Biomedical publications with connected research

Recovery from desensitization in GluA2 AMPA receptors is affected by a single mutation in the N-terminal domain interface.

The Journal of biological chemistry | 2024-03-01 | PMID 38311178

Larsen Andreas Haahr, Perozzo Amanda M, Biggin Philip C and 2 more

Genetic polymorphism of KIAA1217 is functionally associated with lumbar disc herniation in the Chinese population.

Neuro-Chirurgie | 2024-03-01 | PMID 38311218

Dai Jian, Jiang Haitao, Cheng Zhang and 2 more

HSP90: A promising target for NSCLC treatments.

European journal of pharmacology | 2024-03-15 | PMID 38311278

Zhu Yue, Dai Zhaoxia

G1 the common Echinococcus granulosus genotype infected domestic cat (Felis catus) in Iraq.

Journal of veterinary science | 2024-01-01 | PMID 38311322

Al-Ardi Musafer H

Cell fate regulation governed by p53: Friends or reversible foes in cancer therapy.

Cancer communications (London, England) | 2024-03-01 | PMID 38311377

Song Bin, Yang Ping, Zhang Shuyu

Genes: TP53

[Primary myelofibrosis with double mutation in U2AF1].

[Rinsho ketsueki] The Japanese journal of clinical hematology | 2024-01-01 | PMID 38311386

Maeyama Keiko, Nagaharu Keiki, Ino Kazuko and 3 more

Germline predisposition for clonal hematopoiesis.

Seminars in hematology | 2024-02-01 | PMID 38311514

Kubota Yasuo, Viny Aaron D

Clonal hematopoiesis in children with predisposing conditions.

Seminars in hematology | 2024-02-01 | PMID 38311515

Attardi Enrico, Corey Seth J, Wlodarski Marcin W

Current management of uncommon EGFR mutations in non-small cell lung cancer.

Current problems in cancer | 2024-04-01 | PMID 38311523

Trinh Jonathan Q, Abughanimeh Omar

Germline variants in early and late-onset Brazilian prostate cancer patients.

Urologic oncology | 2024-03-01 | PMID 38311546

Coelho Karoline Brito Caetano Andrade, Squire Jeremy A, Duarte Kelly Gomes and 9 more

The use of high-resolution SNP arrays to detect congenital cardiac defects.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians | 2024-12-01 | PMID 38311547

Linhuan Huang, Danlei Cai, Zhiming He and 8 more

[Genetic analysis of eighteen patients from Gansu Province with Tetrahydrobiopterin deficiency].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311548

Zhang Chuan, Tian Xinyuan, Wang Yupei and 8 more

[Application of whole exome sequencing for the inferential analysis of recessive genetic disease carrier status for couples with a child died of Primary immunodeficiency].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311549

Zhang Bing, Yang Ke, Zhang Yuwei and 6 more

[Association of ITGA4 and ICAM-1 gene polymorphisms with the risk and clinicopathological characteristics of Crohn's disease].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311553

Zhang Dingli, Wu Hao, Shao Xiaoxiao and 2 more

[Variant analysis and prenatal diagnosis for two Chinese pedigrees affected with Spinal muscular atrophy with respiratory distress type 1].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311554

Li Huijun, Zhu Xiangyu, Yang Ying and 2 more

[Clinical features and genetic analysis of five children with epilepsies due to variants of SCN8A gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311555

Zhang Xin, Qiu Shiyan, Yang Li and 3 more

[Clinical features and genetic analysis of three patients with Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome due to variants of FOXP3 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311556

Zheng Cuifang, Meng Yingying, Deng Zhaohui and 3 more

[Genetic analysis of a family with epilepsy accompanied by developmental delay and brain deformity due to a de novo variant of TUBB2A gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311557

Zhao Juan, Xu Na, Li Yufen and 4 more

[Prenatal diagnosis and phenotypic analysis of two fetuses harboring heterozygous deletions of SHOX gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311560

Gu Leilei, Liu Wei, Zhu Xiangyu and 1 more

[Genetic and clinical analysis of a child with Shwachman-Diamond syndrome due to compound heterozygous variants of SBDS gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311561

Li Suli, Yu Zhidan, Zhou Fang and 4 more

[Genetic analysis of a case with Adult-onset globoid cell leukodystrophy].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311562

Liang Wenwen, Zhu Zhou, Fang Yongkang

[Genetic analysis of a fetus with Meckel syndrome due to variants of TMEM67 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311563

Tang Hui, Song Xiaoyan, Weng Xin and 2 more

[Clinical and genetic analysis of a child with Canavan disease due to compound heterozygous variants of ASPA gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311564

Niu Shasha, Ma Yanyan, Lyu Yuqiang and 7 more

[Analysis of clinical features and genetic variant in a child with Cowden syndrome 1].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311565

Yan Lulu, Tian Liyun, Zhang Yuxin and 5 more

[Analysis of a child with DIGFAN syndrome due to variant of MORC2 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311566

Xie Bobo, Fan Xin, Wei Xianda and 5 more

[Analysis of a child with 46,XY Disorder of sex development due to a novel variant of NR5A1 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311567

Liu Ailing, Wu Mingli, Li Ping and 4 more

[Clinical phenotype and genetic analysis of a child featuring short stature and multiple skeletal dysplasia].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311568

Lyu Yongxue, Qi Fengfeng, Fei Zhenghua and 2 more

[Genetic analysis of a fetus with Cornelia de Lange syndrome due to variant of SMC3 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2024-02-10 | PMID 38311569

Huang Hui, Chen Peiwen, Feng Qian and 3 more

Dynamic phenotypic reprogramming and chemoresistance induced by lung fibroblasts in small cell lung cancer.

Scientific reports | 2024-02-05 | PMID 38311608

Lu Yuanhua, Li Hui, Zhao Peiyan and 4 more

Spatial analysis of the osteoarthritis microenvironment: techniques, insights, and applications.

Bone research | 2024-02-04 | PMID 38311627

Fan Xiwei, Sun Antonia Rujia, Young Reuben S E and 5 more

Construction and validation of a colon cancer prognostic model based on tumor mutation burden-related genes.

Scientific reports | 2024-02-04 | PMID 38311637

Zou Daoyang, Xu Tianwen

The impact of folate pathway variants on the outcome of methotrexate therapy in rheumatoid arthritis patients.

Clinical rheumatology | 2024-03-01 | PMID 38311638

Nomair Azhar M, Abdelati Abeer, Dwedar Fatma I and 3 more

Low-Dose LPS Modulates Microglia/Macrophages Phenotypic Transformation to Amplify Rehabilitation Effects in Chronic Spinal Cord Injured (CSCI) Mice.

Molecular neurobiology | 2024-09-01 | PMID 38311654

Zhong Juan, He Yingxi, Zhao Qin and 9 more

HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF.

Hormones (Athens, Greece) | 2024-06-01 | PMID 38311659

Xekouki P, Konstantinidou A, Tatsi C and 7 more

Targeting BRCA and PALB2 in Pancreatic Cancer.

Current treatment options in oncology | 2024-03-01 | PMID 38311708

Anbil Sriram, Reiss Kim A

Tumor mutational burden predictability in head and neck squamous cell carcinoma patients treated with immunotherapy: systematic review and meta-analysis.

Journal of translational medicine | 2024-02-04 | PMID 38311741

Rodrigo Juan P, Sánchez-Canteli Mario, Otero-Rosales María and 3 more

Natural genetic variation in GLK1-mediated photosynthetic acclimation in response to light.

BMC plant biology | 2024-02-05 | PMID 38311744

Muino Jose M, Großmann Christopher, Kleine Tatjana and 1 more

Causal associations of COVID-19 on neurosurgical diseases risk: a Mendelian randomization study.

Human genomics | 2024-02-05 | PMID 38311757

Dai Lirui, Lyu Liang, Zhou Peizhi and 1 more

Micronutrients intake and genetic variants associated with premature ovarian insufficiency; MASHAD cohort study.

BMC women's health | 2024-02-04 | PMID 38311764

Mirinezhad Mohammad Reza, Aghsizadeh Maliheh, Ghazizadeh Hamideh and 7 more

In vitro propagation of Indonesian stevia (Stevia rebaudiana) genotype using axenic nodal segments.

BMC research notes | 2024-02-05 | PMID 38311772

Jadid Nurul, Anggraeni Suci, Ramadani Muhammad Rifqi Nur and 2 more

Genetic Diversity and Pathogenicity of the Fusarium Species Complex on Soybean in Serbia.

Plant disease | 2024-06-01 | PMID 38311795

Petrović Kristina, Orzali Laura, Krsmanović Slobodan and 4 more

Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy.

Annals of clinical and translational neurology | 2024-03-01 | PMID 38311799

Donkervoort Sandra, Mohassel Payam, O'Leary Melanie and 20 more

Genes: ACTN2

Recurrent MTOR Mutations in Renal Cell Carcinoma With Fibromyomatous Stroma: A Report of 2 Tumors.

International journal of surgical pathology | 2024-10-01 | PMID 38311893

Palathingal Bava Ejas, Gupta Nilesh, Alruwaii Fatimah I and 2 more

Heterogeneity of sensitization profiles and clinical phenotypes among patients with seasonal allergic rhinitis in Southern European countries-The @IT.2020 multicenter study.

Allergy | 2024-04-01 | PMID 38311961

Dramburg S, Grittner U, Potapova E and 53 more

Myocardial Injury in Peritoneal Dialysis Patients Assessed by Multiparametric MRI: Relationship With Left Ventricular Phenotypes.

Journal of magnetic resonance imaging : JMRI | 2024-11-01 | PMID 38311966

Jin Shiqi, Wang Fan, Tian Zhaoxin and 4 more

[Plasma miRNA expression in patients with genetically confirmed multiple endocrine neoplasia type 1 syndrome and its phenocopies].

Problemy endokrinologii | 2024-01-24 | PMID 38311997

Trukhina D A, Mamedova E O, Nikitin A G and 3 more

Genes: MEN1

The novel HLA-B*35:592 allele, confirmed by Sanger dideoxy nucleotide sequencing in a Russian individual.

HLA | 2024-02-01 | PMID 38312011

Loginova Maria, Makhova Olga, Paramonov Igor

Molecular relapse monitoring reveals the domination of impaired NK cell education over impaired inhibition in missing KIR-ligand recognition in patients after unrelated hematopoietic stem cell transplantation for malignant diseases.

HLA | 2024-02-01 | PMID 38312022

Nowak Jacek, Witkowska Agnieszka, Rogatko-Koroś Marta and 7 more

Mitochondrial D-loop methylation levels inversely correlate with disease duration in amyotrophic lateral sclerosis.

Epigenomics | 2024-02-01 | PMID 38312023

Stoccoro Andrea, Smith Adam R, Mosca Lorena and 6 more

Genes: SOD1

Using molecular characteristics to distinguish multiple primary lung cancers and intrapulmonary metastases.

PeerJ | 2024-01-01 | PMID 38313018

Li Zhenhua, Lv Huilai, Zhang Fan and 7 more

Evaluation of sesame (Sesamum indicum L.) varieties for drought tolerance using agromorphological traits and drought tolerance indices.

PeerJ | 2024-01-01 | PMID 38313022

Yemata Getahun, Bekele Tewachew

Genotyping by sequencing for the construction of oil palm (Elaeis guineensis Jacq.) genetic linkage map and mapping of yield related quantitative trait loci.

PeerJ | 2024-01-01 | PMID 38313025

Mohd Shaha Fakhrur Razi, Liew Pui Ling, Qamaruz Zaman Faridah and 5 more

A rare presentation of childhood interstitial lung disease attributed to KDM3B gene mutation: a case report.

The Pan African medical journal | 2023-01-01 | PMID 38314229

Benslimane Zaineb, Yavuz Sinan, Francis Nader

The predictive effect of family genetic risk scores as an indirect measure of causal effects of one disorder on another.

Psychological medicine | 2024-06-01 | PMID 38314515

Kendler Kenneth S, Ohlsson Henrik, Sundquist Jan and 1 more

A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation.

Hemoglobin | 2024-01-01 | PMID 38314576

Wu Shao-Min, Li Chan, Huang Su-Ran and 2 more

Hb Hebei [α20 (B1) His→Leu; HBA2:C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin.

Hemoglobin | 2024-01-01 | PMID 38314585

Li Wei-Bin, Zheng Li-Hong, Li You-Qiong

Computational evidences of a misfolding event in an aggregation-prone light chain preceding the formation of the non-native pathogenic dimer.

Proteins | 2024-07-01 | PMID 38314653

Desantis Fausta, Miotto Mattia, Milanetti Edoardo and 2 more

Case report: diagnosis of VEXAS syndrome in a patient with therapy-resistant large vessel vasculitis.

Acta clinica Belgica | 2024-04-01 | PMID 38314661

Boret M, Malfait T

A method for isolating contractile smooth muscle cells from cryopreserved tissue.

American journal of physiology. Cell physiology | 2024-03-01 | PMID 38314725

Schultz Matheus L C, Seth Pranjal, Kachmar Linda and 2 more

Pain in Parkinson disease: a deep phenotyping study.

Pain | 2024-07-01 | PMID 38314763

Salabasidou Elena, Binder Tobias, Volkmann Jens and 2 more

A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice.

Sleep | 2024-05-10 | PMID 38314840

Leu Chia-Luen, Lam Daniel D, Salminen Aaro V and 9 more

An expression-directed linear mixed model discovering low-effect genetic variants.

Genetics | 2024-04-03 | PMID 38314848

Li Qing, Bian Jiayi, Qian Yanzhao and 8 more

Landscape of T cell epitopes displays hot mutations of SARS-CoV-2 variant spikes evading cellular immunity.

Journal of medical virology | 2024-02-01 | PMID 38314852

Gan Mengze, Cao Jinge, Zhang Yandi and 6 more

Genetic characterization and molecular epidemiological analysis of enterovirus C99 in China.

Journal of medical virology | 2024-02-01 | PMID 38314919

Cong Ruyi, Xiao Jinbo, Ji Tianjiao and 12 more

Transcriptome-Wide Association Studies (TWAS): Methodologies, Applications, and Challenges.

Current protocols | 2024-02-01 | PMID 38314955

Evans Patrick, Nagai Taylor, Konkashbaev Anuar and 3 more

Overcoming Clinical Resistance to EZH2 Inhibition Using Rational Epigenetic Combination Therapy.

Cancer discovery | 2024-06-03 | PMID 38315003

Kazansky Yaniv, Cameron Daniel, Mueller Helen S and 13 more

Genetic diversity and recombination of bovine enterovirus strains in China.

Microbiology spectrum | 2024-03-05 | PMID 38315051

Chang Xiaoran, Zhang Zhiyuan, Cui Xuyuan and 5 more

Genes: F7, F3

Genetic signatures of suicide attempt behavior: insights and applications.

Expert review of proteomics | 2024-01-01 | PMID 38315076

Drago Antonio

Genes: BDNF, DRD2, HTR2A

Influence of Fluorescence Lifetime Selections and Conformational Flexibility on Brightness of FusionRed Variants.

The journal of physical chemistry letters | 2024-02-15 | PMID 38315162

Mukherjee Srijit, Douglas Nancy, Jimenez Ralph

Variability in plasma rifampicin concentrations and role of SLCO1B1, ABCB1, AADAC2 and CES2 genotypes in Ethiopian patients with tuberculosis.

Infectious diseases (London, England) | 2024-04-01 | PMID 38315168

Sileshi Tesemma, Makonnen Eyasu, Telele Nigus Fikrie and 3 more

Genes: SLCO1B1, ABCB1, AADAC, CES2

Compensatory mutations are associated with increased in vitro growth in resistant clinical samples of Mycobacterium tuberculosis.

Microbial genomics | 2024-02-01 | PMID 38315172

Brunner Viktoria M, Fowler Philip W

CRISPR/Cas9-mediated efficient white genome editing in the black soldier fly Hermetia illucens.

Molecular genetics and genomics : MGG | 2024-02-05 | PMID 38315256

Sui Zhuoxiao, Wu Qi, Geng Jin and 2 more

Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling.

Plant cell reports | 2024-02-05 | PMID 38315261

Min Wang Ki, Kwon Dae Hwan, Song Jong Tae and 1 more

Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers.

Molecular biology reports | 2024-02-05 | PMID 38315301

Ul Mudassir Behjat, Agha Zehra

Characterization and genetic differences analysis in adventitious roots development of 38 Populus germplasm resources.

Plant molecular biology | 2024-02-05 | PMID 38315324

Zhang Min, Zhou Xinglu, Xiang Xiaodong and 3 more

Molecular Determinants of Neurocognitive Deficits in Glioma: Based on 2021 WHO Classification.

Journal of molecular neuroscience : MN | 2024-02-05 | PMID 38315329

Zhang Kun, Yang Tianrui, Xia Yu and 26 more

Clinical heterogeneity and five phenotypes identified in pediatric Behçet's syndrome: a cohort study from Shanghai Behçet's syndrome database.

World journal of pediatrics : WJP | 2024-08-01 | PMID 38315355

Hu Dan, She Chun-Hui, Bao Hua-Fang and 7 more

B10 cells: Development, phenotype, and function in cancer.

Advances in clinical and experimental medicine : official organ Wroclaw Medical University | 2024-11-01 | PMID 38315382

Li Dandan, Ma Yunfeng

Plant-based natural products in cancer therapeutics.

Journal of drug targeting | 2024-04-01 | PMID 38315449

Mahato Rohini, Behera Dillip Kumar, Patra Biswajit and 5 more

Association analysis of the sorting nexin 29 (SNX29) gene copy number variations with growth traits in Diannan small-ear (DSE) pigs.

Animal biotechnology | 2024-11-01 | PMID 38315463

Yang Long, Lin Xiaoding, Chen Yuhan and 6 more

Screening Mutations of the Monogenic Syndromic High Myopia by Whole Exome Sequencing From MAGIC Project.

Investigative ophthalmology & visual science | 2024-02-01 | PMID 38315492

Chen Chong, An Gang, Yu Xiaoguang and 11 more

Genes: CACNA1F, COL2A1, FBN1, FZD4, GJA8, HSF4, MIP, TEK

Noninvasive fetal blood group antigen genotyping.

Blood transfusion = Trasfusione del sangue | 2025-03-01 | PMID 38315532

Clausen Frederik B, van der Schoot C Ellen

Genes: RHD

HLA class I expression on human platelets is highly variable and correlates with distinct allele group frequencies.

Blood transfusion = Trasfusione del sangue | 2024-09-01 | PMID 38315535

Cantisani Rocco, Del Re Valeria, Toraldo Francesca and 4 more

First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.

Blood transfusion = Trasfusione del sangue | 2024-09-01 | PMID 38315540

Mbeti Jeanne Manga Messina, Bénech Caroline, Sack Françoise Ngo and 6 more

Genes: RHD, RHCE, SCD

High-risk HPV prevalence and vaccination coverage among Indigenous women in the Colombian Amazon: Implications for cervical cancer prevention. Cross-sectional study.

PloS one | 2024-01-01 | PMID 38315664

Sarmiento-Medina María Inés, de Amaya Miryam Puerto, Villamizar-Gómez Licet and 2 more

Impact of Different Cofactors on Naturally Acquired Human Papillomavirus Antibody Levels Among Unvaccinated Pregnant Women.

Viral immunology | 2000-01-01 | PMID 38315747

Kirjavainen Laura, Suominen Helmi, Syrjänen Kari and 4 more

Type 2M/2A von Willebrand disease: a shared phenotype between type 2M and 2A.

Blood advances | 2024-04-09 | PMID 38315875

Seidizadeh Omid, Mollica Luca, Zambarbieri Serena and 8 more

Single-Agent Trabectedin Versus Physician's Choice Chemotherapy in Patients With Recurrent Ovarian Cancer With BRCA-Mutated and/or BRCAness Phenotype: A Randomized Phase III Trial.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2024-05-01 | PMID 38315944

Lorusso Domenica, Raspagliesi Francesco, Ronzulli Dominique and 20 more

Comprehensive biomarker diagnostics of unfavorable cancer of unknown primary to identify patients eligible for precision medical therapies.

European journal of cancer (Oxford, England : 1990) | 2024-03-01 | PMID 38316065

Zaun Gregor, Borchert Sabrina, Metzenmacher Martin and 11 more

Effect of disulfidptosis-related genes SLC3A2, SLC7A11 and FLNB polymorphisms on risk of autoimmune thyroiditis in a Chinese population.

International immunopharmacology | 2024-03-10 | PMID 38316082

Wang Qiang, Xiao Zhifu, Hou Zebin and 1 more

PIK3CA-Related Disorders: From Disease Mechanism to Evidence-Based Treatments.

Annual review of genomics and human genetics | 2024-08-01 | PMID 38316164

Morin Gabriel M, Zerbib Lola, Kaltenbach Sophie and 4 more

Genetic diversity of G9, G3, G8 and G1 rotavirus group A strains circulating among children with acute gastroenteritis in Vietnam from 2016 to 2021.

Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2024-03-01 | PMID 38316245

Le Ly K T, Chu Mai N T, Tate Jacqueline E and 10 more

Genetic analysis and QTL mapping of seed hardness trait in a soybean (Glycine max) recombinant inbred line (RIL) population.

Gene | 2024-05-05 | PMID 38316262

Ren Honglei, Zhao Kezhen, Zhang Chunlei and 8 more

Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: A systematic review and meta-analysis.

Gene | 2024-05-15 | PMID 38316264

Regina da Silva Correa da Ronda Carla, Berlofa Visacri Marília, Tiemi Siguemoto Júlia and 8 more

Lifestyle factors, genetic susceptibility to obesity and their interactions on coronary artery disease risk: A cohort study in the UK Biobank.

Preventive medicine | 2024-03-01 | PMID 38316272

Choi Jungyoon, Wen Wanqing, Jia Guochong and 4 more

Genes: CAD

Causal role of immune cell traits in stroke: A Mendelian randomization study.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association | 2024-05-01 | PMID 38316285

Wang Maiqiu, Zhang Xu, Fan Rongli and 1 more

Effects of protein genetic variants on their phosphorylation levels, milk composition, milk proteome, and milk coagulation ability in Chinese Holstein bovine milk.

International journal of biological macromolecules | 2024-03-01 | PMID 38316325

Zhang Wenyuan, Zheng Sifan, Zhu Huiquan and 6 more

Various mutations in icaR, the repressor of the icaADBC locus, occur in mucoid Staphylococcus aureus isolates recovered from the airways of people with cystic fibrosis.

Microbes and infection | 2000-01-01 | PMID 38316375

Schwartbeck Bianca, Rumpf Christine H, Hait Robert Jonathan and 5 more

Echinococcus granulosus sheep strain (G1) as the predominant genotype in definitive host (dogs) isolates in northeastern Iran.

Veterinary parasitology, regional studies and reports | 2024-02-01 | PMID 38316501

Hejazi Seyed-Hossein, Mirbadie Seyed-Reza, Jafari Rasool and 10 more

Genetic Coupling of Mate Recognition Systems in the Genomic Era.

Cold Spring Harbor perspectives in biology | 2024-04-01 | PMID 38316558

Ritchie Michael G, Butlin Roger K