Cheng Ni

1665 Kongjiang Road
Shanghai, 200092, China

Last Updated: 09/26/2026

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Found 17 publications

Antifouling and rechargeable antibacterial polyurethane modified with N-halamine for dental unit waterlines.

Antifouling and rechargeable antibacterial polyurethane modified with N-halamine for dental unit waterlines.

Journal: Journal of materials chemistry. B

Published: May 14, 2026

Corrigendum to "A tumor microenvironment-responsive core-shell tecto dendrimer nanoplatform for magnetic resonance imaging-guided and cuproptosis-promoted chemo-chemodynamic therapy" Acta Biomaterialia 164, 2023, 474-486.

Corrigendum to "A tumor microenvironment-responsive core-shell tecto dendrimer nanoplatform for magnetic resonance imaging-guided and cuproptosis-promoted chemo-chemodynamic therapy" Acta Biomaterialia 164, 2023, 474-486.

Journal: Acta biomaterialia

Published: November 08, 2025

Corrigendum to "Copper-doped layered double hydroxides co-deliver proteins/drugs for cascaded chemodynamic/immunotherapy via dual regulation of tumor metabolism" [Acta Biomaterialia 2025, 195, 350-362].

Corrigendum to "Copper-doped layered double hydroxides co-deliver proteins/drugs for cascaded chemodynamic/immunotherapy via dual regulation of tumor metabolism" [Acta Biomaterialia 2025, 195, 350-362].

Journal: Acta biomaterialia

Published: October 17, 2025

Copper-doped layered double hydroxides co-deliver proteins/drugs for cascaded chemodynamic/immunotherapy via dual regulation of tumor metabolism.

Copper-doped layered double hydroxides co-deliver proteins/drugs for cascaded chemodynamic/immunotherapy via dual regulation of tumor metabolism.

Journal: Acta biomaterialia

Published: December 04, 2024

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report.

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report.

Journal: Frontiers in immunology

Published: April 18, 2024

Identification of deep intronic variants in junctional epidermolysis bullosa using genome sequencing and splicing assays.

Identification of deep intronic variants in junctional epidermolysis bullosa using genome sequencing and splicing assays.

Journal: NPJ genomic medicine

Published: February 26, 2024

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome.

Journal: EMBO molecular medicine

Published: September 02, 2021

Novel and recurrent PHGDH and PSAT1 mutations in Chinese patients with Neu-Laxova syndrome.

Novel and recurrent PHGDH and PSAT1 mutations in Chinese patients with Neu-Laxova syndrome.

Journal: European journal of dermatology : EJD

Published: January 07, 2020

Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese.

Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese.

Journal: Clinical genetics

Published: December 03, 2019

Coinheritance of generalized pustular psoriasis and familial Behçet-like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state.

Coinheritance of generalized pustular psoriasis and familial Behçet-like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state.

Journal: The Journal of dermatology

Published: April 15, 2019

Severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome caused by de novo mutation in the DSP gene misdiagnosed as generalized pustular psoriasis and treatment of acitretin with gabapentin.

Severe dermatitis, multiple allergies and metabolic wasting (SAM) syndrome caused by de novo mutation in the DSP gene misdiagnosed as generalized pustular psoriasis and treatment of acitretin with gabapentin.

Journal: The Journal of dermatology

Published: March 02, 2019

A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.

A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis.

Journal: The Journal of investigative dermatology

Published: May 05, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026