N S Thomas|S T Holgate - JoVE Visualize

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Thorax|September 17, 2005

Tumour necrosis factor (TNFalpha) as a novel therapeutic target in symptomatic corticosteroid dependent asthmaP H Howarth, K S Babu, H S Arshad, et al.

Allergy|July 22, 2014

Stability of phenotypes defined by physiological variables and biomarkers in adults with asthmaM Kupczyk, B Dahlén, P J Sterk, et al.

Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 17, 2004

Prophylactic management of children at risk for recurrent upper respiratory infections: the Preventia I StudyA Grimfeld, S T Holgate, G W Canonica, et al.

Clinical Genetics|June 1, 1990

Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNAM Upadhyaya, R A Smith, N S Thomas, et al.

The Journal of Biological Chemistry|November 5, 1991

Interferon-alpha treatment of Daudi cells down-regulates the octamer binding transcription/DNA replication factors Oct-1 and Oct-2C L Dent, K A Lillycrop, A Bybee, et al.

American Journal of Human Genetics|October 16, 2003

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityS E Roberts, F Maggouta, N S Thomas, et al.

Blood|July 1, 1992

Down-regulation of human protein kinase C alpha is associated with terminal neutrophil differentiationV Devalia, N S Thomas, P J Roberts, et al.

Journal of Medical Genetics|August 1, 1983

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosomeH M Kingston, N S Thomas, P L Pearson, et al.

Journal of Medical Genetics|March 21, 1998

Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implicationsB M Ferguson, N S Thomas, F Munoz, et al.

The Journal of Pediatrics|March 1, 1989

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysisJ Zonana, M Sarfarazi, N S Thomas, et al.

Pageof 66

Showing results (581-590 of 654) with videos related to

Sort By:

Pageof 66

Thorax|September 17, 2005

Tumour necrosis factor (TNFalpha) as a novel therapeutic target in symptomatic corticosteroid dependent asthmaP H Howarth, K S Babu, H S Arshad, et al.

Allergy|July 22, 2014

Stability of phenotypes defined by physiological variables and biomarkers in adults with asthmaM Kupczyk, B Dahlén, P J Sterk, et al.

Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 17, 2004

Prophylactic management of children at risk for recurrent upper respiratory infections: the Preventia I StudyA Grimfeld, S T Holgate, G W Canonica, et al.

Clinical Genetics|June 1, 1990

Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNAM Upadhyaya, R A Smith, N S Thomas, et al.

The Journal of Biological Chemistry|November 5, 1991

Interferon-alpha treatment of Daudi cells down-regulates the octamer binding transcription/DNA replication factors Oct-1 and Oct-2C L Dent, K A Lillycrop, A Bybee, et al.

American Journal of Human Genetics|October 16, 2003

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexityS E Roberts, F Maggouta, N S Thomas, et al.

Blood|July 1, 1992

Down-regulation of human protein kinase C alpha is associated with terminal neutrophil differentiationV Devalia, N S Thomas, P J Roberts, et al.

Journal of Medical Genetics|August 1, 1983

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosomeH M Kingston, N S Thomas, P L Pearson, et al.

Journal of Medical Genetics|March 21, 1998

Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implicationsB M Ferguson, N S Thomas, F Munoz, et al.

The Journal of Pediatrics|March 1, 1989

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysisJ Zonana, M Sarfarazi, N S Thomas, et al.

Pageof 66