Publications by authors named "Xu Manting"

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WTAP promotes the proliferation of multiple myeloma by regulating the hippo pathway through mA modification of MAP6D1.
Han Xu, Manting Xu, Jiamin Ding, Jing Bao

Leuk Lymphoma· November 2025

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Clinical and genetic characterization of -related disorders: insights into genotype-phenotype correlations.
Xu Manting, Li Hua, Huang Sheng, Han Xiaodi, Sun Dan

Front Pediatr· November 2025

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Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in Children.
Xiaodi Han, Hua Li, Jie Deng, Xiuwei Zhuo, Zhimei Liu, Manting Xu

Neurol Sci· November 2024

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Arsenic and Human Health: New Molecular Mechanisms For Arsenic-Induced Cancers.
Alexandra N Nail, Manting Xu, Jonathan C Bastick, Deep P Patel, Max N Rogers

Curr Pollut Rep· December 2023

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Demonstration of in vivo engineered tandem duplications of varying sizes using CRISPR and recombinases in Drosophila melanogaster.
David W Loehlin, Georgia L McClain, Manting Xu, Ria Kedia, Elise Root

G3 (Bethesda)· September 2023

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Demonstration of engineered tandem duplications of varying sizes using CRISPR and recombinases in .
David W Loehlin, Georgia L McClain, Manting Xu, Ria Kedia, Elise Root

bioRxiv· January 2023

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"A fly appeared": sable, a classic Drosophila mutation, maps to Yippee, a gene affecting body color, wings, and bristles.
Derek M Dean, David L Deitcher, Caleigh O Paster, Manting Xu, David W Loehlin

G3 (Bethesda)· May 2022

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Whole genome and exome sequencing identify mutations as a new cause of progressive cavitating leukoencephalopathy.
Zhimei Liu, Li Zhang, Changhong Ren, Manting Xu, Shufang Li

J Med Genet· April 2022

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Clinical implementation of RNA sequencing for Mendelian disease diagnostics.
Vicente A Yépez, Mirjana Gusic, Robert Kopajtich, Christian Mertes, Nicholas H Smith, Manting Xu

Genome Med· April 2022

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Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency.
Huafang Jiang, Ahmad Alahmad, Song Fu, Xiaoling Fu, Zhimei Liu, Manting Xu

J Inherit Metab Dis· March 2022

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Generation of an iPSC line from a patient with early-onset epileptic encephalopathy carrying CARS2 (p.G476R) mutation.
Manting Xu, Xin Duan, Xiaotun Ren, Zhimei Liu, Shuhua Chen

Stem Cell Res· March 2022

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Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndrome.
Manting Xu, Robert Kopajtich, Matthias Elstner, Hua Li, Zhimei Liu

Mitochondrion· January 2022

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Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers' Syndrome Genotypes.
Hua Li, Wei Wang, Xiaodi Han, Yujia Zhang, Lifang Dai, Manting Xu

Front Pharmacol· October 2021

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Biallelic -Variants Leading to Developmental Regression With Progressive Spasticity and Brain Atrophy in a Chinese Patient.
Rui Ban, Zhimei Liu, Masaru Shimura, Xiao Tong, Junling Wang, Manting Xu

Front Genet· July 2021

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Corrigendum: Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With Mutations Presenting With Leigh/Leigh-Like Syndrome.
Junling Wang, Zhimei Liu, Manting Xu, Xiaodi Han, Changhong Ren

Front Pharmacol· June 2021

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Identification of a Novel Variant in Causing MELAS.
Manting Xu, Robert Kopajtich, Matthias Elstner, Zhaoxia Wang, Zhimei Liu

Front Genet· May 2021

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Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With Mutations Presenting With Leigh/Leigh-Like Syndrome.
Junling Wang, Zhimei Liu, Manting Xu, Xiaodi Han, Changhong Ren

Front Pharmacol· March 2021

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Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation.
Hua Li, Fang Fang, Manting Xu, Zhimei Liu, Ji Zhou

Front Pharmacol· December 2019

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Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy.
Katharina Danhauser, Bader Alhaddad, Christine Makowski, Dorota Piekutowska-Abramczuk, Steffen Syrbe, Manting Xu

Am J Hum Genet· November 2018

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[Progress in respiratory function assessment and management for Duchenne muscular dystrophy].
Manting Xu, Fang Fang

Zhonghua Er Ke Za Zhi· November 2014

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[Rare combination of dystrophinopathy and Klinefelter's syndrome in one patient].
Manting Xu, Fang Fang, Jing Xu

Zhonghua Er Ke Za Zhi· July 2014

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