Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
CNNM4 encodes a member of the ancient conserved domain containing protein family. Additionally we are shipping CNNM4 Antibodies (45) and CNNM4 Proteins (7) and many more products for this protein.
these results indicate that CNNM4-dependent Mg(2 (show MUC7 ELISA Kits)+) efflux suppresses tumor progression by regulating energy metabolism.
The c.1312 dupC mutation of CNNM4 leads to a premature termination of amelogenesis resulting in thin, incompletely mineralized enamel, whereas in dentin, only mineralization is disturbed.
CNNM4 is sorted to the basolateral membrane by the complementary function of AP-1A and AP-1B
Data indicate that a mutation in the cystathionine-beta-synthase (CBS (show CBS ELISA Kits)) domains of ancient conserved domain protein 4/cyclin M4 CNNM4 completely abrogated their Mg2 (show MUC7 ELISA Kits)+ efflux functions.
These results demonstrate the crucial importance of Mg(2 (show MUC7 ELISA Kits)+) extrusion by CNNM4 in organismal and topical regulation of magnesium.
Our case shows a unique combination of NF1 (show NF1 ELISA Kits) and Jalili syndrome; clinical examination, but also of molecular genetic analysis, which together provide a precise diagnosis.
This work describes the purification and preliminary crystallographic analysis of the CBS (show CBS ELISA Kits)-pair regulatory domain of the human ancient domain protein 4 (ACDP4), also known as CNNM4.
Identification of CNNM4 as the causative gene for Jalili syndrome, characterized by autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
Since CNNM4 is implicated in metal ion transport, cone-rod dystrophy and amelogenesis imperfecta may originate from abnormal ion homeostasis.
these results indicate that CNNM4-dependent Mg(2 (show MCOLN1 ELISA Kits)+) efflux suppresses tumor progression by regulating energy metabolism.
This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta.
, metal transporter CNNM4
, metal transporter CNNM4-like
, ancient conserved domain protein 4
, ancient conserved domain-containing protein 4