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 8958 of 10600

ATG7 is a haploinsufficient repressor of tumor progression and promoter of metastasis.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-12 | PMID 35867735
Long Jaclyn S, Kania Elżbieta, McEwan David G and 5 more
A method to predict the response to directional selection using a Kalman filter.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-12 | PMID 35867739
Milocco Lisandro, Salazar-Ciudad Isaac
Voltage-gated sodium channel scn8a is required for innervation and regeneration of amputated adult zebrafish fins.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-12 | PMID 35867745
Osorio-Méndez Daniel, Miller Andrew, Begeman Ian J and 8 more
NURR1 expression regulates retinal pigment epithelial-mesenchymal transition and age-related macular degeneration phenotypes.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-12 | PMID 35867766
Yao Pei-Li, Parmar Vipul M, Choudhary Mayur and 1 more
Sequential small cell transformation and T790M mutation in an epidermal growth factor-mutant lung adenocarcinoma: A rare occurrence with significant management implications.
Cytopathology : official journal of the British Society for Clinical Cytology | 2022-11-01 | PMID 35867808
Shastri Malvika, Gupta Parikshaa, Gupta Nalini and 4 more
Allele-specific activation, enzyme kinetics, and inhibitor sensitivities of EGFR exon 19 deletion mutations in lung cancer.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-26 | PMID 35867821
Brown Benjamin P, Zhang Yun-Kai, Kim Soyeon and 9 more
Genes: EGFR
Molecular mechanism of the severe MH/CCD mutation Y522S in skeletal ryanodine receptor (RyR1) by cryo-EM.
Proceedings of the National Academy of Sciences of the United States of America | 2022-07-26 | PMID 35867837
Iyer Kavita A, Hu Yifan, Klose Thomas and 2 more
The direct effect of fibroblast growth factor 23 on vascular smooth muscle cell phenotype and function.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 2023-02-13 | PMID 35867864
Vergara Noemi, de Mier M Victoria Pendón-Ruiz, Rodelo-Haad Cristian and 17 more
Negative regulation of salicylic acid-induced stomatal closure by glutathione in Arabidopsis thaliana.
Bioscience, biotechnology, and biochemistry | 2022-09-23 | PMID 35867881
Akter Fahmida, Munemasa Shintaro, Nakamura Toshiyuki and 2 more
Phenotypic and genotypic characterization of two factor VII deficiency patients from southeastern China.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2022-12-01 | PMID 35867939
Wang Anzi, Su Dongyun, Chen Yanrong and 6 more
Genomic landscapes of canine splenic angiosarcoma (hemangiosarcoma) contain extensive heterogeneity within and between patients.
PloS one | 2022-01-01 | PMID 35867969
Wong Shukmei, Ehrhart E J, Stewart Samuel and 13 more
11 C-Acetate PET/CT Detects Reactive Astrogliosis Helping Glioma Classification.
Clinical nuclear medicine | 2022-10-01 | PMID 35868002
Kim Dongwoo, Chun Joong Hyun, Yi Ju Hyeon and 14 more
Directional mutation and crossover boosted ant colony optimization with application to COVID-19 X-ray image segmentation.
Computers in biology and medicine | 2022-09-01 | PMID 35868049
Qi Ailiang, Zhao Dong, Yu Fanhua and 7 more
Influence of germline test results on surgical decision making in women with invasive breast cancer.
Cancer genetics | 2022-08-01 | PMID 35868102
Vargason Ashlee B, Turner Clesson E, Shriver Craig D and 1 more
Current progress and novel strategies that target CDK12 for drug discovery.
European journal of medicinal chemistry | 2022-10-05 | PMID 35868123
Lei Peng, Zhang Jifa, Liao Peiyu and 3 more
The relationship of 50 bp deletion in the promoter region of SOD1 gene with viscosity and trace elements in chronic gastritis with Helicobacter Pylori: A case study.
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) | 2022-09-01 | PMID 35868167
Duzgun Ergun D, Doganer F, Koc G and 3 more
Genotypic and phenotypic spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency.
Molecular genetics and metabolism | 2000-01-01 | PMID 35868242
Goetz M, Schröter J, Dattner T and 8 more
Establishment of a human induced pluripotent stem cell line, KMUGMCi004-A, from a patient bearing a heterozygous c.1832delG mutation in the APC gene leading familial adenomatous polyposis (FAP).
Stem cell research | 2022-08-01 | PMID 35868288
Ura Hiroki, Togi Sumihito, Hatanaka Hisayo and 1 more
Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene.
Stem cell research | 2022-08-01 | PMID 35868289
Ou-Yang Chih-Hsin, Lin Han-I, Lin Chin-Hsien
Can the "female protective effect" liability threshold model explain sex differences in autism spectrum disorder?
Neuron | 2022-10-19 | PMID 35868305
Dougherty Joseph D, Marrus Natasha, Maloney Susan E and 8 more
Genetic identification of the pleiotropic gene Tasg-D1/2 affecting wheat grain shape by regulating brassinolide metabolism.
Plant science : an international journal of experimental plant biology | 2022-10-01 | PMID 35868348
Zhang Yaoyuan, Miao Hanxiao, Wang Chao and 10 more
Association of OPG and RANKL gene polymorphisms with bone mineral density in Indian women.
Gene | 2022-10-05 | PMID 35868414
Nair Sandhya, Bhadricha Hetal, Patil Anushree and 4 more
Structural, functional analysis and association of MSH6 rs1800932, rs1042821 polymorphisms with clinical outcome in North Indian lung cancer patients treated with platinum-based doublet chemotherapy.
The American journal of the medical sciences | 2022-12-01 | PMID 35868444
Singh Sidhartha, Singh Navneet, Baranwal Manoj and 1 more
Diversity and novel mutations in membrane transporters of Mycobacterium tuberculosis.
Briefings in functional genomics | 2023-04-13 | PMID 35868449
Khan Muhammad Tahir, Khan Taj Ali, Ahmad Irshad and 2 more
Utility and Outcomes of the 2019 American College of Medical Genetics and Genomics-Clinical Genome Resource Guidelines for Interpretation of Copy Number Variants with Borderline Classifications at an Academic Clinical Diagnostic Laboratory.
The Journal of molecular diagnostics : JMD | 2022-10-01 | PMID 35868509
Drackley Andy, Brew Casey, Wlodaver Alissa and 7 more
NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing.
The Journal of molecular diagnostics : JMD | 2022-10-01 | PMID 35868510
Cao Yujie, Ha Shau-Yin, So Chi-Chiu and 13 more
Mutation burden-orthogonal tumor genomic subtypes delineate responses to immune checkpoint therapy.
Journal for immunotherapy of cancer | 2022-07-01 | PMID 35868660
Takamatsu Shiro, Hamanishi Junzo, Brown J B and 7 more
Alagille Syndrome: Current Understanding of Pathogenesis, and Challenges in Diagnosis and Management.
Clinics in liver disease | 2022-08-01 | PMID 35868679
Ayoub Mohammed D, Kamath Binita M
Association of immunoglobulin G N-glycosylation with carotid atherosclerotic plaque phenotypes and actual clinical cardiovascular events: a study protocol for a longitudinal prospective cohort study.
BMJ open | 2022-07-22 | PMID 35868824
Tian Cuihong, Mahara Gehendra, Zhang Hongxia and 1 more
Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Annals of the rheumatic diseases | 2022-10-01 | PMID 35868845
Kozycki Christina Torres, Kodati Shilpa, Huryn Laryssa and 67 more
Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy.
Neuromuscular disorders : NMD | 2022-08-01 | PMID 35868898
Bouman Karlijn, Gubbels Madelief, van den Heuvel Frederik M A and 5 more
Langerhans cell histiocytosis. Advances in pathogenesis and clinical practice.
Anales de pediatria | 2022-08-01 | PMID 35869015
Astigarraga Itziar, García-Obregón Susana, Pérez-Martínez Antonio and 6 more
SMOC2 promotes an epithelial-mesenchymal transition and a pro-metastatic phenotype in epithelial cells of renal cell carcinoma origin.
Cell death & disease | 2022-07-22 | PMID 35869056
Feng Daniel, Gao Peng, Henley Nathalie and 6 more
Structure of DNMT3B homo-oligomer reveals vulnerability to impairment by ICF mutations.
Nature communications | 2022-07-22 | PMID 35869095
Gao Linfeng, Guo Yiran, Biswal Mahamaya and 9 more
The screening for anticoagulant rodenticide gene VKORC1 polymorphism in the rat Rattus norvegicus, Rattus tanezumi and Rattus losea in Hong Kong.
Scientific reports | 2022-07-22 | PMID 35869096
Huang Elaine Y Y, Law Sean T S, Nong Wenyan and 4 more
Genome-wide association study in minority children with asthma implicates DNAH5 in bronchodilator responsiveness.
Scientific reports | 2022-07-22 | PMID 35869121
Joo Jaehyun, Mak Angel C Y, Xiao Shujie and 19 more
Structure-based prediction of BRAF mutation classes using machine-learning approaches.
Scientific reports | 2022-07-22 | PMID 35869122
Krebs Fanny S, Britschgi Christian, Pradervand Sylvain and 6 more
Skull variation in Afro-Eurasian monkeys results from both adaptive and non-adaptive evolutionary processes.
Scientific reports | 2022-07-22 | PMID 35869137
Schroeder Lauren, Elton Sarah, Ackermann Rebecca Rogers
HEM1 Actin Immunodysregulatory Disorder: Genotypes, Phenotypes, and Future Directions.
Journal of clinical immunology | 2022-11-01 | PMID 35869404
Cook Sarah, Lenardo Michael J, Freeman Alexandra F
Investigation of rumen long noncoding RNA before and after weaning in cattle.
BMC genomics | 2022-07-22 | PMID 35869425
Marceau Alexis, Gao Yahui, Baldwin Ransom L and 4 more
Assessing the clinical utility of protein structural analysis in genomic variant classification: experiences from a diagnostic laboratory.
Genome medicine | 2022-07-22 | PMID 35869530
Caswell Richard C, Gunning Adam C, Owens Martina M and 2 more
Identification of phenylketonuria patient genotypes using single-gene full-length sequencing.
Human genomics | 2022-07-22 | PMID 35869558
Gao Jinshuang, Li Xiaole, Guo Yaqing and 8 more
Mendelian randomization analysis identified causal Association of Childhood Obesity with adult major depressive disorder.
Pediatric obesity | 2022-12-01 | PMID 35869568
Yan Shan-Shan, Xu Qian, Han Bai-Xue and 8 more
Genetic Characteristics and Linkage of Virulence Genes of the Puccinia striiformis f. sp. tritici TSA-6 Isolate to Yr5 Host Resistance.
Plant disease | 2023-03-01 | PMID 35869586
Zhang Gensheng, Liu Wei, Wang Lin and 5 more
Virulence Phenotyping and Molecular Genotyping Reveal High Diversity Within and Strong Gene Flow Between the Puccinia striiformis f. sp. tritici Populations Collected from Barberry and Wheat in Shaanxi Province of China.
Plant disease | 2023-03-01 | PMID 35869588
Zhao Yuanyuan, Huang Xueling, Li Qiao and 3 more
Implementation of NUDT15 Genotyping to Prevent Azathioprine-Induced Leukopenia for Patients With Autoimmune Disorders in Chinese Population.
Clinical pharmacology and therapeutics | 2022-11-01 | PMID 35869597
Wang Chuang-Wei, Chi Min-Hui, Tsai Tsen-Fang and 17 more
MITF deficiency and oncogenic GNAQ each promote proliferation programs in zebrafish melanocyte lineage cells.
Pigment cell & melanoma research | 2022-09-01 | PMID 35869673
Phelps Grace B, Amsterdam Adam, Hagen Hannah R and 2 more
Epidemiology-based Analysis of Characteristics of Dual Infection of Tuberculosis /Acquired Immune Deficiency Syndrome (AIDS) and Drug Resistance Mechanism of Related Genes.
Cellular and molecular biology (Noisy-le-Grand, France) | 2022-02-28 | PMID 35869708
Yang Jingjing, Zheng Xiaoyan, Zhang Shuai and 1 more
Multiple insecticide resistance and first evidence of V410L kdr mutation in Aedes (Stegomyia) aegypti (Linnaeus) from Burkina Faso.
Medical and veterinary entomology | 2022-09-01 | PMID 35869781
Toé Hyacinthe K, Zongo Soumanaba, Guelbeogo Moussa W and 7 more
Correlation of p53 immunohistochemistry with TP53 mutational status and overall survival in newly diagnosed acute myeloid leukaemia.
Histopathology | 2022-10-01 | PMID 35869818
Fitzpatrick Megan J, Boiocchi Leonardo, Fathi Amir T and 3 more
FishShapes v1: Functionally relevant measurements of teleost shape and size on three dimensions.
Ecology | 2022-12-01 | PMID 35869828
Price Samantha A, Friedman Sarah T, Corn Katherine A and 26 more
Expanding phenotype of FAM111B-related disease focusing on liver involvement: Literature review, report of a case with end-stage liver disease and proposal for a new acronym.
American journal of medical genetics. Part A | 2022-10-01 | PMID 35869874
Macchiaiolo Marina, Panfili Filippo M, Vecchio Davide and 9 more
Association of TNFSF11 rs2200287 and TNFSF11 rs2148072 gene polymorphisms in preeclampsia.
American journal of reproductive immunology (New York, N.Y. : 1989) | 2022-10-01 | PMID 35869907
Sivaraj Nagarjuna, Kusuma Bunga Papa, Kutikuppala L V Simhachalam and 3 more
An additional patient with SMAD4-Juvenile Polyposis-Hereditary hemorrhagic telangiectasia and connective tissue abnormalities: SMAD4 loss-of-function and gain-of-function pathogenic variants result in contrasting phenotypes.
American journal of medical genetics. Part A | 2022-10-01 | PMID 35869926
Gheewalla Gregory M, Luther Jay, Das Saumya and 5 more
Pathogenic variants identified using whole-exome sequencing in Chinese patients with primary ciliary dyskinesia.
American journal of medical genetics. Part A | 2022-10-01 | PMID 35869935
Ye Yutian, Huang Qijun, Chen Lipeng and 6 more
Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing Technologies.
Clinical chemistry | 2022-09-01 | PMID 35869940
Lansdon Lisa A, Cadieux-Dion Maxime, Herriges John C and 11 more
ARNSHL gene identification: past, present and future.
Molecular genetics and genomics : MGG | 2022-09-01 | PMID 35869994
Imtiaz Ayesha
Prevalence of pathogenic germline variants in the circulating tumor DNA testing.
International journal of clinical oncology | 2022-10-01 | PMID 35870019
Yamamoto Yoshihiro, Fukuyama Keita, Kanai Masashi and 9 more
Genetic analyses of Vietnamese patients with oculocutaneous albinism.
Journal of clinical laboratory analysis | 2022-09-01 | PMID 35870188
Thuong Ma Thi Huyen, Anh Luong Thi Lan, Nhung Vu Phuong and 6 more
Genetic correlation of crizotinib efficacy and resistance in ALK- rearranged non-small-cell lung cancer.
Lung cancer (Amsterdam, Netherlands) | 2022-09-01 | PMID 35870258
Liu Chang, Liu Cuicui, Liao Jiatao and 10 more
Synonymous mutation rs1129293 is associated with PIK3CG expression and PI3Kγ activation in patients with chronic Chagas cardiomyopathy.
Immunobiology | 2022-09-01 | PMID 35870262
Silva Maria Cláudia, Fuzo Carlos Alessandro, Marques Paiva Isadora and 8 more
Functional characterization of novel variants found in patients with suspected Fabry disease.
Clinica chimica acta; international journal of clinical chemistry | 2022-09-01 | PMID 35870541
Varela-Calais Patrícia, Nicolicht Priscila, Paulo Martin Renan and 4 more
Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency.
Biochimie | 2022-10-01 | PMID 35870552
Vamecq Joseph, Masso Vincent, Bancel Léo-Paul and 4 more
Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension.
Kidney international | 2022-11-01 | PMID 35870639
Surapaneni Aditya, Schlosser Pascal, Zhou Linda and 7 more
Encoded Conformational Dynamics of the HIV Splice Site A3 Regulatory Locus: Implications for Differential Binding of hnRNP Splicing Auxiliary Factors.
Journal of molecular biology | 2022-09-30 | PMID 35870649
Chiu Liang-Yuan, Emery Ann, Jain Niyati and 6 more
Comparison of the efficacy and safety of first-line treatments based on clinicopathological characteristics for patients with advanced epidermal growth factor receptor mutated non-small-cell lung cancer: A systematic review and network meta-analysis.
Critical reviews in oncology/hematology | 2022-09-01 | PMID 35870763
Yang Fei, Zhang Wengang, Shang Xiaoling and 6 more
Lacrimo-auriculo-dento-digital syndrome with AIRE mutation: A case report.
Journal of stomatology, oral and maxillofacial surgery | 2022-11-01 | PMID 35870793
Zhu Hui, Yu Guang-Yan
Multiple-trait analyses improved the accuracy of genomic prediction and the power of genome-wide association of productivity and climate change-adaptive traits in lodgepole pine.
BMC genomics | 2022-07-23 | PMID 35870886
Cappa Eduardo P, Chen Charles, Klutsch Jennifer G and 12 more
Novel mutations of the USH2A gene cause Usher syndrome in five Chinese families.
BMC ophthalmology | 2022-07-23 | PMID 35870892
Xing Dongjun, Yu Rongguo, Wang Linni and 5 more
COVID-19 related acute necrotizing encephalopathy with extremely high interleukin-6 and RANBP2 mutation in a patient with recently immunized inactivated virus vaccine and no pulmonary involvement.
BMC infectious diseases | 2022-07-23 | PMID 35870896
Pongpitakmetha Thanakit, Hemachudha Pasin, Rattanawong Wanakorn and 3 more
Knockdown of myorg leads to brain calcification in zebrafish.
Molecular brain | 2022-07-23 | PMID 35870928
Zhao Miao, Lin Xiao-Hong, Zeng Yi-Heng and 7 more
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population.
Italian journal of pediatrics | 2022-07-23 | PMID 35870951
Sarwar Sumbal, Shabana, Tahir Amna and 6 more
Mesenchymal stem cells derived from adipose accelerate the progression of colon cancer by inducing a MT-CAFs phenotype via TRPC3/NF-KB axis.
Stem cell research & therapy | 2022-07-23 | PMID 35870973
Xue Chunling, Gao Yang, Li Xuechun and 6 more
Renal phenotypes correlate with genotypes in unrelated individuals with tuberous sclerosis complex in China.
Orphanet journal of rare diseases | 2022-07-23 | PMID 35870981
Luo Cong, Zhang Ye, Zhang Yu-Shi and 8 more
Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.
Italian journal of pediatrics | 2022-07-23 | PMID 35870983
Zhang Lu, Liu Xiaoliang, Zhao Yunjing and 6 more
Identification of clinical implications and potential prognostic models of chromatin regulator mutations in multiple myeloma.
Clinical epigenetics | 2022-07-23 | PMID 35870987
Zhang Lina, Zhang Run, Wang Jing and 7 more
Usefulness of circulating tumor DNA from cerebrospinal fluid in recurrent high-grade glioma.
Revue neurologique | 2022-11-01 | PMID 35871016
Fontanilles M, Deniel A, Marguet F and 10 more
Risk reducing surgery with peritoneal staging in BRCA1-2 mutation carriers. A prospective study.
European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology | 2022-12-01 | PMID 35871032
Marchetti Claudia, Arcieri Martina, Vertechy Laura and 7 more
Revisiting the concept of childhood preleukemia.
Trends in cancer | 2022-11-01 | PMID 35871053
Cobaleda Cesar, Vicente-Dueñas Carolina, Ramírez-Orellana Manuel and 1 more
UPF1/circRPPH1/ATF3 feedback loop promotes the malignant phenotype and stemness of GSCs.
Cell death & disease | 2022-07-23 | PMID 35871061
Xu Jinkun, Zhang Guoqing, Hu Jinpeng and 6 more
Identification of fusions with potential clinical significance in melanoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2022-12-01 | PMID 35871080
Moran Jakob M T, Le Long P, Nardi Valentina and 10 more
Different AHO phenotype in a Chinese family with a novel GNAS missense variant: a case report.
Italian journal of pediatrics | 2022-07-23 | PMID 35871092
Zhou Qing, Liang Bin, Fu Qing-Xian and 2 more
Sex-biased and parental allele-specific gene regulation by KDM6A.
Biology of sex differences | 2022-07-23 | PMID 35871105
Ma Wenxiu, Fang He, Pease Nicolas and 3 more
Landscape of somatic alterations in large-scale solid tumors from an Asian population.
Nature communications | 2022-07-23 | PMID 35871175
Wu Liqun, Yao Herui, Chen Hui and 51 more
Discovering the drivers of clonal hematopoiesis.
Nature communications | 2022-07-23 | PMID 35871184
Pich Oriol, Reyes-Salazar Iker, Gonzalez-Perez Abel and 1 more
A polygenic score indexing a DRD2-related co-expression network is associated with striatal dopamine function.
Scientific reports | 2022-07-23 | PMID 35871219
D'Ambrosio Enrico, Pergola Giulio, Pardiñas Antonio F and 14 more
Sexual selection for males with beneficial mutations.
Scientific reports | 2022-07-23 | PMID 35871224
Roberts Gilbert, Petrie Marion
Somatic mutations in DCC are associated with genomic instability and favourable outcomes in melanoma patients treated with immune checkpoint inhibitors.
British journal of cancer | 2022-11-01 | PMID 35871235
Li Yuting, Wang Qinghua, Chen Yang and 1 more
CMDB: the comprehensive population genome variation database of China.
Nucleic acids research | 2023-01-06 | PMID 35871305
Li Zhichao, Jiang Xiaosen, Fang Mingyan and 4 more
Early Identification of Different Behavioral Phenotypes in the Behavioral Variant of Frontotemporal Dementia with the Aid of the Mini-Frontal Behavioral Inventory (mini-FBI).
Journal of Alzheimer's disease : JAD | 2022-01-01 | PMID 35871334
Cerami Chiara, Perdixi Elena, Meli Claudia and 4 more
Huntingtin and Its Partner Huntingtin-Associated Protein 40: Structural and Functional Considerations in Health and Disease.
Journal of Huntington's disease | 2022-01-01 | PMID 35871360
Seefelder Manuel, Klein Fabrice A C, Landwehrmeyer Bernhard and 2 more
Phenotypical variability of the sigmoid sinus in translabyrinthine and retrosigmoid surgeries.
Surgical and radiologic anatomy : SRA | 2022-08-01 | PMID 35871409
Al-Fauri Maryna, Lee Daniel, Kelly Paul
Profiling of Fusarium head blight resistance QTL haplotypes through molecular markers, genotyping-by-sequencing, and machine learning.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2022-09-01 | PMID 35871415
Winn Zachary J, Lyerly Jeanette, Ward Brian and 9 more
Atypical TDP-43 protein expression in an ALS pedigree carrying a p.Y374X truncation mutation in TARDBP.
Brain pathology (Zurich, Switzerland) | 2023-01-01 | PMID 35871544
Cooper-Knock Johnathan, Julian Thomas H, Feneberg Emily and 15 more
The mutation features and geographical distributions of the surface glycoprotein (S gene) in SARS-CoV-2 strains: A comparative analysis of the early and current strains.
Journal of medical virology | 2022-11-01 | PMID 35871556
Liu Rang, Lin Xinran, Chen Bing and 8 more
Metastatic Lung Tumors from Colorectal Cancer with EGFR Mutations That Responded to Osimertinib.
Internal medicine (Tokyo, Japan) | 2023-03-01 | PMID 35871578
Yanagisawa Atsushi, Kinehara Yuhei, Kijima Ryo and 4 more
[Association Between TAB2 Gene Polymorphisms and Susceptibility to Cryptorchidism in Han Chinese Population in Southwest China].
Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition | 2022-07-01 | PMID 35871735
Su Min, Li Zhi-Long, Song Ya-Ping and 3 more
Rotavirus vaccine-derived cases in Belgium: Evidence for reversion of attenuating mutations and alternative causes of gastroenteritis.
Vaccine | 2022-08-19 | PMID 35871871
Simsek Ceren, Bloemen Mandy, Jansen Daan and 4 more
From single-omics to interactomics: How can ligand-induced perturbations modulate single-cell phenotypes?
Advances in protein chemistry and structural biology | 2022-01-01 | PMID 35871896
Piochi L F, Gaspar A T, Rosário-Ferreira N and 2 more
Clinician attitudes and practices on pregnancy planning and care in cystic fibrosis.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2023-03-01 | PMID 35871973
Montemayor Kristina, Kazmerski Traci M, Riekert Kristin A and 7 more