Shuxiang X. Lin

Tianjin, China

Last Updated: 09/26/2026

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Found 15 publications

TGF-β1-Mediated Leukocyte Cell-Derived Chemotaxin 2 Is Associated With Liver Fibrosis in Biliary Atresia.

TGF-β1-Mediated Leukocyte Cell-Derived Chemotaxin 2 Is Associated With Liver Fibrosis in Biliary Atresia.

Journal: Frontiers in pediatrics
Published: March 22, 2022

Analysis of bacterial pathogens and clinical characteristics of children with respiratory tract infections in Tianjin

Analysis of bacterial pathogens and clinical characteristics of children with respiratory tract infections in Tianjin

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: October 29, 2021

Alteration of Allergen Fold of Bos d 5 into a Hypoallergenic Vaccine for Immunotherapy of Cow's Milk Allergy.

Alteration of Allergen Fold of Bos d 5 into a Hypoallergenic Vaccine for Immunotherapy of Cow's Milk Allergy.

Journal: International archives of allergy and immunology
Published: March 24, 2021

Analysis of gene variant in a Chinese child affected with dihydropyrimidinase deficiency

Analysis of gene variant in a Chinese child affected with dihydropyrimidinase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 12, 2020

Genetic analysis of a child with very long chain acyl-CoA dehydrogenase deficiency

Genetic analysis of a child with very long chain acyl-CoA dehydrogenase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 21, 2020

Rapid screening of a hotspot variant c.609G>A in MMACHC gene by using PCR-high-resolution melting curve analysis

Rapid screening of a hotspot variant c.609G>A in MMACHC gene by using PCR-high-resolution melting curve analysis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 04, 2020

Genetic analysis of one family with congenital limb malformations

Genetic analysis of one family with congenital limb malformations

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 14, 2019

Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.

Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiency.

Journal: Medicine
Published: January 05, 2019

Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review.

Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review.

Journal: European journal of medical genetics
Published: December 23, 2018

Identification of a novel mutation of UPB1 gene in a Chinese family affected with beta-ureidopropinoase deficiency

Identification of a novel mutation of UPB1 gene in a Chinese family affected with beta-ureidopropinoase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 05, 2018

Component resolved diagnostic study of cow's milk allergy in infants and young children in northern China.

Component resolved diagnostic study of cow's milk allergy in infants and young children in northern China.

Journal: International immunopharmacology
Published: April 10, 2018

Identification of ALDH5A1 gene mutations in a Chinese family affected with succinic semialdehyde dehydrogenase deficiency

Identification of ALDH5A1 gene mutations in a Chinese family affected with succinic semialdehyde dehydrogenase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 11, 2017
Showing 1-12 of 15

Last Updated: 09/26/2026