Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Catina Bernadis"'
Autor:
Farzin Farzaneh, Anna E. Martinez, Magdalena Martinez-Queipo, Havinder Hara, Wei Wang, Adrian J. Thrasher, Alya Abdul-Wahab, Jemima E. Mellerio, Alex Virasami, Su M. Lwin, Waseem Qasim, John A. McGrath, Farhatullah Syed, Dale Moulding, Neil J. Sebire, John I. Harper, Wei Li Di, Tendai Kadiyirire, Anastasia Petrova, Catina Bernadis, M. Zamiri, Dyanne Rampling
Publikováno v:
Human gene therapy. 30(9)
Netherton syndrome (NS) is a rare autosomal recessive skin disorder caused by mutations in SPINK5. It is a debilitating condition with notable mortality in the early years of life. There is no cura...
Autor:
Adrian J. Thrasher, Waseem Qasim, John A. McGrath, Farhatullah Syed, Anna E. Martinez, Su M. Lwin, Jemima E. Mellerio, Wei-Li Di, Catina Bernadis, Anastasia Petrova
Publikováno v:
Journal of Investigative Dermatology. 139:S262
Autor:
Wei-Li Di, Magdalena Martinez-Queipo, John Harper, Waseem Qasim, Farzin Farzaneh, Alya Abdul-Wahab, Anne-Marie McNicol, John A. McGrath, Adrian J. Thrasher, Lucas Chan, S Ghani, Catina Bernadis, Jemima E. Mellerio, Havinder Hara
Publikováno v:
Human Gene Therapy Clinical Development. 24:182-190
Netherton syndrome (NS) is a serious inherited skin disorder caused by mutations in the gene SPINK5 (serine protease inhibitor Kazal type 5) which encodes for a serine protease inhibitor LEKTI (lymphoepithelial Kazal type-related inhibitor). Patients
Autor:
Wei-Li Di, Jemima E Mellerio, Catina Bernadis, John Harper, Alya Abdul-Wahab, Sumera Ghani, Magdalena Martinez-Queipo, Havinder Hara, Anne-Marie McNicol, John McGrath, Adrian J. Thrasher, Waseem Qasim
Publikováno v:
Human gene therapy. Clinical development.
Netherton syndrome (NS) is a serious inherited skin disorder caused by mutations in the gene SPINK5 (serine protease inhibitor Kazal type 5) which encodes for a serine protease inhibitor LEKTI (lymphoepithelial Kazal type-related inhibitor). Patients