User profiles for "author:A Cao"
Anyuan CaoPeking University Verified email at pku.edu.cn Cited by 29670 |
[HTML][HTML] Beta-thalassemia
A Cao, R Galanello - Genetics in medicine, 2010 - Elsevier
Beta-thalassemia is caused by the reduced (beta+) or absent (beta 0) synthesis of the beta
globin chains of the hemoglobin tetramer. Three clinical and hematological conditions of …
globin chains of the hemoglobin tetramer. Three clinical and hematological conditions of …
[HTML][HTML] Metallic biomaterials: current challenges and opportunities
…, J Spoor, R Symes, M Tieppo, C Collins, A Cao… - Materials, 2017 - mdpi.com
Metallic biomaterials are engineered systems designed to provide internal support to
biological tissues and they are being used largely in joint replacements, dental implants …
biological tissues and they are being used largely in joint replacements, dental implants …
The prevention of thalassemia
A Cao, YW Kan - Cold Spring Harbor …, 2013 - perspectivesinmedicine.cshlp.org
The thalassemias are among the most common inherited diseases worldwide, affecting
individuals originating from the Mediterranean area, Middle East, Transcaucasia, Central …
individuals originating from the Mediterranean area, Middle East, Transcaucasia, Central …
[HTML][HTML] Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits
…, P Galan, A Chakravarti, D Schlessinger, A Cao… - PLoS …, 2007 - journals.plos.org
The obesity epidemic is responsible for a substantial economic burden in developed
countries and is a major risk factor for type 2 diabetes and cardiovascular disease. The …
countries and is a major risk factor for type 2 diabetes and cardiovascular disease. The …
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
…, R Collins, RN Bergman, M Uda, J Tuomilehto, A Cao… - Nature …, 2008 - nature.com
To identify genetic variants influencing plasma lipid concentrations, we first used genotype
imputation and meta-analysis to combine three genome-wide scans totaling 8,816 …
imputation and meta-analysis to combine three genome-wide scans totaling 8,816 …
Isolation of NF-E2-related factor 2 (Nrf2), a NF-E2-like basic leucine zipper transcriptional activator that binds to the tandem NF-E2/AP1 repeat of the beta-globin locus …
P Moi, K Chan, I Asunis, A Cao… - Proceedings of the …, 1994 - National Acad Sciences
Hypersensitive site 2 located in the beta-globin locus control region confers high levels of
expression to the genes of the beta-globin cluster. A tandem repeat of the consensus …
expression to the genes of the beta-globin cluster. A tandem repeat of the consensus …
Self‐Assembled 3D flowerlike iron oxide nanostructures and their application in water treatment
An ethylene‐glycol‐mediated self‐assembly process is adopted to synthesize 3D flowerlike
nanostructures of iron oxide (see figure) using inexpensive and nontoxic ferric chloride. A …
nanostructures of iron oxide (see figure) using inexpensive and nontoxic ferric chloride. A …
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
…, D Schlessinger, P Gasparini, D Bonneau, A Cao… - Nature …, 2001 - nature.com
In type I blepharophimosis/ptosis/epicanthus inversus syndrome (BPES), eyelid
abnormalities are associated with ovarian failure. Type II BPES shows only the eyelid …
abnormalities are associated with ovarian failure. Type II BPES shows only the eyelid …
Variants in MTNR1B influence fasting glucose levels
…, M Bochud, LL Bonnycastle, TA Buchanan, A Cao… - Nature …, 2009 - nature.com
To identify previously unknown genetic loci associated with fasting glucose concentrations,
we examined the leading association signals in ten genome-wide association scans …
we examined the leading association signals in ten genome-wide association scans …
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
…, P Baybayan, EY Chen, R Huber, G Neri, A Cao… - Nature …, 1996 - nature.com
Abstract Simpson-Golabi-Behmel syndrome (SGBS) is an X-linked condition characterized
by pre-and postnatal overgrowth with visceral and skeletal anomalies. To identify the …
by pre-and postnatal overgrowth with visceral and skeletal anomalies. To identify the …