نتائج البحث - Curt Scharfe
- يعرض 1 - 13 نتائج من 13
-
1
-
2
-
3
-
4
-
5
-
6
-
7
Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes حسب Curt Scharfe, Henry Horng‐Shing Lu, Jutta K. Neuenburg, Edward A. Allen, Guan-Cheng Li, Thomas Klopstock, Tina M. Cowan, Gregory M. Enns, Ronald W. Davis
منشور في 2009Artigo -
8
Combining newborn metabolic and DNA analysis for second-tier testing of methylmalonic acidemia حسب Gang Peng, Peidong Shen, Neeru Gandotra, Anthony Le, Eula Fung, Laura L. Jelliffe‐Pawlowski, Ronald W. Davis, Gregory M. Enns, Hongyu Zhao, Tina M. Cowan, Curt Scharfe
منشور في 2018Artigo -
9
A systems biology approach identifies the role of dysregulated PRDM6 in the development of hypertension حسب Kushan Gunawardhana, Lingjuan Hong, Trojan Rugira, Severin Uebbing, Joanna Kucharczak, Sameet Mehta, Dineth R. Karunamuni, Brenda Cabrera‐Mendoza, Neeru Gandotra, Curt Scharfe, Renato Polimanti, James P. Noonan, Arya Mani
منشور في 2023Artigo -
10
Acylcarnitine Profiles Reflect Metabolic Vulnerability for Necrotizing Enterocolitis in Newborns Born Premature حسب Karl G. Sylvester, Zachary J. Kastenberg, R.L. Moss, Gregory M. Enns, Tina M. Cowan, Gary M. Shaw, David K. Stevenson, Tiffany J. Sinclair, Curt Scharfe, Kelli K. Ryckman, Laura L. Jelliffe‐Pawlowski
منشور في 2016Artigo -
11
The Role of Selection in the Evolution of Human Mitochondrial Genomes حسب Toomas Kivisild, Peidong Shen, Dennis P. Wall, Bao Do, Raphael Sung, Karen Davis, Giuseppe Passarino, Peter A. Underhill, Curt Scharfe, Antonio Torroni, Rosaria Scozzari, David Modiano, Alfredo Coppa, Peter de Knijff, Marcus W. Feldman, L. L. Cavalli‐Sforza, Peter J. Oefner
منشور في 2005Artigo -
12
Integrative Analysis of the Mitochondrial Proteome in Yeast حسب Holger Prokisch, Curt Scharfe, David Camp, Wenzhong Xiao, Lior David, Christophe Andréoli, Matthew Monroe, Ronald J. Moore, Marina Gritsenko, C. Kozany, Kim Hixson, Heather M. Mottaz, Hans Zischka, Marius Ueffing, Zelek S. Herman, Ronald W. Davis, Thomas Meitinger, Peter J. Oefner, Richard Smith, Lars M. Steinmetz
منشور في 2004Artigo -
13
Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for t... حسب Marni J. Falk, Li Shen, Michael Gonzalez, Jeremy Leipzig, Marie T. Lott, Alphons P. M. Stassen, Maria Angela Diroma, Daniel Navarro-Gomez, Philip E. Yeske, Renkui Bai, Richard G. Boles, Virginia Brilhante, David Ralph, Jeana T. DaRe, Robert Shelton, Sharon F. Terry, Zhe Zhang, William C. Copeland, Mannis van Oven, Holger Prokisch, Douglas C. Wallace, Marcella Attimonelli, Danuta Krotoski, Stephan Züchner, Xiaowu Gai, Sherri J. Bale, Jirair K. Bedoyan, Doron M. Behar, Penelope E. Bonnen, Lisa Brooks, Claudia Calabrese, Sarah E. Calvo, Patrick F. Chinnery, John Christodoulou, Deanna M. Church, Rosanna Clima, Bruce H. Cohen, Richard G.H. Cotton, I.F.M. de Coo, Olga Derbenevoa, Johan T. den Dunnen, David Dimmock, Gregory M. Enns, Giuseppe Gasparre, Amy Goldstein, Iris L. Gonzalez, Katrina Gwinn, Sihoun Hahn, Richard Haas, Hákon Hákonarson, Michio Hirano, Douglas S. Kerr, Dong Li, Maria Lvova, Finley Macrae, Donna Maglott, Elizabeth M. McCormick, Grant Mitchell, Vamsi K. Mootha, Yasushi Okazaki, Aurora Pujol, Melissa A. Parisi, Juan C. Perín, Eric A. Pierce, Vincent Procaccio, Shamima Rahman, Reddi Honey, Heidi L. Rehm, Erin Rooney Riggs, Richard J. Rodenburg, Yaffa Rubinstein, Russell P. Saneto, Mariangela Santorsola, Curt Scharfe, Claire A. Sheldon, Eric A. Shoubridge, Domenico Simone, H.J.M. Smeets, Jan Smeitink, Christine M. Stanley, Anu Suomalainen, Mark A. Tarnopolsky, Isabelle Thiffault, David R. Thorburn, Johan Van Hove, Lynne A. Wolfe, Lee-Jun Wong
منشور في 2014Revisão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Computational biology
Medicine
Computer science
Genome
Internal medicine
Bioinformatics
Disease
Mitochondrial DNA
Mutation
Pediatrics
Allele
DNA sequencing
Endocrinology
Enhancer
Evolutionary biology
Exon
False positive paradox
Function (biology)
Gene expression
Methylmalonic acidemia
Mitochondrial disease
Mitochondrion
Multiplex
Newborn screening
Pathology
Phenotype
Sanger sequencing