AHI1 抗体
(Abelson Helper Integration Site 1 (AHI1))
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008].
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Latest Publications for our AHI1 抗体
: "Identification of tyrosine kinase, HCK, and tumor suppressor, BIN1, as potential mediators of AHI-1 oncogene in primary and transformed CTCL cells." in: Blood, Vol. 113, Issue 19, pp. 4646-55, (2009) (PubMed).: "AHI-1 interacts with BCR-ABL and modulates BCR-ABL transforming activity and imatinib response of CML stem/progenitor cells." in: The Journal of experimental medicine, Vol. 205, Issue 11, pp. 2657-71, (2008) (PubMed).
: "Evidence for an oncogenic role of AHI-1 in Sezary syndrome, a leukemic variant of human cutaneous T-cell lymphomas." in: Leukemia, Vol. 20, Issue 9, pp. 1593-601, (2006) (PubMed).
: "Ahi-1, a novel gene encoding a modular protein with WD40-repeat and SH3 domains, is targeted by the Ahi-1 and Mis-2 provirus integrations." in: Journal of virology, Vol. 76, Issue 18, pp. 9046-59, (2002) (PubMed).
Aliases for AHI1 抗体
Abelson helper integration site 1 (AHI1) 抗体Abelson helper integration site 1 (ahi1) 抗体
Abelson helper integration site 1 (Ahi1) 抗体
1700015F03Rik 抗体
AHI-1 抗体
Ahi-1 抗体
AHI1 抗体
D10Bwg0629e 抗体
dJ71N10.1 抗体
JBTS3 抗体
ORF1 抗体
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