Literature Search

Alkashash(A),Samiei(A),Hu(S),Liao(X),Lin(J),… Am J Surg Pathol 2026-03-01

...MSH2 and MSH6) and p53 overexpression were each identified in 1 case (5.3%). All cases were negative for HER2 and pan-TR...

Fan(Y),Zhang(C),Zhu(M),Xu(Y),Tang(H),Pang(J)… Eur J Med Res 2026-01-19

...MSH2, FANCI, etc.), affecting Fanconi anemia, mismatch repair, PI3K-AKT, and MAPK pathways (P < 0.01). RNA profiling rev...

Bilardi(RA),Flensburg(C),Xu(Z),Derrick(EB),K… Nucleic Acids Res 2026-01-14

...Msh2), evident through elevated rates of CG > TG mutations in Msh6-deficient cells: 2.6-4.8 CG > TG mutations/genome/day...

Roush(SM),Beck(S),Coelho(J),Chirwa(A),Mponda… AIDS 2026-06-01

...MSH2 loss. Integration with a published HIV+ DLBCL dataset revealed recurrent driver mutations including LILRB1 p.R30S, ...

Vazzano Goldstone(J),Logan(SJ),Wilkins(BJ),M… Diagn Pathol 2026-01-22

...MSH2, MSH6, MLH1, PMS2) cause autosomal dominant Lynch syndrome (LS), most commonly manifesting as colonic or endometria...

Parulekar(M),Kim(YN),Kim(K),Lee(S),No(JH),Le… Gynecol Oncol 2026-02-00

...MSH2, MSH6, BRIP1, RAD51C, RAD51D, ATM, and CHEK2) with a variant allele frequency (VAF) of ≥40 %; and (2) exclusion of ...

Shen(M),Chen(G),Cai(F),Ren(Y),Zhang(Y),Shi(J) Int J Colorectal Dis 2026-01-14

...MSH2 and MSH6 proteins to identify patients with pMMR/MSI-H and pMMR/MSS. Multiplex immunofluorescence technology was em...

Chami(AM),Zózimo(TRS),Matosinho(CGR),Silva-F… Einstein (Sao Paulo) None

...MSH2):c.1894_1898del (p.Ile633Lysfs*9), an MSH2 germline variant detected in a family with Lynch syndrome. Clinical eval...

Glykofridis(IE),Dekker(M),Stoepker(C),van Ra… Proc Natl Acad Sci U S A 2026-01-20

...MSH2, MSH6, MLH1, or PMS2. Beyond clearly pathogenic mutations, germline sequencing often reveals variants of uncertain ...

Liu(Y),Ye(S),Liu(Z),Chen(Z),Liang(X) Cancers (Basel) 2026-02-03

...MSH2, MSH6, and PMS2). This approach fails to leverage gene-specific characteristics for precision healthcare delivery. ...