L. Yin

发表

Immunometabolism in the pathogenesis of systemic lupus erythematosus

You-ying Mao, Chenxing Zhang, Huiyu Wang, 2020, Journal of translational autoimmunity.

Addition of cyclosporine/tacrolimus for pediatric relapsed lupus nephritis during mycophenolate mofetil maintenance therapy

Tong-Xin Chen, Wei Zhou, You-ying Mao, 2018, The Journal of international medical research.

Clinical manifestations, immunological features and prognosis of Chinese pediatric systemic lupus erythematosus: A single‐center study

Tong-Xin Chen, W. Zhou, You-ying Mao, 2019, International journal of rheumatic diseases.

Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report

Tingting Yu, Jian Wang, Yufei Xu, 2018, BMC Medical Genomics.

Henoch–Schönlein purpura in 535 Chinese children: clinical features and risk factors for renal involvement

Tong-Xin Chen, W. Zhou, You-ying Mao, 2014, The Journal of international medical research.

Biallelic ERBB3 loss-of-function variants are associated with a novel multisystem syndrome without congenital contracture

Yiping Shen, Tingting Yu, Jian Wang, 2019, Orphanet Journal of Rare Diseases.

Further delineation of primary B cell immunodeficiency caused by novel variants of the BLNK gene in two Chinese patients.

Tingting Yu, Jian Wang, Niu Li, 2020, Clinical immunology.

Microscopic Polyangitis in Pediatric Systemic Lupus Erythematosus: A Unique Presentation of Pulmonary - Renal Syndrome and Case Report of an Overlap Syndrome

Wei Zhou, You-ying Mao, Chenxing Zhang, 2020 .

Clinical and molecular analysis in a cohort of Chinese children with Cornelia de Lange syndrome

Jian Wang, Yufei Xu, Xiumin Wang, 2020, Scientific Reports.

Incidence and clinical features of paediatric vasculitis in Eastern China: 14-year retrospective study, 1999–2013

Tong-Xin Chen, Wei Zhou, You-ying Mao, 2016, The Journal of international medical research.

Characterization of Six Missense Mutations in the Tissue-Nonspecific Alkaline Phosphatase (TNSALP) Gene in Chinese Children with Hypophosphatasia

Yiping Shen, X. Mo, Tingting Yu, 2013, Cellular Physiology and Biochemistry.

A retrospective study of nine patients with progressive pseudorheumatoid dysplasia: to explore early diagnosis and further treatment

Jian Wang, You-ying Mao, Yongguo Yu, 2021, Clinical Rheumatology.

Systematical analysis of nine Chinese patients with progressive pseudorheumatoid dysplasia and assessment of calcitriol treatment

Wei Zhou, Jian Wang, You-ying Mao, 2020 .

A novel mutation in NPHS2 gene identified in a Chinese pedigree with autosomal recessive steroid‐resistant nephrotic syndrome

Wei Zhou, L. Yin, Jian Wang, 2009, Pathology.

Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience

Y. Wang, Yiping Shen, Tingting Yu, 2017, Genetics in Medicine.

Targeted exome sequencing identified a novel mutation hotspot and a deletion in Chinese primary hypertrophic osteoarthropathy patients.

Yiping Shen, Tingting Yu, Jian Wang, 2018, Clinica chimica acta; international journal of clinical chemistry.

Identification of TCIRG1 and CLCN7 gene mutations in a patient with autosomal recessive osteopetrosis.

Tingting Yu, Jian Wang, Yongguo Yu, 2014, Molecular medicine reports.

Novel Mutations in the SCNN1A Gene Causing Pseudohypoaldosteronism Type 1

Tingting Yu, Jian Wang, Yongguo Yu, 2013, PloS one.

Novel variants in CIITA caused type II bare lymphocyte syndrome: A case report.

Tingting Yu, Jian Wang, R. Yao, 2021, Asian Pacific journal of allergy and immunology.

Vincristine alleviates adriamycin-induced nephropathy through stabilizing actin cytoskeleton

W. Zhou, You-ying Mao, Zhen Zhang, 2017, Cell & Bioscience.

Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report

Tingting Yu, Jian Wang, Yufei Xu, 2018, BMC medical genomics.

Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing country: the China experience

Yiping Shen, Tingting Yu, Jian Wang, 2018, Genetics in Medicine.

Treatment and outcome of IgA nephropathy in children from one single center experience

Wei Zhou, You-ying Mao, Chenxing Zhang, 2023, BMC Pediatrics.