Associated Papers
Germ line variants in patients with acute myeloid leukemia without a suspicion of hereditary hematologic malignancy syndrome.
Guijarro F et al.
Blood Advances, 2023
37450374 (PubMed )
Supplement: BLOODA_ADV-2023-009742-mmc2.xlsx › 20220406_291_germline_paired_gn
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances.
Pignata L et al.
Clinical Epigenetics, 2022
35643636 (PubMed )
Supplement: 13148_2022_1292_MOESM4_ESM.pdf
ATP-Binding and Hydrolysis in Inflammasome Activation.
Sandall CF et al.
Molecules (basel, Switzerland), 2020
NLRP2, an inhibitor of the NF-kappaB pathway, is transcriptionally activated by NF-kappaB and exhibits a nonfunctional allelic variant.
Fontalba A et al.
Journal of Immunology (baltimore, Md. : 1950), 2007
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