Citations for
1HAX1
Hax1 regulates neutrophil adhesion and motility through RhoA.
Cavnar PJ, Berthier E, Beebe DJ, Huttenlocher A.
J Cell Biol 193(3):465-73. Epub 2011 Apr 25. 2011
2HAX1, SAV1
hSav1 interacts with HAX1 and attenuates its anti-apoptotic effects in MCF-7 breast cancer cells.
Luo X, Li Z, Li X, Wang G, Liu W, Dong S, Cai S, Tao D, Yan Q, Wang J, Leng Y, Gong J, Hu J.
Int J Mol Med 28(3):349-55. doi: 10.3892/ijmm.2011.692. Epub 2011 May 6. 2011
3HAX1, XIAP
Molecular interaction between HAX-1 and XIAP inhibits apoptosis.
Kang YJ, Jang M, Park YK, Kang S, Bae KH, Cho S, Lee CK, Park BC, Chi SW, Park SG.
Biochem Biophys Res Commun 393(4):794-9. Epub 2010 Feb 18.PMID: 20171186 2010
4EIF3G, HAX1, PELO, SRPX
Pelota interacts with HAX1, EIF3G and SRPX and the resulting protein complexes are associated with the actin cytoskeleton.
Burnicka-Turek O, Kata A, Buyandelger B, Ebermann L, Kramann N, Burfeind P, Hoyer-Fender S, Engel W, Adham IM.
BMC Cell Biol 11:28. 2010
5HAX1
HAX1 deficiency: impact on lymphopoiesis and B-cell development.
Peckl-Schmid D, Wolkerstorfer S, Königsberger S, Achatz-Straussberger G, Feichtner S, Schwaiger E, Zaborsky N, Huemer M, Gratz IK, Schibli R, Lamers M, Crameri R, Moser K, Luger EO, Achatz G.
Eur J Immunol 40(11):3161-72. doi: 10.1002/eji.200940221. Epub 2010 Sep 24. 2010
6HAX1
The anti-apoptotic protein HAX-1 is a regulator of cardiac function.
Zhao W, Waggoner JR, Zhang ZG, Lam CK, Han P, Qian J, Schroder PM, Mitton B, Kontrogianni-Konstantopoulos A, Robia SL, Kranias EG.
Proc Natl Acad Sci U S A roc Natl Acad Sci U S A. 2009 Nov 17. [Epub ahead of print]PMID: 19920172 2009
7HAX1, SCNP3
A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease).
Faiyaz-Ul-Haque M, Al-Jefri A, Abalkhail HA, Toulimat M, Al-Muallimi MA, Pulicat MS, Gaafar A, Alaiya AA, Al-Dayel F, Peltekova I, Zaidi SH.
Clin Genet 76(6):569-72. Epub 2009 Oct 1. No abstract available. PMID: 19796188 2009
8HTRA2, HAX1
Hax1-mediated processing of HtrA2 by Parl allows survival of lymphocytes and neurons.
Chao JR, Parganas E, Boyd K, Hong CY, Opferman JT, Ihle JN.
Nature 452(7183):98-102. Epub 2008 Feb 20. 2008
9HAX1, SCNP3
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene.
Ishikawa N, Okada S, Miki M, Shirao K, Kihara H, Tsumura M, Nakamura K, Kawaguchi H, Ohtsubo M, Yasunaga S, Matsubara K, Sako M, Hara J, Shiohara M, Kojima S, Sato T, Takihara Y, Kobayashi M.
J Med Genet 45(12):802-7. Epub 2008 Jul 8. 2008
10SCNP3, HAX1
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schaffer AA, Rathinam C, Boztug K, Schwinzer B, Rezaei N, Bohn G, Melin M, Carlsson G, Fadeel B, Dahl N, Palmblad J, Henter JI, Zeidler C, Grimbacher B, Welte K.
Nat Genet 39(1):86-92. Epub 2006 Dec 24. 2007
11CASP9, HAX1
Overexpression of HAX-1 protects cardiac myocytes from apoptosis through caspase-9 inhibition.
Han Y, Chen YS, Liu Z, Bodyak N, Rigor D, Bisping E, Pu WT, Kang PM.
Circ Res 99(4):415-23. Epub 2006 Jul 20. 2006
12HAX1
HAX-1, identified by differential display reverse transcription polymerase chain reaction, is overexpressed in lesional psoriasis.
Mirmohammadsadegh A, Tartler U, Michel G, Baer A, Walz M, Wolf R, Ruzicka T, Hengge UR.
J Invest Dermatol 120(6):1045-51. 2003
13BLOM7, HAX1, MCKD1, SYT11, TPM3, UBAP2L
Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.
Fuchshuber A, Kroiss S, Karle S, Berthold S, Huck K, Burton C, Rahman N, Koptides M, Deltas C, Otto E, Ruschendorf F, Feest T, Hildebrandt F.
Genomics 72(3):278-84. 2001
14HAX1
Evidence that HAX-1 is an interleukin-1 alpha N-terminal binding protein.
Yin H, Morioka H, Towle CA, Vidal M, Watanabe T, Weissbach L.
Cytokine 15(3):122-37. 2001