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Trevor Lucas

Showing results (41-50 of 53) with videos related to

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Audiology & Neuro-Otology|December 17, 2003
A novel connexin 26 mutation associated with autosomal recessive sensorineural deafnessKlemens Frei, Trevor Lucas, Reinhard Ramsebner, et al.
International Journal of Cancer|April 12, 2002
Bcl-X(L) is a chemoresistance factor in human melanoma cells that can be inhibited by antisense therapyElisabeth Heere-Ress, Christiane Thallinger, Trevor Lucas, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Cancers|April 30, 2021
PRKCA Overexpression Is Frequent in Young Oral Tongue Squamous Cell Carcinoma Patients and Is Associated with Poor PrognosisThomas Parzefall, Julia Schnoell, Laura Monschein, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
Connexin 26 mutations in cases of sensorineural deafness in eastern AustriaKlemens Frei, Károly Szuhai, Trevor Lucas, et al.
European Journal of Gastroenterology & Hepatology|May 1, 2002
The constitutive expression of galectin-3 is downregulated in the intestinal epithelia of Crohn's disease patients, and tumour necrosis factor alpha decreases the level of galectin-3-specific mRNA in HCT-8 cellsErika Jensen-Jarolim, Regina Gscheidlinger, Georg Oberhuber, et al.
Cardiovascular Research|April 26, 2008
Colony-stimulating factor-1 transfection of myoblasts improves the repair of failing myocardium following autologous myoblast transplantationSeyedhossein Aharinejad, Dietmar Abraham, Patrick Paulus, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 4, 2013
Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter studyReinhard Ramsebner, Martin Ludwig, Trevor Lucas, et al.
Cancer Research|April 4, 2002
The melanocyte-specific isoform of the microphthalmia transcription factor affects the phenotype of human melanomaEdgar Selzer, Volker Wacheck, Trevor Lucas, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Audiology & Neuro-Otology|December 17, 2003
A novel connexin 26 mutation associated with autosomal recessive sensorineural deafnessKlemens Frei, Trevor Lucas, Reinhard Ramsebner, et al.
International Journal of Cancer|April 12, 2002
Bcl-X(L) is a chemoresistance factor in human melanoma cells that can be inhibited by antisense therapyElisabeth Heere-Ress, Christiane Thallinger, Trevor Lucas, et al.
Acta Oto-Laryngologica|November 10, 2016
The role of alternative GJB2 transcription in screening for neonatal sensorineural deafness in AustriaThomas Parzefall, Trevor Lucas, Martin Koenighofer, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Cancers|April 30, 2021
PRKCA Overexpression Is Frequent in Young Oral Tongue Squamous Cell Carcinoma Patients and Is Associated with Poor PrognosisThomas Parzefall, Julia Schnoell, Laura Monschein, et al.
European Journal of Human Genetics : EJHG|July 11, 2002
Connexin 26 mutations in cases of sensorineural deafness in eastern AustriaKlemens Frei, Károly Szuhai, Trevor Lucas, et al.
European Journal of Gastroenterology & Hepatology|May 1, 2002
The constitutive expression of galectin-3 is downregulated in the intestinal epithelia of Crohn's disease patients, and tumour necrosis factor alpha decreases the level of galectin-3-specific mRNA in HCT-8 cellsErika Jensen-Jarolim, Regina Gscheidlinger, Georg Oberhuber, et al.
Cardiovascular Research|April 26, 2008
Colony-stimulating factor-1 transfection of myoblasts improves the repair of failing myocardium following autologous myoblast transplantationSeyedhossein Aharinejad, Dietmar Abraham, Patrick Paulus, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 4, 2013
Identification of a SNP in a regulatory region of GJB2 associated with idiopathic nonsyndromic autosomal recessive hearing loss in a multicenter studyReinhard Ramsebner, Martin Ludwig, Trevor Lucas, et al.
Cancer Research|April 4, 2002
The melanocyte-specific isoform of the microphthalmia transcription factor affects the phenotype of human melanomaEdgar Selzer, Volker Wacheck, Trevor Lucas, et al.
Pageof 6