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N Lamb

Showing results (211-220 of 244) with videos related to

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BMJ Open|March 12, 2026
Top 10 priorities for problematic hip replacement research: a priority setting partnership led by the British Hip Society and the James Lind AllianceTim N Board, Asim Khan, Antony K Sorial, et al.
Plos One|July 23, 2013
Molecular organization of the nanoscale surface structures of the dragonfly Hemianax papuensis wing epicuticleElena P Ivanova, Song Ha Nguyen, Hayden K Webb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2011
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problemsTrilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, et al.
Bioinformatics (Oxford, England)|January 31, 2004
Database model and specification of GermOnline Release 2.0, a cross-species community annotation knowledgebase on germ cell differentiationC Wiederkehr, R Basavaraj, C Sarrauste de Menthière, et al.
ACS Omega|January 17, 2022
Discovery of Potent Peptidomimetic Antagonists for Heterochromatin Protein 1 Family ProteinsKelsey N Lamb, Sarah N Dishman, Jarod M Waybright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Clinical Genetics|March 30, 2010
Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2S Alliman, J Coppinger, J Marcadier, et al.
European Journal of Human Genetics : EJHG|July 1, 2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeAngela L Duker, Blake C Ballif, Erawati V Bawle, et al.
Nature Communications|November 28, 2013
Bactericidal activity of black siliconElena P Ivanova, Jafar Hasan, Hayden K Webb, et al.
Scientific Reports|June 1, 2018
Structure and Chemical Organization in Damselfly Calopteryx haemorrhoidalis Wings: A Spatially Resolved FTIR and XRF Analysis with Synchrotron RadiationSusan Stuhr, Vi Khanh Truong, Jitraporn Vongsvivut, et al.
Pageof 25

Showing results (211-220 of 244) with videos related to

Sort By:
Pageof 25
BMJ Open|March 12, 2026
Top 10 priorities for problematic hip replacement research: a priority setting partnership led by the British Hip Society and the James Lind AllianceTim N Board, Asim Khan, Antony K Sorial, et al.
Plos One|July 23, 2013
Molecular organization of the nanoscale surface structures of the dragonfly Hemianax papuensis wing epicuticleElena P Ivanova, Song Ha Nguyen, Hayden K Webb, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2011
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problemsTrilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, et al.
Bioinformatics (Oxford, England)|January 31, 2004
Database model and specification of GermOnline Release 2.0, a cross-species community annotation knowledgebase on germ cell differentiationC Wiederkehr, R Basavaraj, C Sarrauste de Menthière, et al.
ACS Omega|January 17, 2022
Discovery of Potent Peptidomimetic Antagonists for Heterochromatin Protein 1 Family ProteinsKelsey N Lamb, Sarah N Dishman, Jarod M Waybright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Clinical Genetics|March 30, 2010
Clinical and molecular characterization of individuals with recurrent genomic disorder at 10q22.3q23.2S Alliman, J Coppinger, J Marcadier, et al.
European Journal of Human Genetics : EJHG|July 1, 2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeAngela L Duker, Blake C Ballif, Erawati V Bawle, et al.
Nature Communications|November 28, 2013
Bactericidal activity of black siliconElena P Ivanova, Jafar Hasan, Hayden K Webb, et al.
Scientific Reports|June 1, 2018
Structure and Chemical Organization in Damselfly Calopteryx haemorrhoidalis Wings: A Spatially Resolved FTIR and XRF Analysis with Synchrotron RadiationSusan Stuhr, Vi Khanh Truong, Jitraporn Vongsvivut, et al.
Pageof 25