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LZTR1 encodes a member of the BTB-kelch superfamily. Additionally we are shipping LZTR1 Antibodies (26) and LZTR1 Proteins (3) and many more products for this protein.
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Nerve lesions and LZTR1 germline mutations in segmental schwannomatosis.
Data indicate that molecular analysis of leucine-zipper-like transcription regulator 1 (LZTR1) may contribute to the molecular characterization of schwannomatosis patients.
We show for the first time that an inherited mutation in PBRM1 (show PBRM1 ELISA Kits) predisposes to RCC (show XRCC1 ELISA Kits).
Data confirm the relationship between mutations in LZTR1 and schwannomatosis. They indicate that germline mutations in LZTR1 confer an increased risk of vestibular schwannoma.
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas.
LZTR-1 is the first BTB-kelch protein that exclusively localizes to the Golgi network
This gene encodes a member of the BTB-kelch superfamily. Initially described as a putative transcriptional regulator based on weak homology to members of the basic leucine zipper-like family, the encoded protein subsequently has been shown to localize exclusively to the Golgi network where it may help stabilize the Gogli complex. Deletion of this gene may be associated with DiGeorge syndrome.
leucine-zipper-like transcription regulator 1
, Leucine-zipper-like transcriptional regulator 1
, leucine-zipper-like transcriptional regulator 1
, leucine-zipper-like regulator-1
, leucine-zipper-like transcriptional regulator, 1