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Number of items: 3.

Vahidnezhad, Hassan; Youssefian, Leila; Saeidian, Amir Hossein; Touati, Andrew; Pajouhanfar, Sara; Baghdadi, Taghi; Shadmehri, Azam Ahmadi; Giunta Meyer, Cecilia; Kraenzlin, Marius; Syx, Delfien; Malfait, Fransiska; Has, Cristina; Lwin, Su M; Karamzadeh, Razieh; Liu, Lu; Guy, Alyson; Hamid, Mohammad; Kariminejad, Ariana; Zeinali, Sirous; McGrath, John A; Uitto, Jouni (2019). Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency. Matrix Biology, 81:91-106.

Khosravi, Mohammad Ali; Abbasalipour, Maryam; Concordet, Jean-Paul; vom Berg, Johannes; Zeinali, Sirous; Arashkia, Arash; Azadmanesh, Kayhan; Buch, Thorsten; Karimipoor, Morteza (2019). Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease. European Journal of Pharmacology, 854:398-405.

Khatami, Shohreh; Dehnabeh, Soghra Rouhi; Zeinali, Sirous; Thöny, Beat; Alaei, Mohammadreza; Salehpour, Shadab; Setoodeh, Aria; Rohani, Farzaneh; Hajivalizadeh, Fatemeh; Samavat, Ashraf (2017). Four years of diagnostic challenges with tetrahydrobiopterin deficiencies in Iranian patients. In: Morava, E; Baumgartner, M; Patterson, M; Rahman, S; Zschocke, J; Peters, V. JIMD Reports, Volume 32. Berlin, Heidelberg: Springer, 1-8.

This list was generated on Mon Sep 16 08:17:49 2019 CEST.