檢索結果 - Jayaraman, Vijayakumar

Pro-Inflammatory Chemokine CCL2 (MCP-1) Promotes Healing in Diabetic Wounds by Restoring the Macrophage Response 由 Wood, Stephen, Jayaraman, Vijayakumar, Huelsmann, Erica J., Bonish, Brian, Burgad, Derick, Sivaramakrishnan, Gayathri, Qin, Shanshan, DiPietro, Luisa A., Zloza, Andrew, Zhang, Chunxiang, Shafikhani, Sasha H.

獲取全文 獲取全文 獲取全文

Somatic variation as an incidental finding in the pediatric next-generation sequencing era 由 Melas, Marilena, Mathew, Mariam T., Mori, Mari, Jayaraman, Vijayakumar, Wilson, Sarah A., Martin, Cortlandt, Jacobson-Kelly, Amanda E., Kelly, Ben J., Magrini, Vincent, Mardis, Elaine R., Cottrell, Catherine E., Lee, Kristy

獲取全文 獲取全文 獲取全文

Utility and limitations of exome sequencing in the molecular diagnosis of pediatric inherited platelet disorders 由 Romasko, Edward J., Devkota, Batsal, Biswas, Sawona, Jayaraman, Vijayakumar, Rajagopalan, Ramakrishnan, Dulik, Matthew C., Thom, Christopher S., Choi, Jiwon, Jairam, Sowmya, Scarano, Maria I., Krantz, Ian D., Spinner, Nancy B., Conlin, Laura K., Lambert, Michele P.

獲取全文 獲取全文 獲取全文

Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience 由 Miller, Cecelia R., Lee, Kristy, Pfau, Ruthann B., Reshmi, Shalini C., Corsmeier, Donald J., Hashimoto, Sayaka, Dave-Wala, Ashita, Jayaraman, Vijayakumar, Koboldt, Daniel, Matthews, Theodora, Mouhlas, Danielle, Stein, Maggie, McKinney, Aimee, Grossman, Tom, Kelly, Benjamin J., White, Peter, Magrini, Vincent, Wilson, Richard K., Mardis, Elaine R., Cottrell, Catherine E.

獲取全文 獲取全文 獲取全文

Utility and limitations of exome sequencing as a genetic diagnostic tool for conditions associated with pediatric sudden cardiac arrest/sudden cardiac death 由 Li, Mindy H., Abrudan, Jenica L., Dulik, Matthew C., Sasson, Ariella, Brunton, Joshua, Jayaraman, Vijayakumar, Dugan, Noreen, Haley, Danielle, Rajagopalan, Ramakrishnan, Biswas, Sawona, Sarmady, Mahdi, DeChene, Elizabeth T., Deardorff, Matthew A., Wilkens, Alisha, Noon, Sarah E., Scarano, Maria I., Santani, Avni B., White, Peter S., Pennington, Jeffrey, Conlin, Laura K., Spinner, Nancy B., Krantz, Ian D., Vetter, Victoria L.

獲取全文 獲取全文 獲取全文

Utility and limitations of exome sequencing as a genetic diagnostic tool for children with hearing loss 由 Sheppard, Sarah, Biswas, Sawona, Li, Mindy H., Jayaraman, Vijayakumar, Slack, Ian, Romasko, Edward J., Sasson, Ariella, Brunton, Joshua, Rajagopalan, Ramakrishnan, Sarmady, Mahdi, Abrudan, Jenica L., Jairam, Sowmya, DeChene, Elizabeth T., Ying, Xiahoan, Choi, Jiwon, Wilkens, Alisha, Raible, Sarah E., Scarano, Maria I., Santani, Avni, Pennington, Jeffrey W., Luo, Minjie, Conlin, Laura K., Devkota, Batsal, Dulik, Matthew C., Spinner, Nancy B., Krantz, Ian D.

獲取全文 獲取全文 獲取全文

Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes 由 de Kovel, Carolien G. F., Syrbe, Steffen, Brilstra, Eva H., Verbeek, Nienke, Kerr, Bronwyn, Dubbs, Holly, Bayat, Allan, Desai, Sonal, Naidu, Sakkubai, Srivastava, Siddharth, Cagaylan, Hande, Yis, Uluc, Saunders, Carol, Rook, Martin, Plugge, Susanna, Muhle, Hiltrud, Afawi, Zaid, Klein, Karl-Martin, Jayaraman, Vijayakumar, Rajagopalan, Ramakrishnan, Goldberg, Ethan, Marsh, Eric, Kessler, Sudha, Bergqvist, Christina, Conlin, Laura K., Krok, Bryan L., Thiffault, Isabelle, Pendziwiat, Manuela, Helbig, Ingo, Polster, Tilman, Borggraefe, Ingo, Lemke, Johannes R., van den Boogaardt, Marie-José, Møller, Rikke S., Koeleman, Bobby P. C.

獲取全文 獲取全文 獲取全文