Pages that link to "Q75424240"
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The following pages link to Kostmann syndrome: severe congenital neutropenia associated with defective expression of Bcl-2, constitutive mitochondrial release of cytochrome c, and excessive apoptosis of myeloid progenitor cells (Q75424240):
Displaying 24 items.
- A syndrome with congenital neutropenia and mutations in G6PC3 (Q24655459) (← links)
- Neutrophils: Between host defence, immune modulation, and tissue injury (Q28087227) (← links)
- HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease) (Q28280427) (← links)
- Late-onset neutropenia associated with rituximab therapy: evidence for a maturation arrest at the (pro)myelocyte stage of granulopoiesis (Q33320029) (← links)
- Hax1 lacks BH modules and is peripherally associated to heavy membranes: implications for Omi/HtrA2 and PARL activity in the regulation of mitochondrial stress and apoptosis (Q34991732) (← links)
- 5. Mechanisms of disordered granulopoiesis in congenital neutropenia (Q36543836) (← links)
- Mitochondria in hematopoiesis and hematological diseases. (Q36558011) (← links)
- Myelodysplastic syndromes: the complexity of stem-cell diseases (Q36717910) (← links)
- Genetic heterogeneity in severe congenital neutropenia: how many aberrant pathways can kill a neutrophil? (Q36995948) (← links)
- Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden (Q37292153) (← links)
- Shwachman-Diamond syndrome: implications for understanding the molecular basis of leukaemia (Q37356551) (← links)
- Hax-1: a regulator of calcium signaling and apoptosis progression with multiple roles in human disease (Q37851497) (← links)
- Primary immunodeficiency diseases associated with neurologic manifestations (Q37950942) (← links)
- Cellular stress pathways in pediatric bone marrow failure syndromes: many roads lead to neutropenia (Q38160152) (← links)
- Severe congenital neutropenias (Q39359222) (← links)
- N(alpha)-tosyl-L-phenylalanine chloromethyl ketone induces caspase-dependent apoptosis in transformed human B cell lines with transcriptional down-regulation of anti-apoptotic HS1-associated protein X-1. (Q39812900) (← links)
- Early mitochondrial alterations in ATRA-induced cell death (Q40400306) (← links)
- Aberrant subcellular targeting of the G185R neutrophil elastase mutant associated with severe congenital neutropenia induces premature apoptosis of differentiating promyelocytes. (Q40469524) (← links)
- Survivin expression in the bone marrow of patients with severe congenital neutropenia (Q46345792) (← links)
- Induction of cytokines by radioprotective tocopherol analogs (Q46903824) (← links)
- A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14. (Q50703043) (← links)
- How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel (Q56269950) (← links)
- The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia (Q59636266) (← links)
- HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI (Q82609158) (← links)