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- Yoshida, Sakiko
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- Kanegane, Hirokazu
- Yamamoto, Tatsuo
- Umezu, Hajime
- Nishikomori, Ryuta
- Heike, Toshio
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In:
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Diversity of XMEN Disease: Description of 2 Novel Variants and Analysis of the Lymphocyte Phenotype. [electronic resource] by
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- Chan, Jonathan J
- Marshall, Glenn M
- Mitchell, Richard
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- Ma, Cindy S
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In:
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Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1. [electronic resource] by
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- Dowdy, Jola
- Triplett, Brandon
- Li, Chen
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- Dokmeci, Elif
- Love, James T
- da Matta Ain, Ana C
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- Tang, Xing
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- Ryu, Byoung Y
- De Ravin, Suk See
- Weiss, Mitchell J
- Youngblood, Benjamin
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The New England journal of medicine vol. 380
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Gammaretrovirus-mediated correction of SCID-X1 is associated with skewed vector integration site distribution in vivo. [electronic resource] by
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- Wissler, Manuela
- King, Douglas J S
- Zhang, Fang
- Parsley, Kathryn L
- Gilmour, Kimberly C
- Sinclair, Joanna
- Bayford, Jinhua
- Peraj, Rachel
- Pike-Overzet, Karin
- Staal, Frank J T
- de Ridder, Dick
- Kinnon, Christine
- Abel, Ulrich
- Wagemaker, Gerard
- Gaspar, H Bobby
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Successful reduced-intensity SCT from unrelated cord blood in three patients with X-linked SCID. [electronic resource] by
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- Inamoto, J
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- Sato, T
- Kaneda, M
- Cho, Y
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In:
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Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN disease. [electronic resource] by
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- Collins, Graham Peter
- Hatton, Christian Simon Ross
- Bhole, Malini
- Ferry, Berne
- Chapel, Helen M
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A novel model of SCID-X1 reconstitution reveals predisposition to retrovirus-induced lymphoma but no evidence of gammaC gene oncogenicity. [electronic resource] by
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- Nielsen, Anne A
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- Thrasher, Adrain J
- Cameron, Ewan R
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Producer: 20090807
In:
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Lymphomagenesis in SCID-X1 mice following lentivirus-mediated phenotype correction independent of insertional mutagenesis and gammac overexpression. [electronic resource] by
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- Alexander, Stephen I
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In:
Molecular therapy : the journal of the American Society of Gene Therapy vol. 18
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Sensorineural hearing loss in primary antibody deficiency disorders. [electronic resource] by
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- Meini, Antonella
- Salsi, Daria
- Nicolai, Piero
- Plebani, Alessandro
Producer: 20080813
In:
The Journal of pediatrics vol. 153
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Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene. [electronic resource] by
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- Anover, Stephanie
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- Hermine, Olivier
- Vijay, Shashi
- Gambineri, Eleonora
- Cerf-Bensussan, Nadine
- Fischer, Alain
- Ochs, Hans D
- Goulet, Olivier
- Ruemmele, Frank M
Producer: 20070626
In:
Gastroenterology vol. 132
Availability: No items available.
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