Phenotyping of FGF12AV52H mutation in mouse implies a complex FGF12 network.
Neurobiology of disease | 2024-10-01 | PMID 39142611
Huang Jianyu, Sun Chongyang, Zhu Qian and 9 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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 9556 of 10600
The C-terminal 4CXXC-type zinc finger domain of CDCA7 recognizes hemimethylated DNA and modulates activities of chromatin remodeling enzyme HELLS.
Nucleic acids research | 2024-09-23 | PMID 39142653
Shinkai Akeo, Hashimoto Hideharu, Shimura Chikako and 8 more
Genes: CDCA7, HELLS
Pathogenesis-driven treatment of primary pulmonary alveolar proteinosis.
European respiratory review : an official journal of the European Respiratory Society | 2024-07-01 | PMID 39142709
Lettieri Sara, Bonella Francesco, Marando Vincenzo Alfredo and 3 more
Multi-omic Analyses Shed Light on The Genetic Control of High-altitude Adaptation in Sheep.
Genomics, proteomics & bioinformatics | 2024-07-03 | PMID 39142817
Li Chao, Chen Bingchun, Langda Suo and 31 more
Genes: HBB, HBE1, EGLN1
Genome-wide Studies Reveal Genetic Risk Factors for Hepatic Fat Content.
Genomics, proteomics & bioinformatics | 2024-07-03 | PMID 39142818
Li Yanni, van den Berg Eline H, Kurilshikov Alexander and 12 more
Genes: GCM1, APOE, FTO, PNPLA3, TM6SF2, ZPR1
[Epidemiological characteristics of human respiratory syncytial virus in influenza-like illness in Shenzhen City from 2019 to 2023].
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] | 2024-08-06 | PMID 39142877
Sun Y, Wu W H, Huang Y L and 6 more
[Analysis of virus gene subtypes and drug resistance monitoring results of newly reported HIV/AIDS population in Anhui Province from 2020 to 2023].
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine] | 2024-08-06 | PMID 39142890
Qin Y Z, Shen Y L, Liu A W and 5 more
Occurrence of blaNDM-1, blaNDM-5, blaNDM-7, and blaKPC-2 genes in clinical isolates of enterobacterales with high genetic variability, from colonization and infection in patients with or without COVID-19, from a hospital in Brazil.
Journal of applied microbiology | 2024-08-05 | PMID 39143035
Martins Lamartine Rodrigues, Pimentel Maria Izabely Silva, de Oliveira Érica Maria and 3 more
Genome-wide large-scale multi-trait analysis characterizes global patterns of pleiotropy and unique trait-specific variants.
Nature communications | 2024-08-14 | PMID 39143063
Qi Guanghao, Chhetri Surya B, Ray Debashree and 4 more
Identification of interactions between genetic risk scores and dietary patterns for personalized prevention of kidney dysfunction in a population-based cohort.
Nutrition & diabetes | 2024-08-14 | PMID 39143076
Jang Min-Jae, Tan Li-Juan, Park Min Young and 2 more
Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model.
Nature communications | 2024-08-14 | PMID 39143095
Qiu Hangyuan, Sun Yaxun, Wang Xiaochen and 11 more
Genes: LMNA, SIRT1, RYR2, SUN1
The spectrum of novel ABCB11 gene variations in children with progressive familial intrahepatic cholestasis type 2 in Pakistani cohorts.
Scientific reports | 2024-08-14 | PMID 39143102
Riaz Hafsa, Zheng Bixia, Zheng Yucan and 7 more
Molecular basis of facilitated target search and sequence discrimination of TALE homeodomain transcription factor Meis1.
Nature communications | 2024-08-14 | PMID 39143123
Choi Seo-Ree, Lee Juyong, Seo Yeo-Jin and 6 more
Molecular characteristics and oncogenic role of CHD family genes: a pan-cancer analysis based on bioinformatic and biological analysis.
Scientific reports | 2024-08-15 | PMID 39143142
Lu Yujia, Jiang Jiebang, He Zhihong and 3 more
Saliva-derived DNA is suitable for the detection of clonal haematopoiesis of indeterminate potential.
Scientific reports | 2024-08-14 | PMID 39143154
O'Reilly Robert L, Burke Jared, Harraka Philip and 10 more
Isocitrate dehydrogenase (IDH) 1 and 2 mutations predict better outcome in patients with acute myeloid leukemia undergoing allogeneic hematopoietic cell transplantation: a study of the ALWP of the EBMT.
Bone marrow transplantation | 2024-11-01 | PMID 39143183
Mohty Razan, Bazarbachi Abdul Hamid, Labopin Myriam and 20 more
Origin and evolution of the bread wheat D genome.
Nature | 2024-09-01 | PMID 39143210
Cavalet-Giorsa Emile, González-Muñoz Andrea, Athiyannan Naveenkumar and 68 more
Continuously fluctuating selection reveals fine granularity of adaptation.
Nature | 2024-10-01 | PMID 39143223
Bitter M C, Berardi S, Oken H and 4 more
A lmod1a mutation causes megacystis microcolon intestinal hypoperistalsis in a CRISPR/Cas9-modified zebrafish model.
Pediatric surgery international | 2024-08-14 | PMID 39143337
Kalim Alvin Santoso, Nagata Kouji, Toriigahara Yukihiro and 8 more
E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant?
European journal of pediatrics | 2024-10-01 | PMID 39143349
Orouk Awaad Elham, Khoury Lana, van Straalen Joeri W and 5 more
Genome-wide study identifies novel genes associated with bone toxicities in children with acute lymphoblastic leukaemia.
British journal of haematology | 2024-11-01 | PMID 39143423
Zhu Qianqian, Nambiar Ram, Schultz Emily and 17 more
Active spread of β-thalassemia beyond the thalassemia belt: A study on a Russian population.
Clinical genetics | 2025-01-01 | PMID 39143497
Shchemeleva Ekaterina, Salomashkina Valentina V, Selivanova Daria and 4 more
Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families.
BMC ophthalmology | 2024-08-14 | PMID 39143519
Khan Jahangir, Asif Saaim, Ghani Shamsul and 9 more
Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism.
BMC genomics | 2024-08-14 | PMID 39143522
Zouaghi Yassine, Choudhary Anbreen Mazhar, Irshad Saba and 13 more
Targeted gene sequencing reveals disparate genomic mutations between young and older adults in renal cell carcinoma.
BMC cancer | 2024-08-14 | PMID 39143525
Zhang Baochao, Xie Tianlei, Li Hao and 5 more
Molecular heterogeneity and treatment outcome of EGFR exon 20 insertion mutations in Chinese patients with advanced non-small cell lung cancer: insights from a large-scale real-world study.
BMC cancer | 2024-08-14 | PMID 39143560
Wu Weirui, Yu Silin, Huang Jinsheng and 3 more
PARK2 as a susceptibility factor for nontuberculous mycobacterial pulmonary disease.
Respiratory research | 2024-08-14 | PMID 39143598
Park Youngmok, Hong Ji Won, Ahn Eunsol and 2 more
Mendelian randomization implicates causal association between epigenetic age acceleration and age-related eye diseases or glaucoma endophenotypes.
Clinical epigenetics | 2024-08-14 | PMID 39143611
Chen Jiawei, Yuan Xiang-Ling, Zhou Xiaoyu and 3 more
Unveiling distinct kinematic profiles among total knee arthroplasty candidates through clustering technique.
Journal of orthopaedic surgery and research | 2024-08-14 | PMID 39143616
Abou-Abbas Lina, Hagemeister Nicola, Ouakrim Youssef and 5 more
GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics.
Journal of translational medicine | 2024-08-14 | PMID 39143639
Li Xinxiao, Guo Shengnan, Sun Yangyang and 6 more
Genes: GABRG2
FTO gene polymorphism and susceptibility to polycystic ovary syndrome: A meta-analysis.
The journal of obstetrics and gynaecology research | 2024-09-01 | PMID 39143730
Zhang Chuanhua, Yu Jiali
Non-alcoholic fatty liver disease and heart failure: A comprehensive bioinformatics and Mendelian randomization analysis.
ESC heart failure | 2024-12-01 | PMID 39143741
Zhang Yayun, Feng Lu, Guan Xin and 3 more
[A case report of Danon's disease with dilated phenotype].
Zhonghua xin xue guan bing za zhi | 2024-08-24 | PMID 39143788
Tang Y, Cui C, Yang S J and 1 more
[Research progress of PRKAG2 cardiac syndrome].
Zhonghua xin xue guan bing za zhi | 2024-08-24 | PMID 39143794
Cheng W P, Song X W, Zhang B L
[Gene mutation characteristics of clinical stage ⅠA lung adenocarcinoma and their relations with patients' long-term prognosis].
Zhonghua zhong liu za zhi [Chinese journal of oncology] | 2024-08-23 | PMID 39143798
Zhang L, Liu M W, Li L and 6 more
Association between hypothyroidism and nephrotic syndrome: a bidirectional two-sample Mendelian randomization analysis.
Renal failure | 2024-12-01 | PMID 39143823
Liu Can, Shen Jiaxuan, Ding Zhaoran and 2 more
Genotyping and Antiretroviral Drug Resistance Mutations among HIV Patients in Southern Santa Catarina, Brazil.
Current HIV research | 2024-01-01 | PMID 39143878
Mendes Marcon Chaiana Esmeraldino, Schlindwein Aline Daiane, de Macedo Brigido Luis Fernando and 3 more
Descriptive epidemiology and phylogenetic analysis of highly pathogenic avian influenza H5N1 clade 2.3.4.4b in British Columbia (B.C.) and the Yukon, Canada, September 2022 to June 2023.
Emerging microbes & infections | 2024-12-01 | PMID 39143912
Russell Shannon L, Andrew Cassandra L, Yang Kevin C and 21 more
Targeting Solvent-Front Mutations for Kinase Drug Discovery: From Structural Basis to Design Strategies.
Journal of medicinal chemistry | 2024-09-12 | PMID 39143914
Zhou Yang, Kang Jibo, Lu Xiaoyun
Empirical Therapy Versus Tailored Therapy of Helicobacter pylori in Korea: Results of the K-CREATE Study.
Helicobacter | 2000-01-01 | PMID 39143948
Kim Joon Sung, Kim Byung-Wook, Kim Jin Il and 15 more
Evaluating the causal effect of circulating proteome on the risk of inflammatory bowel disease-related traits using Mendelian randomization.
Frontiers in immunology | 2024-01-01 | PMID 39144148
Li Beining, Hu Ping, Liang Hongyan and 5 more
MED23 pathogenic variant: genomic-phenotypic analysis.
Journal of medicine and life | 2024-05-01 | PMID 39144687
Bamaga Ahmed, Muthaffar Osama, Alyazidi Anas and 7 more
Trends and characteristics of the metabolically healthy obese phenotype in an Arab population.
Frontiers in public health | 2024-01-01 | PMID 39145170
Wani Kaiser, Kumar Balvir, Al-Daghri Nasser M and 1 more
Sex Dimorphism in Pulmonary Arterial Hypertension Associated With Autoimmune Diseases.
Arteriosclerosis, thrombosis, and vascular biology | 2024-10-01 | PMID 39145392
Krzyżewska Anna, Kurakula Kondababu
MAPT mutations associated with familial tauopathies lead to formation of conformationally distinct oligomers that have cross-seeding ability.
Protein science : a publication of the Protein Society | 2024-09-01 | PMID 39145409
Bhopatkar Anukool A, Bhatt Nemil, Haque Md Anzarul and 4 more
Genes: MAPT
Strategies for the prevention or reversal of PARP inhibitor resistance.
Expert review of anticancer therapy | 2024-10-01 | PMID 39145413
Mitri Zahi, Goodyear Shaun M, Mills Gordon
Overexpression of the transcription factor ANAC017 results in a genomes uncoupled phenotype under lincomycin.
The Plant journal : for cell and molecular biology | 2024-10-01 | PMID 39145415
Zhu Yanqiao, Narsai Reena, He Cunman and 5 more
Mendelian randomization of plasma lipidome, inflammatory proteome and heart failure.
ESC heart failure | 2024-12-01 | PMID 39145416
Zheng Zequn, Tan Xuerui
Biochemical characterization of naturally occurring mutations in SARS-CoV-2 RNA-dependent RNA polymerase.
Protein science : a publication of the Protein Society | 2024-09-01 | PMID 39145418
Danda Matěj, Klimešová Anna, Kušková Klára and 6 more
Interference of default mode on attention networks in adults with attention-deficit/hyperactivity disorder and its association with genetic variants and treatment outcomes.
CNS neuroscience & therapeutics | 2024-08-01 | PMID 39145420
Liu Lu, Chen Di, Huang Fang and 10 more
SLC44A2-mediated phenotypic switch of vascular smooth muscle cells contributes to aortic aneurysm.
The Journal of clinical investigation | 2024-08-15 | PMID 39145443
Xing Mengen, Chen Wanqi, Ji Yachen and 1 more
Genes: SLC44A2, ITGB3, NRP1
Mouse sarcopenia model reveals sex- and age-specific differences in phenotypic and molecular characteristics.
The Journal of clinical investigation | 2024-06-11 | PMID 39145448
Kerr Haiming L, Krumm Kora, Anderson Barbara and 14 more
Human genetics and epigenetics of alcohol use disorder.
The Journal of clinical investigation | 2024-08-15 | PMID 39145449
Zhou Hang, Gelernter Joel
Rare genetic variants provide a mechanistic basis for immune imbalance in IgG4-related disease.
The Journal of clinical investigation | 2024-08-15 | PMID 39145453
Ciavatta Dominic J
Genes: IKZF1, UBR4
The association between the single-nucleotide polymorphism of site rs1333040 in region 9p21 and the risk of coronary heart disease in Chinese population.
Acta cardiologica | 2024-09-01 | PMID 39145594
Zhao Chen-Hui
Natural selection and recombination at host-interacting lipoprotein loci drive genome diversification of Lyme disease and related bacteria.
mBio | 2024-09-11 | PMID 39145656
Akther Saymon, Mongodin Emmanuel F, Morgan Richard D and 17 more
Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial.
ESC heart failure | 2024-12-01 | PMID 39145700
Garcia-Pavia Pablo, Lakdawala Neal K, Sinagra Gianfranco and 10 more
Vitreoretinopathy in Asymptomatic Children With CTNNB1 Syndrome.
JAMA ophthalmology | 2024-09-01 | PMID 39145965
Bedoukian Emma C, Forbes Grace, Scoles Drew
Genes: CTNNB1
Identification of pathways to high-level vancomycin resistance in Clostridioides difficile that incur high fitness costs in key pathogenicity traits.
PLoS biology | 2024-08-01 | PMID 39146240
Buddle Jessica E, Thompson Lucy M, Williams Anne S and 6 more
Genetic structure of black soldier flies in northern Iran.
PloS one | 2024-01-01 | PMID 39146257
Boukan Afrooz, Nozari Jamasb, Naseri Karimi Nazanin and 3 more
Evaluation of the binding interactions between Plasmodium falciparum Kelch-13 mutant recombinant proteins with artemisinin.
PloS one | 2024-01-01 | PMID 39146276
Md Yusuf Noorazian, Azman Aisya Nazura, Abdul Aziz Amirul Adli and 3 more
Phytochemical profiling of soybean genotypes using GC-MS and UHPLC-DAD/MS.
PloS one | 2024-01-01 | PMID 39146325
Li Shuxian, Wang Mei, Lee Joseph
Finemap-MiXeR: A variational Bayesian approach for genetic finemapping.
PLoS genetics | 2024-08-01 | PMID 39146375
Akdeniz Bayram Cevdet, Frei Oleksandr, Shadrin Alexey and 5 more
Sequence typing of Haemophilus ducreyi isolated from patients in the Namatanai region of Papua New Guinea: Infections by Class I and Class II strain types differ in ulcer duration and resurgence of infection after azithromycin treatment.
PLoS neglected tropical diseases | 2024-08-01 | PMID 39146379
Medappa Monica, Pospíšilová Petra, John Lucy N and 4 more
Comprehensive analysis of the functional impact of single nucleotide variants of human CHEK2.
PLoS genetics | 2024-08-01 | PMID 39146382
McCarthy-Leo Claire E, Brush George S, Pique-Regi Roger and 3 more
Clinical and molecular features of early onset pancreatic adenocarcinoma.
International journal of cancer | 2024-12-01 | PMID 39146492
Rémond Maxime, Smolenschi Cristina, Tarabay Anthony and 16 more
Genes: BRCA1, CDKN2A, KRAS
Alzheimer's disease risk gene CD2AP is a dose-sensitive determinant of synaptic structure and plasticity.
Human molecular genetics | 2024-10-07 | PMID 39146503
Pavešković Matea, De-Paula Ruth B, Ojelade Shamsideen A and 16 more
Genes: CD2AP, CD2
RNF43 in cancer: Molecular understanding and clinical significance in immunotherapy.
The journal of gene medicine | 2024-08-01 | PMID 39146560
Huo Xingfa, Han Weizhong, Yang Zhen and 3 more
Genes: RNF43
The antitumor activity of osimertinib plus palbociclib in non-small cell lung cancer patient-derived xenograft (PDX)/2D/3D culture models harboring EGFR amplification and CDKN2A/2B homozygous deletions.
Neoplasia (New York, N.Y.) | 2024-11-01 | PMID 39146623
Fu Jen-Fen, Hsu Cheng-Lung, Hsu Ping-Chih
The significance of recurrent de novo amino acid substitutions that emerged during chronic SARS-CoV-2 infection: an observational study.
EBioMedicine | 2024-09-01 | PMID 39146693
Ip Jonathan Daniel, Chu Wing-Ming, Chan Wan-Mui and 11 more
The epilepsy phenotype of KCNK4-related neurodevelopmental disease.
Seizure | 2024-10-01 | PMID 39146707
Krygier Magdalena, Ziętkiewicz Szymon, Talaśka-Liczbik Weronika and 5 more
Phenotypic and genotypic characteristics of children with PCDH19 clustering epilepsy in China.
Seizure | 2024-10-01 | PMID 39146709
Feng Weixing, Wang Zihan, Wang Xiaohui and 6 more
Factors associated with Edinburgh Cognitive and Behavioural ALS Screen (ECAS) alteration at time of diagnosis, in amyotrophic lateral sclerosis.
Clinical neurology and neurosurgery | 2024-10-01 | PMID 39146722
Ginanneschi Federica, Pucci Barbara, Casali Stefania and 3 more
Pathophysiology of the ascending aorta: Impact of dilation and valve phenotype on large-scale blood flow coherence detected by 4D flow MRI.
Computer methods and programs in biomedicine | 2024-10-01 | PMID 39146759
Calò Karol, Guala Andrea, Mazzi Valentina and 7 more
Genomic patterns of somatic mutations provide new prognostic, therapeutic, and biological insights in cancer.
Cell genomics | 2024-08-14 | PMID 39146802
Tseitline Dana, Cohen Yuval, Adar Sheera
Streptococcus pneumoniae carriage, serotypes, genotypes, and antimicrobial resistance trends among children in Portugal, after introduction of PCV13 in National Immunization Program: A cross-sectional study.
Vaccine | 2024-09-17 | PMID 39146858
Candeias Catarina, Almeida Sónia T, Paulo A Cristina and 8 more
Implication of Apolipoprotein E gene variants in pediatric-onset multiple sclerosis: Possible association with disease susceptibility and its clinical characteristics, in a Hellenic cohort.
Multiple sclerosis and related disorders | 2024-10-01 | PMID 39146895
Skarlis Charalampos, Markoglou Nikolaos, Artemiadis Artemios and 4 more
Comparative phenotypic and transcriptomic analysis reveals genotypic differences in nitrogen use efficiency in sorghum.
Plant physiology and biochemistry : PPB | 2024-10-01 | PMID 39146913
Liu Chunjuan, Gu Wendong, Liu Chang and 3 more
Molecular impact of mutations in RNA splicing factors in cancer.
Molecular cell | 2024-10-03 | PMID 39146933
Zhang Qian, Ai Yuxi, Abdel-Wahab Omar
Genes: RBM10, SF3B1, SRSF2, U2AF1
Genomic dynamics of the Lower Yellow River Valley since the Early Neolithic.
Current biology : CB | 2024-09-09 | PMID 39146937
Du Panxin, Zhu Kongyang, Wang Minghui and 43 more
Extensive immune receptor repertoire diversity in disease-resistant rice landraces.
Current biology : CB | 2024-09-09 | PMID 39146939
Gladieux Pierre, van Oosterhout Cock, Fairhead Sebastian and 11 more
Genomic stasis over millions of years in subseafloor sediment.
Environmental microbiology | 2024-07-01 | PMID 39146976
Garber Arkadiy I, Ramírez Gustavo A, D'Hondt Steven
Association between obesity phenotypes and dietary patterns: A two-step cluster analysis based on the China multi-ethnic cohort study.
Preventive medicine | 2024-10-01 | PMID 39146982
Hu Yuxin, Zhang Yuxin, Zhong Jianqin and 3 more
Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutation.
Gene | 2024-12-20 | PMID 39147111
Chen Yingqi, Wei Xiaoyang, Ci Xiaorui and 2 more
NOD1 and NOD2 genetic variants: Impact on hepatocellular carcinoma susceptibility and progression in Moroccan population.
Gene | 2024-12-30 | PMID 39147112
Zerrad Chaimaa, Lkhider Mustapha, Bouqdayr Meryem and 6 more
Genetic admixture predictors of fetal alcohol spectrum disorders (FASD) in a South African population.
Gene | 2024-12-30 | PMID 39147113
Carter R Colin, Yang Zikun, Akkaya-Hocagil Tugba and 8 more
The interaction between TMEM161B (rs768705) and paranoid personality traits in relation to the risk of major depressive disorder: Results form a longitudinal study of 7642 Chinese freshmen.
Journal of affective disorders | 2024-11-15 | PMID 39147160
Luo Linlin, Xu Ruixue, Mu Fuqin and 9 more
Spatially Resolved Niche and Tumor Microenvironmental Alterations in Gastric Cancer Peritoneal Metastases.
Gastroenterology | 2024-12-01 | PMID 39147169
Zhao Joseph J, Ong Chin-Ann Johnny, Srivastava Supriya and 39 more
Genes: GC, CDH1, CLDN18, ELF3, PIGR
Harmonized coexistence of intragenomic variations in diatom Skeletonema strains.
Environmental research | 2024-12-01 | PMID 39147184
Liu Shuya, Ding Xiangxiang, Liu Kuiyan and 1 more
The first Brazilian clinical report of Kleefstra syndrome, including semicircular canals agenesis as a possible phenotype expansion.
European journal of medical genetics | 2024-10-01 | PMID 39147273
Da Cás Eduardo, Pires Lucas V L, Linnenkamp Bianca D W and 6 more
Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia.
The Journal of allergy and clinical immunology | 2024-11-01 | PMID 39147326
Soomann Maarja, Bily Viktor, Elgizouli Magdeldin and 27 more
Identification of whole-genome mutations and structural variations of bile cell-free DNA in cholangiocarcinoma.
Genomics | 2024-09-01 | PMID 39147332
Yin Lei, Duan Anqi, Zhang Wei and 18 more
Genes: KRAS, TP53
Radix Isatidis polysaccharide (RIP) alleviates QX-genotype infectious bronchitis virus-induced interstitial nephritis through the Nrf2/NLRP3/Caspase-3 signaling pathway.
International journal of biological macromolecules | 2024-10-01 | PMID 39147344
Xiang Xuelian, Huang Yamei, Shen Yuxi and 8 more
Unravelling the genomic and environmental diversity of the ubiquitous Solirubrobacter.
Environmental microbiology | 2024-07-01 | PMID 39147372
Jara-Servin Angélica, Mejia Gerardo, Romero Miguel F and 2 more
Heterogenetic mechanism in multidimensional pit mud with different fermentation years: From microbial structure dynamic succession to metabolism phenotypes.
Food research international (Ottawa, Ont.) | 2024-09-01 | PMID 39147493
Ren Dongliang, Liu Shuangping, Qin Hui and 4 more
Regional variation and adaptive evolution in Bifidobacterium pseudocatenulatum: Insights into genomic and functional diversity in human gut.
Food research international (Ottawa, Ont.) | 2024-09-01 | PMID 39147525
Wu Qiong, Li Weicheng, Kwok Lai-Yu and 3 more
Benchmarking bulk and single-cell variant-calling approaches on Chromium scRNA-seq and scATAC-seq libraries.
Genome research | 2024-09-20 | PMID 39147582
Wiens Matthew, Farahani Hossein, Scott R Wilder and 2 more
Sotos Syndrome: Deep Neuroimaging Phenotyping Reveals a High Prevalence of Malformations of Cortical Development.
AJNR. American journal of neuroradiology | 2024-10-03 | PMID 39147584
Neeman Bar, Sudhakar Sniya, Biswas Asthik and 17 more
Genes: NSD1
Evaluating the evidence for genotype-informed Bayesian dosing of tacrolimus in children undergoing solid organ transplantation: A systematic literature review.
British journal of clinical pharmacology | 2024-11-01 | PMID 39147586
Khatri Dhrita, Felmingham Ben, Moore Claire and 6 more
Effect of CYP3A5 Gene Polymorphisms on Tacrolimus Blood Concentrations and Adverse Events in Allogeneic Hematopoietic Stem Cell Transplant Patients.
Transplantation proceedings | 2024-09-01 | PMID 39147616
Jiang Jia, Luan Jiajie