J. Tubb

Extended core sequences from the cHS4 insulator are necessary for protecting retroviral vectors from silencing position effects.

G. Stamatoyannopoulos, G. Felsenfeld, H. Kiem, 2007, Human gene therapy.

Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

M. Kay, D. Bellinger, T. Nichols, 1999, Nature Medicine.

Topological constraints governing the use of the chicken HS4 chromatin insulator in oncoretrovirus vectors.

G. Stamatoyannopoulos, E. Yannaki, M. Aker, 2002, Molecular therapy : the journal of the American Society of Gene Therapy.

Development of virus vectors for gene therapy of beta chain hemoglobinopathies: flanking with a chromatin insulator reduces gamma-globin gene silencing in vivo.

G. Stamatoyannopoulos, Qiliang Li, E. Yannaki, 2002, Blood.

Development of virus vectors for gene therapy of (cid:1) chain hemoglobinopathies: flanking with a chromatin insulator reduces (cid:2) -globin gene silencing in vivo

G. Stamatoyannopoulos, E. Yannaki, D. W. Emery, 2002 .

Selection with a regulated cell growth switch increases the likelihood of expression for a linked gamma-globin gene.

G. Stamatoyannopoulos, C. A. Blau, D. W. Emery, 2005, Blood cells, molecules & diseases.

Partial correction of murine β-thalassemia with a gammaretrovirus vector for human γ-globin

D. W. Emery, Tamon Nishino, J. Tubb, 2006 .

A chromatin insulator protects retrovirus vectors from chromosomal position effects.

G. Stamatoyannopoulos, E. Yannaki, D. W. Emery, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Integration bias of gammaretrovirus vectors following transduction and growth of primary mouse hematopoietic progenitor cells with and without selection.

Daniel G. Miller, G. Stamatoyannopoulos, M. Aker, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Use of the hereditary persistence of fetal hemoglobin 2 enhancer to increase the expression of oncoretrovirus vectors for human gamma-globin

N. Anagnou, M. Fragkos, D. W. Emery, 2005, Gene Therapy.

Strain related variations in adenovirally mediated transgene expression from mouse hepatocytes in vivo: comparisons between immunocompetent and immunodeficient inbred strains.

M. Kay, A. Lieber, A. Scaria, 1995, Gene therapy.