Results 111 to 120 of about 16,067 (252)

E3 Ubiquitin Ligases in MASH‐Associated Liver Fibrosis: Mechanisms and Therapeutic Opportunities

Liver International, Volume 46, Issue 10, October 2026.
ABSTRACT Metabolic dysfunction‐associated steatohepatitis (MASH) is a major cause of progressive liver fibrosis and can ultimately lead to cirrhosis and hepatocellular carcinoma (HCC). MASH‐associated liver fibrosis develops through a complex interplay among lipotoxic hepatocyte injury, oxidative and endoplasmic reticulum stress, inflammatory ...
Ah‐Reum Oh, Yelin Jeong, Young Hoon Jung, Young Un Kim, HyunJoon Gi, Do‐Wan Kim, Young Du Choi, Sang Bae Lee, KyeongJin Kim   +8 more
wiley   +1 more source

Dynamic Remodeling of Oocyte‐Granulosa Cell Communication During Bovine Folliculogenesis Revealed by Transcriptomic Meta‐Analyses

The FASEB Journal, Volume 40, Issue 18, 30 September 2026.
Bidirectional communication between oocytes and granulosa cells undergoes progressive remodeling during bovine folliculogenesis. Integrative transcriptomic analysis identified stage‐specific ligand‐receptor signaling networks coordinating structural, metabolic, and developmental processes.
Noemi Monferini, Ludovica Donadini, Pritha Dey, Federica Franciosi, Valentina Lodde, Maria Belen Rabaglino, Alberto Maria Luciano   +6 more
wiley   +1 more source

椎间盘组织中炎症因子水平、MMPs/TIMPs表达与腰椎间盘突出症的关系研究

Zhongguo shiyan zhenduanxue, 2018
目的探讨椎间盘组织中炎症因子水平、基质金属蛋白酶/金属蛋白酶组织抑制因子(MMPs/TIMPs)表达与腰椎间盘突出症的关系,为腰椎间盘突出症的预防和治疗方案选择提供参考。方法选择2015年3月—2017年2月在我院行腰椎间盘突出症手术治疗的56例腰椎间盘突出症患者为观察组,另选择同期我院收治的腰椎爆裂性骨折手术患者52例为对照组。两组患者均于术中获取腰椎组织,并检测炎症因子(IL-6、CRP、PCT、CNF-α)水平和MMPs/TIMPs表达(MMP-1、MMP-2、MMP-8、MMP-9、TIMP-1、
侯桂红, 李倩, 谢燕
doaj  

Quality Thresholds for Angiogenesis Under Acoustic Manipulation in Engineered Vascular Tissues

Advanced Science, Volume 13, Issue 52, 18 September 2026.
Defined biological and physical quality thresholds achieved through acoustic manipulation regulate cellular alignment and spatial organization, promoting self‐assembling vasculature, extracellular matrix deposition, and angiogenic responses, thereby establishing critical acoustic patterning requirements for engineered vascular tissue development in ...
Oscar O'Dwyer Lancaster‐Jones, Russell Quinn, Niloofar Khoshdel Rad, Kilian Paul, Andrea Frank, Daniela F. Duarte Campos   +5 more
wiley   +1 more source

An Exploratory Study of Vitamin D and Matrix Metalloproteinase and Their Regulators in Polyendocrine Metabolic Ovarian Syndrome. [PDF]

Pharmaceuticals (Basel)
Zainalabedin M, Smahi N, Sathyapalan T, Butler AE, Atkin SL.   +4 more
europepmc   +1 more source

Diagnostic Odyssey of Atypical Long‐Chain 3‐Hydroxyacyl‐CoA Dehydrogenase Deficiency (LCHADD) Explained by Three Allelic Products From Two Pathogenic Variants

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2128-2135, September 2026.
ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta, Lynette C. Rives, T. Andrew Burrow, Thomas A. Cassini, Rory J. Tinker, Amy K. Robertson, Kimberly M. Ezell, Rizwan Hamid, Joy D. Cogan, John A. Phillips III   +9 more
wiley   +1 more source

Look what you make my tissues do: The role of metalloproteinases and their inhibitors in Bothrops snakebites. [PDF]

PLoS Negl Trop Dis
Ferreira Neves JC, Magalhães-Gama F, Ibiapina HNS, Seixas KB, Barbosa ÊS, Malheiro A, Sachett JAG, Campi-Azevedo AC, Martins-Filho OA, Teixeira-Carvalho A, Sartim MA, Monteiro W, Costa AG.   +12 more
europepmc   +1 more source

Response of an Infant With Presumed Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) to Ketone Supplementation

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2140-2150, September 2026.
ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta, Kaitlyn N. Bloom, Jerry Vockley, Angela R. Grochowsky, Neena S. Agrawal, Ellen W. Strickler, Natalie N. Owen, Erica T. Gray, B. Lakshitha A. Perera, Eric R. Gamazon, Lynette C. Rives, Hua‐Chang Chen, Qi Liu, Rizwan Hamid, Joy D. Cogan, John A. Phillips III, Thomas A. Cassini, Bryce A. Schuler   +17 more
wiley   +1 more source

Hidradenitis suppurativa: epidemiology, diagnosis, molecular pathogenesis and therapy. [PDF]

Mol Biomed
Lolli MG, Sanna L, Belli R, Dattolo A, Fania L, Colonna L, Marchetti P, Albanesi C, Mercurio L, Madonna S.   +9 more
europepmc   +1 more source

Preoperative Glucose‐to‐Albumin Ratio as a Prognostic Marker for Survival in Pancreatic Cancer Patients Undergoing Pancreatectomy

Cancer Medicine, Volume 15, Issue 9, September 2026.
ABSTRACT Background Pancreatic cancer (PC) disrupts metabolic and nutritional processes, including glucose homeostasis and albumin levels. Both hyperglycemia and hypoalbuminemia have been linked to poorer outcomes in various cancers, including PC. This study investigates the preoperative glucose‐to‐albumin ratio (GAR) as a potential prognostic marker ...
Andrea Feci, Isabel Lavine, Sophia Shah, Matthew Kraft, Benjamin Varughese, Elijah Hoffman, Navin Rana, Harish Lavu, Wilbur Bowne, Charles J. Yeo, Avinoam Nevler   +10 more
wiley   +1 more source