Xiaomeng M. Yang

Jinan, 250022, China

Last Updated: 09/26/2026

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Found 54 publications

A multicenter study on effect of delayed chemotherapy on prognosis of Burkitt lymphoma in children

A multicenter study on effect of delayed chemotherapy on prognosis of Burkitt lymphoma in children

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

Published: September 27, 2024

Current situation of surgical treatment of gallbladder polyps and some problems that should be paid attention to

Current situation of surgical treatment of gallbladder polyps and some problems that should be paid attention to

Journal: Zhonghua yi xue za zhi

Published: August 28, 2024

Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.

Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.

Journal: Scientific reports

Published: August 12, 2024

Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi055-A from a patient with NEDSDV carrying a heterozygote mutation in the CTNNB1 gene.

Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi055-A from a patient with NEDSDV carrying a heterozygote mutation in the CTNNB1 gene.

Journal: Stem cell research

Published: December 23, 2023

Generation and characterization of an induced pluripotent stem cell (iPSC) line SDQLCHi063-A from peripheral blood mononuclear cells of a patient with Maturity-onset diabetes of the young type 2 carrying GCK exon 1 deletion.

Generation and characterization of an induced pluripotent stem cell (iPSC) line SDQLCHi063-A from peripheral blood mononuclear cells of a patient with Maturity-onset diabetes of the young type 2 carrying GCK exon 1 deletion.

Journal: Stem cell research

Published: November 11, 2023

Generation of a human induced pluripotent stem cell line (SDQLCHi057-A) from an Isovaleric aciduria patient carrying novel compound heterozygous mutations in the IVD gene.

Generation of a human induced pluripotent stem cell line (SDQLCHi057-A) from an Isovaleric aciduria patient carrying novel compound heterozygous mutations in the IVD gene.

Journal: Stem cell research

Published: October 29, 2023

Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene.

Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene.

Journal: Stem cell research

Published: October 25, 2023

An induced pluripotent stem cell line (SDQLCHi062-A) from a patient carrying a mutation in the PAX2 gene.

An induced pluripotent stem cell line (SDQLCHi062-A) from a patient carrying a mutation in the PAX2 gene.

Journal: Stem cell research

Published: September 21, 2023

Establishment of human induced pluripotent stem cell line (SDQLCHi060-A) from a patient with AUTS2 syndrome carrying a heterozygous mutation in AUTS2 gene.

Establishment of human induced pluripotent stem cell line (SDQLCHi060-A) from a patient with AUTS2 syndrome carrying a heterozygous mutation in AUTS2 gene.

Journal: Stem cell research

Published: July 25, 2023

Establishment of induced pluripotent stem cell line SDPHi003-A from a healthy male donor.

Establishment of induced pluripotent stem cell line SDPHi003-A from a healthy male donor.

Journal: Stem cell research

Published: March 29, 2023

Establishment of a controlled induced pluripotent stem cell line SDPHi004-A from a healthy male donor.

Establishment of a controlled induced pluripotent stem cell line SDPHi004-A from a healthy male donor.

Journal: Stem cell research

Published: March 29, 2023

Generation of a transgene-free iPS cell line (SDQLCHi053-A) from a young girl carrying a heterozygous mutation (c.427C > T) in SYNGAP1 gene.

Generation of a transgene-free iPS cell line (SDQLCHi053-A) from a young girl carrying a heterozygous mutation (c.427C > T) in SYNGAP1 gene.

Journal: Stem cell research

Published: March 05, 2023

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Last Updated: 09/26/2026