✦ LIBER ✦

A point mutation affecting an SP1 binding site in the promoter of the ferrochelatase gene impairs gene transcription and causes erythropoietic protoporphyria

✍ Scribed by Elena Di Pierro; Maria Domenica Cappellini; Renata Mazzucchelli; Valeria Moriondo; Daniela Mologni; Barbara Zanone Poma; Agostino Riva

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A point mutation in an Sp1 binding motif

✍ Yoshiko Murakami; Antonio Almeida; Mark Layton; Peter Hillmen; Yusuke Maeda; Ana 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 81 KB

Functional significance of a putative Sp

✍ M. V. Mityaev; E. P. Kopantzev; A. A. Buzdin; T. V. Vinogradova; E. D. Sverdlov 📂 Article 📅 2008 🏛 Springer 🌐 English ⚖ 336 KB

Basal transcription activity of the dysk

✍ Rüdiger Salowsky; Nina S Heiss; Axel Benner; Rainer Wittig; Annemarie Poustka 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 735 KB

Association Between a Polymorphism Affec

✍ C. Sobacchi; P. Vezzoni; D. M. Reid; F. E. A. McGuigan; A. Frattini; M. Mirolo; 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 132 KB

A newly identified mutation in an IPF1 b

✍ M. T. Malecki; P. Lebrun; M. Pezzolesi; J. H. Warram; A. S. Krolewski; U. S. Jha 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 120 KB

Characterization of a promoter mutation

✍ Lodi, T. ;Petrochilo, E. ;Gaisne, M. ;Verdière, J. 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 424 KB