Wen-qi Chen

Hebei Key Laboratory Of Maternal And Fetal Medicine, Shijiazhuang Key Laboratory Of Reproductive Health
Shijiazhuang, China

Last Updated: 09/26/2026

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Found 13 publications

SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.

SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.

Journal: Communications biology

Published: October 09, 2024

Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection.

Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection.

Journal: Molecular genetics & genomic medicine

Published: March 31, 2024

Identification of novel variations in three cases with rare inherited neuromuscular disorder.

Identification of novel variations in three cases with rare inherited neuromuscular disorder.

Journal: Experimental and therapeutic medicine

Published: December 18, 2023

RBM25 induces trophoblast epithelial-mesenchymal transition and preeclampsia disorder by enhancing the positive feedback loop between Grhl2 and RBM25.

RBM25 induces trophoblast epithelial-mesenchymal transition and preeclampsia disorder by enhancing the positive feedback loop between Grhl2 and RBM25.

Journal: Experimental biology and medicine (Maywood, N.J.)

Published: September 20, 2023

SGMS1 facilitates osteogenic differentiation of MSCs and strengthens osteogenesis-angiogenesis coupling by modulating Cer/PP2A/Akt pathway.

SGMS1 facilitates osteogenic differentiation of MSCs and strengthens osteogenesis-angiogenesis coupling by modulating Cer/PP2A/Akt pathway.

Journal: iScience

Published: September 11, 2023

Identification of Novel NSD1 variations in four Pediatric cases with sotos Syndrome.

Identification of Novel NSD1 variations in four Pediatric cases with sotos Syndrome.

Journal: BMC medical genomics

Published: August 22, 2023

Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).

Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).

Journal: Molecular genetics & genomic medicine

Published: August 07, 2023

NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway.

NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway.

Journal: Cell death discovery

Published: June 01, 2023

Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.

Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.

Journal: Molecular genetics & genomic medicine

Published: December 20, 2022

Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.

Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.

Journal: Genes

Published: July 27, 2022

Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia.

Genome sequencing identified a novel exonic microdeletion in the RUNX2 gene that causes cleidocranial dysplasia.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: December 16, 2021

Metabolic and biophysical study of the MFN2Ile213Thr mutant causing Hereditary Motor and Sensory Neuropathy (HMSN).

Metabolic and biophysical study of the MFN2Ile213Thr mutant causing Hereditary Motor and Sensory Neuropathy (HMSN).

Journal: American journal of translational research

Published: March 25, 2021

Showing 1-12 of 13

Last Updated: 09/26/2026