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The Journal of Biological Chemistry|July 29, 1994
Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gatingK L Gunderson, R R KopitoCell|July 28, 1995
Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysisK L Gunderson, R R KopitoThe Journal of Biological Chemistry|September 17, 1999
Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gatingM A Harrington, K L Gunderson, R R KopitoGenome Research|December 10, 1998
Mutation detection by ligation to complete n-mer DNA arraysK L Gunderson, X C Huang, M S Morris, et al.American Journal of Medical Genetics. Part A|March 3, 2007
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and reviewP A Lennon, M L Cooper, D A Peiffer, et al.Science (New York, N.Y.)|March 29, 1996
Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATPM M Reddy, P M Quinton, C Haws, et al.Clinical Genetics|October 6, 2007
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridizationN Brunetti-Pierri, D K Grange, Z Ou, et al.Clinical Genetics|June 30, 2009
Identification of critical regions for clinical features of distal 10q deletion syndromeS A Yatsenko, M C Kruer, P I Bader, et al.Blood Cancer Journal|April 11, 2015
Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell developmentE N Smith, E M Ghia, C M DeBoever, et al.Pageof 1