Tian Pu

Wuxi, 214131, China

Last Updated: 09/26/2026

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Found 14 publications

Integrated sludge resources hierarchical recovery: enhancing VFAs production through pilot scale liquid-state anaerobic fermentation by sludge residues-based biochar.

Integrated sludge resources hierarchical recovery: enhancing VFAs production through pilot scale liquid-state anaerobic fermentation by sludge residues-based biochar.

Journal: Bioresource technology

Published: April 05, 2026

Research on Output Characteristics of Microscale BST Laminate Structure Based on Mixed Finite Element Method.

Research on Output Characteristics of Microscale BST Laminate Structure Based on Mixed Finite Element Method.

Journal: Micromachines

Published: March 06, 2023

COVID-19 treated with oral Nirmatrelvir-Ritonavir in 3 children

COVID-19 treated with oral Nirmatrelvir-Ritonavir in 3 children

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: November 01, 2022

Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy.

Exome sequencing identifies a FHOD3 p.S527del mutation in a Chinese family with hypertrophic cardiomyopathy.

Journal: The journal of gene medicine

Published: July 16, 2019

Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.

Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family.

Journal: Molecular genetics & genomic medicine

Published: May 30, 2019

Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease.

Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease.

Journal: Twin research and human genetics : the official journal of the International Society for Twin Studies

Published: December 02, 2017

CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children.

CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children.

Journal: DNA and cell biology

Published: April 25, 2017

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.

Journal: Molecular genetics and genomics : MGG

Published: January 13, 2017

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity.

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity.

Journal: Scientific reports

Published: April 11, 2016

Exome sequencing identifies a c.148-1G>C mutation of TBX5 in a Holt-Oram family with unusual genotype-phenotype correlations.

Exome sequencing identifies a c.148-1G>C mutation of TBX5 in a Holt-Oram family with unusual genotype-phenotype correlations.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Published: August 26, 2015

Patients carrying 9q31.1-q32 deletion share common features with Cornelia de Lange Syndrome.

Patients carrying 9q31.1-q32 deletion share common features with Cornelia de Lange Syndrome.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Published: November 11, 2014

Inactivation and identification of three genes encoding glycosyltransferase required for biosynthesis of nogalamycin.

Inactivation and identification of three genes encoding glycosyltransferase required for biosynthesis of nogalamycin.

Journal: Biotechnology and applied biochemistry

Published: October 26, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026