Zobrazeno 1 - 10
of 16
pro vyhledávání: '"H B, Gaspar"'
Autor:
A. Magnani, M. Semeraro, F. Adam, C. Booth, L. Dupré, E. C. Morris, A. Gabrion, C. Roudaut, D. Borgel, A. Toubert, E. Clave, C. Abdo, G. Gorochov, R. Petermann, M. Guiot, M. Miyara, D. Moshous, E. Magrin, A. Denis, F. Suarez, C. Lagresle, A. M. Roche, J. Everett, A. Trinquand, M. Guisset, J. Xu Bayford, S. Hacein-Bey-Abina, A. Kauskot, R. Elfeky, C. Rivat, S. Abbas, H. B. Gaspar, E. Macintyre, C. Picard, F. D. Bushman, A. Galy, A. Fischer, E. Six, A. J. Thrasher, M. Cavazzana
Publikováno v:
Nature Medicine. 28:2217-2217
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f6d0103ef72fa0ff75e2c16a1b251e1
https://doi.org/10.1038/s41591-022-01985-y
https://doi.org/10.1038/s41591-022-01985-y
Autor:
S. Hacein-Bey Abina, S.-Y. Pai, H. B. Gaspar, M. Armant, J. Bayford, C. Berry, S. Blanche, J. Bleesing, J. Blondeau, H. de Boer, K. Buckland, L. Caccavelli, G. Cros, S. de Oliveira, K. Fernandez, D.J. Guo, C. E. Harris, G. Hopkins, L. E. Lehmann, A. Lim, W. B. London, J. C.M. van der Loo, N. Malani, F. Male, P. Malik, M. A. Marinovic, A.-M. McNichol, D. Moshous, B. Neven, M. Oleastro, C. Picard, J. Ritz, C. Rivat, A. Schambach, K. L. Shaw, E. Sherman, L. E. Silberstein, E. Six, F. Touzot, A. Tsytsykova
Publikováno v:
Submitted, not yet published.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=erc_________::0a61b15554e8cd19d5591656455aae7e
Autor:
S. Hacein-Bey-Abina, H. B. Gaspar, J. Blondeau, L. Caccavelli, S. Charrier, K. Buckland, C. Picard, E. Six, N. Himoudi, K. Gilmour, A.-M. McNicol, H. Hara, J. Xu-Bayford, C. Rivat, F. Touzot, F. Mavilio, A. Lim, S. Hxe9ritier, F. Lefrxe8re, J. Magalon, I. Pengue-Koyi, G. Honnet, S. Blanche, E. Sherman, F. Male, C. Berry, N. Malani, F. D, Bushman, A. Fischer, A. J. Trasher, A. Galy, M, Cavazzana
Publikováno v:
Submitted, not yet published.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=erc_________::e0775f26335f7e5a1c3ecb42e1d0a62e
Autor:
B L, Alexander, R R, Ali, E W F, Alton, J W, Bainbridge, S, Braun, S H, Cheng, T R, Flotte, H B, Gaspar, M, Grez, U, Griesenbach, M G, Kaplitt, M G, Ott, R, Seger, M, Simons, A J, Thrasher, A Z, Thrasher, S, Ylä-Herttuala
Publikováno v:
Gene therapy. 14(20)
Over the last two decades gene therapy has moved from preclinical to clinical studies for many diseases ranging from single gene disorders such as cystic fibrosis and Duchenne muscular dystrophy, to more complex diseases such as cancer and cardiovasc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::040bc50dd9c6bfb955b46178b0b543b6
https://pubmed.ncbi.nlm.nih.gov/17909539
https://pubmed.ncbi.nlm.nih.gov/17909539
Autor:
H B, Gaspar, P, Amrolia, A, Hassan, D, Webb, A, Jones, N, Sturt, G, Vergani, A, Pagliuca, G, Mufti, N, Hadzic, G, Davies, P, Veys
Publikováno v:
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer. 159
Allogeneic haematopoietic stem cell transplantation (HSCT) can be a highly successful treatment option for individuals with congenital immunodeficiency states. The strategy for HSCT is varied but in cases where there is preservation of residual T cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49ee54828c592d45db73c62c6fdb2cb2
https://pubmed.ncbi.nlm.nih.gov/11785837
https://pubmed.ncbi.nlm.nih.gov/11785837
Publikováno v:
Advances in experimental medicine and biology. 486
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86b20a371b7bfe4e0677f3b4911b2cb8
https://pubmed.ncbi.nlm.nih.gov/11783527
https://pubmed.ncbi.nlm.nih.gov/11783527
Autor:
W, Qasim, K C, Gilmour, S, Heath, E, Ashton, T, Cranston, A, Thomas, A, Finn, E G, Davies, A J, Thrasher, C, Kinnon, A, Jones, H B, Gaspar
Publikováno v:
British journal of haematology. 113(4)
Mutations in the gene encoding the Wiskott-Aldrich syndrome protein (WASp) give rise to Wiskott-Aldrich syndrome (WAS), a condition that exhibits a wide spectrum of clinical severity. Patients may develop mild thrombocytopenia or suffer from a wide r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06bc48c0b069ad1af9b45befd046e517
https://pubmed.ncbi.nlm.nih.gov/11442475
https://pubmed.ncbi.nlm.nih.gov/11442475
Autor:
K C, Gilmour, T, Cranston, S, Loughlin, J, Gwyther, T, Lester, T, Espanol, M, Hernandez, G, Savoldi, E G, Davies, M, Abinun, C, Kinnon, A, Jones, H B, Gaspar
Publikováno v:
British journal of haematology. 112(3)
The severe combined immunodeficiencies (SCID) are a heterogeneous group of conditions arising from a variety of molecular defects. The X-linked form of SCID (X-SCID) is caused by defects in the common gamma chain (gammac), and is characterized by a T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::91f66106049e0c98321653d9ed555ff0
https://pubmed.ncbi.nlm.nih.gov/11260071
https://pubmed.ncbi.nlm.nih.gov/11260071
Publikováno v:
Archives of disease in childhood. 84(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a93e581ff49c9b04f7399e5b85bff278
https://pubmed.ncbi.nlm.nih.gov/11159300
https://pubmed.ncbi.nlm.nih.gov/11159300
Autor:
K C, Gilmour, T, Cranston, A, Jones, E G, Davies, D, Goldblatt, A, Thrasher, C, Kinnon, K E, Nichols, H B, Gaspar
Publikováno v:
European journal of immunology. 30(6)
X-linked lymphoproliferative disease (XLP) is an inherited immunodeficiency in which affected boys show abnormal responses to Epstein-Barr virus infection. The gene defective in XLP has been identified and designated SH2D1A and encodes a protein term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1b474250cb917800f04623c91a996ea
https://pubmed.ncbi.nlm.nih.gov/10898506
https://pubmed.ncbi.nlm.nih.gov/10898506