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C Alexander Valencia

Showing results (21-30 of 68) with videos related to

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PNAS Nexus|July 24, 2024
DNA-encoded probe-based assay for profiling plant kinase activitiesYuan-Chi Chien, C Alexander Valencia, Han Yong Lee, et al.
Journal of Clinical Immunology|September 11, 2014
Combined immune deficiency in a patient with a novel NFKB2 mutationAndrew W Lindsley, Yaping Qian, C Alexander Valencia, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 21, 2005
Scanning the human proteome for calmodulin-binding proteinsXinchun Shen, C Alexander Valencia, Jack W Szostak, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2007
Proteome-wide identification of family member-specific natural substrate repertoire of caspasesWujian Ju, C Alexander Valencia, Hao Pang, et al.
Journal of Genetic Counseling|December 18, 2016
Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual UnderstandingLeandra K Tolusso, Kathleen Collins, Xue Zhang, et al.
Human Mutation|October 18, 2014
Clinical applications and implications of common and founder mutations in Indian subpopulationsArunkanth Ankala, Parag M Tamhankar, C Alexander Valencia, et al.
Cell Calcium|September 15, 2007
Ca(2+)/Calmodulin-binding proteins from the C. elegans proteomeXinchun Shen, C Alexander Valencia, Weiyi Gao, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 21, 2020
An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticistRafael Mena, Esperanza Mendoza, Maria Gomez Peña, et al.
Blood|June 12, 2014
Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosisKejian Zhang, Shanmuganathan Chandrakasan, Heather Chapman, et al.
Pediatric Diabetes|November 5, 2015
Bilateral cataracts in a 6-yr-old with new onset diabetes: a novel presentation of a known INS gene mutationHalley Wasserman, Robert B Hufnagel, Virginia Miraldi Utz, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
PNAS Nexus|July 24, 2024
DNA-encoded probe-based assay for profiling plant kinase activitiesYuan-Chi Chien, C Alexander Valencia, Han Yong Lee, et al.
Journal of Clinical Immunology|September 11, 2014
Combined immune deficiency in a patient with a novel NFKB2 mutationAndrew W Lindsley, Yaping Qian, C Alexander Valencia, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 21, 2005
Scanning the human proteome for calmodulin-binding proteinsXinchun Shen, C Alexander Valencia, Jack W Szostak, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2007
Proteome-wide identification of family member-specific natural substrate repertoire of caspasesWujian Ju, C Alexander Valencia, Hao Pang, et al.
Journal of Genetic Counseling|December 18, 2016
Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual UnderstandingLeandra K Tolusso, Kathleen Collins, Xue Zhang, et al.
Human Mutation|October 18, 2014
Clinical applications and implications of common and founder mutations in Indian subpopulationsArunkanth Ankala, Parag M Tamhankar, C Alexander Valencia, et al.
Cell Calcium|September 15, 2007
Ca(2+)/Calmodulin-binding proteins from the C. elegans proteomeXinchun Shen, C Alexander Valencia, Weiyi Gao, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 21, 2020
An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticistRafael Mena, Esperanza Mendoza, Maria Gomez Peña, et al.
Blood|June 12, 2014
Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosisKejian Zhang, Shanmuganathan Chandrakasan, Heather Chapman, et al.
Pediatric Diabetes|November 5, 2015
Bilateral cataracts in a 6-yr-old with new onset diabetes: a novel presentation of a known INS gene mutationHalley Wasserman, Robert B Hufnagel, Virginia Miraldi Utz, et al.
Pageof 7