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L Wenger

Showing results (171-180 of 221) with videos related to

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Circulation Research|June 1, 1980
Procainamide delivery to ischemic canine myocardium following rapid intravenous administrationT L Wenger, D J Browning, C E Masterton, et al.
Genomics|May 1, 1996
Chromosomal mapping of the human M6 genesS Olinsky, B T Loop, A DeKosky, et al.
The Journal of Biological Chemistry|February 7, 2001
Wild type and mutant p53 differentially regulate the gene expression of human collagenase-3 (hMMP-13)Y Sun, J M Cheung, J Martel-Pelletier, et al.
Neoreviews|March 1, 2024
Ethical and Legal Issues Surrounding Genetic Testing in the NICUKatharine P Callahan, Ellen W Clayton, Amy A Lemke, et al.
American Journal of Medical Genetics|April 15, 2000
Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22sS L Wenger, L Y Boone, J H Cummins, et al.
Human Genetics|January 28, 1999
Relaxation of imprinting in Prader-Willi syndromeP K Rogan, J R Seip, L M White, et al.
Clinical Case Reports|February 14, 2022
Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapyPrasanth Pattisapu, Tara L Wenger, John P Dahl, et al.
Human Molecular Genetics|December 10, 2003
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocorneaVera A Voronina, Elena A Kozhemyakina, Christina M O'Kernick, et al.
Scientific Reports|January 20, 2016
The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum DisorderTara L Wenger, Charlly Kao, Donna M McDonald-McGinn, et al.
American Journal of Medical Genetics. Part A|January 20, 2017
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndromeTara L Wenger, Penny Chow, Stephanie C Randle, et al.
Pageof 23

Showing results (171-180 of 221) with videos related to

Sort By:
Pageof 23
Circulation Research|June 1, 1980
Procainamide delivery to ischemic canine myocardium following rapid intravenous administrationT L Wenger, D J Browning, C E Masterton, et al.
Genomics|May 1, 1996
Chromosomal mapping of the human M6 genesS Olinsky, B T Loop, A DeKosky, et al.
The Journal of Biological Chemistry|February 7, 2001
Wild type and mutant p53 differentially regulate the gene expression of human collagenase-3 (hMMP-13)Y Sun, J M Cheung, J Martel-Pelletier, et al.
Neoreviews|March 1, 2024
Ethical and Legal Issues Surrounding Genetic Testing in the NICUKatharine P Callahan, Ellen W Clayton, Amy A Lemke, et al.
American Journal of Medical Genetics|April 15, 2000
Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22sS L Wenger, L Y Boone, J H Cummins, et al.
Human Genetics|January 28, 1999
Relaxation of imprinting in Prader-Willi syndromeP K Rogan, J R Seip, L M White, et al.
Clinical Case Reports|February 14, 2022
Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapyPrasanth Pattisapu, Tara L Wenger, John P Dahl, et al.
Human Molecular Genetics|December 10, 2003
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocorneaVera A Voronina, Elena A Kozhemyakina, Christina M O'Kernick, et al.
Scientific Reports|January 20, 2016
The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum DisorderTara L Wenger, Charlly Kao, Donna M McDonald-McGinn, et al.
American Journal of Medical Genetics. Part A|January 20, 2017
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndromeTara L Wenger, Penny Chow, Stephanie C Randle, et al.
Pageof 23