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Suzanne E Clements

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American Journal of Medical Genetics. Part A|August 15, 2009
Importance of PORCN and Wnt signaling pathways in embryogenesisSuzanne E Clements
Archives of Dermatology|March 19, 2008
Molecular genetics as a diagnostic and prognostic aid in the assessment of neonates with red, scaly genodermatoses: work still in progressSuzanne E Clements, John A McGrath
The Practitioner|June 22, 2005
Skin signs of internal diseaseSharizan Abdul Ghaffar, Suzanne E Clements, Jennifer Yell
Clinical Medicine (London, England)|January 18, 2006
Modern management of psoriasisSharizan Abdul Ghaffar, Suzanne E Clements, Christopher E M Griffiths
British Journal of Hospital Medicine (London, England : 2005)|May 10, 2006
Biological therapy for psoriasisSuzanne E Clements, Sharizan Abdul-Ghaffar, Christopher E M Griffiths
Journal of Dermatological Science|October 24, 2007
Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN geneSuzanne E Clements, Vesarat Wessagowit, Joey E Lai-Cheong, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II)J Timothy Wright, Clark Morris, Suzanne E Clements, et al.
The Journal of Investigative Dermatology|April 2, 2010
Revertant mosaicism in recessive dystrophic epidermolysis bullosaNoor Almaani, Nikoletta Nagy, Lu Liu, et al.
The American Journal of Pathology|September 19, 2009
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activationJoey E Lai-Cheong, Maddy Parsons, Akio Tanaka, et al.
Human Molecular Genetics|March 28, 2008
A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromesTuula Rinne, Suzanne E Clements, Evert Lamme, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|August 15, 2009
Importance of PORCN and Wnt signaling pathways in embryogenesisSuzanne E Clements
Archives of Dermatology|March 19, 2008
Molecular genetics as a diagnostic and prognostic aid in the assessment of neonates with red, scaly genodermatoses: work still in progressSuzanne E Clements, John A McGrath
The Practitioner|June 22, 2005
Skin signs of internal diseaseSharizan Abdul Ghaffar, Suzanne E Clements, Jennifer Yell
Clinical Medicine (London, England)|January 18, 2006
Modern management of psoriasisSharizan Abdul Ghaffar, Suzanne E Clements, Christopher E M Griffiths
British Journal of Hospital Medicine (London, England : 2005)|May 10, 2006
Biological therapy for psoriasisSuzanne E Clements, Sharizan Abdul-Ghaffar, Christopher E M Griffiths
Journal of Dermatological Science|October 24, 2007
Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN geneSuzanne E Clements, Vesarat Wessagowit, Joey E Lai-Cheong, et al.
American Journal of Medical Genetics. Part A|August 15, 2009
Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II)J Timothy Wright, Clark Morris, Suzanne E Clements, et al.
The Journal of Investigative Dermatology|April 2, 2010
Revertant mosaicism in recessive dystrophic epidermolysis bullosaNoor Almaani, Nikoletta Nagy, Lu Liu, et al.
The American Journal of Pathology|September 19, 2009
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activationJoey E Lai-Cheong, Maddy Parsons, Akio Tanaka, et al.
Human Molecular Genetics|March 28, 2008
A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromesTuula Rinne, Suzanne E Clements, Evert Lamme, et al.
Pageof 2