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A Geiger

Showing results (131-140 of 157) with videos related to

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Anatomical Record (Hoboken, N.J. : 2007)|August 31, 2012
A histological comparison of the original and regenerated tail in the green anole, Anolis carolinensisRebecca E Fisher, Lauren A Geiger, Laura K Stroik, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathyHung-Chun Yu, Curtis R Coughlin, Elizabeth A Geiger, et al.
Physical Review Letters|June 9, 2018
Observation and Uses of Position-Space Bloch Oscillations in an Ultracold GasZachary A Geiger, Kurt M Fujiwara, Kevin Singh, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndromeChad R Haldeman-Englert, Taiyabah Naeem, Elizabeth A Geiger, et al.
Journal of Medicinal Chemistry|November 7, 2000
Inhibition of protein synthesis by didemnins: cell potency and SARD Ahuja, A Geiger, J M Ramanjulu, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Chad R Haldeman-Englert, Kimberly A Chapman, Hillary Kruger, et al.
Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.
Arthritis and Rheumatism|July 15, 1998
Fcgamma receptor IIa polymorphism in Caucasian patients with systemic lupus erythematosus: association with clinical symptomsK Manger, R Repp, B M Spriewald, et al.
Journal of Neurosurgery|September 17, 2022
Use of heparin to rescue immunosuppressive monocyte reprogramming by glioblastoma-derived extracellular vesiclesBenjamin T Himes, Cori E Fain, Zachariah P Tritz, et al.
European Journal of Medical Genetics|December 23, 2008
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delayChad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, et al.
Pageof 16

Showing results (131-140 of 157) with videos related to

Sort By:
Pageof 16
Anatomical Record (Hoboken, N.J. : 2007)|August 31, 2012
A histological comparison of the original and regenerated tail in the green anole, Anolis carolinensisRebecca E Fisher, Lauren A Geiger, Laura K Stroik, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathyHung-Chun Yu, Curtis R Coughlin, Elizabeth A Geiger, et al.
Physical Review Letters|June 9, 2018
Observation and Uses of Position-Space Bloch Oscillations in an Ultracold GasZachary A Geiger, Kurt M Fujiwara, Kevin Singh, et al.
American Journal of Medical Genetics. Part A|July 18, 2009
A 781-kb deletion of 13q12.3 in a patient with Peters plus syndromeChad R Haldeman-Englert, Taiyabah Naeem, Elizabeth A Geiger, et al.
Journal of Medicinal Chemistry|November 7, 2000
Inhibition of protein synthesis by didemnins: cell potency and SARD Ahuja, A Geiger, J M Ramanjulu, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21Chad R Haldeman-Englert, Kimberly A Chapman, Hillary Kruger, et al.
Human Molecular Genetics|May 15, 2015
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain developmentPeter M Van Laarhoven, Leif R Neitzel, Anita M Quintana, et al.
Arthritis and Rheumatism|July 15, 1998
Fcgamma receptor IIa polymorphism in Caucasian patients with systemic lupus erythematosus: association with clinical symptomsK Manger, R Repp, B M Spriewald, et al.
Journal of Neurosurgery|September 17, 2022
Use of heparin to rescue immunosuppressive monocyte reprogramming by glioblastoma-derived extracellular vesiclesBenjamin T Himes, Cori E Fain, Zachariah P Tritz, et al.
European Journal of Medical Genetics|December 23, 2008
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delayChad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, et al.
Pageof 16