Search Results - "Ginwalla, Aasiya"

Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSC by Erzurumluoglu, A Mesut, Alsaadi, Muslim M, Rodriguez, Santiago, Alotaibi, Tahani S, Guthrie, Philip A I, Lewis, Sian, Ginwalla, Aasiya, Gaunt, Tom R, Alharbi, Khalid K, Alsaif, Fahad M, Alsaadi, Basma M, Day, Ian N M

“…Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early onset periodontitis and palmoplantar hyperkeratosis. A…”
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Regulation of Scaffold Cell Adhesion Using Artificial Membrane Binding Proteins by Burke, Madeline, Armstrong, James P. K., Goodwin, Andrew, Deller, Robert C., Carter, Benjamin M., Harniman, Robert L., Ginwalla, Aasiya, Ting, Valeska P., Davis, Sean A., Perriman, Adam W.

“…The rapid pace of development in biotechnology has placed great importance on controlling cell–material interactions. In practice, this involves attempting to…”
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Proxy Molecular Diagnosis from Whole-Exome Sequencing Reveals Papillon-Lefevre Syndrome Caused by a Missense Mutation in CTSC: e0121351 by Erzurumluoglu, A Mesut, Alsaadi, Muslim M, Rodriguez, Santiago, Alotaibi, Tahani S, Guthrie, Philip AI, Lewis, Sian, Ginwalla, Aasiya, Gaunt, Tom R, Alharbi, Khalid K, Alsaif, Fahad M

“…Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early onset periodontitis and palmoplantar hyperkeratosis. A…”
Get full text