Works matching DE "GENETIC techniques"

Results: 5000

Application and prospects of genetic engineering in CAR-NK cell therapy.

Published in:

Frontiers in Immunology, 2025, p. 1, doi. 10.3389/fimmu.2025.1600411

By:

Hu, Caidong;
Lai, Wenhong;
Tian, Bin;
Xu, Xi;
Xie, Shuiling;
Zhong, Wenting;
Kang, Huiqiang;
Chen, Xiaoyun;
Li, Hailiang;
Xu, Jingxin;
Liu, Liping

Publication type:

Article

Traditional contraceptive practices: survey of medicinal plants used to control birth in four states in Nigeria.

Published in:

BMC Complementary Medicine & Therapies, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12906-025-04935-6

By:

Ibrahim, Mutiat B.;
Odewo, Akinniyi S.;
Lawal, Bilqis A.;
Oyedeji, Oluseye F.;
Balogun, Noimot A.;
Tijani, Wakilat A.;
Abdulraheem, Abdullahi S.;
Shafiyi, Jubril;
Ilomuanya, Margaret O.

Publication type:

Article

VEXAS syndrome through a rheumatologist's lens: insights from a Spanish national cohort.

Published in:

Rheumatology, 2025, v. 64, n. 6, p. 3747, doi. 10.1093/rheumatology/keaf094

By:

García-Escudero, Paula;
López-Gómez, Marta;
López, Berta Magallares;
Dorta, Alicia García;
Frade-Sosa, Beatriz;
Lizarzaburu, Meritxell Sallés;
Rúa-Figueroa, Íñigo;
Fiallo, Dolly Viviana;
Miera, Francisco Javier Toyos Sáenz de;
Melero-Gonzalez, Rafael Benito;
Santos, Diego Dios;
Miranda, José Alberto;
Belando, Clara García;
Boselli, Giuliano;
Boteanu, Alina Lucica;
Villalobos, Lourdes;
Selaya, Cristina Corrales;
Santos, Cristiana Sieiro;
Álvarez, Elvira Díez;
Font, Judit

Publication type:

Article

The genetic landscape of pediatric postural orthostatic tachycardia syndrome.

Published in:

Clinical Autonomic Research, 2025, v. 35, n. 3, p. 431, doi. 10.1007/s10286-025-01110-2

By:

Qu, Huiqi;
Qu, Jingchun;
Chang, Xiao;
Williams, Nolan;
Mentch, Frank;
Snyder, James;
Lemma, Maria;
Nguyen, Kenny;
Behr, Meckenzie;
March, Michael;
Connolly, John;
Glessner, Joseph;
Boris, Jeffrey R.;
Hakonarson, Hakon

Publication type:

Article

Experimental Approaches to Visualize Effector Protein Translocation During Host‐Pathogen Interactions.

Published in:

BioEssays, 2025, v. 47, n. 4, p. 1, doi. 10.1002/bies.202400188

By:

Fritsch, Verena Nadin;
Hensel, Michael

Publication type:

Article

Differentially expressed genes in the placentas with pre-eclampsia and fetal growth restriction using RNA sequencing and verification.

Published in:

Journal of Perinatal Medicine, 2025, v. 53, n. 5, p. 595, doi. 10.1515/jpm-2025-0025

By:

Chen, Haiying;
Li, Xiaoqing;
Xu, Xiaoming;
Hu, Yanjun;
Zheng, Jianqiong

Publication type:

Article

Substitution of Glutamic Acid at Position 71 of DRβ1*04:01 and Collagen‐Specific Tolerance Without Alloreactivity.

Published in:

Arthritis & Rheumatology, 2025, v. 77, n. 5, p. 526, doi. 10.1002/art.43067

By:

Jha, Vibha;
Freed, Brian M.;
Sunderhaus, Elizabeth R.;
Lee, Jessica E.;
Prage, Edward B.;
Miglani, Manjula;
Rosloniec, Edward F.;
Matsuda, Jennifer L.;
Coulombe, Marilyne G.;
McKee, Amy S.;
Roark, Christina L.

Publication type:

Article

The PancreasView gemcitabine transcriptomic signature predicts response to gemcitabine in patients with resected pancreatic ductal adenocarcinoma.

Published in:

Oncologist, 2025, v. 30, n. 5, p. 1, doi. 10.1093/oncolo/oyaf083

By:

Bolm, Louisa;
Fraunhoffer, Nicolas;
Dusetti, Nelson;
Straesser, Julia;
Petruch, Natalie;
Castillo, Carlos Fernandez del;
Iovanna, Juan

Publication type:

Article

Assessment of the association of miR-499 and miR-146a polymorphisms with systemic lupus erythematosus in Egyptians.

Published in:

Egyptian Rheumatology & Rehabilitation, 2025, v. 52, n. 1, p. 1, doi. 10.1186/s43166-025-00329-1

By:

Sayed Abdel-Tawab, Marwa;
Mohamed, Alaa A.;
Sayed, Marwa Tantawy;
Kamal El Din Abed El Rahman, Shaymaa;
Salah Gaber, Safy;
Taha Osman, Shimaa;
Othman, Asmaa M.;
Abdel-Salam, Soha Mahmoud;
Ramadan Reyad, Hoda

Publication type:

Article

The role of probiotics in modulating the microbiota of the nose and paranasal sinuses and reducing chronic inflammation of the paranasal sinuses.

Published in:

Polish Otorhinolaryngological Review / Polski Przegląd Otorynolaryngologiczny (Index Copernicus), 2025, v. 14, n. 1, p. 26, doi. 10.5604/01.3001.0054.9412

By:

Zblewski, Jakub;
Kozakiewicz, Bartosz;
Dalke, Krzysztof;
Górna, Aleksandra

Publication type:

Article

The Pharmacokinetics, Dosage, Preparation Forms, and Efficacy of Orally Administered Melatonin for Non-Organic Sleep Disorders in Autism Spectrum Disorder During Childhood and Adolescence: A Systematic Review.

Published in:

Children, 2025, v. 12, n. 5, p. 648, doi. 10.3390/children12050648

By:

Paditz, Ekkehart;
Renner, Bertold;
Koch, Rainer;
Schneider, Barbara M.;
Schlarb, Angelika A.;
Ipsiroglu, Osman S.

Publication type:

Article

Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review.

Published in:

Clinical Medicine Insights: Case Reports, 2025, p. 1, doi. 10.1177/11795476251342637

By:

Aamir, Muhammad;
Faizullah, Fahad;
Khan, Malik W. Z.;
Azeem, Touba;
Khan, Muhammad Awais

Publication type:

Article

Morphological Markers of Chromosomal Instability: A Useful Aid in Effusion Cytology.

Published in:

Journal of Cytology, 2025, v. 42, n. 2, p. 95, doi. 10.4103/joc.joc_15_24

By:

Buch, Archana;
Agarwal, Mallika;
Londhe, Mangesh;
Singh, Madhuri;
Raj, Akshi;
Gore, Charusheela

Publication type:

Article

Identification and Characterization of a Rare Exon 22 Duplication in CFTR in Two Families.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 10, p. 4487, doi. 10.3390/ijms26104487

By:

Ahting, Simone;
Henn, Constance;
vom Hove, Maike;
Strehlow, Vincent;
Duffek, Patricia;
Behrendt, Sophie;
Drukewitz, Stephan;
Berger, Jasmin;
Graeber, Simon Y.;
Hentschel, Julia

Publication type:

Article

An attempt to explain what intrinsically disordered TCF4 does in its spare time when PTHS-related mutations prevent it from doing its job.

Published in:

Cell Communication & Signaling, 2025, v. 23, n. 1, p. 1, doi. 10.1186/s12964-025-02265-1

By:

Sozańska, Nikola;
Krupnik, Viktoryia;
Greb-Markiewicz, Beata;
Ożyhar, Andrzej;
Tarczewska, Aneta

Publication type:

Article

Ophthalmologists weigh if gene therapy is the future of wet AMD treatment.

Published in:

Ocular Surgery News, 2025, v. 43, n. 10, p. 18

By:

Cimberle, Michela

Publication type:

Article

FROM IMPLEMENTATION TO DISSEMINATION OF KANGAROO CARE IN SANTA CATARINA: A FOUCAULT'S ANALYSIS.

Published in:

Texto & Contexto Enfermagem, 2023, v. 32, p. 1, doi. 10.1590/1980-265X-TCE-2022-0327en

By:

dos Passos Aires, Luana Cláudia;
Wilhelm, Laís Antunes;
de Lima, Margarete Maria;
Boscoli de Oliveira Alves, Isadora Ferrante;
Delgado, Bruna Schiphorst;
Costa, Roberta

Publication type:

Article

EXEQUIBILIDADE DA ATENÇÃO INTEGRAL EM GENÉTICA CLÍNICA NO SISTEMA ÚNICO DE SAÚDE: AMPLIANDO O DEBATE.

Published in:

Texto & Contexto Enfermagem, 2014, v. 23, n. 4, p. 1130, doi. 10.1590/0104-07072014002120012

By:

Lopes-Júnior, Luís Carlos;
Flória-Santos, Milena;
Ferraz, Victor Evangelista de Faria;
Villa, Tereza Cristina Scatena;
Palha, Pedro Fredemir;
Bomfim, Emiliana de Omena;
Abrahão, Camila Aparecida;
da Silva, Sara

Publication type:

Article

Gleason 6 Cancer Is Still Cancer.

Published in:

2014

By:

ICZKOWSKI, KENNETH A.;
LA ROSA, FRANCISCO G.

Publication type:

Opinion

Genetic Testing in Gastrointestinal Cancers: A Case-Based Approach.

Published in:

Oncology (08909091), 2012, v. 26, n. 5, p. 433

By:

SCHRADER, KASMINTAN;
OFFIT, KENNETH;
STADLER, ZSOFIA K.

Publication type:

Article

Joseph Sparano on Gene Expression Assays for Breast Cancer.

Published in:: 2011
Publication type:: Interview

Inflammatory Breast Cancer: What Progress Have We Made?

Published in:

Oncology (08909091), 2011, v. 25, n. 3, p. 264

By:

Dawood, Shaheenah;
Cristofanilli, Massimo

Publication type:

Article

Isoform-specific potentiation of stem and progenitor cell engraftment by AML1/RUNX1.

Published in:

2007

By:

Tsuzuki, Shinobu;
Dengli Hong;
Gupta, Rajeev;
Matsuo, Keitaro;
Seto, Masao;
Enver, Tariq;
Hong, Dengli

Publication type:

journal article

Palladin mutation causes familial pancreatic cancer: absence in European families.

Published in:

2007

By:

Slater, Emily;
Amrillaeva, Vera;
Fendrich, Volker;
Bartsch, Detlef;
Earl, Julie;
Vitone, Louis J.;
Neoptolemos, John P.;
Greenhalf, William

Publication type:

Letter

In celiac disease, a subset of autoantibodies against transglutaminase binds toll-like receptor 4 and induces activation of monocytes.

Published in:

2006

By:

Zanoni, Giovanna;
Navone, Riccardo;
Lunardi, Claudio;
Tridente, Giuseppe;
Bason, Caterina;
Sivori, Simona;
Beri, Ruggero;
Dolcino, Marzia;
Valletta, Enrico;
Corrocher, Roberto;
Puccetti, Antonio

Publication type:

journal article

Immune protection of nonhuman primates against Ebola virus with single low-dose adenovirus vectors encoding modified GPs.

Published in:

2006

By:

Sullivan, Nancy J.;
Geisbert, Thomas W.;
Geisbert, Joan B.;
Shedlock, Devon J.;
Ling Xu;
Lamoreaux, Laurie;
Custers, Jerome H. H. V.;
Popernack, Paul M.;
Zhi-Yong Yang;
Pau, Maria G.;
Roederer, Mario;
Koup, Richard A.;
Goudsmit, Jaap;
Jahrling, Peter B.;
Nabel, Gary J.;
Xu, Ling;
Yang, Zhi-Yong

Publication type:

journal article

Crystallized or Liquid Phenol Application in Pilonidal Sinus Treatment.

Published in:

2015

By:

Kayaalp, Cuneyt;
Tolan, Kerem

Publication type:

Letter

Clinical Profile, Pathology, and Molecular Typing of Gliomas with Oligodendroglial Morphology: A Single Institutional Experience.

Published in:

2022

By:

Lavanya, Garapati;
Uppin, Megha;
Alugolu, Rajesh;
Bhattacharjee, Suchanda;
Saradhi, Mudumba;
Yeramneni, Vamsi;
Uppin, Megha Shantveer;
Saradhi, Mudumba Vijaya;
Yeramneni, Vamsi Krishna

Publication type:

Journal Article

Drug-resistant 'Non-Lesional' Visual Sensitive Epilepsies of Childhood - Electroclinical Phenotype-Genotype Associations.

Published in:

2021

By:

Menon, Ramshekhar;
Nambiar, Poornima;
Keni, R;
Baishya, Jitupam;
Radhakrishnan, Ashalatha;
Cherian, Ajith;
Nampoothiri, Sheela;
Madhavilatha, G;
Kotecha, Udaya;
Thomas, Sanjeev;
Menon, Ramshekhar N;
Nambiar, Poornima N;
Keni, R Ravish;
Madhavilatha, G K;
Kotecha, Udaya H;
Thomas, Sanjeev V

Publication type:

journal article

Enigma of tropical spastic paraplegia.

Published in:

2020

By:

Gourie-Devi, M

Publication type:

journal article

The Relationship Between Tumor Necrosis Factor-Alpha (-308G/A, +488G/A, -857C/T, and -1031T/C) Gene Polymorphisms and Risk of Intracerebral Hemorrhage in the North Indian Population: A Hospital-Based Case-Control Study.

Published in:

2020

By:

Kumar, Pradeep;
Misra, Shubham;
Kumar, Amit;
Faruq, Mohammad;
Vivekanandhan, Subiah;
Srivastava, Achal;
Prasad, Kameshwar;
Srivastava, Achal K

Publication type:

journal article

Schwartz-Jampel Syndrome Mimicking Myotonia Congenita.

Published in:

2019

By:

Padmanabha, Hansashree;
Mathew, Thomas;
Manjusha T.;
Manjusha, T

Publication type:

Case Study

Novel genotype-electroclinical phenotype correlations in sporadic early-onset childhood myoclonic-atonic epilepsy.

Published in:

2019

By:

Babu, Suresh;
Menon, Ramshekhar;
Asranna, Ajay;
Nampoothiri, Sheela;
Radhakrishnan, Ashalatha;
Cherian, Ajith;
Thomas, Sanjeev;
Babu, Suresh P;
Menon, Ramshekhar N;
Thomas, Sanjeev V

Publication type:

Case Study

The origin and possible mechanism of embryonic cell-free DNA release in spent embryo culture media: a review.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 6, p. 1231, doi. 10.1007/s10815-023-02813-z

By:

Handayani, Nining;
Aubry, Daniel;
Boediono, Arief;
Wiweko, Budi;
Sirait, Batara;
Sini, Ivan;
Polim, Arie A;
Dwiranti, Astari;
Bowolaksono, Anom

Publication type:

Article

Ethics in pre-ART genetics: a missed X-linked Menkes disease case.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 4, p. 811, doi. 10.1007/s10815-023-02778-z

By:

Gerdes, A.-M. A.;
Møller, L. Birk;
Horn, N.

Publication type:

Article

Roche: Computers Map Genes 1,000x Faster.

Published in:

Bio-IT World, 2004, v. 3, n. 12, p. 16

By:

Ueling, Mark D.

Publication type:

Article

A Hip Approach to Gene Hunting.

Published in:

Bio-IT World, 2004, v. 3, n. 6, p. 34

By:

Goldman, Michael A.

Publication type:

Article

Useful Medications for Oral Conditions.

Published in:: 2016
Publication type:: journal article

Breeding for water-use efficiency in wheat: progress, challenges and prospects.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09345-4

By:

Hafeez, Aqsa;
Ali, Shehzad;
Javed, Muhammad Ammar;
Iqbal, Rashid;
Khan, Muhammad Nauman;
ÇIĞ, Fatih;
Sabagh, Ayman EL;
Abujamel, Turki;
Harakeh, Steve;
Ercisli, Sezai;
Ali, Baber

Publication type:

Article

Simulation–Optimization Approach for Optimal Cut-Off Design Under the Hydraulic Structure.

Published in:

Geotechnical & Geological Engineering, 2024, v. 42, n. 1, p. 465, doi. 10.1007/s10706-023-02583-6

By:

Hassan, Waqed H.;
Nile, Basim K.;
Zwain, Haider M.

Publication type:

Article

A novel method of male sex identification of human ancient skeletal remains.

Published in:

Chromosome Research, 2020, v. 28, n. 3/4, p. 277, doi. 10.1007/s10577-020-09634-1

By:

Navarro-Romero, María Teresa;
Muñoz, María de Lourdes;
Alcala-Castañeda, Enrique;
Terreros-Espinosa, Eladio;
Domínguez-de-la-Cruz, Eduardo;
García-Hernández, Normand;
Moreno-Galeana, Miguel Ángel

Publication type:

Article

Testing for Differentiation of Microbial Communities Using Phylogenetic Methods: Accounting for Uncertainty of Phylogenetic Inference and Character State Mapping.

Published in:

Microbial Ecology, 2006, v. 52, n. 3, p. 408, doi. 10.1007/s00248-006-9002-7

By:

Jones, Ryan T.;
Martin, Andrew P.

Publication type:

Article

Exome-wide screening identifies novel rare risk variants for bone mineral density.

Published in:

Osteoporosis International, 2023, v. 34, n. 5, p. 965, doi. 10.1007/s00198-023-06710-0

By:

He, D.;
Pan, C.;
Zhao, Y.;
Wei, W.;
Qin, X.;
Cai, Q.;
Shi, S.;
Chu, X.;
Zhang, N.;
Jia, Y.;
Wen, Y.;
Cheng, B.;
Liu, H.;
Feng, R.;
Zhang, F.;
Xu, P.

Publication type:

Article

Association between gut microbiota, bone metabolism, and fracture risk in postmenopausal Japanese women.

Published in:

Osteoporosis International, 2021, v. 32, n. 1, p. 145, doi. 10.1007/s00198-020-05728-y

By:

Ozaki, D.;
Kubota, R.;
Maeno, T.;
Abdelhakim, M.;
Hitosugi, N.

Publication type:

Article

LRP5 gene polymorphisms and radiographic joint damage in rheumatoid arthritis patients.

Published in:

Osteoporosis International, 2018, v. 29, n. 10, p. 2355, doi. 10.1007/s00198-018-4625-3

By:

Costa, L.;
Bernardes, M.;
Simões-Ventura, F.;
Ramos, I.;
Machado, J. C.;
Durães, C.;
Martins, M. J.;
Oliveira, A.;
Pereira, J. G.;
Lucas, R.

Publication type:

Article

Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2.

Published in:

Osteoporosis International, 2018, v. 29, n. 7, p. 1643, doi. 10.1007/s00198-018-4499-4

By:

Butscheidt, S.;
Delsmann, A.;
Rolvien, T.;
Barvencik, F.;
Al-Bughaili, M.;
Mundlos, S.;
Schinke, T.;
Amling, M.;
Kornak, U.;
Oheim, R.

Publication type:

Article

Network based subcellular proteomics in monocyte membrane revealed novel candidate genes involved in osteoporosis.

Published in:

Osteoporosis International, 2017, v. 28, n. 10, p. 3033, doi. 10.1007/s00198-017-4146-5

By:

Zeng, Y.;
Zhang, L.;
Zhu, W.;
He, H.;
Sheng, H.;
Tian, Q.;
Deng, F.-Y.;
Zhang, L.-S.;
Hu, H.-G.;
Deng, H.-W.

Publication type:

Article

Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.

Published in:

Osteoporosis International, 2017, v. 28, n. 10, p. 2985, doi. 10.1007/s00198-017-4143-8

By:

Liu, Y.;
Asan;
Ma, D.;
Lv, F.;
Xu, X.;
Wang, J.;
Xia, W.;
Jiang, Y.;
Wang, O.;
Xing, X.;
Yu, W.;
Sun, J.;
Song, L.;
Zhu, Y.;
Yang, H.;
Li, M.

Publication type:

Article

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants.

Published in:

Osteoporosis International, 2017, v. 28, n. 10, p. 3023, doi. 10.1007/s00198-017-4150-9

By:

Kämpe, A.;
Costantini, A.;
Mäkitie, R.;
Jäntti, N.;
Valta, H.;
Mäyränpää, M.;
Kröger, H.;
Pekkinen, M.;
Taylan, F.;
Jiao, H.;
Mäkitie, O.

Publication type:

Article

A novel large fragment deletion in PLS3 causes rare X-linked early-onset osteoporosis and response to zoledronic acid.

Published in:

Osteoporosis International, 2017, v. 28, n. 9, p. 2691, doi. 10.1007/s00198-017-4094-0

By:

Lv, F.;
Ma, M.;
Liu, W.;
Xu, X.;
Song, Y.;
Li, L.;
Jiang, Y.;
Wang, O.;
Xia, W.;
Xing, X.;
Qiu, Z.;
Li, M.

Publication type:

Article