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HAX1
Gene Information from Publications |
| Publication Link |
Summary of findings |
| 18055975 |
important role of HAX1 on neural development as well as myelopoiesis. |
| 17929250 |
HAX1, an anti-apoptotic protein, inhibits the HIV-1 rev function by altering is subcellular localization. |
| 16971486 |
These findings reveal that nuclear localization of pre-IL-1alpha depends on the binding to HAX-1 and that biological activities might be elicited by the binding to both HAX-1 and IL-1RII in SSc fibroblasts. |
| 17187068 |
HAX1 is a major regulator of myeloid homeostasis and mutant proteins cause autosomal recessive severe congenital neutropenia. |
| 12787133 |
In psoriasis, the epidermal differentiation could be disturbed due to the increased expression of HAX-1 and hence a prolonged resistance to terminal differentiation |
| 16857965 |
HAX-1 is a newly identified anti-apoptotic factor and its mechanism of action is through caspase-9 inhibition. |
| 15159385 |
HAX-1 binds bile salt export protein (BSEP), cortactin, MDR1, and MDR2. HAX-1 and cortactin regulate BSEP abundance in the apical membrane of cells. |
Recent Publications on HAX1: |  |
Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities.
Kostmann disease or severe congenital neutropenia (SCN) is an autosomal... | 14th October, 2009
| Childhood Cancer Research Unit, Department of Woman and Child Health,
| Pediatr Blood Cancer. 2009 Dec;53(6):1143-6.
DOI Direct Link |
Neutropenia and primary immunodeficiency diseases.
Primary immunodeficiency diseases (PID) are a heterogeneous group of... | 9th October, 2009
| Center of Excellence for Pediatrics, Children's Medical Center, Tehran
| Int Rev Immunol. 2009;28(5):335-66.
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Hepatitis C virus core protein and cellular protein HAX-1 promote 5-fluorouracil-mediated hepatocyte growth inhibition.
Hepatitis C virus (HCV) often causes chronic infection and may lead to... | 8th October, 2009
| Department of Internal Medicine, Saint Louis University, St. Louis,
| J Virol. 2009 Oct;83(19):9663-71. Epub 2009 Jul 15.
DOI Direct Link |
A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease).
Primary immunodeficiency diseases (PID) are a heterogeneous group of... | 3rd October, 2009
| Department of Pathology and Laboratory Medicine, King Faisal Specialist
| Clin Genet. 2009 Oct 1.
DOI Direct Link |
Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia.
Severe congenital neutropenia (SCN) is a genetically heterogeneous... | 25th September, 2009
| Division of Oncology, Department of Medicine, Washington University School
| Br J Haematol. 2009 Nov;147(4):535-42. Epub 2009 Sep 22.
DOI Direct Link |
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