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Kolbe

Showing results (1121-1130 of 1,381) with videos related to

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Glia|September 3, 2020
Diacylglycerol lipase alpha in astrocytes is involved in maternal care and affective behaviorsLena-Louise Schuele, Sandra Glasmacher, Jürg Gertsch, et al.
Communications Biology|November 4, 2022
ATP-binding and hydrolysis of human NLRP3Rebecca Brinkschulte, David M Fußhöller, Florian Hoss, et al.
International Journal of Cosmetic Science|May 12, 2020
Validation of a new in vitro Sun Protection Factor method to include a wide range of sunscreen product emulsion typesM Pissavini, C Tricaud, G Wiener, et al.
Breathe (Sheffield, England)|August 26, 2015
Optimising inhaled mannitol for cystic fibrosis in an adult populationPatrick A Flume, Moira L Aitken, Diana Bilton, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 2009
Dendritic cells require STAT-1 phosphorylated at its transactivating domain for the induction of peptide-specific CTLAndreas Pilz, Wolfgang Kratky, Silvia Stockinger, et al.
Bone Marrow Transplantation|August 18, 2009
Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantationR G Meyer, E M Wagner, A Konur, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.
The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 14, 2025
Biomechanical Corneal Parameters in Eyes With Chronic Ocular Hypotony and in Non-Hypotonic Eyes. Self-Controlled Case Series StudyRachid Bouchikh-El Jarroudi, Kolbe Roche Fernández, Pau Romera Romero, et al.
Pageof 139

Showing results (1121-1130 of 1,381) with videos related to

Sort By:
Pageof 139
Glia|September 3, 2020
Diacylglycerol lipase alpha in astrocytes is involved in maternal care and affective behaviorsLena-Louise Schuele, Sandra Glasmacher, Jürg Gertsch, et al.
Communications Biology|November 4, 2022
ATP-binding and hydrolysis of human NLRP3Rebecca Brinkschulte, David M Fußhöller, Florian Hoss, et al.
International Journal of Cosmetic Science|May 12, 2020
Validation of a new in vitro Sun Protection Factor method to include a wide range of sunscreen product emulsion typesM Pissavini, C Tricaud, G Wiener, et al.
Breathe (Sheffield, England)|August 26, 2015
Optimising inhaled mannitol for cystic fibrosis in an adult populationPatrick A Flume, Moira L Aitken, Diana Bilton, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 2009
Dendritic cells require STAT-1 phosphorylated at its transactivating domain for the induction of peptide-specific CTLAndreas Pilz, Wolfgang Kratky, Silvia Stockinger, et al.
Bone Marrow Transplantation|August 18, 2009
Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantationR G Meyer, E M Wagner, A Konur, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.
The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 14, 2025
Biomechanical Corneal Parameters in Eyes With Chronic Ocular Hypotony and in Non-Hypotonic Eyes. Self-Controlled Case Series StudyRachid Bouchikh-El Jarroudi, Kolbe Roche Fernández, Pau Romera Romero, et al.
Pageof 139