Literature Search

Blasco(M),Quiroga(B),García-Aznar(JM),Castro… Am J Kidney Dis 2024-12-00

...PAX2, UMOD, MUC1, and INF2 (7.3%, 5.9%, 2.5%, 2.5%, and 2.5%, respectively). Overall, 87 novel variants classified as P/...

Li(L),Hossain(SM),Eccles(MR) Int J Mol Sci 2024-06-19

...PAX2 and PAX8, in the three most common RCC subtypes, including ccRCC, papillary RCC (PRCC), and chromophobe RCC (ChRCC)...

Mahmoud(AH),Talaat(IM),Tlili(A),Hamoudi(R) Front Med (Lausanne) 2024-00-00

...PAX2, TBX18, NRIP1, REX, SIX2, BMP4, and chromosome 17 cause CAKUT. Over 50 genes have been identified as the root cause...

X Zhang(G),Yang(B) Histopathology 2024-11-00

...PAX2 expression than loss of PAX2 (92.3% versus 7.7%), regardless of somatic or germline mutations. Loss of PAX2 was obs...

Zhong(J),Wang(W),Li(Y),Wei(J),Cui(S),Song(N)… Genes (Basel) 2024-07-09

...Pax2/5/8, Pax3/7, and Pax4/6 subfamilies. We believe that Pax1/9 has an effect on the growth traits of buffalo and domes...

Nagao(S),Matsuura(M),Kurokawa(S),Tamate(M),A… Case Rep Oncol Med 2024-00-00

...PAX2] [-], and estrogen receptor [ER] [-]). In patients with cancer, histopathology and immunohistochemistry are importa...

Hu(X),Lin(W),Luo(Z),Zhong(Y),Xiao(X),Tang(R) Mol Genet Genomic Med 2024-09-00

Paired box gene 2 (PAX2) heterozygous mutations can cause renal coloboma syndrome, but its role in patients with focal s...

Uribe-Montes(LC),Sanabria-Camargo(CA),Piñero… PLoS One 2024-00-00

...pax2, ATPα1a.1), structural abnormalities were evident. Differences between wild-type and mutation-carriers suggest a ha...

Shao(H),Liao(Y),Xiang(M),Hu(D),Liu(S) Cell Mol Biol (Noisy-le-grand) 2024-06-05

...PAX2) carbonic anhydrase IX were biomolecules closely linked with ccRCC development and outcomes of multiple malignancie...

Lee(SY),Park(JM),Rhim(WK),Lee(EH),Lee(SH),Ki… Nano Converg 2024-10-26

...PAX2 for distal tubules in the renal defect model. With these, structural regeneration and functional recovery were achi...