Results 271 to 280 of about 982,148 (390)

Nanosensors in Leukemia Management: Pioneering Real‐Time Biomarker Detection for Precision Oncology

Nano Select, EarlyView.
This review highlights pioneering nanosensors designed for real‐time leukemia biomarker detection, integrating advanced nanomaterials such as liposomes, polymeric nanoparticles and quantum dots. It examines electrochemical, optical and magnetic detection mechanisms, the applications across AML, ALL, CML, and CLL subtypes, and clinical translation ...
Hamed Soleimani Samarkhazan, Mohammad Navid Khaksari, Amirhossein Mirzazadeh, Mohammad Siavashi, Niloofar Pilehvari, Mohammad Hossein Mohammadi   +5 more
wiley   +1 more source

Chromosome translocations involving band 7q35 or 7p15 in childhood T- cell leukemia/lymphoma [PDF]

, 1988
Y Kaneko, Nobuo Maseki, Chieko Homma, M Sakurai, Shuki Mizutani, Takeo Takeda, T Shikano, T Fujimoto, K Yaoi, T Shimokawa   +9 more
openalex   +1 more source

Chromosomal translocation master genes, mouse models and experimental therapeutics

Oncogene, 2001
T. Rabbitts
semanticscholar   +1 more source

Nephroprotective Effects of Fraxinus Hookeri Wenz. Against Renal Toxicity and DNA Oxidative Damages Induced by CCl4 in Rats

ChemistryOpen, EarlyView.
This study evaluates the nephroprotective potential of Fraxinus hookeri Wenz. (F. hookeri), a medicinal plant of the Oleaceae family, against CCl4‐induced oxidative stress. The findings demonstrate its ability to restore antioxidant defenses, renal function markers, and DNA integrity while reducing lipid peroxidation and histopathological damage.
Raheela Sarwar, Bashir Ahmad, Ayman M. Al‐Qaaneh, Shumaila Rauf, Laiba Ahmad, Mounir M. Bekhit, Said Hassan, Nadeem Ullah, Gokhan Zengin, Arshad Farid   +9 more
wiley   +1 more source

A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia. [PDF]

Cells, 2019
Erkilic N, Gatinois V, Torriano S, Bouret P, Sanjurjo-Soriano C, Luca V, Damodar K, Cereso N, Puechberty J, Sanchez-Alcudia R, Hamel CP, Ayuso C, Meunier I, Pellestor F, Kalatzis V.   +14 more
europepmc   +1 more source

A complex double translocation involving four chromosomes and five breakpoints in a child with mild mental retardation. [PDF]

, 1983
D A Couzin, J L Watt, I.A. Auchterlonie
openalex   +1 more source

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.
Yan Lü, Yi Yu, Jiazhen Chang, Mengmeng Li, Xueting Yang, Xiya Zhou, Na Hao, Hua Meng, Zhenghong Li, Lishuang Ma, Hui You, Shan Jian, Ying Wang, Shengjie Li, Yiqing Yu, Kaili Yin, Mingming Wang, Yulin Jiang, Qingwei Qi   +18 more
wiley   +1 more source

The influence of mutations on chromosome 17 upon the segregation of homologues in female mice heterozygous for Robertsonian translocations [PDF]

, 1987
A. Ruvinsky, Sergei I. Agulnik, Alexander I. Agulnik, D. K. Belyaev   +3 more
openalex   +1 more source

A green-brown plaque on the dorsal hand. [PDF]

, 2019
de Feraudy, Sebastien, Elsensohn, Ashley, Hosking, Anna-Marie, Kassira, Sama, Pouldar, Delila, Smith, Janellen   +5 more
core  

A Prospective Evaluation of the Diagnostic Utility for Low‐Coverage Genome Sequencing in Prenatal Samples: A Comparison With Chromosomal Microarray Analysis

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective The present study aimed to evaluate the efficacy of LC‐GS in detecting clinically relevant chromosomal abnormalities in comparison with conventional CMA within a prenatal context. Methods We conducted a prospective study involving 200 amniotic fluid samples.
Yan Yin, Yuxia He, Chun Chen, Yanyan He, Jin Wang, Shengfang Qin, Hongna Wang, Kun Ma, Dahui Hu, Rui Xiao, Gang Wang, Xueyan Wang   +11 more
wiley   +1 more source