Yuting J. Lou

No. 88 Jiefang Road
Hangzhou, 310009, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 32 publications

KCNB1 mutation impairs neuronal differentiation by disrupting gene expression temporal regulation and neuron-specific pathways.

KCNB1 mutation impairs neuronal differentiation by disrupting gene expression temporal regulation and neuron-specific pathways.

Journal: Frontiers in neurology

Published: November 04, 2025

Surface mechanics and compressive stress impact mammalian follicle development.

Surface mechanics and compressive stress impact mammalian follicle development.

Journal: Nature communications

Published: May 01, 2025

Stress anisotropy in axisymmetric 3D active curved structures.

Stress anisotropy in axisymmetric 3D active curved structures.

Journal: Physical review. E

Published: April 17, 2025

Multiscale mechanisms driving tissue rupture by invading cells.

Multiscale mechanisms driving tissue rupture by invading cells.

Journal: Developmental cell

Published: February 19, 2025

Novel Loss of Function Variant in SOST From Chinese Family Results in Sclerosteosis 1.

Novel Loss of Function Variant in SOST From Chinese Family Results in Sclerosteosis 1.

Journal: Molecular genetics & genomic medicine

Published: November 28, 2024

Hysteresis induced by incomplete relaxation under finite-rate disturbance.

Hysteresis induced by incomplete relaxation under finite-rate disturbance.

Journal: Physical review. E

Published: November 03, 2024

Hemizygous splicing variant in CNKSR2 results in X-linked intellectual developmental disorder.

Hemizygous splicing variant in CNKSR2 results in X-linked intellectual developmental disorder.

Journal: Molecular genetics & genomic medicine

Published: October 29, 2023

Video-based evaluation system for tic action in Tourette syndrome: modeling, detection, and evaluation.

Video-based evaluation system for tic action in Tourette syndrome: modeling, detection, and evaluation.

Journal: Health information science and systems

Published: April 26, 2023

Generation of a human iPSC line (ZJSHDPi001-A) from peripheral blood mononuclear cells of a patient with Developmental epileptic encephalopathy-47 carrying FGF12 gene mutation (c.334G > A).

Generation of a human iPSC line (ZJSHDPi001-A) from peripheral blood mononuclear cells of a patient with Developmental epileptic encephalopathy-47 carrying FGF12 gene mutation (c.334G > A).

Journal: Stem cell research

Published: February 15, 2023

Appetizer on soft matter physics concepts in mechanobiology.

Appetizer on soft matter physics concepts in mechanobiology.

Journal: Development, growth & differentiation

Published: December 13, 2022

A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family.

A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family.

Journal: Cytogenetic and genome research

Published: November 23, 2022

Abnormal dynamics of brain functional networks in children with Tourette syndrome.

Abnormal dynamics of brain functional networks in children with Tourette syndrome.

Journal: Journal of psychiatric research

Published: September 16, 2022

Showing 1-12 of 32

Last Updated: 09/26/2026