Xiaxin Li

Overview

Explore the profile of Xiaxin Li including associated specialties, affiliations and a list of published articles.

Snapshot

Articles 17

Citations 973

Followers 0

Related Specialties

Hematology

Allergy & Immunology

General Medicine

Top 10 Co-Authors

D Wade Clapp

Attilio Orazi

Laura S Haneline

Brian Freie

Ping Hong

Edward F Srour

Hal E Broxmeyer

P Artur Plett

Eliane Gluckman

Yanzhu Yang

Published In

Blood

J Biol Chem

Biol Blood Marrow Transplant

Br J Haematol

J Exp Med

Affiliations

Soon will be listed here.

Recent Articles

11.

Acute graft-versus-host disease in patients with Fanconi anemia or acquired aplastic anemia undergoing bone marrow transplantation from HLA-identical sibling donors: risk factors and influence on outcome

Guardiola P, Socie G, Li X, Ribaud P, Devergie A, Esperou H, et al.

Blood . 2003 Aug; 103(1):73-7. PMID: 12946993

To assess whether Fanconi anemia (FA) patients might be at risk for acute graft-versus-host disease (AGvHD) despite using low-intensity conditionings, we retrospectively analyzed the incidence of AGvHD and its impact...

12.

Fanconi anemia type C and p53 cooperate in apoptosis and tumorigenesis

Freie B, Li X, Ciccone S, Nawa K, Cooper S, Vogelweid C, et al.

Blood . 2003 Jul; 102(12):4146-52. PMID: 12855557

Fanconi anemia (FA) is a recessive genomic instability syndrome characterized by developmental defects, progressive bone marrow failure, and cancer. FA is genetically heterogeneous, however; the proteins encoded by different FA...

13.

Fanconi anemia type C-deficient hematopoietic stem/progenitor cells exhibit aberrant cell cycle control

Li X, Plett P, Yang Y, Hong P, Freie B, Srour E, et al.

Blood . 2003 May; 102(6):2081-4. PMID: 12763929

The pathogenesis of bone marrow failure in Fanconi anemia is poorly understood. Suggested mechanisms include enhanced apoptosis secondary to DNA damage and altered inhibitory cytokine signaling. Recent data determined that...

14.

Stromal cell-derived factor-1/CXCL12 directly enhances survival/antiapoptosis of myeloid progenitor cells through CXCR4 and G(alpha)i proteins and enhances engraftment of competitive, repopulating stem cells

Broxmeyer H, Kohli L, Kim C, Lee Y, Mantel C, Cooper S, et al.

J Leukoc Biol . 2003 Apr; 73(5):630-8. PMID: 12714578

Stromal cell-derived factor-1 (SDF-1/CXCL12) enhances survival of myeloid progenitor cells. The two main questions addressed by us were whether these effects on the progenitors were direct-acting and if SDF-1/CXCL12 enhanced...

15.

Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia

Li X, Leteurtre F, Rocha V, Guardiola P, Berger R, Daniel M, et al.

Br J Haematol . 2003 Mar; 120(5):836-45. PMID: 12614219

Fanconi's anaemia (FA) is an autosomal recessive disorder characterized by progressive bone marrow failure and a susceptibility to cancer. Haematopoietic stem cell transplantation is the only curative method for restoring...

16.

Locatelli F, Rocha V, Reed W, Bernaudin F, Ertem M, Grafakos S, et al.

Blood . 2002 Nov; 101(6):2137-43. PMID: 12424197

Allogeneic bone marrow transplantation (BMT) from HLA-identical siblings is an accepted treatment for both thalassemia and sickle cell disease (SCD). However, it is associated with decided risk of both transplant-related...

17.

Retroviral-mediated expression of recombinant Fancc enhances the repopulating ability of Fancc-/- hematopoietic stem cells and decreases the risk of clonal evolution

Haneline L, Li X, Ciccone S, Hong P, Yang Y, Broxmeyer H, et al.

Blood . 2002 Oct; 101(4):1299-307. PMID: 12393504

Fanconi anemia (FA) is a chromosomal instability disorder characterized by a progressive bone marrow (BM) failure and an increased incidence of myeloid leukemias. Children with FA are currently being enrolled...