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This study showed that MAD1L1 (show MAD1L1 Proteins) as a susceptibility gene for both of these genetically overlapping disorders is associated with a decreased bottom-up responsiveness of the mesolimbic reward system and related cortical regions involved in the salience network as well as with reduced top-down control processes.
Results show that low DNA methylation (show HELLS Proteins) levels of LINC00682, MAD1L1 (show MAD1L1 Proteins), and LINE-2 was strongly correlated with hepatocellular carcinomas recurrence, patient disease-free survival, and/or overall survival.
MAD1L1 (show MAD1L1 Proteins) positive expression may be associated with tumour progression and metastasis in small-cell lung cancer (SCLC) and may thus serve as a new biomarker for prognosis in these patients.
In this review, we highlight a novel Mad1 role in chromosome alignment, which is the first conserved mechanism that links the spindle assembly checkpoint and kinesin-mediated chromosome gliding.
MAD1L1 (show MAD1L1 Proteins) Arg558His and MAD2L1 (show MAD2L1 Proteins) Leu84Met interaction with smoking increase the risk of colorectal cancer
Deubiquitylase POH1 stabilizes E2F1 protein through binding (show E2F1 Proteins)to and deubiquitylating E2F1 in liver cancer.
MAD1L1 rs12666575 polymorphism may play a protective role against schizophrenia (SCZ) in the Chinese population. rs12666575 may be associated with general psychopathology and thought disturbance in SCZ patients.
We also show that replication perturbations result in relocalization of MAD1 (show MXD1 Proteins)/MAD2 (show MAD2L1 Proteins) in human cells, suggesting that the role of SAC (show ADCY10 Proteins) in DNA repair is conserved.
Mad1 (show MXD1 Proteins) has a role in secretion and cell migration.
MAD1 (show MXD1 Proteins) kinetochore localization dictates the spindle assembly checkpoint in metaphase.
Conditional knockout of Poh1 alleles results in reduced E2F1 (show E2F1 Proteins) expression in primary mouse liver cells.
These results identify a novel mechanism of Mitf (show MITF Proteins) regulation in osteoclasts by POH1.
This gene encodes a component of the 26S proteasome. The 26S proteasome is a large multiprotein complex that catalyzes the degradation of ubiquitinated intracellular proteins. The encoded protein is a component of the 19S regulatory cap complex of the 26S proteasome and mediates substrate deubiquitination. A pseudogene of this gene is also located on the long arm of chromosome 2.
, regulatory particle non-ATPase 11
, yippee interacting protein 5
, MAD1-like protein 1
, mitotic arrest deficient 1-like protein 1
, mitotic checkpoint MAD1 protein homolog
, mitotic spindle assembly checkpoint protein MAD1
, mitotic-arrest deficient 1, yeast, homolog-like 1
, tax-binding protein 181
, tumor protein p53 inducible protein 9
, 26S proteasome non-ATPase regulatory subunit 14
, 26S proteasome regulatory subunit rpn11
, 26S proteasome-associated PAD1 homolog 1
, proteasome 26S subunit, non-ATPase 14
, 26S proteasome non-ATPase subunit
, 26S proteasome-associated pad1 homolog