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Showing results (651-660 of 694) with videos related to

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European Journal of Human Genetics : EJHG|September 20, 2019
MNS1 variant associated with situs inversus and male infertilityJoseph S Leslie, Lettie E Rawlins, Barry A Chioza, et al.
Free Radical Biology & Medicine|December 13, 2025
Rapid design and production of Alpha-1 antitrypsin fusion proteins in a plant-based cell-free expression systemAnindya Karmaker, Faris Alyami, Connor A Randolph, et al.
Parkinsonism & Related Disorders|December 1, 2020
Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoformOlivia J Rickman, Claire G Salter, Adam C Gunning, et al.
Communications Biology|December 13, 2022
Tissue registration and exploration user interfaces in support of a human reference atlasKaty Börner, Andreas Bueckle, Bruce W Herr, et al.
American Journal of Human Genetics|October 26, 2010
Defective mitochondrial mRNA maturation is associated with spastic ataxiaAndrew H Crosby, Heema Patel, Barry A Chioza, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 27, 2016
Key Matrix Proteins Within the Pancreatic Islet Basement Membrane Are Differentially Digested During Human Islet IsolationS E Cross, R H Vaughan, A J Willcox, et al.
Molecular Cancer Therapeutics|December 6, 2014
Optimizing the sequence of anti-EGFR-targeted therapy in EGFR-mutant lung cancerCatherine B Meador, Hailing Jin, Elisa de Stanchina, et al.
Diabetes|May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-ChannelRachel J Salisbury, Bing Han, Rachel E Jennings, et al.
Plos Genetics|September 27, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorderZineb Ammous, Lettie E Rawlins, Hannah Jones, et al.
American Journal of Human Genetics|November 19, 2013
Mutations in KPTN cause macrocephaly, neurodevelopmental delay, and seizuresEmma L Baple, Reza Maroofian, Barry A Chioza, et al.
Pageof 70

Showing results (651-660 of 694) with videos related to

Sort By:
Pageof 70
European Journal of Human Genetics : EJHG|September 20, 2019
MNS1 variant associated with situs inversus and male infertilityJoseph S Leslie, Lettie E Rawlins, Barry A Chioza, et al.
Free Radical Biology & Medicine|December 13, 2025
Rapid design and production of Alpha-1 antitrypsin fusion proteins in a plant-based cell-free expression systemAnindya Karmaker, Faris Alyami, Connor A Randolph, et al.
Parkinsonism & Related Disorders|December 1, 2020
Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoformOlivia J Rickman, Claire G Salter, Adam C Gunning, et al.
Communications Biology|December 13, 2022
Tissue registration and exploration user interfaces in support of a human reference atlasKaty Börner, Andreas Bueckle, Bruce W Herr, et al.
American Journal of Human Genetics|October 26, 2010
Defective mitochondrial mRNA maturation is associated with spastic ataxiaAndrew H Crosby, Heema Patel, Barry A Chioza, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 27, 2016
Key Matrix Proteins Within the Pancreatic Islet Basement Membrane Are Differentially Digested During Human Islet IsolationS E Cross, R H Vaughan, A J Willcox, et al.
Molecular Cancer Therapeutics|December 6, 2014
Optimizing the sequence of anti-EGFR-targeted therapy in EGFR-mutant lung cancerCatherine B Meador, Hailing Jin, Elisa de Stanchina, et al.
Diabetes|May 2, 2015
Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-ChannelRachel J Salisbury, Bing Han, Rachel E Jennings, et al.
Plos Genetics|September 27, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorderZineb Ammous, Lettie E Rawlins, Hannah Jones, et al.
American Journal of Human Genetics|November 19, 2013
Mutations in KPTN cause macrocephaly, neurodevelopmental delay, and seizuresEmma L Baple, Reza Maroofian, Barry A Chioza, et al.
Pageof 70