibbs, Richard, Boerwinkle, Eric, Venkata, Manjunath Gorentla, Yu, Fuli

Získat plný text Získat plný text Získat plný text

ChloroplastDB: the Chloroplast Genome Database Autor Cui, Liying, Veeraraghavan, Narayanan, Richter, Alexander, Wall, Kerr, Jansen, Robert K., Leebens-Mack, Jim, Makalowska, Izabela, dePamphilis, Claude W.

Získat plný text Získat plný text Získat plný text

The Genome Sequence of Lone Star Virus, a Highly Divergent Bunyavirus Found in the Amblyomma americanum Tick Autor Swei, Andrea, Russell, Brandy J., Naccache, Samia N., Kabre, Beniwende, Veeraraghavan, Narayanan, Pilgard, Mark A., Johnson, Barbara J. B., Chiu, Charles Y.

Získat plný text Získat plný text Získat plný text

Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses Autor James, Kiely N., Clark, Michelle M., Camp, Brandon, Kint, Cyrielle, Schols, Peter, Batalov, Sergey, Briggs, Benjamin, Veeraraghavan, Narayanan, Chowdhury, Shimul, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

A framework for collaborative analysis of ENCODE data: Making large-scale analyses biologist-friendly Autor Blankenberg, Daniel, Taylor, James, Schenck, Ian, He, Jianbin, Zhang, Yi, Ghent, Matthew, Veeraraghavan, Narayanan, Albert, Istvan, Miller, Webb, Makova, Kateryna D., Hardison, Ross C., Nekrutenko, Anton

Získat plný text Získat plný text Získat plný text

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease Autor Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease Autor Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease Autor Sweeney, Nathaly M., Nahas, Shareef A., Chowdhury, Shimul, Batalov, Sergey, Clark, Michelle, Caylor, Sara, Cakici, Julie, Nigro, John J., Ding, Yan, Veeraraghavan, Narayanan, Hobbs, Charlotte, Dimmock, David, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome Autor Polfus, Linda M., Boerwinkle, Eric, Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Grove, Megan, Shete, Sanjay, Wallace, Stephanie, Milewicz, Dianna, Hanchard, Neil, Lupski, James R., Hashmi, Syed Shahrukh, Gupta-Malhotra, Monesha

Získat plný text Získat plný text Získat plný text

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline Autor Reid, Jeffrey G, Carroll, Andrew, Veeraraghavan, Narayanan, Dahdouli, Mahmoud, Sundquist, Andreas, English, Adam, Bainbridge, Matthew, White, Simon, Salerno, William, Buhay, Christian, Yu, Fuli, Muzny, Donna, Daly, Richard, Duyk, Geoff, Gibbs, Richard A, Boerwinkle, Eric

Získat plný text Získat plný text Získat plný text

Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease Autor Li, Alexander H, Morrison, Alanna C, Kovar, Christie, Cupples, L Adrienne, Brody, Jennifer A, Polfus, Linda M, Yu, Bing, Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Liu, Xiaoming, Lumley, Thomas, Mosley, Thomas H, Gibbs, Richard A, Boerwinkle, Eric

Získat plný text Získat plný text Získat plný text

Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility Autor Kim, Jihoon, Shimizu, Chisato, Kingsmore, Stephen F., Veeraraghavan, Narayanan, Levy, Eric, Ribeiro dos Santos, Andre M., Yang, Hai, Flatley, Jay, Hoang, Long Truong, Hibberd, Martin L., Tremoulet, Adriana H., Harismendy, Olivier, Ohno-Machado, Lucila, Burns, Jane C.

Získat plný text Získat plný text Získat plný text

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization Autor Farnaes, Lauge, Hildreth, Amber, Sweeney, Nathaly M., Clark, Michelle M., Chowdhury, Shimul, Nahas, Shareef, Cakici, Julie A., Benson, Wendy, Kaplan, Robert H., Kronick, Richard, Bainbridge, Matthew N., Friedman, Jennifer, Gold, Jeffrey J., Ding, Yan, Veeraraghavan, Narayanan, Dimmock, David, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine Levels and Incident Coronary Heart Disease Autor Yu, Bing, Li, Alexander H., Muzny, Donna, Veeraraghavan, Narayanan, de Vries, Paul S., Bis, Joshua C., Musani, Solomon K., Alexander, Danny, Morrison, Alanna C., Franco, Oscar H., Uitterlinden, André, Hofman, Albert, Dehghan, Abbas, Wilson, James G., Psaty, Bruce M., Gibbs, Richard, Wei, Peng, Boerwinkle, Eric

Získat plný text Získat plný text Získat plný text

Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation Autor Eicher, John D., Chen, Ming-Huei, Pitsillides, Achilleas N., Lin, Honghuang, Veeraraghavan, Narayanan, Brody, Jennifer A., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Becker, Diane M., Becker, Lewis C., Faraday, Nauder, Mathias, Rasika A., Yanek, Lisa R., Boerwinkle, Eric, Cupples, L. Adrienne, Johnson, Andrew D.

Získat plný text Získat plný text Získat plný text

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants Autor Petrikin, Josh E., Cakici, Julie A., Clark, Michelle M., Willig, Laurel K., Sweeney, Nathaly M., Farrow, Emily G., Saunders, Carol J., Thiffault, Isabelle, Miller, Neil A., Zellmer, Lee, Herd, Suzanne M., Holmes, Anne M., Batalov, Serge, Veeraraghavan, Narayanan, Smith, Laurie D., Dimmock, David P., Leeder, J. Steven, Kingsmore, Stephen F.

Získat plný text Získat plný text Získat plný text

A Novel Rhabdovirus Associated with Acute Hemorrhagic Fever in Central Africa Autor Grard, Gilda, Fair, Joseph N., Lee, Deanna, Slikas, Elizabeth, Steffen, Imke, Muyembe, Jean-Jacques, Sittler, Taylor, Veeraraghavan, Narayanan, Ruby, J. Graham, Wang, Chunlin, Makuwa, Maria, Mulembakani, Prime, Tesh, Robert B., Mazet, Jonna, Rimoin, Anne W., Taylor, Travis, Schneider, Bradley S., Simmons, Graham, Delwart, Eric, Wolfe, Nathan D., Chiu, Charles Y., Leroy, Eric M.

Získat plný text Získat plný text Získat plný text