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 9164 of 10600

Report of Consensus Panel 3 from the 11th International workshop on Waldenström's Macroglobulinemia: Recommendations for molecular diagnosis in Waldenström's Macroglobulinemia.
Seminars in hematology | 2023-03-01 | PMID 37099028
Garcia-Sanz Ramón, Varettoni Marzia, Jiménez Cristina and 19 more
Dynamic ctDNA Mutational Complexity in Patients with Melanoma Receiving Immunotherapy.
Molecular diagnosis & therapy | 2023-07-01 | PMID 37099071
Fitzgerald Sandra, Blenkiron Cherie, Stephens Rosalie and 12 more
DNA Repair Enzyme XRCC4 30 bp Indel Intron 3 Locus Significant Association with Predisposition of Cataract in Senility.
Applied biochemistry and biotechnology | 2024-01-01 | PMID 37099126
Kafeel Sanober, Bizenjo Neelam, Shivji Shams Salman and 3 more
Production of MSTN knockout porcine cells using adenine base-editing-mediated exon skipping.
In vitro cellular & developmental biology. Animal | 2023-04-01 | PMID 37099179
Yang Shuai-Peng, Zhu Xiang-Xing, Qu Zi-Xiao and 18 more
Causal relationship between cannabis use and cancer: a genetically informed perspective.
Journal of cancer research and clinical oncology | 2023-09-01 | PMID 37099198
Huang Peng, Zhang Peng Fei, Li Qiu
HAMLET effect on cell death and mitochondrial respiration in colorectal cancer cell lines with KRAS/BRAF mutations.
Journal of cancer research and clinical oncology | 2023-09-01 | PMID 37099199
Žilinskas Justas, Stukas Darius, Jasukaitienė Aldona and 8 more
Metabolomic Evenness Underlies Intraspecific Differences Among Lineages of a Wetland Grass.
Journal of chemical ecology | 2023-08-01 | PMID 37099216
Salgado Ana L, Glassmire Andrea E, Sedio Brian E and 6 more
An association of epidermal growth factor receptor mutation subtypes with prognostic prediction and site-specific recurrence in advanced stage lung cancer patients.
Molecular biology reports | 2023-06-01 | PMID 37099232
Joshi Jigna, Pandit Apexa, Tarapara Bhoomi and 4 more
Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis.
Clinical journal of the American Society of Nephrology : CJASN | 2023-07-01 | PMID 37099456
Zhang Changming, Han Xu, Jin Ying and 23 more
Diagnostic performance of the GenoType MTBDRplus VER 2.0 line probe assay for the detection of isoniazid resistant Mycobacterium tuberculosis in Ethiopia.
PloS one | 2023-01-01 | PMID 37099514
Moga Shewki, Bobosha Kidist, Fikadu Dinka and 6 more
Premature senescence of the liver in Alagille patients.
PloS one | 2023-01-01 | PMID 37099537
Jannone Giulia, de Magnée Catherine, Tambucci Roberto and 4 more
Study investigating executive function in schizophrenia patients and their unaffected siblings.
PloS one | 2023-01-01 | PMID 37099556
Xu Feifei, Xian Zhenping
The 3' UTR polymorphisms rs3742330 in DICER1 and rs10719 in DROSHA genes are not associated with primary open-angle and angle-closure glaucoma: As case-control study.
PloS one | 2023-01-01 | PMID 37099569
Kondkar Altaf A, Azad Taif A, Sultan Tahira and 4 more
Molecular Characterization and Phylogenetic Analysis of Dengue Fever Viruses in Three Outbreaks in Tanzania Between 2017 and 2019.
PLoS neglected tropical diseases | 2023-04-01 | PMID 37099594
Kelly Maria Ezekiely, Msafiri Frank, Affara Muna and 10 more
Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice.
Blood advances | 2023-09-26 | PMID 37099686
Nagai Koki, Niihori Tetsuya, Muto Akihiko and 4 more
twas_sim, a Python-based tool for simulation and power analysis of transcriptome-wide association analysis.
Bioinformatics (Oxford, England) | 2023-05-04 | PMID 37099718
Wang Xinran, Lu Zeyun, Bhattacharya Arjun and 2 more
Adagrasib in Advanced Solid Tumors Harboring a KRASG12C Mutation.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2023-09-01 | PMID 37099736
Bekaii-Saab Tanios S, Yaeger Rona, Spira Alexander I and 9 more
KRAS Mutation Testing on Endoscopic Ultrasound-Guided Fine-Needle Aspiration Samples Improves the Diagnostic Accuracy of Pancreatic Cancer.
Pancreas | 2000-01-01 | PMID 37099780
Yeung Maximus C F, Shek Tony W H
Circ_0058058 Drives the Malignant Phenotypes and Immune Evasion of Pancreatic Cancer by the MicroRNA-557-Dependent Regulation of PDL1.
Pancreas | 2000-01-01 | PMID 37099790
Lin Lin, Xiao Liang, Jin Chang'e and 5 more
Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy.
Pediatric neurology | 2023-07-01 | PMID 37099824
Casas-Alba Dídac, Aguilar Anna, Alonso Itziar and 3 more
Epidemiological investigations and multilocus sequence typing of Mycoplasma synoviae isolates from chicken farms in China.
Poultry science | 2023-06-01 | PMID 37099877
Wei Xiaona, Chen Wei, Sun Qianjin and 6 more
Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A.
Stem cell research | 2023-06-01 | PMID 37099934
Ukaji Takao, Takahashi-Shibata Mikako, Arai Daisuke and 7 more
Tumour mutational burden as a biomarker in patients with mismatch repair deficient/microsatellite instability-high metastatic colorectal cancer treated with immune checkpoint inhibitors.
European journal of cancer (Oxford, England : 1990) | 2023-07-01 | PMID 37099945
Manca Paolo, Corti Francesca, Intini Rossana and 17 more
Efficacy and tolerability of isocitrate dehydrogenase inhibitors in patients with acute myeloid leukemia: A systematic review of clinical trials.
Leukemia research | 2023-06-01 | PMID 37100025
Aiman Wajeeha, Ali Muhammad Ashar, Basit Muhammad Abdul and 11 more
Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype.
Human heredity | 2023-01-01 | PMID 37100044
Bureau Alexandre, Tian Yuang, Levallois Patrick and 3 more
Selective killing of the human gastric pathogen Helicobacter pylori by mitochondrial respiratory complex I inhibitors.
Cell chemical biology | 2023-05-18 | PMID 37100053
Lettl Clara, Schindele Franziska, Mehdipour Ahmad Reza and 10 more
Integrative genetic analysis identifies FLVCR1 as a plasma-membrane choline transporter in mammals.
Cell metabolism | 2023-06-06 | PMID 37100056
Kenny Timothy C, Khan Artem, Son Yeeun and 9 more
Intestinal epigenotype of Atlantic salmon (Salmo salar) associates with tenacibaculosis and gut microbiota composition.
Genomics | 2023-05-01 | PMID 37100093
Hansen Søren B, Bozzi Davide, Mak Sarah S T and 6 more
Waiting times in a branching process model of colorectal cancer initiation.
Theoretical population biology | 2023-06-01 | PMID 37100121
Zhang Ruibo, Ukogu Obinna A, Bozic Ivana
Omicron Spike Protein is Vulnerable to Reduction.
Journal of molecular biology | 2023-07-01 | PMID 37100168
Yao Zhong, Geng Betty, Marcon Edyta and 8 more
Machine learning-based immune phenotypes correlate with STK11/KEAP1 co-mutations and prognosis in resectable NSCLC: a sub-study of the TNM-I trial.
Annals of oncology : official journal of the European Society for Medical Oncology | 2023-07-01 | PMID 37100205
Rakaee M, Andersen S, Giannikou K and 22 more
Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?
European journal of medical genetics | 2023-07-01 | PMID 37100236
Sarma Asodu Sandeep, Peter Mathew Rohan, Dalal Ashwin and 2 more
Ferric uptake regulator (Fur) binds a [2Fe-2S] cluster to regulate intracellular iron homeostasis in Escherichia coli.
The Journal of biological chemistry | 2023-06-01 | PMID 37100285
Fontenot Chelsey R, Ding Huangen
Targeting CDK12 obviates the malignant phenotypes of colorectal cancer through the Wnt/β-catenin signaling pathway.
Experimental cell research | 2023-07-01 | PMID 37100369
Liu Shenglan, Wu Junhong, Lu Xiaolu and 9 more
Early-Onset Pectus Excavatum Is More Likely to Be Part of a Genetic Variation.
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie | 2024-08-01 | PMID 37100424
Billar Ryan, Heyman Stijn, Kant Sarina and 4 more
The African Turquoise Killifish: A Scalable Vertebrate Model for Aging and Other Complex Phenotypes.
Cold Spring Harbor protocols | 2024-03-01 | PMID 37100468
Boos Felix, Chen Jingxun, Brunet Anne
Enriching representation learning using 53 million patient notes through human phenotype ontology embedding.
Artificial intelligence in medicine | 2023-05-01 | PMID 37100502
Daniali Maryam, Galer Peter D, Lewis-Smith David and 6 more
Vitamin D receptor genetic polymorphisms in severe and recurrent tuberculosis in children.
The Indian journal of tuberculosis | 2023-04-01 | PMID 37100582
Shah Ira, Shetty Naman S, Chigari Prameeta and 5 more
Willingness of people with cystic fibrosis receiving elexacaftor/tezacaftor/ivacaftor (ETI) to participate in randomized modulator and inhaled antimicrobial clinical trials.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2023-07-01 | PMID 37100705
VanDevanter D R, Zemanick E T, Konstan M W and 5 more
Targeted locus amplification reveals heterogeneity between and within CFTR genotypes and association with CFTR function in patient-derived intestinal organoids.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2023-05-01 | PMID 37100706
Lefferts J W, Boersma V, Nieuwenhuijze N D A and 10 more
Reversion of mutations in a live mycoplasma vaccine alters its metabolism.
Vaccine | 2023-05-16 | PMID 37100722
Klose Sara M, De Souza David P, Disint Jillian F and 5 more
Semaphorin 3A levels in vascular and nonvascular phenotypes in systemic sclerosis.
Laboratory medicine | 2023-11-02 | PMID 37100766
Kayaalp Mehmet, Erden Abdulsamet, Apaydin Hakan and 7 more
A CRISPR/Cas9-generated mutation in the zebrafish orthologue of PPP2R3B causes idiopathic scoliosis.
Scientific reports | 2023-04-26 | PMID 37100808
Seda Marian, Crespo Berta, Corcelli Michelangelo and 2 more
Genotype-phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea.
Scientific reports | 2023-04-26 | PMID 37100867
Kim Ji Hyun, Lim Seon Hee, Song Ji Yeon and 23 more
SRSF2-P95H decreases JAK/STAT signaling in hematopoietic cells and delays myelofibrosis development in mice.
Leukemia | 2023-06-01 | PMID 37100881
Willekens Christophe, Laplane Lucie, Dagher Tracy and 23 more
Relationship between food-derived antioxidant vitamin intake and breast cancer risk: a mendelian randomized study.
European journal of nutrition | 2023-09-01 | PMID 37100890
Zhao Hang, Wu Shengnan, Liu Hailong and 3 more
Reducing brassinosteroid signalling enhances grain yield in semi-dwarf wheat.
Nature | 2023-05-01 | PMID 37100915
Song Long, Liu Jie, Cao Beilu and 23 more
CircHIPK2 facilitates phenotypic switching of vascular smooth muscle cells in hypertension.
Journal of human hypertension | 2023-11-01 | PMID 37100987
Liu Chi, Li Nan, Li Fangcun and 6 more
Association of DRB1*11 and DRB1*12 alleles of the HLA system with the evolution of the Hepatitis B virus infection in Burkina Faso.
Molecular biology reports | 2023-06-01 | PMID 37101005
Zongo Sidnooma Véronique, Djigma Florencia Wendkuuni, Yonli Albert Théophane and 13 more
Physiological traits and expression profile of genes associated with nitrogen and phosphorous use efficiency in wheat.
Molecular biology reports | 2023-06-01 | PMID 37101006
Sagwal Vijeta, Kumar Upendra, Sihag Pooja and 3 more
Comparative genomics revealed that Vibrio furnissii and Vibrio fluvialis have mutations in genes related to T6SS1 and T6SS2.
Archives of microbiology | 2023-04-26 | PMID 37101014
Sun Jiakai, Su Haochen, Zhang Wenhui and 3 more
Two simple methods to improve the accuracy of the genomic selection methodology.
BMC genomics | 2023-04-26 | PMID 37101112
Montesinos-López Osval A, Kismiantini, Montesinos-López Abelardo
Impact of pharmacogenomic DPYD variant guided dosing on toxicity in patients receiving fluoropyrimidines for gastrointestinal cancers in a high-volume tertiary centre.
BMC cancer | 2023-04-26 | PMID 37101114
Lau David K, Fong Caroline, Arouri Faten and 14 more
Priors, population sizes, and power in genome-wide hypothesis tests.
BMC bioinformatics | 2023-04-26 | PMID 37101120
Cai Jitong, Zhan Jianan, Arking Dan E and 1 more
Influence of herd immunity on norovirus: a long-term field study of repeated viral gastroenteritis outbreaks at the same facilities.
BMC infectious diseases | 2023-04-26 | PMID 37101126
Kumazaki Makoto, Usuku Shuzo
Ischaemic stroke with multi-focal venous and arterial thrombosis due to hyperhomocysteinemia: anabolic androgenic steroid use and MTHFR c.667 C > T variant - a case report.
BMC neurology | 2023-04-26 | PMID 37101129
Chen Jpk, Rees A, Coughlan C H and 3 more
Two patients with ZAP-70 deficiency in China present with a different genetic, immunological, and clinical phenotype.
BMC pediatrics | 2023-04-26 | PMID 37101133
Luo Xianze, Liu Qing, Zhou Lina and 3 more
MDSi: Multi-omics Database for Setaria italica.
BMC plant biology | 2023-04-27 | PMID 37101150
Li Xukai, Hou Siyu, Feng Mengmeng and 6 more
Genetic evidence implicating natriuretic peptide receptor-3 in cardiovascular disease risk: a Mendelian randomization study.
BMC medicine | 2023-04-26 | PMID 37101178
Cronjé Héléne T, Karhunen Ville, Hovingh G Kees and 4 more
TP53 somatic mutations in Asian breast cancer are associated with subtype-specific effects.
Breast cancer research : BCR | 2023-04-26 | PMID 37101199
Ragu Mohana Eswari, Lim Joanna Mei Ch'wan, Ng Pei-Sze and 4 more
A comprehensive map of human glucokinase variant activity.
Genome biology | 2023-04-26 | PMID 37101203
Gersing Sarah, Cagiada Matteo, Gebbia Marinella and 12 more
Multiple PIK3CA mutation clonality correlates with outcomes in taselisib + fulvestrant-treated ER+/HER2-, PIK3CA-mutated breast cancers.
Genome medicine | 2023-04-26 | PMID 37101291
Hutchinson Katherine E, Chen Jessica W, Savage Heidi M and 11 more
Genetic associations between circulating metabolic biomarkers and lung cancer in East Asians and Europeans.
European journal of medical research | 2023-04-26 | PMID 37101305
Liu Kai, Wang Shangshang, Zhou Yuhan and 4 more
Gene-level association analysis of bivariate ordinal traits with functional regressions.
Genetic epidemiology | 2023-09-01 | PMID 37101379
Wang Shuqi, Chiu Chi-Yang, Wilson Alexander F and 6 more
Genes: ARMS2, CFH
Suppression of ZEAXANTHIN EPOXIDASE 1 restricts stripe rust growth in wheat.
Plant communications | 2023-09-11 | PMID 37101397
Chang Chao-Yan, Yang Shu-Xian, Zhang Mei-Qi and 14 more
Examining the Extent of Contamination, Antibiotic Resistance, and Genetic Diversity of Clostridioides (Clostridium) difficile Strains in Meat and Feces of Some Native Birds of Iran.
BioMed research international | 2023-01-01 | PMID 37101693
Ansarian Barezi Akbar, Shakerian Amir, Rahimi Ebrahim and 1 more
The novel HLA-DRB1*14:251 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual.
HLA | 2023-08-01 | PMID 37102197
Hao Cai-Xia, Zheng Zhong-Zheng, Du Ke-Ming and 2 more
GRAMM: A new method for analysis of HLA in families.
HLA | 2023-10-01 | PMID 37102220
Ansbacher-Feldman Zuriya, Israeli Sapir, Maiers Martin and 4 more
Assessment of genomic breeding values and their accuracies for carcass traits in Jeju Black cattle using whole-genome SNP chip panels.
Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie | 2023-09-01 | PMID 37102238
Haque Md Azizul, Iqbal Asif, Bae Haechang and 4 more
[Clinical characteristics and genetic analysis of two children with Autosomal dominant mental retardation type 21 due to variants of CTCF gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102286
Lyu Yuqiang, Song Fengling, Zhang Kaihui and 6 more
[Genetic analysis of a Chinese pedigree affected with Congenital coagulation factor XII deficiency due to a c.1A>G start codon variant of F12 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102287
Ji Weidan, Lin Sen, Chen Jie and 5 more
[Analysis of clinical features and PAK1 gene variant in a child with epilepsy and global developmental delay].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102288
Yuan Meng, Zhang Jia, Li Yang and 3 more
[Genetic analysis of a child with Charlevoix-Saguenay spastic ataxia due to variant of SACS gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102289
Luo Huan, Chen Xiaolu, Rao Xueyi and 4 more
[Analysis of MYRF gene variant in a fetus with Cardiac-urogenital syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102290
Sun Hairui, Zhang Hongjia, He Yihua
[Analysis of clinical phenotype and pathogenic variant of a fetus with Cornelia de Lange syndrome type II].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102291
Huang Hailong, Hou Jiaru, Zhou Yangzi and 2 more
[Prenatal diagnosis for a fetus with Walker-Warburg syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102292
Ma Panpan, Chen Xue, Hui Ling and 7 more
[Analysis of CYP2U1 gene variants in a child with Hereditary spastic paraplegia type 56].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102293
Zhang Guangyu, Li Sansong, Yang Lei and 3 more
[Clinical characteristics and genetic analysis of a fetus with Melnick-Needles syndrome due to variant of FLNA gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102294
Zou Jinghui, Zhang Yisheng, Liu Yan and 3 more
[Clinical phenotype and genetic analysis of a child with 14q12q13 microdeletion syndrome manifesting as congenital hypothyroidism].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102297
Wang Jie, Li Hongjuan, Yuan Shuhua and 3 more
[Phenotypic and genetic analysis of a child with partial trisomy 7q].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102298
Wang Chaojie, Li Dongxiao, Zhang Yaodong and 5 more
[Analysis of frequency and molecular genetics of Jk (a-b-) phenotype among blood donors from Jining area].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-05-10 | PMID 37102299
Zhang Na, Gao Huanhuan, Gao Hongjun
TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia.
Genes, chromosomes & cancer | 2023-07-01 | PMID 37102302
Hara Yusuke, Shiba Norio, Yoshida Kenichi and 21 more
Mapping Genetic Susceptibility to Stenosis in the Proximal Airway.
The Laryngoscope | 2023-11-01 | PMID 37102306
Sharif Kayvon, Tierney William S, Davis Ruth J and 7 more
[Barlow's disease with arrhythmic phenotype: a case report].
Giornale italiano di cardiologia (2006) | 2023-05-01 | PMID 37102353
Mengoni Marco, Conti Serenella, Dell'Uomo Marco and 5 more
Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2023-04-01 | PMID 37102386
Nartisa Inga, Kirsteina Rasa, Neiburga Katrina Daila and 11 more
Understanding immunoactinopathies: A decade of research on WAS gene defects.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology | 2023-04-01 | PMID 37102395
Vieira Rhaissa Calixto, Pinho Lia Goncalves, Westerberg Lisa S
The potential of trait data to increase the availability of bioindicators: A case study using plant conservatism values.
Ecological applications : a publication of the Ecological Society of America | 2023-07-01 | PMID 37102427
Crisfield Varina E, Ficken Cari D, Allen Brandon E and 2 more
A synonymous codon variant altering splicing of RBCK1 expands the phenotype and genotype spectra of polyglucosan body myopathy 1.
Clinical genetics | 2023-09-01 | PMID 37102570
Wen Qi, Zhu Wenjia, Wen Xinmei and 13 more
Shedder status-An analysis over time and assessment of various contributing factors.
Journal of forensic sciences | 2023-07-01 | PMID 37102619
Lee Li Yen Candy, Tan Jiayu, Lee Yong Sheng and 1 more
Association of CYP4A22 gene polymorphisms with cerebral stroke risk in the Chinese Han population.
The journal of gene medicine | 2023-08-01 | PMID 37102626
Zhuo Qingqing, Zhong Xiaoji, Wen Jiangling and 1 more
Behçet syndrome: The disturbed balance between anti- (CLEC12A, CLC) and proinflammatory (IFI27) gene expressions.
Immunity, inflammation and disease | 2023-04-01 | PMID 37102643
Oğuz Ali Kemal, Oygür Çağdaş Şahap, Taşır Seda and 2 more
Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes.
Development (Cambridge, England) | 2023-04-15 | PMID 37102702
Redhead Yushi, Gibbins Dorota, Lana-Elola Eva and 7 more
Role of the NaHCO3 Transporter MpsABC in the NaHCO3-β-Lactam-Responsive Phenotype in Methicillin-Resistant Staphylococcus aureus.
Microbiology spectrum | 2023-06-15 | PMID 37102972
Fan Sook-Ha, Proctor Richard A, Ersoy Selvi C and 5 more
Endoplasmic Reticulum Stress and the Lysosomal Pathway Play Crucial Roles in the Progression of βB2-Crystallin Mutation-Induced Congenital Cataracts in Mice.
Investigative ophthalmology & visual science | 2023-04-03 | PMID 37103007
Xiao Wei, Yang Weimin, Zhang Xinyu and 2 more
A Pilot Study of the Association VDR Polymorphisms With Primary Hyperparathyroidism.
In vivo (Athens, Greece) | 2000-01-01 | PMID 37103067
Chorti Angeliki, Achilla Charoula, Tsalkatidou Despoina and 4 more
Co-mutation of ASXL1 and SF3B1 Predicts Poorer Overall Survival Than Isolated ASXL1 or SF3B1 Mutations.
In vivo (Athens, Greece) | 2000-01-01 | PMID 37103105
Song Jinming, Moscinski Lynn, Yang Ethan and 3 more
Positive Impact of Implementing a Comprehensive Genetic Testing Protocol for Prostate Cancer Patients in a Multi-disciplinary Uro-oncology Practice.
Urology practice | 2023-01-01 | PMID 37103436
Ramanathan Siddharth, Korman Andrew, Ramanathan Sadhna and 6 more
No association of NAFLD-related polymorphisms in PNPLA3 and TM6SF2 with all-cause and cardiovascular mortality in an Austrian population study.
Wiener klinische Wochenschrift | 2024-05-01 | PMID 37103556
Semmler Georg, Balcar Lorenz, Wernly Sarah and 7 more
Genetic and physical localization of a major susceptibility gene to Pyrenophora teres f. maculata in barley.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2023-04-27 | PMID 37103563
Alhashel Abdullah F, Fiedler Jason D, Nandety Raja Sekhar and 5 more
Irritability and risk of lung cancer: a Mendelian randomization and mediation analysis.
Journal of cancer research and clinical oncology | 2023-09-01 | PMID 37103569
Qi Ao, Jiao Lijing, Zhang Yilu and 5 more