Yuan(X),Jia(D),Wan(G),Wang(C),Liu(K),Meng(... Clin Biochem 2025-12-00

...HEXB and down regulated HBA1, while DHRS2 was significantly different in the urine of the two subtypes.

Tsourmas(KI),Butler(CA),Kwang(NE),Sloane(Z... Nat Commun 2025-08-27

...Hexb). Although Hexb expression in the brain is specific to microglia, SD primarily affects neurons. To investigate how ...

Ha(Tae Kwang),Kim(Yeon-Gu),Lee(Gyun Min) Biotechnol Bioeng 2016-03-14

...hexb, neu1, and neu3) were up-regulated over 1.5 times in the culture with ammonium addition after 5 days of culture; ho...

Tao(J),Liu(W),Shang(G),Zheng(Y),Huang(J),L... Neuroscience 2016-06-01

...Hexb, Bcl2, etc. MiR-207 and miR-352 were mainly downregulated after ischemic stroke, followed by a slight return to bas...

Richardson(Katie),Livieratos(Achilleas),Du... Behav Brain Res 2016-09-20

...Hexb knockout, Hexb(-/-)) disease using wheel-running activity measurement, neuropathology and clock gene expression ana...

Gerovska(Daniela),Araúzo-Bravo(Marcos J) Mol Hum Reprod 2016-11-09

...Hexb, Slc1a1, Svip, Liph and Mier3), six new stable PE markers (Sdc4, Cpn1, Dkk1, Havcr1, F2r/Par1 and Slc7a6os) as well...

Tropak(Michael B),Yonekawa(Sayuri),Karumut... Mol Ther Methods Clin Dev 2016-03-11

Tay-Sachs or Sandhoff disease result from mutations in either the evolutionarily related HEXA or HEXB genes encoding res...

Yang(Won Ho),Aziz(Peter V),Heithoff(Dougla... Proc Natl Acad Sci U S A 2016-03-02

...HexB), possess hydrolytic activities that temporally remodel N-glycan structures, progressively exposing different sacch...

Tiribuzi(Roberto),D'Angelo(Francesco),Bera... Cell Biochem Funct 2015-08-24

In an attempt to investigate whether the genetic defect in the HEXA and HEXB genes (which causes the absence of the lyso...

Masri(Amira),Liao(Jun),Kornreich(Ruth),Hag... Eur J Paediatr Neurol 2015-02-12

...HEXB) gene. Here, we investigated the clinical characteristics and molecular basis of Sandhoff disease in an infant fema...