000 | nab a22 7a 4500 | ||
---|---|---|---|
999 |
_c16715 _d16715 |
||
003 | PC16715 | ||
005 | 20220202130759.0 | ||
008 | 220202b xxu||||| |||| 00| 0 eng d | ||
040 | _cH12O | ||
041 | _aeng | ||
100 |
_91219 _aRodríguez Peralto, José Luis _eAnatomía Patológica |
||
245 | 0 | 0 |
_aWhole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation. _h[artículo] |
260 |
_bLeukemia, _c2014 |
||
300 | _a28(6):1334-40. | ||
500 | _aFormato Vancouver: Martínez N, Almaraz C, Vaqué JP, Varela I, Derdak S, Beltran S et al. Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation. Leukemia. 2014 Jun;28(6):1334-40. | ||
501 | _aPMID: 24296945 | ||
504 | _aContiene 49 referencias | ||
520 | _aSplenic marginal zone lymphoma (SMZL) is a B-cell neoplasm whose molecular pathogenesis remains fundamentally unexplained, requiring more precise diagnostic markers. Previous molecular studies have revealed 7q loss and mutations of nuclear factor κB (NF-κB), B-cell receptor (BCR) and Notch signalling genes. We performed whole-exome sequencing in a series of SMZL cases. Results confirmed that SMZL is an entity distinct from other low-grade B-cell lymphomas, and identified mutations in multiple genes involved in marginal zone development, and others involved in NF-κB, BCR, chromatin remodelling and the cytoskeleton. | ||
710 |
_9330 _aServicio de Anatomía Patológica |
||
856 |
_uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc16715.pdf _ySolicitar documento |
||
942 |
_2ddc _cART _n0 |