Xiaxin Li
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Explore the profile of Xiaxin Li including associated specialties, affiliations and a list of published articles.
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17
Citations
973
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Recent Articles
1.
Zhang S, Xu W, Wu L, Li X, Liu X, Wu X, et al.
Adv Healthc Mater
. 2024 May;
13(26):e2401095.
PMID: 38794821
Enamel has good optical and mechanical properties because of its multiscale hierarchical structure. Biomimetic construction of enamel-like 3D bulk materials at nano-, micro-, mesh- and macro-levels is a challenge. A...
2.
Zhao L, Fu G, Pang W, Li X, Pan C, Hu Z
Chemosphere
. 2023 Feb;
321:138157.
PMID: 36796520
We undertook a lab-scale evaluation of a novel autotrophic denitrification and nitrification integrated constructed wetland (ADNI-CW) for improved carbon (C), nitrogen (N), and sulfur (S) cycling to treat mariculture wastewater....
3.
Li X, Brazauskas R, Wang Z, Al-Seraihy A, Baker K, Cahn J, et al.
Biol Blood Marrow Transplant
. 2014 Jan;
20(4):587-92.
PMID: 24388803
We conducted a nested case-control study within a cohort of 6244 patients to assess risk factors for avascular necrosis (AVN) of bone in children and adolescents after allogeneic transplantation. Eligible...
4.
Pulliam-Leath A, Ciccone S, Nalepa G, Li X, Si Y, Miravalle L, et al.
Blood
. 2010 Jul;
116(16):2915-20.
PMID: 20606166
Fanconi anemia (FA) is an inherited chromosomal instability syndrome characterized by bone marrow failure, myelodysplasia (MDS), and acute myeloid leukemia (AML). Eight FA proteins associate in a nuclear core complex...
5.
Li X, Alexander S
Pediatr Blood Cancer
. 2008 Nov;
52(3):403-5.
PMID: 18985745
Hereditary persistence of alpha-fetoprotein (HPAFP) is a rare benign autosomal dominant disorder. Here we report a 7-year-old healthy female who was found to have elevated alpha-fetoprotein (AFP) of 55-88 ng/ml...
6.
Broxmeyer H, Orschell C, Clapp D, Hangoc G, Cooper S, Plett P, et al.
J Exp Med
. 2005 Apr;
201(8):1307-18.
PMID: 15837815
Improving approaches for hematopoietic stem cell (HSC) and hematopoietic progenitor cell (HPC) mobilization is clinically important because increased numbers of these cells are needed for enhanced transplantation. Chemokine stromal cell...
7.
Schubbert S, Lieuw K, Rowe S, Lee C, Li X, Loh M, et al.
Blood
. 2005 Mar;
106(1):311-7.
PMID: 15761018
PTPN11 encodes the protein tyrosine phosphatase SHP-2, which relays signals from growth factor receptors to Ras and other effectors. Germline PTPN11 mutations underlie about 50% of Noonan syndrome (NS), a...
8.
Li X, Le Beau M, Ciccone S, Yang F, Freie B, Chen S, et al.
Blood
. 2005 Jan;
105(9):3465-71.
PMID: 15644418
Current strategies for genetic therapy using Moloney retroviruses require ex vivo manipulation of hematopoietic cells to facilitate stable integration of the transgene. While many studies have evaluated the impact of...
9.
Freie B, Ciccone S, Li X, Plett P, Orschell C, Srour E, et al.
J Biol Chem
. 2004 Sep;
279(49):50986-93.
PMID: 15377654
Fanconi anemia (FA) is a complex, heterogeneous genetic disorder composed of at least 11 complementation groups. The FA proteins have recently been found to functionally interact with the cell cycle...
10.
Li X, Yang Y, Yuan J, Hong P, Freie B, Orazi A, et al.
Blood
. 2004 Apr;
104(4):1204-9.
PMID: 15113761
Fanconi anemia (FA) is characterized by bone marrow (BM) failure and cancer susceptibility. Identification of the cDNAs of many FA complementation types allows the potential of using gene transfer technology...