Results 161 to 170 of about 41,126 (213)

Cat Eye Syndrome in a Sudanese Infant: Congenital Cataract in the Absence of Iris Coloboma: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT We report the first Cat Eye Syndrome case from Sudan: a 5‐month‐old female with growth retardation, craniofacial dysmorphism, congenital cataract without iris coloboma, and ventricular septal defect. Cytogenetics confirmed 47,XX,+idic(22)(q11.2).
Rayan Khalid, Imad Fadl‐Elmula
wiley   +1 more source

The Extrachromosomal DNA Fusion Factory: Extrachromosomal Genesis of Oncogenic Fusion Transcripts. [PDF]

Research (Wash D C)
Maimaitiyiming Y, Yang C, Hua Naranmandura.   +2 more
europepmc   +1 more source

Unveiling Candidate Markers for Drug Resistance or Synthetic Lethality in Cervical Cancer: Integrative Analysis of Genetic and Pharmacoprofiling

Cancer Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Introduction Systemic cervical cancer management continues to be challenging. Numerous chemotherapies have been approved, but predicting response is difficult due to the lack of biomarkers. Here, we analyze the genetic and protein profiles of 20 cervical cancer cell lines (CCCLs) and explore their correlation with drug response patterns to ...
Suzy Scholl, Elaine Del Nery, Pierre Gestraud, Maral Halladjian, Elodie Girard, Adèle Soria, Elodie Anthony, Leanne De Koning, Nicolas Servant, Els Berns, Maud Kamal   +10 more
wiley   +1 more source

A Fitness Burden Drives the Reversion of in vitro Acquired Doxycycline Resistance in <i>V. cholerae</i> O1. [PDF]

Infect Drug Resist
Shoukair DH, Turk AZ, Kurdi A, Matar GM, Abou Fayad AG.   +4 more
europepmc   +1 more source

Standardized Pipeline for Metabolism and Cognition in GO‐DS21 Mouse Model: Investigating Down Syndrome Comorbidities

Current Protocols, Volume 6, Issue 6, June 2026.
Abstract Down syndrome (DS) is the most prevalent form of intellectual disability (ID) globally, with an incidence rate of approximately 1 in 1000 births, affecting over 5 million individuals worldwide. DS is characterized by a genetic profile that predisposes individuals to a range of medical and cognitive conditions, including ID and obesity, which ...
Mohammed Selloum, Patricia da Silva‐Buttkus, Fabrice Riet, Nathalia R. V. Dragano, Lillian Garrett, Hugues Jacobs, Sabine M. Hölter, Nicolas Torquet, Birgit Rathkolb, Loic Lindner, Valerie Gailus‐Durner, Guillaume Pavlovic, Li Chan, Johannes Beckers, Benoit Petit Demoulière, Helmut Fuchs, Elodie Ey, Tania Sorg, Martin Hrabe de Angelis, Yann Herault, the GO‐DS21 Consortium   +20 more
wiley   +1 more source

Core temperature-dependent leukocyte and neutrophil responses during prolonged heat exposure. [PDF]

Front Immunol
Xu Y, Wang H, Wang FF.
europepmc   +1 more source

Inverse Association Between Dietary Niacin Intake and Prevalence of Depressive Symptoms in Adults With Metabolic‐Associated Fatty Liver Disease: A Cross‐Sectional Study

Food Science &Nutrition, Volume 14, Issue 6, June 2026.
This cross‐sectional study included adults with MAFLD. Logistic regression and smooth curve fitting were used to evaluate the association between dietary and supplemental niacin intake (mg/day) and depression (PHQ‐9 score ≥ 10). The results indicate that moderate niacin intake may reduce the risk of depression in individuals with MAFLD, with a ...
Xiaoxian Yang, Haiyi Yan, Xueying Qin, Yan Chen   +3 more
wiley   +1 more source

Performance of EUCAST disc diffusion and supplementary methods to detect reduced susceptibility to linezolid in enterococci- the NordicAST LRE-study. [PDF]

J Antimicrob Chemother
Haldorsen BC, Augustinussen MH, Matuschek E, Småbrekke L, Skjold F, Hegstad J, Holzknecht BJ, Helgason KO, Ilmavirta H, Kahlmeter G, Sundsfjord A, Hegstad K, NordicAST 2023 LRE-TRE Study Group .   +12 more
europepmc   +1 more source

Cytogenetic and Molecular Analysis of a “Double‐Hit” RUNX1 Including a RUNX1 p.Trp279* and a Cryptic Novel t(6;21)(q25;q22)/RUNX1::ARID1B in Acute Myeloid Leukemia

Genes, Chromosomes and Cancer, Volume 65, Issue 6, June 2026.
ABSTRACT Introduction Alterations involving RUNX1 are recurrent in hematologic malignancies and contribute to disease pathogenesis via dysregulation of transcriptional factors essential for hematopoiesis. Here, we report an acquired alteration in both alleles of RUNX1; one is a truncating mutation and the second is a novel RUNX1::ARID1B identified in ...
Rolando García, Jing Xu, Lan Yu, Kalayarasan Srinivasan, Sharon Koorse Germans, Olga Weinberg, Franklin Fuda, Weina Chen, Prasad Koduru   +8 more
wiley   +1 more source

Learning curve in image-based robotic assisted total knee arthroplasty: a MAKO-robot experience. [PDF]

Eur J Orthop Surg Traumatol
Granata F, Bosco F, Cobisi CD, Nasca F, Giai Via R, Carlino M, Vigdorchik JM, Burgio C.   +7 more
europepmc   +1 more source