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T Strachan

Showing results (61-70 of 138) with videos related to

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American Journal of Human Genetics|July 1, 1993
Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndromeM Tassabehji, T Strachan, M Sharland, et al.
Gene|October 3, 1998
Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lungM Lako, T Strachan, P Bullen, et al.
Molecular Pharmacology|November 26, 2009
Genetic deletion of p90 ribosomal S6 kinase 2 alters patterns of 5-hydroxytryptamine 2A serotonin receptor functional selectivityRyan T Strachan, Noah Sciaky, Mark R Cronan, et al.
Human Molecular Genetics|May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrainM Lako, S Lindsay, P Bullen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Human Genetics|March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency familiesP J Sinnott, C Livieri, M Sampietro, et al.
Heart Rhythm|January 28, 2021
Right ventricular insertion promotes reinitiation of ventricular fibrillation in defibrillation failureKenichi Iijima, Hanyu Zhang, Matthew T Strachan, et al.
Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.
Journal of Medical Genetics|June 1, 1995
Diagnostic issues in a family with late onset type 2 neurofibromatosisD G Evans, D Bourn, A Wallace, et al.
The EMBO Journal|May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypesS Collier, P J Sinnott, P A Dyer, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|July 1, 1993
Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndromeM Tassabehji, T Strachan, M Sharland, et al.
Gene|October 3, 1998
Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lungM Lako, T Strachan, P Bullen, et al.
Molecular Pharmacology|November 26, 2009
Genetic deletion of p90 ribosomal S6 kinase 2 alters patterns of 5-hydroxytryptamine 2A serotonin receptor functional selectivityRyan T Strachan, Noah Sciaky, Mark R Cronan, et al.
Human Molecular Genetics|May 23, 1998
A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrainM Lako, S Lindsay, P Bullen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.
Human Genetics|March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency familiesP J Sinnott, C Livieri, M Sampietro, et al.
Heart Rhythm|January 28, 2021
Right ventricular insertion promotes reinitiation of ventricular fibrillation in defibrillation failureKenichi Iijima, Hanyu Zhang, Matthew T Strachan, et al.
Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.
Journal of Medical Genetics|June 1, 1995
Diagnostic issues in a family with late onset type 2 neurofibromatosisD G Evans, D Bourn, A Wallace, et al.
The EMBO Journal|May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypesS Collier, P J Sinnott, P A Dyer, et al.
Pageof 14