Works matching AU Qin, Zailong

Results: 53

Novel mutations in ZMYND15 are associated with male infertility with oligozoospermia/azoospermia.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 5, p. 1601, doi. 10.1007/s10815-025-03480-y

By:

Wei, Chunjia;
Lu, Yingchi;
Yi, Sibing;
Liang, Yaoqiong;
Meng, Lanlan;
Tan, Chen;
Du, Juan;
Lin, Ge;
Tan, Yue-Qiu;
Gan, Xianyou;
Tu, Chaofeng;
Qin, Zailong

Publication type:

Article

LINC00470 promotes malignant progression of testicular germ cell tumors.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-10083-w

By:

Liu, Zhizhong;
Lv, Shanshan;
Qin, Zailong;
Shu, Jinhui;
Zhu, Fang;
Luo, Yanwei;
Fan, Liqing;
Chen, Mengqian;
Bo, Hao;
Liu, Lvjun

Publication type:

Article

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study.

Published in:

Human Mutation, 2022, v. 43, n. 5, p. 568, doi. 10.1002/humu.24347

By:

Sun, Yu;
Peng, Jing;
Liang, Desheng;
Ye, Xiantao;
Xu, Na;
Chen, Linlin;
Yan, Dan;
Zhang, Huiwen;
Xiao, Bing;
Qiu, Wenjuan;
Shen, Yiping;
Pang, Nan;
Liu, Yingdi;
Liang, Chen;
Qin, Zailong;
Luo, Jingsi;
Chen, Fei;
Wang, Jingmin;
Zhang, Zhixin;
Wei, Haiyan

Publication type:

Article

Novel germline variants in KMT2C in Chinese patients with Kleefstra syndrome-2.

Published in:

Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1340458

By:

Qi Yang;
Qiang Zhang;
Sheng Yi;
Shujie Zhang;
Shang Yi;
Xunzhao Zhou;
Zailong Qin;
Biyan Chen;
Jingsi Luo

Publication type:

Article

Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0462-0

By:

Su, Jiasun;
Fu, Huayu;
Xie, Bobo;
Lu, Weiliang;
Li, Wei;
Wei, Yuan;
Zhang, Qiang;
Wei, Shengkai;
Chen, Qiuli;
Lu, Yingchi;
Jiang, Tingting;
Luo, Jingsi;
Qin, Zailong

Publication type:

Article

Mosaic UPD(7q)mat in a patient with silver Russell syndrome.

Published in:

Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0337-1

By:

Jiasun Su;
Jin Wang;
Xin Fan;
Chunyun Fu;
ShuJie Zhang;
Yue Zhang;
Zailong Qin;
Hongdou Li;
Jingsi Luo;
Chuan Li;
Tingting Jiang;
Yiping Shen

Publication type:

Article

De Novo SMARCC2 Variant in a Chinese Woman with Coffin-Siris Syndrome 8: a Case Report with Mild Intellectual Disability and Endocrinopathy.

Published in:

Journal of Molecular Neuroscience, 2022, v. 72, n. 6, p. 1293, doi. 10.1007/s12031-022-02010-0

By:

Yi, Sheng;
Li, Mengting;
Yang, Qi;
Qin, Zailong;
Yi, Shang;
Xu, Juanjuan;
Chen, Junjie;
Wei, Hao;
Jiang, Yaoyao;
Wei, Rongmin;
Zhang, Qinle;
Yang, Chengyun;
Chen, Biyan;
Luo, Jingsi

Publication type:

Article

Epstein-Barr Virus miR-BART6-3p Inhibits the RIG-I Pathway.

Published in:

Journal of Innate Immunity, 2017, v. 9, n. 6, p. 574, doi. 10.1159/000479749

By:

Lu, Yuanjun;
Qin, Zailong;
Wang, Jia;
Zheng, Xiang;
Lu, Jianhong;
Zhang, Xuemei;
Wei, Lingyu;
Peng, Qiu;
Zheng, Ying;
Ou, Chunlin;
Ye, Qiurong;
Xiong, Wei;
Li, Guiyuan;
Fu, Yuxin;
Yan, Qun;
Ma, Jian

Publication type:

Article

Lactoferrin Deficiency Promotes Colitis-Associated Colorectal Dysplasia in Mice.

Published in:

PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0103298

By:

Ye, Qiurong;
Zheng, Ying;
Fan, Songqing;
Qin, Zailong;
Li, Nan;
Tang, Anliu;
Ai, Feiyan;
Zhang, Xuemei;
Bian, Yanhui;
Dang, Wei;
Huang, Jing;
Zhou, Ming;
Zhou, Yanhong;
Xiong, Wei;
Yan, Qun;
Ma, Jian;
Li, Guiyuan

Publication type:

Article

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature.

Published in:

BMC Medical Genomics, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s12920-020-00842-6

By:

Zhang, Qiang;
Qin, Zailong;
Yi, Shang;
Wei, Hao;
Zhou, Xun Zhao;
Su, Jiasun

Publication type:

Article

Clinical application of whole-exome sequencing: A retrospective, single-center study.

Published in:

Experimental & Therapeutic Medicine, 2021, v. 22, n. 1, p. N.PAG, doi. 10.3892/etm.2021.10185

By:

Zhang, Qiang;
Qin, Zailong;
Yi, Shang;
Wei, Hao;
Zhou, Xun Zhao;
Su, Jiasun

Publication type:

Article

Suppression Colitis and Colitis-Associated Colon Cancer by Anti-S100a9 Antibody in Mice.

Published in:

Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01774

By:

Xuemei Zhang;
Lingyu Wei;
Jing Wang;
Zailong Qin;
Jia Wang;
Yuanjun Lu;
Xiang Zheng;
Qiu Peng;
Qiurong Ye;
Feiyan Ai;
Peishan Liu;
Siwen Wang;
Guiyuan Li;
Shourong Shen;
Jian Ma

Publication type:

Article

Phenotypic Spectrum of Trisomy 18 Mosaicism: a New Patient and Literature Review.

Published in:

Clinical Laboratory, 2023, v. 69, n. 3, p. 625, doi. 10.7754/Clin.Lab.2022.220610

By:

Weijia Sun;
Linlin Wang;
Tiansheng Liu;
Luping Ouyang;
Wangshang Qin;
Jingsi Luo;
Zailong Qin

Publication type:

Article

Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.

Published in:

Brain: A Journal of Neurology, 2023, v. 146, n. 8, p. 3347, doi. 10.1093/brain/awad071

By:

Liu, Fang;
Liang, Chen;
Li, Zhengchang;
Zhao, Sen;
Yuan, Haiming;
Yao, Ruen;
Qin, Zailong;
Shangguan, Shaofang;
Zhang, Shujie;
Zou, Li-Ping;
Chen, Qian;
Gao, Zhijie;
Wen, Suiwen;
Peng, Jing;
Yin, Fei;
Chen, Fei;
Qiu, Xiaoxia;
Luo, Jingsi;
Xie, Yingjun;
Lu, Dian

Publication type:

Article

A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5.

Published in:

BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01039-5

By:

Li, Wei;
Fan, Xin;
Zhang, Yue;
Huang, Limei;
Jiang, Tingting;
Qin, Zailong;
Su, Jiasun;
Luo, Jingrong;
Yi, Shang;
Zhang, Shujie;
Shen, Yiping

Publication type:

Article

Inflammation-induced S100A8 activates Id3 and promotes colorectal tumorigenesis.

Published in:

International Journal of Cancer, 2015, v. 137, n. 12, p. 2803, doi. 10.1002/ijc.29671

By:

Zhang, Xuemei;
Ai, Feiyan;
Li, Xiayu;
She, Xiaoling;
Li, Nan;
Tang, Anliu;
Qin, Zailong;
Ye, Qiurong;
Tian, Li;
Li, Guiyuan;
Shen, Shourong;
Ma, Jian

Publication type:

Article

Unmasking a Recessive Allele by a Rare Interstitial Deletion at 10q26.13q26.2: Prenatal Diagnosis of MMP21 ‐Related Disorder and Further Refine INSYN2A Involvement in the Postnatal Cognitive Phenotype.

Published in:

Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 2, p. 1, doi. 10.1002/mgg3.70082

By:

Su, Jiasun;
Zhang, Shujie;
Li, Wei;
Wei, Yuan;
Lin, Fei;
Zhou, Chaofan;
Tang, Xianglian;
Lan, Yueyun;
Huang, Minpan;
Zhang, Qiang;
Yi, Shang;
Yang, Qi;
Yi, Sheng;
Zhou, Xunzhao;
Qin, Zailong;
Huang, Peng

Publication type:

Article

Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, café‐au‐lait spots, and metabolic abnormality.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 2, p. 1, doi. 10.1002/mgg3.2408

By:

Yang, Qi;
Ou, Shan;
Zhou, Xunzhao;
Yi, Sheng;
Lin, Li;
Yi, Shang;
Zhang, Shujie;
Qin, Zailong;
Luo, Jingsi

Publication type:

Article

A genetic variant in the MAST1 gene is associated with mega‐corpus‐callosum syndrome with hypoplastic cerebellar vermis, in a fetus.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2358

By:

Yi, Sheng;
Tang, Xianglian;
Chen, Fei;
Wang, Linlin;
Chen, Junjie;
Yang, Zuojian;
Huang, Minpan;
Yi, Shang;
Huang, Limei;
Yang, Qi;
Yang, Shuihua;
Pan, Pingshan;
Qin, Zailong;
Luo, Jingsi

Publication type:

Article

Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing‐site variant and a missense variant in the ROBO3 gene.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 9, p. 1, doi. 10.1002/mgg3.2215

By:

Yi, Sheng;
Qin, Zailong;
Zhou, Xunzhao;
Chen, Junjie;
Yi, Shang;
Chen, Qiuli;
Huang, Limei;
Zhang, Qinle;
Chen, Biyan;
Luo, Jingsi

Publication type:

Article

A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 6, p. 1, doi. 10.1002/mgg3.1683

By:

Yi, Sheng;
Zhang, Yue;
Qin, Zailong;
Yi, Shang;
Zheng, Haiyang;
Luo, Jingsi;
Li, Qifei;
Wang, Jin;
Yang, Qi;
Li, Mengting;
Chen, Fei;
Zhang, Qiang;
Zhang, Qinle;
Shen, Yiping

Publication type:

Article

Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1624

By:

Su, Jiasun;
Lu, Weiliang;
Li, Mengting;
Zhang, Qiang;
Chen, Fei;
Yi, Shang;
Yang, Qi;
Yi, Sheng;
Zhou, Xunzhao;
Huang, Limei;
Shen, Yiping;
Luo, Jingsi;
Qin, Zailong

Publication type:

Article

Whole‐exome sequencing identified novel compound heterozygous variants in a Chinese neonate with liver failure and review of literature.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1515

By:

Qin, Zailong;
Yang, Qi;
Yi, Shang;
Huang, Limei;
Shen, Yiping;
Luo, Jingsi

Publication type:

Article

Two novel mutations in DNAJC12 identified by whole‐exome sequencing in a patient with mild hyperphenylalaninemia.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1303

By:

Li, Mengting;
Yang, Qi;
Yi, Sheng;
Qin, Zailong;
Luo, Jingsi;
Fan, Xin

Publication type:

Article

Novel compound heterozygous pathogenic variants in ASCC1 in a Chinese patient with spinal muscular atrophy with congenital bone fractures 2 : Evidence supporting a "Definitive" gene‐disease relationship.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 5, p. 1, doi. 10.1002/mgg3.1212

By:

Lu, Weiliang;
Liang, Mingxing;
Su, Jiasun;
Wang, Jin;
Li, Lingxiao;
Zhang, Shujie;
Qin, Zailong;
Huang, Limei;
Lu, Yingchi;
Yi, Shang;
Yi, Sheng;
Xie, BoBo;
Zheng, Haiyang;
Luo, Jingsi;
Gao, Xiaoyan;
Shen, Yiping

Publication type:

Article

Case Report: Christianson Syndrome Caused by SLC9A6 Mutation: From Case to Genotype-Phenotype Analysis.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.783841

By:

Lan, Yueyun;
Yi, Sheng;
Li, Mengting;
Wang, Jinqiu;
Yang, Qi;
Yi, Shang;
Chen, Fei;
Huang, Limei;
Ruan, Yiyan;
Shen, Yiping;
Luo, Jingsi;
Qin, Zailong

Publication type:

Article

Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.732621

By:

Zhang, Qiang;
Qin, Zailong;
Yi, Shang;
Wei, Hao;
Zhou, Xun zhao;
Shen, Fei

Publication type:

Article

MicroRNAs Provide Feedback Regulation of Epithelial-Mesenchymal Transition Induced by Growth Factors.

Published in:

Journal of Cellular Physiology, 2016, v. 231, n. 1, p. 120, doi. 10.1002/jcp.25060

By:

Qin, Zailong;
He, Wei;
Tang, Jingqun;
Ye, Qiurong;
Dang, Wei;
Lu, Yuanjun;
Wang, Jia;
Li, Guiyuan;
Yan, Qun;
Ma, Jian

Publication type:

Article

Phenotypic and genotypic characterization of NPRL3‐related epilepsy: Two case reports and literature review.

Published in:

Epilepsia Open, 2024, v. 9, n. 1, p. 33, doi. 10.1002/epi4.12856

By:

Yang, Dongling;
Wang, Jinqiu;
Qin, Zailong;
Feng, Juntan;
Mao, Chengyun;
Chen, Yuyi;
Huang, Xuelin;
Ruan, Yiyan

Publication type:

Article

De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome.

Published in:

Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.811092

By:

Yang, Qi;
Zhang, Qinle;
Yi, Shang;
Qin, Zailong;
Shen, Fei;
Ou, Shang;
Luo, Jingsi;
He, Sheng

Publication type:

Article

De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome.

Published in:

Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.811092

By:

Yang, Qi;
Zhang, Qinle;
Yi, Shang;
Qin, Zailong;
Shen, Fei;
Ou, Shang;
Luo, Jingsi;
He, Sheng

Publication type:

Article

Novel compound heterozygous variant of BSCL2 identified by whole exome sequencing and multiplex ligation-dependent probe amplification in an infant with congenital generalized lipodystrophy.

Published in:

Molecular Medicine Reports, 2020, v. 21, n. 6, p. 2296, doi. 10.3892/mmr.2020.11036

By:

BOBO XIE;
XIN FAN;
YAQIN LEI;
SHANG YI;
QI YANG;
JIN WANG;
ZAILONG QIN;
FEI SHEN;
JINGSI LUO;
YIPING SHEN

Publication type:

Article

Two novel pathogenic variants of L1CAM gene in two fetuses with isolated X-linked hydrocephaly: A case report.

Published in:

Molecular Medicine Reports, 2018, v. 18, n. 6, p. 5760, doi. 10.3892/mmr.2018.9583

By:

Xie, Bobo;
Luo, Jingsi;
Lei, Yaqin;
Yang, Qi;
Li, Mengting;
Yi, Shang;
Luo, Shiyu;
Wang, Jin;
Qin, Zailong;
Yang, Zuojian;
Wei, Hongwei;
Fan, Xin

Publication type:

Article

A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1.

Published in:

Molecular Medicine Reports, 2018, v. 17, n. 3, p. 4433, doi. 10.3892/mmr.2018.8436

By:

Yang, Qi;
Xu, Hong;
Luo, Jinsi;
Zhang, Qinle;
Xie, Bobo;
Yi, ShENg;
Rong, Xiuliang;
Wang, Jin;
Qin, Zailong;
Jiang, Tingting;
Lin, Li;
Zuo, Yangjin;
Fan, Xin

Publication type:

Article

Upregulation of CALD1 predicted a poor prognosis for platinum-treated ovarian cancer and revealed it as a potential therapeutic resistance target.

Published in:

BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-10056-0

By:

Li, Wei;
Huang, Limei;
Qi, Nana;
Zhang, Qinle;
Qin, Zailong

Publication type:

Article

Identification of Differentially Expressed lncRNAs in a CpG ODN-Activated Macrophage.

Published in:

2020

By:

Zheng, Ying;
Luo, Xi;
Qin, Zailong;
Zhou, Zhiguang

Publication type:

journal article

Whole-exome sequencing identified a novel heterozygous variant in UBAP2L in a Chinese family with neurodevelopmental disorder characterized by impaired language, behavioral abnormalities, and dysmorphic facies.

Published in:

2024

By:

Yang, Qi;
Zhang, Qiang;
Zhou, Xunzhao;
Feng, Juntan;
Zhang, Shujie;
Lin, Li;
Yi, Shang;
Qin, Zailong;
Luo, Jingsi

Publication type:

Case Study

Integration of single-cell and bulk RNA sequencing data reveals that CYTOR is a potential prognostic and immunotherapeutic response marker for skin cutaneous melanoma.

Published in:

Journal of Cancer, 2024, v. 15, n. 12, p. 3890, doi. 10.7150/jca.94823

By:

Ming Zhang;
Yikun Ju;
Lei Xue;
Xueheng Zhao;
Xuezheng Xu;
Geng Wu;
Hao Bo;
Zailong Qin

Publication type:

Article

Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutations.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0842-7

By:

Yang, Qi;
Yi, Sheng;
Li, Mengting;
Xie, Bobo;
Luo, Jinsi;
Wang, Jin;
Rong, Xiuliang;
Zhang, Qinle;
Qin, Zailong;
Hang, Limei;
Feng, Shihan;
Fan, Xin

Publication type:

Article

A novel variant in NSUN2 causes intellectual disability in a Chinese family.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01883-x

By:

Yang, Qi;
Zhang, Qiang;
Qin, Zailong;
Yi, Shang;
Luo, Jingsi

Publication type:

Article

Clinical features and molecular genetic investigation of infantile-onset ascending hereditary spastic paralysis (IAHSP) in two Chinese siblings caused by a novel splice site ALS2 variation.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01805-x

By:

Zhang, Qiang;
Yang, Qi;
Luo, Jingsi;
Zhou, Xunzhao;
Yi, Shang;
Tan, Shuyin;
Qin, Zailong

Publication type:

Article

Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.

Published in:

BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01567-y

By:

Yang, Qi;
Zhang, Qiang;
Qin, Zailong;
Zhang, Shujie;
Yi, Sheng;
Yi, Shang;
Zhang, Qinle;
Luo, Jingsi

Publication type:

Article

Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.

Published in:

2023

By:

Yang, Qi;
Zhang, Qiang;
Qin, Zailong;
Zhang, Shujie;
Yi, Sheng;
Yi, Shang;
Zhang, Qinle;
Luo, Jingsi

Publication type:

Case Study

Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.

Published in:

2023

By:

Yang, Qi;
Zhang, Qiang;
Qin, Zailong;
Zhang, Shujie;
Yi, Sheng;
Yi, Shang;
Zhang, Qinle;
Luo, Jingsi

Publication type:

Case Study

Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.

Published in:

2023

By:

Yang, Qi;
Zhang, Qiang;
Qin, Zailong;
Zhang, Shujie;
Yi, Sheng;
Yi, Shang;
Zhang, Qinle;
Luo, Jingsi

Publication type:

Case Study

Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients.

Published in:

Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2024.1429586

By:

Qi Yang;
Xunzhao Zhou;
Sheng Yi;
XiaoLing Li;
Qiang Zhang;
Shujie Zhang;
Li Lin;
Shang Yi;
Biyan Chen;
Zailong Qin;
Jingsi Luo

Publication type:

Article

Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients.

Published in:

Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2024.1429586

By:

Qi Yang;
Xunzhao Zhou;
Sheng Yi;
XiaoLing Li;
Qiang Zhang;
Shujie Zhang;
Li Lin;
Shang Yi;
Biyan Chen;
Zailong Qin;
Jingsi Luo

Publication type:

Article

Novel loss-of-function variants in WDR26 cause Skraban-Deardorff syndrome in two Chinese patients.

Published in:

Frontiers in Pediatrics, 2024, p. 01, doi. 10.3389/fped.2024.1429586

By:

Qi Yang;
Xunzhao Zhou;
Sheng Yi;
XiaoLing Li;
Qiang Zhang;
Shujie Zhang;
Li Lin;
Shang Yi;
Biyan Chen;
Zailong Qin;
Jingsi Luo

Publication type:

Article

Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome.

Published in:

Frontiers in Genetics, 2020, v. 11, p. 1, doi. 10.3389/fgene.2020.00592

By:

Qin, Zailong;
Su, Jiasun;
Li, Mengting;
Yang, Qi;
Yi, Shang;
Zheng, Haiyang;
Zhang, Qiang;
Chen, Fei;
Yi, Sheng;
Lu, Weiliang;
Li, Wei;
Huang, Limei;
Xu, Jing;
Shen, Yiping;
Luo, Jingsi

Publication type:

Article

Lactoferrin is required for early B cell development in C57BL/6 mice.

Published in:

2021

By:

Wei, Lingyu;
Liu, Can;
Wang, Jia;
Zheng, Xiang;
Peng, Qiu;
Ye, Qiurong;
Qin, Zailong;
Li, Zhengshuo;
Zhang, Xiaoyue;
Wu, Yangge;
Wen, Yuqing;
Zhang, Xuemei;
Yan, Qun;
Ma, Jian

Publication type:

Letter