Results 141 to 150 of about 54,811 (219)

Harnessing the Therapeutic Potential of Cell Secretomes and Extracellular Vesicles for Craniofacial Regenerative Applications

Journal of Periodontal Research, EarlyView.
The scoping review summarizes the current preclinical and clinical evidence for the use of “cell‐free” therapies in craniofacial (periodontal, bone and soft‐tissue) regeneration. It also aims to highlight key challenges and strategies towards the clinical translation of these therapies.
Siddharth Shanbhag, Magdalena Mayol, Danijel Domic, Madhusudhan Reddy Bobbili, Johannes Grillari, Mariano Sanz, Reinhard Gruber   +6 more
wiley   +1 more source

miR-132-3p靶向调控PTEN/Akt信号通路对缺氧/复氧诱导海马神经元HT22细胞损伤的影响

Zhongguo shiyan zhenduanxue
目的 研究miR-132-3p靶向调控第10号染色体缺失的磷酸酶基因(PTEN)/蛋白激酶B(Akt)信号通路对缺氧/复氧(H/R)诱导海马神经元HT22细胞损伤的影响。方法 体外培养HT22细胞并随机分为对照组、H/R组、阴性对照(miR-132-3p mimics阴性对照+空载质粒)组、miR-132-3p mimics组(miR-132-3p mimics)、PTEN敲低组(PTEN siRNA质粒)、miR-132-3p mimics+PTEN过表达组(miR-132-3p mimics ...
程宝仓, 齐林, 曾利敏
doaj  

Extramedullary Disease—Achilles Heel in Myeloma?

American Journal of Hematology, Volume 101, Issue 3, Page 521-536, March 2026.
ABSTRACT Despite advances in therapy, extramedullary disease (EMD) remains an aggressive form of multiple myeloma associated with poor outcomes. Patients with true EMD, in which plasmacytomas have become completely independent of bone, have a particularly poor prognosis. The pathogenesis of EMD is driven by complex mechanisms involving loss of adhesion
Shaji Kumar, Joshua Richter, Saad Z. Usmani, Yael C. Cohen, Jing Christine Ye, María‐Victoria Mateos, Vania Hungria, Elena Zamagni   +7 more
wiley   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

miRNA Expression and HCC Occurrence in HCV Cirrhotic Patients Treated with Direct Acting Antivirals [PDF]

Background: The risk of hepatocarcinoma in HCV cirrhotic patient responders after treatment with DAAs decrease, but HCC still occurs. A correlation between specific miRNAs and the development of hepatocarcinoma have been highlighted.
Andreone P., Angeli P., Boix L., Brocca A., Bruix J., Calvino V., Ceolotto G., Cillo U., Guarneri V., Lens S., Marino Z., Parisi S. G., Perez-del-Pulgar S., Piano S., Reig M., Romano A., Romero P. P., Russo F. P., Vukotic R., Zilio G.   +19 more
core   +1 more source

Human Cyclophilins—An Emerging Class of Drug Targets

Medicinal Research Reviews, Volume 46, Issue 2, Page 475-512, March 2026.
ABSTRACT Cyclophilins are a family of enzymes with peptidyl‐prolyl isomerase activity found in all cells of all organisms. To date, 17 cyclophilin isoforms have been identified in the human body, participating in diverse biological processes. Consequently, cyclophilins have emerged as promising targets for drug development to address a wide array of ...
Katarina Jurkova, Hana Navratilova, Kamil Musilek, Ondrej Benek   +3 more
wiley   +1 more source

Utility of microRNA analysis in exhaled breath condensate of sarcoidosis and mediastinal tuberculosis patients: a pilot study

ERJ Open Research
Background Sarcoidosis and tuberculosis (TB) are the two most common causes of granulomatous mediastinal lymphadenopathy. These often exhibit overlapping clinical and radiological characteristics, rendering accurate diagnosis difficult.
Bijay Pattnaik, Sryma PB, Naveen Bhatraju, Saurabh Mittal, Sudheer Arava, Deepali Jain, Baibaswata Nayak, Pavan Tiwari, Vijay Hadda, Anant Mohan, Anurag Agrawal, Randeep Guleria, Karan Madan   +12 more
doaj   +1 more source

Local Anesthetics in Cancer: Mechanisms and Translational Perspectives

MedComm – Oncology, Volume 5, Issue 1, March 2026.
Local anesthetics demonstrate multifaceted antitumor effects that collectively contribute to cancer suppression. Beyond canonical sodium channel blockade, these agents exert the following pharmacological actions: inhibition of tumor cell proliferation, suppression of migration and invasion, induction of proapoptotic pathways, attenuation of ...
Wan‐li Wang, Tu Huang, Yi‐hang Hao, Min Zheng, Xin‐hua Liang   +4 more
wiley   +1 more source

Microscopic and molecular aspects of skeletal muscle alterations in cerebral palsy

Developmental Medicine &Child Neurology, Volume 68, Issue 3, Page 343-357, March 2026.
Cerebral palsy, caused by non‐progressive brain injury, is frequently accompanied by skeletal muscle alterations. This review synthesizes current evidence from muscle biopsy studies, revealing cellular and molecular adaptations in muscle tissue. Abstract Cerebral palsy (CP), the most prevalent childhood‐onset motor disability, frequently entails ...
Sebastian Edman, Oscar Horwath, Eva Pontén, Sudarshan Dayanidhi, Ferdinand von Walden   +4 more
wiley   +1 more source

miR-132-3p靶向调控PTEN/Akt信号通路对缺氧/复氧诱导海马神经元HT22细胞损伤的影响 附视频

Zhongguo shiyan zhenduanxue
目的 研究miR-132-3p靶向调控第10号染色体缺失的磷酸酶基因(PTEN)/蛋白激酶B(Akt)信号通路对缺氧/复氧(H/R)诱导海马神经元HT22细胞损伤的影响。方法 体外培养HT22细胞并随机分为对照组、H/R组、阴性对照(miR-132-3p mimics阴性对照+空载质粒)组、miR-132-3p mimics组(miR-132-3p mimics)、PTEN敲低组(PTEN siRNA质粒)、miR-132-3p mimics+PTEN过表达组(miR-132-3p mimics ...
doaj   +2 more sources