Results 121 to 130 of about 1,415 (230)

Dowling-Degos Disease with Multiple Seborrheic Keratosis: An Atypical Presentation in Two Siblings. [PDF]

Indian Dermatol Online J
Ankita, Singhal A, Bisherwal K, Sharma S, Singal A.   +4 more
europepmc   +1 more source

Advanced Sorbent Materials in Solid‐Phase Extraction: A Decade of Innovation and Future Perspectives

Chemistry–Methods, Volume 6, Issue 8, August 2026.
This review systematically summarizes five families of advanced sorbent materials for solid‐phase extraction (SPE): nanocarbons, porous frameworks (MOFs/COFs), smart polymers, biomass‐derived sorbents, and multifunctional composites. Key molecular interactions (π–π stacking, hydrogen bonding, electrostatic attraction, host–guest recognition) are ...
Xingchen Wang, Linling Guo, Jingyi Yue, Wenxiao Zhuo, Shunli Ji   +4 more
wiley   +1 more source

Dyschromatosis universalis hereditaria: Dermoscopic insights in a patient with intellectual disability. [PDF]

JAAD Case Rep
Elizabeth Rosales Martínez Z, Yamileth Reyes Cueva J, María Maza de Franco A, Anett Mejía Rodríguez S.   +3 more
europepmc   +1 more source

Harnessing Repurposed Drugs to Enhance Temozolomide Efficacy in Glioblastoma

Cancer Reports, Volume 9, Issue 8, August 2026.
ABSTRACT Background Glioblastoma (GB) is the most aggressive primary malignant brain tumor in adults and remains associated with poor survival despite surgical resection followed by radiotherapy and temozolomide (TMZ) chemotherapy. Intrinsic and acquired resistance to TMZ, including MGMT‐dependent DNA repair and activation of pro‐survival pathways ...
Ali Nakhaei, Atefeh Taghavi, Amir R. Afshari, Farzaneh Davoudi, Elaheh Gheybi, Mohammad Jalili‐Nik   +5 more
wiley   +1 more source

Progressive scattered and reticular pigmentation lesions. [PDF]

JAAD Case Rep
Zhou Y, Huang L, Yang C, Xu Z, Elbendary A, Xue R.   +5 more
europepmc   +1 more source

CLRN1 Variants in Müller Cells Cause Mitochondrial Dysfunction in USH3A Retinal Organoids

CNS Neuroscience &Therapeutics, Volume 32, Issue 8, August 2026.
We generated retinal organoids from a patient with USH3A and performed single‐cell RNA sequencing. CLRN1 was specifically expressed in Müller cells, where its variants led to mitochondrial dysfunction and photoreceptor degeneration. ABSTRACT Background Usher syndrome 3A (USH3A), caused by mutations in the CLRN1 gene, leads to retinitis pigmentosa and ...
Rui Zhang, Xinbo Ji, Han Yu, Jingwen Xu, Yu Wang, Ping Sun, Yingxin Wang, Yao Tang, Zexin Zhan, Yichang Jiao, Didi Shan, Pengfei Lin, Dong‐dong Wang, Yuying Zhao, Xianyang Liu, Chuanzhu Yan, Jianqiao Li, Mingfeng Li, Fuchen Liu, Shengping Hou   +19 more
wiley   +1 more source

LC-OCT Features of Confluent and Reticulated Papillomatosis of Gougerot-Carteaud Syndrome. [PDF]

Case Rep Dermatol Med
Traini DO, Palmisano G, Paradisi A, Vigilante M, Maccari A, Stefani AD.   +5 more
europepmc   +1 more source

Myocardial Lipid Metabolism Imbalance: The Pathological Core and Novel Diagnostic‐Therapeutic Directions of Cardiovascular Diseases

Journal of Biochemical and Molecular Toxicology, Volume 40, Issue 8, August 2026.
In cardiac cells, Plin5/AMPK regulate lipid homeostasis; excess CD36‐mediated uptake drives lipotoxicity, mitochondrial dysfunction, and CVDs (e.g., heart failure). Biomarkers (ApoB/ApoA‐1) and therapies (SGLT2 inhibitors) target this cascade. ABSTRACT Cardiac lipid metabolism is fundamental to myocardial energy homeostasis, with fatty acid oxidation ...
Peiyun Xie, Qun Zeng, Hongrui Wang, Meihua She   +3 more
wiley   +1 more source

Reticulate acropigmentation of Kitamura with café-au-lait macules: a rare case report. [PDF]

Front Med (Lausanne)
Gao B, Wang H, Fan Q, Cong L, Zhang G, Liu X.   +5 more
europepmc   +1 more source

Impacts of N‐glycanase1 (NGLY1) Down Regulation on the Function of Mitochondria

Journal of Cellular Biochemistry, Volume 127, Issue 8, August 2026.
ABSTRACT N‐glycanase 1 (NGLY1) is involved in intracellular misfolded protein degradation, releasing a de‐N‐glycosylated protein and a complete N‐oligosaccharide. Enzymatic defects in NGLY1 may cause NGLY1‐related congenital disorder of deglycosylation (NGLY1‐CDDG). NGLY1 patients exhibit cognition and coordination defects, and the regulatory impact of
Yanwen Chen, Ruijie Liu, Shaoxing Zhang, Yuxin Zhang, Qiange Lin, Yilin Ye, Shuying Yuan, Xinrong Lu, Linfei Wang, Li Chen, Guiqin Sun   +10 more
wiley   +1 more source