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T Strachan

Showing results (71-80 of 138) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 1999
Probability of bilateral disease in people presenting with a unilateral vestibular schwannomaD G Evans, R Lye, W Neary, et al.
American Journal of Human Genetics|August 27, 1998
Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosisD G Evans, A J Wallace, C L Wu, et al.
Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.
Annales De L'Institut Pasteur. Immunologie|January 1, 1985
Allelism in the HLA class I multigene familyR Sodoyer, C Nguyen, T Strachan, et al.
The Journal of Biological Chemistry|December 24, 2008
Ribosomal S6 kinase 2 directly phosphorylates the 5-hydroxytryptamine 2A (5-HT2A) serotonin receptor, thereby modulating 5-HT2A signalingRyan T Strachan, Douglas J Sheffler, Belinda Willard, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
IJTLD Open|December 16, 2024
Disseminated TB associated with acute severe malnutrition in a Roma childP Kunč, J Fábry, P Ferenc, et al.
Physiological Research|July 14, 2023
Association of selected inflammatory biomarkers with cough reflex sensitivity in asthmatic childrenP Kunč, J Fábry, M Grendár, et al.
Human Immunology|October 1, 1991
Characterization of an expressible nonclassical class I HLA geneM A Pook, V Woodcock, M Tassabehji, et al.
Gene|April 11, 1997
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25T D Bui, M Lako, S Lejeune, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 1999
Probability of bilateral disease in people presenting with a unilateral vestibular schwannomaD G Evans, R Lye, W Neary, et al.
American Journal of Human Genetics|August 27, 1998
Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosisD G Evans, A J Wallace, C L Wu, et al.
Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.
Annales De L'Institut Pasteur. Immunologie|January 1, 1985
Allelism in the HLA class I multigene familyR Sodoyer, C Nguyen, T Strachan, et al.
The Journal of Biological Chemistry|December 24, 2008
Ribosomal S6 kinase 2 directly phosphorylates the 5-hydroxytryptamine 2A (5-HT2A) serotonin receptor, thereby modulating 5-HT2A signalingRyan T Strachan, Douglas J Sheffler, Belinda Willard, et al.
Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.
IJTLD Open|December 16, 2024
Disseminated TB associated with acute severe malnutrition in a Roma childP Kunč, J Fábry, P Ferenc, et al.
Physiological Research|July 14, 2023
Association of selected inflammatory biomarkers with cough reflex sensitivity in asthmatic childrenP Kunč, J Fábry, M Grendár, et al.
Human Immunology|October 1, 1991
Characterization of an expressible nonclassical class I HLA geneM A Pook, V Woodcock, M Tassabehji, et al.
Gene|April 11, 1997
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25T D Bui, M Lako, S Lejeune, et al.
Pageof 14