Liu(W),Ping(J),Deng(L),Wang(K),Xu(J),Peng(... Nat Immunol 2026-05-00

...Xk-related protein 8 (XKR8), a plasma membrane phospholipid scramblase, as a pivotal regulator of NETs formation. Upon N...

Miltenberger-Miltenyi(G),Conceição(VA),Lab... Mov Disord 2026-07-00

XK disease is a multisystem neurodegenerative disorder caused by mutations in the XK gene that codes for the lipid scram...

de Los Santos(KAC),Loyola(ML),Miro(EDP) Acta Crystallogr A Found Ad... 2026-07-01

...Xk, ΓK) of number-theoretic origin. Specifically, we analyze the shift space Xk, defined as the closure of the set Vk of...

Xu(D),Wang(Y),Li(Q),Wang(L) Clin Nucl Med 2026-09-01

...XK mutation (c.664C>T, p.(Arg222*)), confirming McLeod syndrome. This case highlights that bilateral striatal hypometabo...

Li(S),Gao(T),Hao(W),Chen(H),Hu(X),Qi(R),Ch... Cell Mol Life Sci 2026-07-15

...XK-type nuclease domain, designated EndoDinGs, has remained uncharacterized. Here, we report the first structural and fu...

Hu(B),Álvarez(D),Rocha-Roa(C),Guyard(V),Li... Cell 2026-08-06

...XK at near-atomic resolution. VPS13A interacts with XK via its pleckstrin homology domain, priming VPS13A's bridge-like ...

Wang(MB),Yang(LL),Chen(HX),Lv(HB),Liang(LP... Pathol Res Pract 2025-10-00

...XK ESCC. Our findings highlight novel mutation loci that may explain the aggressive nature of XK ESCC. These insights co...

Thalhammer(J),Engström(C),Strahm(B),Speckm... J Hum Immun 2025-09-01

...XK, CYBB, and DYNLT3, leading to CGD, Duchenne muscular dystrophy, and MLP, was scheduled for HSCT with the need of Kx- ...

Davison(CL),Denomme(GA) Immunohematology 2025-09-01

...XK follows a similar theme with an ever-increasing number of new alleles, all encoding the Kx- (null) phenotype. The rev...

Garnier(M),Nectoux(J),Smol(T),Bauchet(A),V... Neuromuscul Disord 2025-08-00

...XK protein, resulting in impaired XK protein expression. This case expands the phenotypic spectrum of MLS and underscore...