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Kaindl

Showing results (381-390 of 543) with videos related to

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Physical Review Letters|January 22, 2002
Far-infrared optical conductivity gap in superconducting MgB2 filmsRobert A Kaindl, Marc A Carnahan, Joseph Orenstein, et al.
Stem Cells Translational Medicine|November 21, 2018
Zooming in on Cryopreservation of hiPSCs and Neural Derivatives: A Dual-Center Study Using Adherent VitrificationJohanna Kaindl, Ina Meiser, Julia Majer, et al.
Journal of Translational Medicine|January 16, 2022
First evidence of long-term effects of transcranial pulse stimulation (TPS) on the human brainEva Matt, Lisa Kaindl, Saskia Tenk, et al.
Human Mutation|August 10, 2005
Homozygous microdeletion of chromosome 4q11-q12 causes severe limb-girdle muscular dystrophy type 2E with joint hyperlaxity and contracturesAngela M Kaindl, Sibylle Jakubiczka, Thomas Lücke, et al.
Nature Chemical Biology|March 11, 2020
Activation of the α<sub>2B</sub> adrenoceptor by the sedative sympatholytic dexmedetomidineDaopeng Yuan, Zhongmin Liu, Jonas Kaindl, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Orphanet Journal of Rare Diseases|November 16, 2013
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutationHeba Gamal Farag, Sebastian Froehler, Konrad Oexle, et al.
Clinical Genetics|November 10, 2015
Genetic causes of MCPH in consanguineous Pakistani familiesNadine Kraemer, Sylvie Picker-Minh, Ansar A Abbasi, et al.
Frontiers in Ophthalmology|March 14, 2025
Ocular symptoms in COVID-19 patients with a history of hospitalization in the first pandemic wave in Styria, AustriaAndreas Guttmann, Astrid Heidinger, Nora Woltsche, et al.
Journal of Neurosurgery. Pediatrics|April 10, 2026
Characteristics of repeated untethering pattern in patients with myelomeningocele from infancy to adolescenceJoanna Schneider, Gesa Cohrs, Magín de la Flor, et al.
Pageof 55

Showing results (381-390 of 543) with videos related to

Sort By:
Pageof 55
Physical Review Letters|January 22, 2002
Far-infrared optical conductivity gap in superconducting MgB2 filmsRobert A Kaindl, Marc A Carnahan, Joseph Orenstein, et al.
Stem Cells Translational Medicine|November 21, 2018
Zooming in on Cryopreservation of hiPSCs and Neural Derivatives: A Dual-Center Study Using Adherent VitrificationJohanna Kaindl, Ina Meiser, Julia Majer, et al.
Journal of Translational Medicine|January 16, 2022
First evidence of long-term effects of transcranial pulse stimulation (TPS) on the human brainEva Matt, Lisa Kaindl, Saskia Tenk, et al.
Human Mutation|August 10, 2005
Homozygous microdeletion of chromosome 4q11-q12 causes severe limb-girdle muscular dystrophy type 2E with joint hyperlaxity and contracturesAngela M Kaindl, Sibylle Jakubiczka, Thomas Lücke, et al.
Nature Chemical Biology|March 11, 2020
Activation of the α<sub>2B</sub> adrenoceptor by the sedative sympatholytic dexmedetomidineDaopeng Yuan, Zhongmin Liu, Jonas Kaindl, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 23, 2008
[Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]A M Kaindl, U-P Guenther, S Rudnik-Schöneborn, et al.
Orphanet Journal of Rare Diseases|November 16, 2013
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutationHeba Gamal Farag, Sebastian Froehler, Konrad Oexle, et al.
Clinical Genetics|November 10, 2015
Genetic causes of MCPH in consanguineous Pakistani familiesNadine Kraemer, Sylvie Picker-Minh, Ansar A Abbasi, et al.
Frontiers in Ophthalmology|March 14, 2025
Ocular symptoms in COVID-19 patients with a history of hospitalization in the first pandemic wave in Styria, AustriaAndreas Guttmann, Astrid Heidinger, Nora Woltsche, et al.
Journal of Neurosurgery. Pediatrics|April 10, 2026
Characteristics of repeated untethering pattern in patients with myelomeningocele from infancy to adolescenceJoanna Schneider, Gesa Cohrs, Magín de la Flor, et al.
Pageof 55