The association of vascular endothelial growth factor related SNPs and circulating iron levels might depend on body mass index.
Frontiers in bioscience (Landmark edition) | 2022-01-18 | PMID 35090332
Chedid Pia, Salami Ali, Ibrahim Mariam and 2 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 8823 of 10600
Genetic variants in obesity-related genes and the risk of osteoporotic fracture. The Hortega Follow-up Study.
Frontiers in bioscience (Landmark edition) | 2022-01-18 | PMID 35090337
Usategui-Martín Ricardo, Pérez-Castrillón Jose Luis, Briongos-Figuero Laisa and 7 more
Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.
BMC endocrine disorders | 2022-01-28 | PMID 35090434
Liu Qingxu, Yin Xiaoqin, Li Pin
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC medical informatics and decision making | 2022-01-28 | PMID 35090449
Yu Jingzhi, Pacheco Jennifer A, Ghosh Anika S and 19 more
Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Reproductive biology and endocrinology : RB&E | 2022-01-28 | PMID 35090489
Li Peng, Ji Zhiyong, Zhi Erlei and 12 more
Mendelian randomization highlights significant difference and genetic heterogeneity in clinically diagnosed Alzheimer's disease GWAS and self-report proxy phenotype GWAX.
Alzheimer's research & therapy | 2022-01-28 | PMID 35090530
Liu Haijie, Hu Yang, Zhang Yan and 7 more
Transcriptome analysis of Echinococcus granulosus sensu stricto protoscoleces reveals differences in immune modulation gene expression between cysts found in cattle and sheep.
Veterinary research | 2022-01-28 | PMID 35090558
Pereira Ismael, Hidalgo Christian, Stoore Caroll and 9 more
Mouse models characterize GNAO1 encephalopathy as a neurodevelopmental disorder leading to motor anomalies: from a severe G203R to a milder C215Y mutation.
Acta neuropathologica communications | 2022-01-28 | PMID 35090564
Silachev Denis, Koval Alexey, Savitsky Mikhail and 4 more
SNP-based breeding for broiler resistance to ascites and evaluation of correlated production traits.
Hereditas | 2022-01-28 | PMID 35090566
Lee Katie Pepper, Anthony Nicholas B, Orlowski Sara K and 1 more
Trans-ancestral fine-mapping of MHC reveals key amino acids associated with spontaneous clearance of hepatitis C in HLA-DQβ1.
American journal of human genetics | 2022-02-03 | PMID 35090584
Valencia Ana, Vergara Candelaria, Thio Chloe L and 30 more
Harnessing tissue-specific genetic variation to dissect putative causal pathways between body mass index and cardiometabolic phenotypes.
American journal of human genetics | 2022-02-03 | PMID 35090585
Leyden Genevieve M, Shapland Chin Yang, Davey Smith George and 4 more
Natural and human-driven selection of a single non-coding body size variant in ancient and modern canids.
Current biology : CB | 2022-02-28 | PMID 35090588
Plassais Jocelyn, vonHoldt Bridgett M, Parker Heidi G and 23 more
SARS-CoV-2 mRNA vaccine induces robust specific and cross-reactive IgG and unequal neutralizing antibodies in naive and previously infected people.
Cell reports | 2022-02-01 | PMID 35090596
Narowski Tara M, Raphel Kristin, Adams Lily E and 7 more
The rising tide of early-onset colorectal cancer: a comprehensive review of epidemiology, clinical features, biology, risk factors, prevention, and early detection.
The lancet. Gastroenterology & hepatology | 2022-03-01 | PMID 35090605
Patel Swati G, Karlitz Jordan J, Yen Timothy and 2 more
Inflammatory response in relation to COVID-19 and other prothrombotic phenotypes.
Reumatologia clinica | 2022-01-01 | PMID 35090606
Páramo José A
Neural network-based integration of polygenic and clinical information: development and validation of a prediction model for 10-year risk of major adverse cardiac events in the UK Biobank cohort.
The Lancet. Digital health | 2022-02-01 | PMID 35090679
Steinfeldt Jakob, Buergel Thore, Loock Lukas and 12 more
Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia.
Brain & development | 2022-05-01 | PMID 35090779
Ayaz Akif, Uzunhan Tugce Aksu, Aydin Kursad
Association of MTOR and PDGFRA gene polymorphisms with different degrees of myopia severity.
Experimental eye research | 2022-04-01 | PMID 35090889
Li Xuan, Long Jianxiong, Liu Yue and 5 more
Towards unveiling the nature of short SERPINA1 transcripts: Avoiding the main ORF control to translate alpha1-antitrypsin C-terminal peptides.
International journal of biological macromolecules | 2022-04-01 | PMID 35090941
Maslakova A A, Didych D A, Golyshev S A and 7 more
Are we finally getting personal? Moving towards a personalized approach in chronic lymphocytic leukemia.
Seminars in cancer biology | 2022-09-01 | PMID 35090979
Albi Elisa, Capasso Antonella, Schiattone Luana and 2 more
Vitamin D modulates cortical transcriptome and behavioral phenotypes in an Mecp2 heterozygous Rett syndrome mouse model.
Neurobiology of disease | 2022-04-01 | PMID 35091041
Ribeiro Mayara C, MacDonald Jessica L
Allele С (rs5186) of at1r is associated with the severity of COVID-19 in the Ukrainian population.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2022-03-01 | PMID 35091110
Izmailova O, Shlykova O, Vatsenko A and 4 more
Recurrent missense variant in the nuclear export signal of FMR1 associated with FXS-like phenotype including intellectual disability, ASD, facial abnormalities.
European journal of medical genetics | 2022-03-01 | PMID 35091116
Mangano Giuseppe Donato, Fontana Antonina, Salpietro Vincenzo and 3 more
The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies.
European journal of medical genetics | 2022-03-01 | PMID 35091117
Arnaud Lionel, Abi Warde Marie-Thérèse, Barcia Giulia and 22 more
Estimation of co-variance components and genetic parameters of fertility and production traits in crossbred cattle of Kerala.
Theriogenology | 2022-03-15 | PMID 35091173
Valsalan Jamuna, Sadan Tina, Anilkumar Kulangara and 1 more
Analysis of mixed DNA profiles from the RapidHIT™ ID platform using probabilistic genotyping software STRmix™.
Forensic science international. Genetics | 2022-05-01 | PMID 35091215
Ward Denise, Henry Julianne, Taylor Duncan
Pharmacological antagonism of EP2 receptor does not modify basal cardiovascular and respiratory function, blood cell counts, and bone morphology in animal models.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie | 2022-03-01 | PMID 35091236
Rawat Varun, Banik Avijit, Amaradhi Radhika and 5 more
Generation of three lines from multiorgan venous and lymphatic defect syndrome patients.
Stem cell research | 2022-04-01 | PMID 35091306
Hu Xiaojun, Mao Junjie, Zhang Ke and 6 more
Establishment of the induced pluripotent stem cell line PLAFMCi006-A from peripheral blood mononuclear cells of polycystic kidney disease patients with PKD2 gene mutation.
Stem cell research | 2022-04-01 | PMID 35091308
Ma Yuxiang, Shang Shunlai, Shi Meihan and 3 more
Generation of human induced pluripotent stem cells from cystic fibrosis patient carrying nonsense mutation (p.S308X) in CFTR gene.
Stem cell research | 2022-04-01 | PMID 35091309
Khor Winnie, Hwang Tzyh-Chang, Wang Chih-Chien and 4 more
Association between Fok1 and TaqI polymorphisms of vitamin D receptor gene with the severity of stenosis and calcification in carotid bulb in patients with ischemic stroke.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2022-03-01 | PMID 35091316
Foroughinia Farzaneh, Morovati Najmeh, Safari Anahid and 5 more
Clonal hematopoiesis: Molecular and clinical implications.
Leukemia research | 2022-02-01 | PMID 35091334
Kusne Yael, Xie Zhuoer, Patnaik Mrinal M
Early-onset Parkinson's disease with atypical molecular imaging abnormalities in a patient carrying the de novo PRKCG mutation.
Parkinsonism & related disorders | 2022-02-01 | PMID 35091391
Chen Yueting, Liu Peng, Cen Zhidong and 3 more
Application of liquid biopsy-based targeted capture sequencing analysis to improve the precision treatment of non-small cell lung cancer by tyrosine kinase inhibitors.
BMJ open respiratory research | 2022-01-01 | PMID 35091437
Zhang Lei, Coffin John, Formenti Kim and 2 more
Comparative Analysis and Isoform-Specific Therapeutic Vulnerabilities of KRAS Mutations in Non-Small Cell Lung Cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2022-04-14 | PMID 35091439
Ricciuti Biagio, Son Jieun, Okoro Jeffrey J and 23 more
Phase II Study of Ponatinib in Advanced Gastrointestinal Stromal Tumors: Efficacy, Safety, and Impact of Liquid Biopsy and Other Biomarkers.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2022-04-01 | PMID 35091442
George Suzanne, von Mehren Margaret, Fletcher Jonathan A and 8 more
Classical RAS proteins are not essential for paradoxical ERK activation induced by RAF inhibitors.
Proceedings of the National Academy of Sciences of the United States of America | 2022-02-01 | PMID 35091470
Lai Lick Pui, Fer Nicole, Burgan William and 6 more
Biallelic SEPSECS variants in two siblings with pontocerebellar hypoplasia type 2D underscore the relevance of splice-disrupting synonymous variants in disease.
Cold Spring Harbor molecular case studies | 2022-02-01 | PMID 35091508
Ramadesikan Swetha, Hickey Scott, De Los Reyes Emily and 9 more
Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder.
Cold Spring Harbor molecular case studies | 2022-02-01 | PMID 35091509
Hunter Jesse M, Massingham Lauren J, Manickam Kandamurugu and 10 more
Documented Viral Illness at the Time of Splenic Sequestration Does Not Affect the Odds of Recurrence in Children With Sickle Cell Disease.
Journal of pediatric hematology/oncology | 2022-03-01 | PMID 35091513
Clement Omoyeni, Fishbein Joanna, Appiah-Kubi Abena and 1 more
Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brain.
Translational psychiatry | 2022-01-28 | PMID 35091539
Holmgren Asbjørn, Hansson Lars, Bjerkaas-Kjeldal Kristine and 4 more
Depletion of mitochondrial methionine adenosyltransferase α1 triggers mitochondrial dysfunction in alcohol-associated liver disease.
Nature communications | 2022-01-28 | PMID 35091576
Barbier-Torres Lucía, Murray Ben, Yang Jin Won and 19 more
Phloem iron remodels root development in response to ammonium as the major nitrogen source.
Nature communications | 2022-01-28 | PMID 35091578
Liu Xing Xing, Zhang Hai Hua, Zhu Qing Yang and 8 more
Whole-genome single nucleotide variant phylogenetic analysis of Mycobacterium tuberculosis Lineage 1 in endemic regions of Asia and Africa.
Scientific reports | 2022-01-28 | PMID 35091638
Netikul Thidarat, Thawornwattana Yuttapong, Mahasirimongkol Surakameth and 4 more
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese families.
Journal of human genetics | 2022-07-01 | PMID 35091664
Ando Masahiro, Higuchi Yujiro, Okamoto Yuji and 17 more
What genes are differentially expressed in individuals with schizophrenia? A systematic review.
Molecular psychiatry | 2022-03-01 | PMID 35091668
Merikangas Alison K, Shelly Matthew, Knighton Alexys and 3 more
The BCL-2 family member BOK promotes KRAS-driven lung cancer progression in a p53-dependent manner.
Oncogene | 2022-02-01 | PMID 35091677
Meinhardt Anna-Lena, Munkhbaatar Enkhtsetseg, Höckendorf Ulrike and 12 more
Oncogenesis induced by combined Phf6 and Idh2 mutations through increased oncometabolites and impaired DNA repair.
Oncogene | 2022-03-01 | PMID 35091680
Chen Tsung-Chih, Yao Chi-Yuan, Chen Yu-Ren and 9 more
The expanded spectrum of arthritis in children with familial Mediterranean fever.
Clinical rheumatology | 2022-05-01 | PMID 35091781
Avar-Aydın Pinar Ozge, Ozcakar Zeynep Birsin, Aydın Fatma and 3 more
Toll-Like Receptors (TLRs) in Health and Disease: An Overview.
Handbook of experimental pharmacology | 2022-01-01 | PMID 35091824
Kumar Vijay, Barrett James E
The role of mitonuclear incompatibilities in allopatric speciation.
Cellular and molecular life sciences : CMLS | 2022-01-29 | PMID 35091831
Burton Ronald S
Genetic parameters for body weight and milk production of dairy Gyr herds.
Tropical animal health and production | 2022-01-28 | PMID 35091866
Hortolani Bruna, Bernardes Priscila Arrigucci, Filho Aníbal Eugênio Vercesi and 2 more
Single nucleotide variants around the connective tissue growth factor (CTGF/CCN2) gene and their association with multiple sclerosis risk, disability scores, and rate of disease progression.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022-06-01 | PMID 35091888
Can Demirdöğen Birsen, Kılıç Osman Oğuzhan, Karagülle Elif Naz and 2 more
Probability of high-risk genetic matching with oocyte and semen donors: complete gene analysis or genotyping test?
Journal of assisted reproduction and genetics | 2022-02-01 | PMID 35091964
Molina Romero Marta, Yoldi Chaure Alberto, Gañán Parra Miguel and 6 more
Novel mutations in NLRP5 and PATL2 cause female infertility characterized by primarily oocyte maturation abnormality and consequent early embryonic arrest.
Journal of assisted reproduction and genetics | 2022-03-01 | PMID 35091966
Huang Lingli, Wang Yu, Lu Fangting and 6 more
Quantification of Helicobacter pylori and its oncoproteins in the oral cavity: A cross-sectional study.
Oral diseases | 2023-05-01 | PMID 35092112
Sekar Ramya, Murali Preethi, Junaid Mohammed
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility.
American journal of medical genetics. Part A | 2022-05-01 | PMID 35092149
Murad Andrea M, Hill Hannah L, Wang Yu and 12 more
Plasmodium falciparum Kelch13 and its artemisinin-resistant mutants assemble as hexamers in solution: a SAXS data-driven modelling study.
The FEBS journal | 2022-08-01 | PMID 35092154
Goel Nainy, Dhiman Kanika, Kalidas Nidhi and 3 more
Long-term follow-up findings in a Turkish girl with osteogenesis imperfecta type XX caused by a homozygous MESD variant.
American journal of medical genetics. Part A | 2022-05-01 | PMID 35092157
Uludağ Alkaya Dilek, Uyguner Zehra Oya, Güneş Nilay and 1 more
Identification of the novel HLA-E*01:03:02:25 allele in an acute lymphoblastic leukemia patient.
HLA | 2022-07-01 | PMID 35092184
Williams Hawys B, Lucas Jonathan A M, Georgiou Xenia and 2 more
Characterization of the novel HLA-A*02:01:01:206 allele in a Northern European individual.
HLA | 2022-07-01 | PMID 35092187
Williams Hawys B, Lucas Jonathan A M, Cambridge Charlotte A and 2 more
Detection of the HLA-DRB1*14:05:05 allele, a variant of HLA-DRB1*14, in a Taiwanese bone marrow donor.
HLA | 2022-06-01 | PMID 35092192
Yang Kuo-Liang, Li Chi-Cheng, Lin Py-Yu
Genetic risk scores used in cardiovascular disease prediction models: a systematic review.
Reviews in cardiovascular medicine | 2022-01-11 | PMID 35092200
Yun Hyunok, Noh Nan Iee, Lee Eun Young
SIRT1 rs7896005 polymorphism affects major vascular outcomes, not all-cause mortality, in Caucasians with type 2 diabetes: A 13-year observational study.
Diabetes/metabolism research and reviews | 2022-05-01 | PMID 35092334
Dardano Angela, Lucchesi Daniela, Garofolo Monia and 6 more
Exon skipping caused by a complex structural variation in SH2D1A resulted in X-linked lymphoproliferative syndrome type 1.
Molecular genetics & genomic medicine | 2022-03-01 | PMID 35092357
Wu Liwen, Yang Feng, Wang Jia and 3 more
Association of Estrogen-Related Polygenetic Risk Scores with Breast Cancer and Interactions with Alcohol Intake, Early Menarche, and Nulligravida.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092367
Song Sang Shin, Kang Suna, Park Sunmin
Association between VDR Gene Polymorphisms and Melanoma Susceptibility in a Colombian Population.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092374
Aristizabal-Pachon Andres Felipe, Gonzalez-Giraldo Yeimy, Garcia Angela Yazmin and 3 more
Detecting Human Papillomavirus Type 16 in Cervical Cancer Patients with Molecular Variation of Gene L1 in Riau Province Indonesia.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092375
Savira Maya, S Donel, Putra Andani Eka and 2 more
TP53 and EGFR Mutational Status in Thymoma: A Genetic Sequencing Study.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092378
Syahruddin Elisna, Zaini Jamal, Sembiring Ruth and 3 more
Rapid Detection of N-RAS Gene Common Mutations in Acute Myeloid Leukemia (AML) Using High Resolution Melting (HRM) Method.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092380
Zaka Khosravi Saeed, Moonesi Mohammadreza, Moradabadi Alireza and 3 more
Correlation between Programmed Death Ligand-1(PD-L1) Expression and Driver Gene Mutations in Non-Small Cell Lung Carcinoma- Adenocarcinoma Phenotype.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092381
Pandey Rahul Kumar, Shukla Saumya, Husain Nuzhat and 4 more
Association of Leptin Receptor Q223R Gene Polymorphism and Breast Cancer Patients: A Case Control Study.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092386
Atoum Manar F, Hamaid Alparrey Ala'a Abdel
Exome Sequencing with Validations and Expression of p16/CDKN2A Shows no Association with HPV in Oral Cancers.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092388
Shyamsundar Vidyarani, Thangaraj Soundara Viveka, Krishnamurthy Arvind and 5 more
Molecular Detection of Genetic Susceptibility to Bladder Cancer in Egyptian Patients.
Asian Pacific journal of cancer prevention : APJCP | 2022-01-01 | PMID 35092392
Mamdouh Samah, Khorshed Fatma, Hammad Gehan and 4 more
AtOZF1 positively regulates JA signaling and SA-JA cross-talk in Arabidopsis thaliana.
Journal of biosciences | 2022-01-01 | PMID 35092410
Singh Nidhi, Nandi Ashis Kumar
MaSTR™: an effective probabilistic genotyping tool for interpretation of STR mixtures associated with differentially degraded DNA.
International journal of legal medicine | 2022-03-01 | PMID 35092470
Holland Mitchell M, Tiedge Teresa M, Bender Abigail J and 2 more
Examining the prevalence of homologous recombination repair defects in ER+ breast cancers.
Breast cancer research and treatment | 2022-04-01 | PMID 35092538
Moore Grace M, Powell Simon N, Higginson Daniel S and 1 more
Heritability: What's the point? What is it not for? A human genetics perspective.
Genetica | 2022-08-01 | PMID 35092541
Robette Nicolas, Génin Emmanuelle, Clerget-Darpoux Françoise
Unraveling novel and rare mutations for alpha-amylase and key transcription factors in EMS-induced wheat mutants for amylose by TILLING.
Molecular biology reports | 2022-06-01 | PMID 35092561
Sharma Vinita, Mishra Ankita, Sharma Himanshu and 2 more
Heritability of social behavioral phenotypes and preliminary associations with autism spectrum disorder risk genes in rhesus macaques: A whole exome sequencing study.
Autism research : official journal of the International Society for Autism Research | 2022-03-01 | PMID 35092647
Gunter Chris, Harris R Alan, Kovacs-Balint Zsofia and 6 more
High-resolution melting PCR analysis for genotyping the gene polymorphism of TNF-α, TGF-β1, IL-10, and IFN-γ in lung transplant recipients.
Advances in clinical and experimental medicine : official organ Wroclaw Medical University | 2022-05-01 | PMID 35092650
Mu Hui-Jun, Zou Jian, Zhang Ji and 1 more
Novel insertion mutation in the PLA2G6 gene in an Iranian family with infantile neuroaxonal dystrophy.
Journal of clinical laboratory analysis | 2022-03-01 | PMID 35092705
Rostampour Dorsa, Zolfaghari Mohammad Reza, Gholami Milad
Probability of HBsAg loss after nucleo(s)tide analogue withdrawal depends on HBV genotype and viral antigen levels.
Journal of hepatology | 2022-05-01 | PMID 35092743
Sonneveld Milan J, Chiu Shao-Ming, Park Jun Yong and 23 more
Circulating tumor DNA tracking in patients with pancreatic cancer using next-generation sequencing.
Gastroenterologia y hepatologia | 2022-10-01 | PMID 35092761
Herreros-Villanueva Marta, Bujanda Luis, Ruiz-Rebollo Lourdes and 4 more
A new insight into the SNP genotyping using high-resolution melting method after the correlation analysis of the SNPs with WSSV-resistant traits.
Fish & shellfish immunology | 2022-03-01 | PMID 35092808
Shi Ruixue, Yang Siqi, Li Yanhe
Fruit transcriptional profiling of the contrasting genotypes for shelf life reveals the key candidate genes and molecular pathways regulating post-harvest biology in cucumber.
Genomics | 2022-03-01 | PMID 35092817
Pradeepkumara N, Sharma Parva Kumar, Munshi A D and 11 more
Impact of resistance mutations on efficacy of dolutegravir plus rilpivirine or plus lamivudine as maintenance regimens: a cohort study.
Journal of global antimicrobial resistance | 2022-03-01 | PMID 35092828
Gagliardini Roberta, Baccini Michela, Modica Sara and 12 more
Genetic structure and phylogeography of Echinococcus granulosus sensu stricto genotypes G1 and G3 in Pakistan and other regions of the world based on nad5 gene.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2022-03-01 | PMID 35092843
Mehmood Naunain, Muqaddas Hira, Ullah Muhammad Irfan and 2 more
Polymorphisms of the filaggrin gene are associated with atopic dermatitis in the Caucasian population of Central Russia.
Gene | 2022-04-15 | PMID 35092857
Churnosov Mikhail, Belyaeva Tatyana, Reshetnikov Evgeny and 2 more
A Drosophila insulator interacting protein suppresses enhancer-blocking function and modulates replication timing.
Gene | 2022-04-20 | PMID 35092858
Stow Emily C, Simmons James R, An Ran and 3 more
Genome-wide detection of selective signals for fecundity traits in goats (Capra hircus).
Gene | 2022-04-15 | PMID 35092859
Wang Jun-Jie, Li Zheng-Dao, Zheng Li-Qing and 3 more
Identification of the most damaging nsSNPs in the human CFL1 gene and their functional and structural impacts on cofilin-1 protein.
Gene | 2022-04-20 | PMID 35092861
Halder Sajal Kumar, Rafi Md Oliullah, Shahriar Esha Binte and 5 more
Let-7i-5p promotes a malignant phenotype in nasopharyngeal carcinoma via inhibiting tumor-suppressive autophagy.
Cancer letters | 2022-04-10 | PMID 35092862
You Bo, Zhang Panpan, Gu Miao and 9 more
Regorafenib enhances antitumor immune efficacy of anti-PD-L1 immunotherapy on oral squamous cell carcinoma.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie | 2022-03-01 | PMID 35092865
Chiang I-Tsang, Lee Yuan-Hao, Tan Zhao-Lin and 2 more
The FLT3 internal tandem duplication mutation at disease diagnosis is a negative prognostic factor in myelodysplastic syndrome patients.
Leukemia research | 2022-02-01 | PMID 35092883
Sumiyoshi Ritsu, Tashiro Haruko, Shirasaki Ryosuke and 5 more
The clinical aspect of NTRK-fusions in pediatric papillary thyroid cancer.
Cancer genetics | 2022-04-01 | PMID 35092884
Ricarte-Filho Julio C, Halada Stephen, O'Neill Alison and 4 more
The influence of host genetics on liver microbiome composition in patients with NAFLD.
EBioMedicine | 2022-02-01 | PMID 35092912
Pirola Carlos Jose, Salatino Adrian, Quintanilla Maria Florencia and 3 more
Cranial autonomic symptoms: prevalence, phenotype and laterality in migraine and two potentially new symptoms.
The journal of headache and pain | 2022-01-29 | PMID 35093009
Karsan Nazia, Nagaraj Karthik, Goadsby Peter J
Prenatal diagnosis of Roberts syndrome in a Chinese family based on ultrasound findings and whole exome sequencing: a case report.
BMC medical genomics | 2022-01-29 | PMID 35093090
Zhu LiFen, Cao DingYa, Chen Min and 3 more
Gene expression predicts dormant metastatic breast cancer cell phenotype.
Breast cancer research : BCR | 2022-01-29 | PMID 35093137
Ren Qihao, Khoo Weng Hua, Corr Alexander P and 3 more