Dietary carbohydrate types, genetic predisposition, and risk of adult-onset asthma: A longitudinal cohort study.
International journal of biological macromolecules | 2024-03-01 | PMID 38290630
Zhang Hehua, Zhang Xiangsu, Yang Huijun and 5 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 9368 of 10600
Exploring the role of sporadic BRAF and KRAS mutations during colorectal cancer pathogenesis: A spotlight on the contribution of the endosome-lysosome system.
Cancer letters | 2024-03-31 | PMID 38290660
Tang Jingying, Lam Giang T, Brooks Robert D and 15 more
Appetitive and psychological phenotypes of pediatric patients with obesity.
Pediatric obesity | 2024-04-01 | PMID 38290813
Fox Claudia K, Molitor Stephen J, Vock David M and 3 more
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.
Journal of medical genetics | 2024-05-21 | PMID 38290825
Morison Lottie D, Kennis Milou G P, Rots Dmitrijs and 14 more
Chorea-acanthocytosis.
Practical neurology | 2024-05-29 | PMID 38290845
Rashid Sana, Malek Naveed, Krommyda Magdalini
Using Multi-phase CT Radiomics Features to Predict EGFR Mutation Status in Lung Adenocarcinoma Patients.
Academic radiology | 2024-06-01 | PMID 38290884
Zhang Guojin, Man Qiong, Shang Lan and 9 more
Cluster analysis of phenotypes, job exposure, and inflammatory patterns in elderly and nonelderly asthma patients.
Allergology international : official journal of the Japanese Society of Allergology | 2024-04-01 | PMID 38290901
Chuang Yung-Chi, Tsai Hsin-Hua, Lin Meng-Chih and 3 more
Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modeling.
Schizophrenia research | 2024-11-01 | PMID 38290943
Tordai Csongor, Hathy Edit, Gyergyák Hella and 11 more
Fine-scale genetic structure in the orchid Gymnadenia conopsea is not associated with local density of flowering plants.
American journal of botany | 2024-02-01 | PMID 38290971
Sletvold Nina, Joffard Nina, Söderquist Linus
GenomeMUSter mouse genetic variation service enables multitrait, multipopulation data integration and analysis.
Genome research | 2024-02-07 | PMID 38290977
Ball Robyn L, Bogue Molly A, Liang Hongping and 26 more
Oxidative stress accelerates intestinal tumorigenesis by enhancing 8-oxoguanine-mediated mutagenesis in MUTYH-deficient mice.
Genome research | 2024-02-07 | PMID 38290979
Ohno Mizuki, Takano Noriko, Hidaka Kyoko and 7 more
Mulberrin extends lifespan in Caenorhabditis elegans through detoxification function.
Journal of applied toxicology : JAT | 2024-06-01 | PMID 38291015
Gao Xiaoyan, Yu Jing, Zhang Lijun and 8 more
VEXAS syndrome is characterized by inflammasome activation and monocyte dysregulation.
Nature communications | 2024-01-30 | PMID 38291039
Kosmider Olivier, Possémé Céline, Templé Marie and 31 more
Genes: TNF, UBA1
Diagnostic evaluation in bone marrow failure disorders: what have we learnt to help inform the transplant decision in 2024 and beyond?
Bone marrow transplantation | 2024-04-01 | PMID 38291125
Ciangola Giulia, Santinelli Enrico, McLornan Donal P and 2 more
A genome-wide association study reveals the relationship between human genetic variation and the nasal microbiome.
Communications biology | 2024-01-30 | PMID 38291185
Liu Xiaomin, Tong Xin, Zou Leying and 14 more
Correlation between neuroimaging, neurological phenotype, and functional outcomes in Wilson's disease.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2024-07-01 | PMID 38291197
Moura João, Pinto Catarina, Freixo Pedro and 11 more
GenoBaits®WheatplusEE: a targeted capture sequencing panel for quick and accurate identification of wheat-Thinopyrum derivatives.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2024-01-31 | PMID 38291310
Deng Pingchuan, Du Xin, Wang Yanzhen and 11 more
A genome-wide association study identifies 25(OH)D3-associated genetic variants in the prediabetic Chinese population.
Endocrine | 2024-06-01 | PMID 38291318
Wang Fei, Yu Jingwen, Lin Leweihua and 3 more
Genes: SLC22A1, SLC22A3
DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
EMBO reports | 2024-03-01 | PMID 38291337
Taglini Francesca, Kafetzopoulos Ioannis, Rolls Willow and 16 more
Genes: DNMT3B, DNMT3A
Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature.
BMC infectious diseases | 2024-01-30 | PMID 38291356
Tao Chaoxin, Zhao Min, Zhang Xiaohui and 7 more
When the second comes first- rhabdomyosarcoma preceding heritable retinoblastoma- a case report.
BMC ophthalmology | 2024-01-30 | PMID 38291358
Tripathy Devjyoti, Moulin Alexandre, Bijon Jacques and 4 more
LOGGIC/FIREFLY-2: a phase 3, randomized trial of tovorafenib vs. chemotherapy in pediatric and young adult patients with newly diagnosed low-grade glioma harboring an activating RAF alteration.
BMC cancer | 2024-01-30 | PMID 38291372
van Tilburg Cornelis M, Kilburn Lindsay B, Perreault Sébastien and 23 more
Cryptosporidium species and subtypes identified in human domestic cases through the national microbiological surveillance programme in Sweden from 2018 to 2022.
BMC infectious diseases | 2024-01-30 | PMID 38291399
Bujila Ioana, Troell Karin, Ögren Jessica and 5 more
Behavioral variant frontotemporal dementia associated with GRN and ErbB4 gene mutations: a case report and literature review.
BMC medical genomics | 2024-01-30 | PMID 38291418
Cai Youde, Peng Zhongyong, He Qiansong and 1 more
Rett syndrome in Ireland: a demographic study.
Orphanet journal of rare diseases | 2024-01-31 | PMID 38291497
Zade Komal, Campbell Ciara, Bach Snow and 2 more
Genes: MECP2
Weight development from childhood to motherhood-embodied experiences in women with pre-pregnancy obesity: a qualitative study.
Reproductive health | 2024-01-30 | PMID 38291504
Sandsæter Heidi L, Eik-Nes Trine Tetlie, Getz Linn Okkenhaug and 4 more
Association of the C allele of rs479200 in the EGLN1 gene with COVID-19 severity in Indian population: a novel finding.
Human genomics | 2024-01-30 | PMID 38291512
Harit Renuka, De Sajal, Singh Piyoosh Kumar and 9 more
Evaluation of Combined p57KIP2 Immunohistochemistry and Fluorescent in situ Hybridization Analysis for Hydatidiform Moles Compared with Genotyping Diagnosis.
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists | 2024-09-01 | PMID 38291567
Usui Hirokazu, Hoshimoto Kazufusa, Sato Asuka and 4 more
Inherited thrombophilia gene mutations and risk of venous thromboembolism in patients with cancer: A systematic review and meta-analysis.
American journal of hematology | 2024-04-01 | PMID 38291601
Roy Danielle Carole, Wang Tzu-Fei, Lun Ronda and 6 more
A Molecular Dynamics Simulation Study of the Effects of βGln114 Mutation on the Dynamic Behavior of the Catalytic Site of the Tryptophan Synthase.
Journal of chemical information and modeling | 2024-02-12 | PMID 38291608
Roy Anupom, Karttunen Mikko
Phenotypic switching of vascular smooth muscle cells in atherosclerosis, hypertension, and aortic dissection.
Journal of cellular physiology | 2024-04-01 | PMID 38291732
Elmarasi Mohamed, Elmakaty Ibrahim, Elsayed Basel and 4 more
Residue coevolution and mutational landscape for OmpR and NarL response regulator subfamilies.
Biophysical journal | 2024-03-19 | PMID 38291753
Shibata Mayu, Lin Xingcheng, Onuchic José N and 2 more
Development of a novel five-dye panel for human identification insertion/deletion (INDEL) polymorphisms.
Journal of forensic sciences | 2024-05-01 | PMID 38291825
Avellaneda Lucio L, Johnson Damani T, Gutierrez Ryan and 5 more
DHDDS and NUS1: A Converging Pathway and Common Phenotype.
Movement disorders clinical practice | 2024-01-01 | PMID 38291835
Williams Laura J, Waller Sophie, Qiu Jessica and 9 more
Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia.
Movement disorders : official journal of the Movement Disorder Society | 2024-04-01 | PMID 38291924
Cao Yuwen, Zheng Haoran, Zhu Zeyu and 3 more
A SNP-based genotyping strategy to detect the abuse of homologous blood transfusion from dried blood spots.
Drug testing and analysis | 2024-11-01 | PMID 38291987
Donati Francesco, Natalucci Alice, Concetti Livia and 2 more
Mosaic GJB2 mutations in widespread porokeratotic adnexal ostial nevus: Report of two patients.
The Journal of dermatology | 2024-08-01 | PMID 38292003
Zhao Anqi, Wang Yumeng, Jia Ning and 12 more
Evaluating NetMHCpan performance on non-European HLA alleles not present in training data.
Frontiers in immunology | 2023-01-01 | PMID 38292493
Atkins Thomas Karl, Solanki Arnav, Vasmatzis George and 2 more
Impact of PNPLA3 and TM6SF2 polymorphisms on the prognosis of patients with MASLD and type 2 diabetes mellitus.
Liver international : official journal of the International Association for the Study of the Liver | 2024-04-01 | PMID 38293718
Lavrado Natália Coelho, Salles Gil Fernando, Cardoso Claudia Regina Lopes and 4 more
Family-based genetic analysis in schizophrenia by whole-exome sequence to identify rare pathogenic variants.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2024-07-01 | PMID 38293813
Shang Binli, Yang Runxu, Lian Kun and 7 more
Genes: PKHD1L1, PRKDC, SNAI2, ST18, TFAP2B, TFEB
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.
Genetics in medicine : official journal of the American College of Medical Genetics | 2024-06-01 | PMID 38293907
Zeitz Christina, Navarro Julien, Azizzadeh Pormehr Leila and 21 more
HLA-B gene methylation and expression in Behçet's syndrome: a potential role of epigenetics in the pathogenesis.
Clinical and experimental rheumatology | 2024-10-01 | PMID 38293994
Özkılınç Önen Merve, Everest Elif, Demirci Turna and 6 more
Genetically proxied low-density lipoprotein cholesterol lowering via PCSK9-inhibitor drug targets and risk of congenital malformations.
European journal of preventive cardiology | 2024-06-03 | PMID 38294056
Ardissino Maddalena, Slob Eric A W, Reddy Rohin K and 7 more
Genes: PCSK9
Obesity/cardiometabolic phenotype of heart failure with preserved ejection fraction: mechanisms to recent trials.
Current opinion in cardiology | 2024-03-01 | PMID 38294186
Verma Raj, Dhingra Nitish K, Connelly Kim A
Inducing vulnerability to InhA inhibition restores isoniazid susceptibility in drug-resistant Mycobacterium tuberculosis.
mBio | 2024-03-13 | PMID 38294237
Harrison Gregory A, Wang Erin R, Cho Kevin and 5 more
Prevalence, risk factors and genotyping of chlamydia trachomatis from endocervical specimens of infertile women at a tertiary care hospital, Vietnam.
International journal of STD & AIDS | 2024-05-01 | PMID 38294256
Nguyen Hoa, Do Ngoc Anh, Nguyen Le Van and 5 more
The Extracellular Niche and Tumor Microenvironment Enhance KRAS Inhibitor Efficacy in Pancreatic Cancer.
Cancer research | 2024-04-01 | PMID 38294344
Kumarasamy Vishnu, Wang Jianxin, Frangou Costakis and 7 more
Green Revolution dwarfing Rht genes negatively affected wheat floral traits related to cross-pollination efficiency.
The Plant journal : for cell and molecular biology | 2024-05-01 | PMID 38294345
Schierenbeck Matías, Alqudah Ahmad M, Lantos Edit and 3 more
The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis.
Genetic testing and molecular biomarkers | 2024-01-01 | PMID 38294355
Shen Hao, Gao Zhigang, Ye Qing
[Physical activity: Tools for customized assessment and prescription].
La Revue du praticien | 2023-11-01 | PMID 38294455
d'Alessandro Eugénie
New insights from the genetic work-up in early onset nephrotic syndrome: report from a registry in western India.
Pediatric nephrology (Berlin, Germany) | 2024-07-01 | PMID 38294522
Sharma Jyoti, Saha Anshuman, Ohri Alpana and 16 more
Fetal Diagnosis of Supravalvular Aortic Stenosis and Pulmonary Stenosis in a Family with Non-Syndromic Elastin Mutation.
Pediatric cardiology | 2024-06-01 | PMID 38294523
Kiener Alexander, Lantin M Regina L, Lawrence Emily J and 2 more
Lactase can target cellular differentiation of Acanthamoeba castellanii belonging to the T4 genotype.
Parasitology research | 2024-01-31 | PMID 38294565
Simau Fathimath Afaaf, Ahmed Usman, Khan Khalid Mohammed and 5 more
Impact of heterozygous ALK1 mutations on the transcriptomic response to BMP9 and BMP10 in endothelial cells from hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension donors.
Angiogenesis | 2024-05-01 | PMID 38294582
Al Tabosh T, Liu H, Koça D and 19 more
Genes: BMP10, PAH, LFNG
Antioxidant Genes Variants and Their Association with Sperm DNA Fragmentation.
Biochemical genetics | 2024-12-01 | PMID 38294591
Sharif Fadel A, Ashour Mohammed J, Abuwarda Hadeer N and 4 more
Therapeutic Strategies for Angiogenesis Based on Endothelial Cell Epigenetics.
Journal of cardiovascular translational research | 2024-08-01 | PMID 38294628
Cai Yue, Li Lihua, Shao Chen and 2 more
A novel likely pathogenetic variant p.(Cys235Arg) of the MEN1 gene in multiple endocrine neoplasia type 1 with multifocal glucagonomas.
Journal of endocrinological investigation | 2024-07-01 | PMID 38294658
Smirne C, Giacomini G M, Berton A M and 10 more
Rise of oligodendroglioma hypermutator phenotype from a subclone harboring TP53 mutation after TMZ treatment.
Brain tumor pathology | 2024-04-01 | PMID 38294664
Higuchi Fumi, Uzuka Takeo, Matsuda Hadzki and 6 more
The Impact of Inherited Genetic Variation on DNA Methylation in Prostate Cancer and Benign Tissues of African American and European American Men.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology | 2024-04-03 | PMID 38294689
Delgado Dayana, Gillard Marc, Tong Lin and 8 more
Genes: IMPACT
Detection of polymorphisms in six genes and their association analysis with litter size in sheep.
Animal biotechnology | 2024-11-01 | PMID 38294691
Liu Kai, Liu Yufang, Chu Mingxing
NRAS Mutant Dictates AHCYL1-Governed ER Calcium Homeostasis for Melanoma Tumor Growth.
Molecular cancer research : MCR | 2024-04-02 | PMID 38294692
Cai Chufan, Tu Jiayi, Najarro Jeronimo and 13 more
Optic Neuropathy Associated with POLG Mutations: A Case Series and Literature Review.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society | 2024-12-01 | PMID 38294884
Reitinger Jeremy C, Mackay Devin D
Genes: POLG
What's new in pediatric asthma and rhinitis phenotypes and endotypes?
Current opinion in allergy and clinical immunology | 2024-04-01 | PMID 38295125
Roberto Giulia, Barberi Salvatore, Marseglia Gian Luigi and 1 more
A connection between the ribosome and two S. pombe tRNA modification mutants subject to rapid tRNA decay.
PLoS genetics | 2024-01-01 | PMID 38295128
De Zoysa Thareendra, Hauke Alayna C, Iyer Nivedita R and 6 more
Cerebrospinal Fluid cfDNA Sequencing for Classification of Central Nervous System Glioma.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2024-07-15 | PMID 38295147
Iser Florian, Hinz Felix, Hoffmann Dirk C and 25 more
Rapid and accurate remethylation of DNA in Dnmt3a-deficient hematopoietic cells with restoration of DNMT3A activity.
Science advances | 2024-02-02 | PMID 38295174
Li Yang, Abel Haley J, Cai Michelle and 6 more
Prognostic impact of cooccurring mutations in FLT3-ITD pediatric acute myeloid leukemia.
Blood advances | 2024-05-14 | PMID 38295280
Tarlock Katherine, Gerbing Robert B, Ries Rhonda E and 14 more
Genes: FLT3, EFS, NSD1, NUP98, NPM1, WT1
The glutaminase inhibitor CB-839 targets metabolic dependencies of JAK2-mutant hematopoiesis in MPN.
Blood advances | 2024-05-14 | PMID 38295283
Usart Marc, Hansen Nils, Stetka Jan and 8 more
Genes: JAK2, GLS, CD34, JAK1
Feasibility and Clinical Utility of Reporting Hereditary Cancer Predisposition Pathogenic Variants Identified in Research Germline Sequencing: A Prospective Interventional Study.
JCO precision oncology | 2024-01-01 | PMID 38295319
Hutchcraft Megan L, Zhang Shulin, Lin Nan and 11 more
A Computational Approach: The Functional Effects of Thyroid Peroxidase Variants in Thyroid Cancer and Genetic Disorders.
JCO clinical cancer informatics | 2024-01-01 | PMID 38295322
Sobitan Adebiyi, Gebremedhin Brhan, Yao Qiaobin and 4 more
GxE interaction effects of HCRTR2 single nucleotide polymorphism and adverse childhood experiences on methamphetamine use disorder.
The American journal of drug and alcohol abuse | 2024-01-02 | PMID 38295363
Chen Kai-Ting, Huang Ming-Chyi, Lin Chun and 2 more
Genes: HCRTR2
Identification of Mayaro Virus Genotype D in Rondônia, Brazil.
The American journal of tropical medicine and hygiene | 2024-03-06 | PMID 38295410
Pimentel Edilene Pereira, Queiroz Jackson Alves da Silva, Ribeiro Jessiane Rodrigues and 5 more
CLCLSA: Cross-omics linked embedding with contrastive learning and self attention for integration with incomplete multi-omics data.
Computers in biology and medicine | 2024-03-01 | PMID 38295477
Zhao Chen, Liu Anqi, Zhang Xiao and 6 more
A One Health perspective on the use of genotypic methods for antimicrobial resistance prediction.
Journal of the American Veterinary Medical Association | 2024-03-01 | PMID 38295518
Maddock Kelli J, Burbick Claire R, Cole Stephen D and 7 more
Prevalence of Fabry disease and GLA variants in young patients with acute stroke: The challenge to widen the screening. The Fabry-Stroke Italian Registry.
Journal of the neurological sciences | 2024-02-15 | PMID 38295534
Romani Ilaria, Sarti Cristina, Nencini Patrizia and 62 more
Comparative transcriptome elucidates key genes and pathways related to golden phenotype of Crassostrea gigas.
Comparative biochemistry and physiology. Part D, Genomics & proteomics | 2024-03-01 | PMID 38295536
Min Yue, Li Qi, Yu Hong and 2 more
The occurrence rate of Haarlem and Beijing genotypes among Middle Eastern isolates of multi drug resistant Mycobacterium tuberculosis: A systematic review and meta-analysis.
Respiratory investigation | 2024-03-01 | PMID 38295613
Ferdosnejad Kianoosh, Sholeh Mohammad, Abdolhamidi Rouhollah and 3 more
Harmonizing the forensic nomenclature for STR loci D6S474 and DYS612.
Forensic science international. Genetics | 2024-05-01 | PMID 38295652
Bodner Martin, Ballard David, Borsuk Lisa A and 4 more
Implication of androgen receptor gene dysfunction in human Müllerian duct anomalies.
European journal of obstetrics, gynecology, and reproductive biology | 2024-03-01 | PMID 38295708
Li Lin, Chen Shuya, Li Shenghui and 3 more
Social environment and anogenital distance length phenotype interact to explain testosterone levels in a communally rearing rodent: Part 2: The female side.
Hormones and behavior | 2024-04-01 | PMID 38295731
Correa Loreto A, Aspillaga-Cid Antonia, León Cecilia and 5 more
Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome.
Stem cell research | 2024-03-01 | PMID 38295749
Wang Yi-Bo, Lv Ya-Feng, Zhang Ye and 1 more
The Effects of Myo-Inositol and D-Chiro-Inositol in a Ratio 40:1 on Hormonal and Metabolic Profile in Women with Polycystic Ovary Syndrome Classified as Phenotype A by the Rotterdam Criteria and EMS-Type 1 by the EGOI Criteria.
Gynecologic and obstetric investigation | 2024-01-01 | PMID 38295772
Pustotina Olga, Myers Samuel H, Unfer Vittorio and 1 more
Association Study between SNPs in MST1 and MST2 and H. pylori Infection as well as Noncardia Gastric Carcinogenesis.
Digestive diseases (Basel, Switzerland) | 2024-01-01 | PMID 38295774
Ma Licong, Gao Fang, Dong Wenjie and 2 more
Lipocalin 2 (LCN2) confers acquired resistance to almonertinib in NSCLC through LCN2-MMP-9 signaling pathway.
Pharmacological research | 2024-03-01 | PMID 38295916
Shi Chen, Wang Cong, Fu Zhiwen and 6 more
Genes: LCN2, EGFR, AR
LAT1-dependent placental methionine uptake is a key player in fetal programming of metabolic disease.
Metabolism: clinical and experimental | 2024-04-01 | PMID 38295946
Schroeder Mariana, Fuenzalida Barbara, Yi Nan and 9 more
Women's reproductive risk and genetic predisposition in type 2 diabetes: A prospective cohort study.
Diabetes research and clinical practice | 2024-02-01 | PMID 38295999
Liu Xiaojing, Liu Xiaowen, Huang Ninghao and 6 more
First molecular detection and characterization of Enterocytozoon bieneusi different genotypes in human patients from Italy.
Acta tropica | 2024-04-01 | PMID 38296015
Guadano-Procesi Isabel, Berrilli Federica, Cave David Di
Recurrent MECR R258W causes adult-onset optic atrophy: A case report.
European journal of medical genetics | 2024-04-01 | PMID 38296034
Jia Nan, Yu Shuiqing, Zhang Geng and 3 more
Next-Generation Sequencing Trends among Adult Patients with Select Advanced Tumor Types: A Real-World Evidence Evaluation.
The Journal of molecular diagnostics : JMD | 2024-04-01 | PMID 38296192
Ferreira-Gonzalez Andrea, Hocum Brian, Ko Gilbert and 3 more
[Wolfram-like syndrome: a case report].
[Zhonghua yan ke za zhi] Chinese journal of ophthalmology | 2024-02-11 | PMID 38296324
Zhu B X, Zhang L, Wang H Y and 2 more
Correlation of polymorphism in Toll-Like Receptor (TLR1 and TLR2) genes with susceptibility of pulmonary tuberculosis in Doda region of India.
The Indian journal of tuberculosis | 2024-01-01 | PMID 38296390
Zargar Azhar Saleem, Borole Kumudini, Rai Rohit
Clinical Challenges of Emerging Acquired Autoinflammatory Diseases, Including VEXAS Syndrome.
Internal medicine (Tokyo, Japan) | 2025-01-01 | PMID 38296470
Kirino Yohei
A 70-year-old Woman with Asymptomatic Ferroportin Disease.
Internal medicine (Tokyo, Japan) | 2024-09-01 | PMID 38296485
Ishikawa Tetsuya, Tatsumi Yasuaki, Kato Koichi and 8 more
Association of hTERT Gene Polymorphism and Colorectal Cancer (CRC) Risk in the Chinese Han Population.
The Tohoku journal of experimental medicine | 2024-06-28 | PMID 38296486
Fu Xianxian, Xiong Yanyan, Tang Renjin and 3 more
Relationship of Toll-Like Receptor 7, 9, and 10 Polymorphisms and the Severity of Coronavirus Disease 2019.
Japanese journal of infectious diseases | 2024-05-23 | PMID 38296538
Bayyurt Burcu, Baltacı Sevgi, Şahin Nil Özbilüm and 2 more
Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People.
International heart journal | 2024-01-01 | PMID 38296580
Miura Aya, Yamamoto Takuma, Funayama Kazuhisa and 4 more
Gut Microbiome and Stroke: a Bidirectional Mendelian Randomisation Study in East Asian and European Populations.
Stroke and vascular neurology | 2024-12-30 | PMID 38296585
Cheng Shiyao, Zheng Hao, Wei Yuandan and 7 more
Stepwise genetic approach for the diagnosis of primary ciliary dyskinesia in highly consanguineous populations.
Archives of disease in childhood | 2024-04-18 | PMID 38296613
Gatt Dvir, Golan Tripto Inbal, Levanon Eran and 5 more
Genes: DNAAF3, DNAAF5, DNAL1, ZMYND10
[Progress of BRAF Gene Alteration in Non-small Cell Lung Cancer].
Zhongguo fei ai za zhi = Chinese journal of lung cancer | 2024-01-20 | PMID 38296628
Deng Libian, Yang Yaxian, Huang Jian
Molecular diagnosis, clinical evaluation and phenotypic spectrum of Townes-Brocks syndrome: insights from a large Chinese hearing loss cohort.
Journal of medical genetics | 2024-04-19 | PMID 38296632
Yan Xiaohong, Wang Jing, Yang Wen and 11 more
Genes: SALL1, DACT1