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Jennifer Kirkham

Showing results (51-60 of 63) with videos related to

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Human Molecular Genetics|December 10, 2013
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfectaJames A Poulter, Steven J Brookes, Roger C Shore, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfectaClaire El Smith, Laura LE Whitehouse, James A Poulter, et al.
Human Molecular Genetics|May 27, 2014
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfectaJames A Poulter, Gina Murillo, Steven J Brookes, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.
Head & Neck Oncology|October 7, 2010
Raman spectroscopy in head and neck cancerAndrew T Harris, Andrew Rennie, Haroon Waqar-Uddin, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
American Journal of Human Genetics|October 27, 2009
Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfectaWalid El-Sayed, David A Parry, Roger C Shore, et al.
The American Journal of Pathology|June 15, 2013
Enamel defects reflect perinatal exposure to bisphenol AKatia Jedeon, Muriel De la Dure-Molla, Steven J Brookes, et al.
Head & Neck Oncology|September 19, 2009
Potential for Raman spectroscopy to provide cancer screening using a peripheral blood sampleAndrew T Harris, Anxhela Lungari, Christopher J Needham, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|December 10, 2013
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfectaJames A Poulter, Steven J Brookes, Roger C Shore, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfectaClaire El Smith, Laura LE Whitehouse, James A Poulter, et al.
Human Molecular Genetics|May 27, 2014
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfectaJames A Poulter, Gina Murillo, Steven J Brookes, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.
Head & Neck Oncology|October 7, 2010
Raman spectroscopy in head and neck cancerAndrew T Harris, Andrew Rennie, Haroon Waqar-Uddin, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
American Journal of Human Genetics|October 27, 2009
Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfectaWalid El-Sayed, David A Parry, Roger C Shore, et al.
The American Journal of Pathology|June 15, 2013
Enamel defects reflect perinatal exposure to bisphenol AKatia Jedeon, Muriel De la Dure-Molla, Steven J Brookes, et al.
Head & Neck Oncology|September 19, 2009
Potential for Raman spectroscopy to provide cancer screening using a peripheral blood sampleAndrew T Harris, Anxhela Lungari, Christopher J Needham, et al.
Pageof 7