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HAX-1 overexpression in multiple myeloma is associated with poor survival.
Feng X, Kwiecinska A, Rossmann E, Bottai M, Ishikawa T, Patarroyo M, Österborg A, Porwit A, Zheng C, Fadeel B. Feng X, et al. Among authors: fadeel b. Br J Haematol. 2019 Apr;185(1):179-183. doi: 10.1111/bjh.15430. Epub 2018 Jun 19. Br J Haematol. 2019. PMID: 29923187 Free article. No abstract available.
Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells.
Carlsson G, Aprikyan AA, Tehranchi R, Dale DC, Porwit A, Hellström-Lindberg E, Palmblad J, Henter JI, Fadeel B. Carlsson G, et al. Among authors: fadeel b. Blood. 2004 May 1;103(9):3355-61. doi: 10.1182/blood-2003-04-1011. Epub 2004 Feb 5. Blood. 2004. PMID: 14764541 Free article.
An endothelial laminin isoform, laminin 8 (alpha4beta1gamma1), is secreted by blood neutrophils, promotes neutrophil migration and extravasation, and protects neutrophils from apoptosis.
Wondimu Z, Geberhiwot T, Ingerpuu S, Juronen E, Xie X, Lindbom L, Doi M, Kortesmaa J, Thyboll J, Tryggvason K, Fadeel B, Patarroyo M. Wondimu Z, et al. Among authors: fadeel b. Blood. 2004 Sep 15;104(6):1859-66. doi: 10.1182/blood-2004-01-0396. Epub 2004 Jun 1. Blood. 2004. PMID: 15172971 Free article.
Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations.
Meeths M, Bryceson YT, Rudd E, Zheng C, Wood SM, Ramme K, Beutel K, Hasle H, Heilmann C, Hultenby K, Ljunggren HG, Fadeel B, Nordenskjöld M, Henter JI. Meeths M, et al. Among authors: fadeel b. Pediatr Blood Cancer. 2010 Apr;54(4):563-72. doi: 10.1002/pbc.22357. Pediatr Blood Cancer. 2010. PMID: 19953648
291 results