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Prdm3 (show MECOM ELISA Kits) and prdm16 are strongly expressed in the pharyngeal arches during cranioskeletal development, and their knockdown leads to defects in both the viscerocranium and the neurocranium.
Animals with the homozygote PRDM16 genotype had lower body weight and average daily gain than those with the other genotypes.
The genetic variation within PRDM16 gene in 1031 Chinese indigenous bovine, was analyzed.
Flow cytometric analysis and western blot analysis of apoptosisassociated proteins indicated that PRDM16 has an antiapoptotic role in prostatic cancer cells. In addition, the spliced form, sPRDM16/MEL1S, was detected to be overexpressed in PCa (show FLVCR1 ELISA Kits) cell lines. In conclusion, the present study indicated an important oncogenic role in prostate cancer.
A single risk variant, rs2651899 in PRDM16, was significantly associated with efficacy of triptans in migraine patients
High PRDM16 expression is associated with astrocytoma.
Our results suggest that K568 SUMOylation of sPRDM16 plays an important role in the progression of acute myeloid leukemia (show BCL11A ELISA Kits).
Results show that PRDM16 overexpression was highly recurrent in de novo paediatric AML (show RUNX1 ELISA Kits) and is associated with adverse outcome
PRDM16 might contribute to maintain adipose tissue "white fat" gene expression profile and systemic metabolic homeostasis.
EVI1 (show MECOM ELISA Kits) and MEL1 are homolog genes whose transcriptional activations by chromosomal translocations have roles in Japanese pediatric acute myeloid leukemia (show BCL11A ELISA Kits)
Three novel loci were identified in East Asians with cardiac arrhythmias: rs2483280 (PRDM16 locus) and rs335206 (PRDM6 (show PRDM6 ELISA Kits) locus) were associated with QRS (show QARS ELISA Kits) duration; and rs17026156 (SLC8A1 (show SLC8A1 ELISA Kits) locus) correlated with PR interval.
Genetic analyses uncovered the importance of the PRDM16 gene in the regulation of lean body mass.
MED1 (show MED1 ELISA Kits) is required for optimal PRDM16-induced Ucp1 (show UCP1 ELISA Kits) expression
We further show that Cdkn1c (show CDKN1C ELISA Kits) is required for post-transcriptional accumulation of the brown fat determinant PR domain containing 16 (PRDM16) and that CDKN1C (show CDKN1C ELISA Kits) and PRDM16 co-localise to the nucleus of rare label-retaining cell within iBAT (show SLC10A2 ELISA Kits).
PRDM16-induced C2C12 transdifferentiation is associated with alterations in CpG methylation of myogenic factors, and PR domain affects both myogenesis and adipogenesis with modified histone methylation marks on MyoD (show MYOD1 ELISA Kits) and PPARgamma (show PPARG ELISA Kits) promoters
PRDM16 deficiency in BAT (show BAAT ELISA Kits) reduces MED1 (show MBD4 ELISA Kits) binding at PRDM16 target sites and causes a fundamental change in chromatin architecture at key brown fat-selective genes
Prdm16 and Prdm3 (show MECOM ELISA Kits) control postnatal BAT (show BAAT ELISA Kits) identity and function.
Study reveals that Prdm16 expression is regulated through Gcn5 (show KAT2A ELISA Kits)/PCAF (show KAT2B ELISA Kits) during brown adipogenesis.
these studies define the transcriptional pathways involved in HOXB4 (show HOXB4 ELISA Kits) HSC (show FUT1 ELISA Kits) expansion in vivo and identify repression of Prdm16 transcription as a mechanism by which expanding HSCs avoid leukemic transformation.
miR (show MLXIP ELISA Kits)-133 links to energy balance through targeting Prdm16.
These findings indicate that PRDM16 and beige (show LYST ELISA Kits) adipocytes are required for the "browning" of white fat and the healthful effects of subcutaneous adipose tissue.
adult satellite cells give rise to brown adipocytes and that microRNA-133 regulates the choice between myogenic and brown adipose determination by targeting the 3'UTR (show UTS2R ELISA Kits) of Prdm16.
When expressed at elevated levels in brown fat, TLE3 counters Prdm16, suppressing brown-selective genes and inducing white-selective genes, resulting in impaired fatty acid oxidation and thermogenesis.
The reciprocal translocation t(1\;3)(p36\;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported.
PR domain containing 16
, PR domain zinc finger protein 16-like
, MDS1/EVI1-like gene 1
, PR domain zinc finger protein 16
, transcription factor MEL1
, PR domain-containing protein 16
, line 27