Works matching DE "GENES"

Results: 5000

Relationship Between Masticatory Dysfunction and Salivary Microbiota.

Published in:

Journal of Oral Rehabilitation, 2025, v. 52, n. 7, p. 991, doi. 10.1111/joor.13963

By:

Liu, Tsunglin;
Wu, Mu‐Heng;
Hu, Po‐Hsiang;
Chuang, Yu‐Ching;
Tsai, Pei‐Fang;
Ko, Nai‐Ying;
Ko, Wen‐Chien;
Chen, Yen‐Chin;
Wang, Jiun‐Ling

Publication type:

Article

Therapeutic potential of miR-204-5p in intervertebral disc degeneration: targeting the SSRP1/NF-κB pathway to inhibit apoptosis.

Published in:

Journal of Orthopaedic Surgery & Research, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13018-025-05999-3

By:

Zhao, Chenhao;
Li, Qiuwei;
Shen, Cailiang

Publication type:

Article

Long Noncoding RNAs Papillary Thyroid Carcinoma Susceptibility Candidate 3 Antisense 1 and Papillary Thyroid Carcinoma Susceptibility Candidate 3 Synergistically Regulate ZC3H12A mRNA Stability via Vimentin at 14q13.3 Thyroid Cancer Locus.

Published in:

Thyroid, 2025, v. 35, n. 6, p. 662, doi. 10.1089/thy.2024.0674

By:

Zhang, Yutong;
Shi, Xiuzhi;
Cheng, Shengqi;
Liu, Jing;
Shi, Jianyun;
An, Zhekun;
Yao, Jiali;
Zou, Binbin;
Gao, Ming;
Cheng, Xiaolong;
Wang, Yanqiang

Publication type:

Article

CLIC1 Supports Mechanisms Related to Platelet Activation and Thrombosis.

Published in:

Transfusion Medicine & Hemotherapy, 2025, v. 52, n. 3, p. 178, doi. 10.1159/000544115

By:

Knowles, Lynn M.;
Ampofo, Emmanuel;
Menger, Michael D.;
Drawz, Anna;
Eichler, Hermann;
Pilch, Jan

Publication type:

Article

Single-Tube Multiplex PCR-SSP for the Detection of RHD Variant Alleles Commonly Found in Serologically D− Phenotype Individuals in a Thai Population.

Published in:

Transfusion Medicine & Hemotherapy, 2025, v. 52, n. 3, p. 169, doi. 10.1159/000544107

By:

Pittayabumrung, Ornuma;
Leelayuwat, Chanvit;
Romphruk, Amornrat V.;
Simtong, Piyapong

Publication type:

Article

A Novel c.459_460insC Variation in the XK Gene Associated with McLeod Syndrome.

Published in:

Transfusion Medicine & Hemotherapy, 2025, v. 52, n. 3, p. 211, doi. 10.1159/000539875

By:

Zhang, Bing;
Yu, Shifang;
Hong, Xiaozhen;
Xu, Xianguo;
Zhu, Faming

Publication type:

Article

Effect on DNA Stability of a Novel Pellet Storing Method for Liquid-Based Cytology Specimens Fixed Using an Alcohol-Based Preservation Solution: Studies Using EGFR Mutation Detection on a Lung Adenocarcinoma Cell Line.

Published in:

Acta Cytologica, 2025, v. 69, n. 3, p. 259, doi. 10.1159/000545062

By:

Matsuo, Yukiko;
Yoshida, Tsutomu;
Yamashita, Kazuya;
Satoh, Yukitoshi

Publication type:

Article

Molecular Characterization of Newcastle Disease Virus Circulating in Pakistan.

Published in:

Cyprus Journal of Medical Sciences, 2025, v. 10, p. 1, doi. 10.4274/cjms.2025.2024-146

By:

Siddique, Uswa;
Ali, Ijaz

Publication type:

Article

Investigation of Single Nucleotide Polymorphisms within the FSHR Gene and Biological Network Analysis of Non-Coding RNAs in Polycystic Ovary Syndrome Patients.

Published in:

Cyprus Journal of Medical Sciences, 2025, v. 10, p. 1, doi. 10.4274/cjms.2025.2024-106

By:

Madhher, Sana;
Ostad-Hasanzadeh, Bita;
Özbakır, Burcu;
Özay, Ali Cenk;
Tulay, Pınar

Publication type:

Article

An Uncharacterized Domain Within the N‐Terminal Tail of Histone H3 Regulates the Transcription of FLO1 via Cyc8.

Published in:

Molecular Microbiology, 2025, v. 123, n. 6, p. 547, doi. 10.1111/mmi.15362

By:

Singh, Ranu;
Tomar, Raghuvir Singh

Publication type:

Article

The role and mechanism of CRISPLD2 in skin fibrosis of systemic sclerosis.

Published in:

Rheumatology, 2025, v. 64, n. 5, p. 3134, doi. 10.1093/rheumatology/keae541

By:

Ding, Liqing;
Bao, Ding;
Dai, Bingying;
Meng, Qiming;
Lv, Chunliu;
Luo, Hui;
Zhu, Honglin

Publication type:

Article

Gene Selection Algorithms in a Single-Cell Gene Decision Space Based on Self-Information.

Published in:

Mathematics (2227-7390), 2025, v. 13, n. 11, p. 1829, doi. 10.3390/math13111829

By:

Fang, Yan;
Lin, Yonghua;
Huang, Chuanbo;
Li, Zhaowen

Publication type:

Article

Perioperative Strategies in Resectable Non-Squamous Non-Small Cell Lung Cancer with EGFR Mutations and ALK Rearrangement.

Published in:

Cancers, 2025, v. 17, n. 11, p. 1844, doi. 10.3390/cancers17111844

By:

Petrella, Francesco;
Cara, Andrea;
Cassina, Enrico Mario;
Degiovanni, Sara;
Libretti, Lidia;
Lo Torto, Sara;
Pirondini, Emanuele;
Raveglia, Federico;
Spinelli, Francesca;
Tuoro, Antonio;
Rizzo, Stefania

Publication type:

Article

Clinical and Morphological Features of ER-Positive HER2-Negative Breast Tumors with PIK3CA Mutations in Russian Patients.

Published in:

Cancers, 2025, v. 17, n. 11, p. 1833, doi. 10.3390/cancers17111833

By:

Sokolova, Tatyana N.;
Yanus, Grigory A.;
Aleksakhina, Svetlana N.;
Belysheva, Yana V.;
Chernyakova, Aleksandra P.;
Zharnakova, Yulia S.;
Nikitina, Alisa S.;
Stebneva, Tatyana M.;
Martianov, Aleksandr S.;
Goryainova, Alla Yu.;
Gluzman, Mark I.;
Orlova, Rashida V.;
Stukan', Anastasiya I.;
Zyuzyukina, Alena V.;
Zukov, Ruslan A.;
Korzun, Polina R.;
Binnatova, Jeyla O.;
Abuzova, Anastasia S.;
Murunova, Yulia N.;
Sultanbaev, Aleksandr V.

Publication type:

Article

From Sanger to Oxford Nanopore MinION Technology: The Impact of Third-Generation Sequencing on Genetic Hematological Diagnosis.

Published in:

Cancers, 2025, v. 17, n. 11, p. 1811, doi. 10.3390/cancers17111811

By:

Larráyoz, María José;
Luri-Martin, Pablo;
Mañu, Amagoia;
Churruca, Oihane;
Gordillo, Natalia;
Erdozain, Irache;
Esteban-Figuerola, Ada;
de Miguel, Carlos;
Robles, Diego;
García-Fortes, María;
Rifón Roca, José;
Alfonso-Pierola, Ana;
Prósper, Felipe;
Ariceta, Beñat;
Calasanz, María José

Publication type:

Article

The Roles of STAT3 and STAT5 in Breast Cancer.

Published in:

Cancers, 2025, v. 17, n. 11, p. 1781, doi. 10.3390/cancers17111781

By:

Temple, Alexandra E.;
Walker, Sarah R.

Publication type:

Article

Effect of Alpha-1 Antitrypsin Deficiency on Zinc Homeostasis Gene Regulation and Interaction with Endoplasmic Reticulum Stress Response-Associated Genes.

Published in:

Nutrients, 2025, v. 17, n. 11, p. 1913, doi. 10.3390/nu17111913

By:

Liuzzi, Juan P.;
Gonzales, Samantha;
Barbieri, Manuel A.;
Vidal, Rebecca;
Yoo, Changwon

Publication type:

Article

The pathogenic role of calcitonin gene‐related peptide and predictors of new‐onset migraine and long‐term outcomes after transcatheter atrial septal defect closure.

Published in:

Headache: The Journal of Head & Face Pain, 2025, v. 65, n. 5, p. 791, doi. 10.1111/head.14885

By:

Su, Tzu‐Hsuan;
Wang, Jou‐Kou;
Kuo, Ping‐Hung;
Chang, Shu‐Hui;
Chiou, Lih‐Chu;
Lee, Wang‐Tso;
Fan, Pi‐Chuan

Publication type:

Article

Causal relationships between alterations in shear stress-related genes and aneurysmal subarachnoid hemorrhage.

Published in:

Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03784-3

By:

Wu, Xiaoxin;
Dai, Yuanyuan;
Niu, Xingyang;
Zhang, Minghao;
Li, Jiaoxing;
Xie, Yi;
Sheng, Wenli;
Ye, Fei

Publication type:

Article

Dissimilar Effects of Selenite and Selenium Nanoparticles on Skeletal Muscle Development Unrelated to GPx1 Activity During Adolescence in Rats.

Published in:

Nutrients, 2025, v. 17, n. 11, p. 1841, doi. 10.3390/nu17111841

By:

Nogales, Fátima;
Pajuelo, Eloísa;
Gallego-López, María del Carmen;
Romero-Herrera, Inés;
Merchán, Francisco;
Carreras, Olimpia;
Ojeda, María Luisa

Publication type:

Article

Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 705, doi. 10.1111/cge.14725

By:

Essid, Miriam;
Karoui, Sana;
Zribi, Mouna;
Ben Younes, Thouraya;
Januel, Louis;
Lafont, Estelle;
Labalme, Audrey;
Ben Hafsa, Meriem;
Hun Seo, Go;
Khatrouch, Safa;
Boudabous, Hela;
Ben Chehida, Amel;
Sanlaville, Damien;
Jilani, Houweyda;
Benjemaa, Lamia;
Kraoua, Ichraf;
Lesca, Gaetan;
Chatron, Nicolas

Publication type:

Article

Digenic Inheritance of Monoallelic MUTYH and POLE Germline Variants in Adrenocortical Carcinoma: Implications for Tumorigenesis and Immunotherapy.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 699, doi. 10.1111/cge.14721

By:

Lopez, Jonathan;
Buisson, Adrien;
Ounnas, Adel;
Tachon, Gaelle;
Viari, Alain;
De Fraipont, Florence;
Albuisson, Juliette;
Barritault, Marc;
Bringuier, Pierre‐Paul;
Feugeas, Jean‐Paul;
Mc Leer, Anne;
Bouras, Ahmed

Publication type:

Article

Comprehensive Clinical and Genetic Characterization of a Spanish Cohort of 22 Patients With Bainbridge–Ropers Syndrome.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 646, doi. 10.1111/cge.14701

By:

Trujillano, Laura;
Valenzuela, Irene;
Costa‐Roger, Mar;
Cuscó, Ivon;
Fernandez‐Alvarez, Paula;
Cueto‐González, Anna;
Lasa‐Aranzasti, Amaia;
Masotto, Bárbara;
Abulí, Anna;
Codina‐Solà, Marta;
del Campo, Miguel;
Ruiz Moreno, Juan Antonio;
Pardo Domínguez, Cristina;
Palma Milla, Carmen;
Pérez de la Fuente, Rubén;
Quesada‐Espinosa, Juan Francisco;
Núñez‐Enamorado, Noemí;
Gener, Blanca;
Ballesta‐Martínez, María Juliana;
Brea‐Fernández, Alejandro J.

Publication type:

Article

Balanced Translocation t(3;12) Disrupting HMGA2 and NAALADL2 Genes in Twins With Silver–Russell Syndrome and Intellectual Disability.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 694, doi. 10.1111/cge.14699

By:

de Souza, Vanessa Sodré;
Wawruk, Halinna Dornelles;
Mehrjouy, Mana M.;
Bak, Mads;
da Cunha, Gabriela Corassa Rodrigues;
Gonçalves, Ana Caroline Gabriel;
Cordoba, Mara Santos;
Tommerup, Niels;
Mazzeu, Juliana F.

Publication type:

Article

Novel Phenotypes and Genotype–Phenotype Correlations in a Large Clinical Cohort of Patients With Kleefstra Syndrome.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 636, doi. 10.1111/cge.14697

By:

Frazier, Zoë J.;
Kilic, Seyda;
Osika, Hailey;
Mo, Alisa;
Quinn, Meg;
Ballal, Sonia;
Katz, Tamar;
Shearer, A. Eliot;
Horlbeck, Max A.;
Pais, Lynn S.;
Dies, Kira A.;
O'Donnell‐Luria, Anne;
Kossowsky, Joe;
Lipton, Jonathan O.;
Kleefstra, Tjitske;
Srivastava, Siddharth

Publication type:

Article

Identification of Novel SCMC Gene Variants Associated With Early Embryonic Arrest.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 680, doi. 10.1111/cge.14696

By:

Zhang, Changlong;
Zhao, Shuai;
Zhang, Honghui;
Su, Wei;
Wang, Yang;
Cui, Ying;
Yang, Bohan;
Wang, Yikun;
Zhao, Han

Publication type:

Article

Hereditary Spastic Paraplegia Linked to Abnormal Splicing From an AIMP1 Missense Variant.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 668, doi. 10.1111/cge.14690

By:

Morais, Sara;
Leal Loureiro, José;
Brandão, Eva;
Sequeiros, Jorge;
Stevanin, Giovanni;
Santos, Mariana

Publication type:

Article

A Unique Case of MBD5 and CCM2 Deletions Leading to a Severe Neurological Phenotype With Prolonged Status Epilepticus.

Published in:

Clinical Genetics, 2025, v. 107, n. 6, p. 663, doi. 10.1111/cge.14685

By:

Silva, Sebastián;
Venegas, Viviana;
Valenzuela, Marcela;
Retamales‐Moreno, Álvaro;
Muñoz‐Castro, Carolina;
Acevedo, Hernán;
Marengo, Juan‐José;
Okubo, Mariko;
Takada, Sanami;
Miyake, Noriko

Publication type:

Article

Research Progress on Embryonic Development, Genetic Regulation and Clinical Management of Congenital Middle Ear Malformations.

Published in:

Flavour & Fragrance Journal, 2025, v. 40, n. 3, p. 393, doi. 10.1002/ffj.3836

By:

Gao, Xiaochen;
Li, Chengzhilin;
Yuan, Fanyu;
Cao, Xue;
Liu, Chengcheng;
Qi, Wenwen;
Xie, Fengyang;
Xia, Ming

Publication type:

Article

Margin weighted robust discriminant score for feature selection in imbalanced gene expression classification.

Published in:

PLoS ONE, 2025, v. 20, n. 6, p. 1, doi. 10.1371/journal.pone.0325147

By:

Gul, Sheema;
Muhammad Khan, Dost;
Aldahmani, Saeed;
Khan, Zardad

Publication type:

Article

Genome-wide identification and characterisation of the glycoside hydrolase gene family in Penicillium expansum.

Published in:

New Zealand Journal of Crop & Horticultural Science, 2025, v. 53, n. 3, p. 587, doi. 10.1080/01140671.2025.2481686

By:

Wang, Kaili;
Pan, Tengxia;
Song, Yusi;
Chen, Hongbin;
Wang, Hua;
Ackah, Michael;
Godana, Esa Abiso;
Yang, Qiya;
Zhang, Hongyin

Publication type:

Article

Phenotypic variability in two siblings with Poretti-Boltshauser syndrome.

Published in:

Global Medical Genetics, 2025, v. 12, n. 1, p. 1, doi. 10.1016/j.gmg.2024.100010

By:

Moura Raftopoulos, Karolyne Michele;
Nascimento Chiang, Fernanda Sousa;
de Melo Gama, Lorena;
Farage, Luciano;
Neves Medina, Cristina Touguinha

Publication type:

Article

A de novo SALL4 mutation causes unilateral renal agenesis by misregulating genes involved in kidney development.

Published in:

Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03833-x

By:

Zhao, Rong;
Fan, Yali;
Li, Jieyan;
Li, Lin;
Yin, Chenghong

Publication type:

Article

In vitro activity of ceftazidime-avibactam and meropenemvaborbactam against carbapenem-resistant Enterobacterales in Egyptian Hospitals: A challenge for clinical practice.

Published in:

Microbes & Infectious Diseases, 2025, v. 6, n. 2, p. 752, doi. 10.21608/MID.2024.323549.2247

By:

ElFeky, Dalia Saad;
Awad, Alaa Reda;
Raafat Hamed, Reham Mohammad;
Baddour, Manal Mohamed;
Mowafy, Hagar Lotfy

Publication type:

Article

Correction to: Season-specific dominance broadly stabilizes polymorphism under symmetric and asymmetric multivoltinism Free.

Published in:: 2025
Publication type:: Correction Notice

Diploidy confers genomic instability in Schizosaccharomyces pombeOpen Access.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf078

By:

Park, Joshua M;
Pinski, Daniel F;
Forsburg, Susan L

Publication type:

Article

Parameters that influence bipartite reporter system expression in Caenorhabditis elegans.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf076

By:

Knoebel, Emma;
Brinck, Anna;
Nonet, Michael L

Publication type:

Article

Improved sampling of genotypes and species reveals new insights on de novo gene history and regulatory origins.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf074

By:

Blair, Logan K;
Cridland, Julie M;
Luo, Yige;
Begun, David J;
Kopp, Artyom

Publication type:

Article

Causal network inference of cis- and trans-gene regulation of expression quantitative trait loci across human tissues.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf064

By:

Kvamme, Jarred;
Badsha, Md Bahadur;
Martin, Evan A;
Wu, Jiayu;
Wang, Xiaoyue;
Fu, Audrey Qiuyan

Publication type:

Article

Identification of regions required for allelic specificity at the cell wall remodeling allorecognition checkpoint in Neurospora crassaOpen Access.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf062

By:

Rico-Ramirez, Adriana M;
Glass, N Louise

Publication type:

Article

Fork-barrier-independent roles of topoisomerase I in the ribosomal DNA.

Published in:

Genetics, 2025, v. 230, n. 2, p. 1, doi. 10.1093/genetics/iyaf052

By:

Molinar, Temistocles;
Sultanov, Daniel;
Klein, Hannah;
Hochwagen, Andreas

Publication type:

Article

Clinical Features of Seven COL2A1 Variations in Chinese Children With Type II Collagen Disorders.

Published in:

Acta Paediatrica, 2025, v. 114, n. 7, p. 1720, doi. 10.1111/apa.70029

By:

Zhan, Shumin;
He, Qin;
Yuan, Jinna;
Xu, Xiaoqin;
Huang, Ke;
Dong, Guanping;
Fu, Junfen;
Wu, Dingwen;
Wu, Wei

Publication type:

Article

FTO Aggravates the Infiltration of Inflammatory Cells and Pulmonary Fibrosis in Silicosis Though Inducing the Imbalance of Macrophages Polarization.

Published in:

Microbiology & Immunology, 2025, v. 69, n. 6, p. 339, doi. 10.1111/1348-0421.13216

By:

Fan, Jian‐min;
Zhang, Xu

Publication type:

Article

Targeting NLRC4 for potential therapeutic strategies in lung adenocarcinoma.

Published in:

Discover Oncology, 2025, v. 16, n. 1, p. 1, doi. 10.1007/s12672-025-02839-y

By:

Xu, Xue;
Zhang, Meng-Yu;
Fan, Jia-Qi;
Li, Guo-Dong;
Li, Jun-Yi;
Chen, Xiao

Publication type:

Article

Siblings With Abnormal Thyroid Function Tests.

Published in:

Clinical Pediatrics, 2025, v. 64, n. 7, p. 1037, doi. 10.1177/00099228241304511

By:

Gornisiewicz, Savanna;
Kessler, Aleeza;
Dayton, Kristin

Publication type:

Article

Congenital Hypothyroidism with Thyroid in situ: A Case Report with NKX2-1 and DUOX2 Hypomorphic Variants.

Published in:

Hormone Research in Paediatrics, 2025, v. 98, n. 3, p. 289, doi. 10.1159/000538895

By:

Uehara, Erika;
Hori, Naoaki;
Tanase-Nakao, Kanako;
Akiba, Kazuhisa;
Sueoka, Hidefumi;
Matsubara, Keiko;
Narumi, Satoshi

Publication type:

Article

Mir-509-3p targets SLC25A13 to regulate ferroptosis and protect retinal endothelial cells in diabetic retinopathy.

Published in:

Acta Diabetologica, 2025, v. 62, n. 6, p. 831, doi. 10.1007/s00592-024-02400-3

By:

Ren, Meiqing;
Xu, Qian;
Luan, Jie;
Ni, Yan;
Xie, Bo

Publication type:

Article

國際家畜基因編輯規範之趨勢.

Published in:

Journal of the Chinese Society of Animal Science, 2024, v. 53, p. 186

By:

杜清富;
楊天樹

Publication type:

Article

Clinical manifestation of autosomal dominant hyper-IgE syndrome with associated autism.

Published in:

Polish Journal of Allergology / Alergologia Polska, 2025, v. 12, n. 2, p. 140, doi. 10.5114/pja.2025.151308

By:

Muciek, Adrianna;
Rutkowska-Zapała, Magdalena;
Szaflarska, Anna

Publication type:

Article

Genetic factors predisposing to atopic dermatitis: selected genes related to the skin barrier and immune response.

Published in:

Polish Journal of Allergology / Alergologia Polska, 2025, v. 12, n. 2, p. 126, doi. 10.5114/pja.2025.151305

By:

Nowak, Tomasz;
Cieśla, Dominika

Publication type:

Article