Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A C Nicholls

Showing results (11-20 of 58) with videos related to

Pageof 6
Sort By:
Lancet (London, England)|January 29, 1983
Pregnancy and Ehlers-Danlos syndrome type IVF M Pope, A C Nicholls
Scandinavian Journal of Respiratory Diseases|August 1, 1979
Serological diagnosis of tuberculosis. Evaluation of two years' experienceG W Bradley, A C Nicholls, L Banfield
British Medical Journal (Clinical Research Ed.)|January 14, 1984
An abnormal collagen alpha chain containing cysteine in autosomal dominant osteogenesis imperfectaA C Nicholls, F M Pope, D Craig
Lancet (London, England)|June 2, 1979
Biochemical heterogeneity of osteogenesis imperfecta: New variantA C Nicholls, F M Pope, H Schloon
Journal of Clinical Pathology|June 1, 1975
A study of the agglutinin response in 40 cases of bacterial pneumoniaA C Nicholls, P E Pease, I D Green
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1976
The nature of the cross-linking of proteins by glutaraldehyde. Part I. Interaction of glutaraldehyde with the amino-groups of 6-aminohexanoic acid and of alpha-N-acetyl-lysineP M Hardy, A C Nicholls, H N Rydon
Journal of Clinical Pathology|April 1, 1975
Agglutinin response to bacterial infection in acute exacerbations of chronic bronchitisA C Nicholls, P E Pease, I D Green
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1997
Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IVA M Lund, A C Nicholls, M Schwartz, et al.
Journal of the Royal Society of Medicine|December 1, 1983
Molecular abnormalities of collagen: a reviewF M Pope, A C Nicholls, J Dorling, et al.
Journal of Medical Genetics|April 6, 2001
Homozygosity for a splice site mutation of the COL1A2 gene yields a non-functional pro(alpha)2(I) chain and an EDS/OI clinical phenotypeA C Nicholls, D Valler, S Wallis, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
Lancet (London, England)|January 29, 1983
Pregnancy and Ehlers-Danlos syndrome type IVF M Pope, A C Nicholls
Scandinavian Journal of Respiratory Diseases|August 1, 1979
Serological diagnosis of tuberculosis. Evaluation of two years' experienceG W Bradley, A C Nicholls, L Banfield
British Medical Journal (Clinical Research Ed.)|January 14, 1984
An abnormal collagen alpha chain containing cysteine in autosomal dominant osteogenesis imperfectaA C Nicholls, F M Pope, D Craig
Lancet (London, England)|June 2, 1979
Biochemical heterogeneity of osteogenesis imperfecta: New variantA C Nicholls, F M Pope, H Schloon
Journal of Clinical Pathology|June 1, 1975
A study of the agglutinin response in 40 cases of bacterial pneumoniaA C Nicholls, P E Pease, I D Green
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1976
The nature of the cross-linking of proteins by glutaraldehyde. Part I. Interaction of glutaraldehyde with the amino-groups of 6-aminohexanoic acid and of alpha-N-acetyl-lysineP M Hardy, A C Nicholls, H N Rydon
Journal of Clinical Pathology|April 1, 1975
Agglutinin response to bacterial infection in acute exacerbations of chronic bronchitisA C Nicholls, P E Pease, I D Green
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1997
Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IVA M Lund, A C Nicholls, M Schwartz, et al.
Journal of the Royal Society of Medicine|December 1, 1983
Molecular abnormalities of collagen: a reviewF M Pope, A C Nicholls, J Dorling, et al.
Journal of Medical Genetics|April 6, 2001
Homozygosity for a splice site mutation of the COL1A2 gene yields a non-functional pro(alpha)2(I) chain and an EDS/OI clinical phenotypeA C Nicholls, D Valler, S Wallis, et al.
Pageof 6