Uveal melanoma-associated mutations in PLCβ4 are constitutively activating and promote melanocyte proliferation and tumorigenesis.
Science signaling | 2021-12-14 | PMID 34905385
Phan Hoa T N, Kim Nam Hoon, Wei Wenhui 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 8783 of 10600
Arterial Chemotherapy of Oxaliplatin Plus Fluorouracil Versus Sorafenib in Advanced Hepatocellular Carcinoma: A Biomolecular Exploratory, Randomized, Phase III Trial (FOHAIC-1).
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2022-02-10 | PMID 34905388
Lyu Ning, Wang Xun, Li Ji-Bin and 7 more
Trade-Offs (and Constraints) in Organismal Biology.
Physiological and biochemical zoology : PBZ | 2000-01-01 | PMID 34905443
Garland Theodore, Downs Cynthia J, Ives Anthony R
Differences in Outcomes between Heart Failure Phenotypes in Patients with Coexistent Chronic Obstructive Pulmonary Disease: A Cohort Study.
Annals of the American Thoracic Society | 2022-06-01 | PMID 34905461
Gulea Claudia, Zakeri Rosita, Quint Jennifer K
Nuclear receptor binding SET domain protein 1 promotes epithelial-mesenchymal transition in paclitaxel-resistant breast cancer cells via regulating nuclear factor kappa B and F-box and leucine-rich repeat protein 11.
Bioengineered | 2021-12-01 | PMID 34905470
Chen Yi, Tang Weiwei, Zhu Xuedan and 8 more
Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
JCI insight | 2022-01-25 | PMID 34905512
Tang Clara Sze Man, Mononen Mimmi, Lam Wai-Yee and 11 more
TM2D genes regulate Notch signaling and neuronal function in Drosophila.
PLoS genetics | 2021-12-01 | PMID 34905536
Salazar Jose L, Yang Sheng-An, Lin Yong Qi and 5 more
Molecular surveillance of resistance to pyrethroids insecticides in Colombian Aedes aegypti populations.
PLoS neglected tropical diseases | 2021-12-01 | PMID 34905537
Granada Yurany, Mejía-Jaramillo Ana María, Zuluaga Sara and 1 more
Nationwide screening for Fabry disease in unselected stroke patients.
PloS one | 2021-01-01 | PMID 34905550
Tomek Aleš, Petra Reková, Paulasová Schwabová Jaroslava and 29 more
Attack of the dark clones the genetics of reproductive and color traits of South African honey bees (Apis mellifera spp.).
PloS one | 2021-01-01 | PMID 34905583
Patterson Rosa Laura, Eimanifar Amin, Kimes Abigail G and 2 more
Development of an efficient Sanger sequencing-based assay for detecting SARS-CoV-2 spike mutations.
PloS one | 2021-01-01 | PMID 34905589
Lim Ho Jae, Park Min Young, Jung Hye Soo and 8 more
The Hippo Pathway Effectors YAP and TAZ Regulate LH Release by Pituitary Gonadotrope Cells in Mice.
Endocrinology | 2022-01-01 | PMID 34905605
Lalonde-Larue Ariane, Boyer Alexandre, Dos Santos Esdras Corrêa and 3 more
Hypofibrinogenemia with preserved hemostasis and protection from thrombosis in mice with an Fga truncation mutation.
Blood | 2022-03-03 | PMID 34905618
Hur Woosuk S, Paul David S, Bouck Emma G and 13 more
Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients.
Journal of pediatric endocrinology & metabolism : JPEM | 2022-03-28 | PMID 34905667
Wasim Muhammad, Khan Haq N, Ayesha Hina and 10 more
SARS-CoV-2 variant Omicron (B.1.1.529) is in a rising trend of mutations increasing the positive electric charge in crucial regions of the spike protein S.
Acta biochimica Polonica | 2021-12-14 | PMID 34905671
Pawłowski Piotr
Reading Frame Repair of TTN Truncation Variants Restores Titin Quantity and Functions.
Circulation | 2022-01-18 | PMID 34905694
Romano Robert, Ghahremani Shahnaz, Zimmerman Talia and 5 more
Demographic decline and lineage-specific adaptations characterize New Zealand kiwi.
Proceedings. Biological sciences | 2021-12-22 | PMID 34905706
Bemmels Jordan B, Mikkelsen Else K, Haddrath Oliver and 3 more
Pharmacogenetic loci for rosuvastatin are associated with intima-media thickness change and coronary artery disease risk.
Pharmacogenomics | 2022-01-01 | PMID 34905955
Kononov Stanislav, Mal Galina, Azarova Iuliia and 4 more
PRPH2-Associated Macular Dystrophy in 4 Family Members with a Novel Mutation.
Ophthalmic genetics | 2022-04-01 | PMID 34906036
Choi Hanna, Cloutier Alan, Lally David
EGFR Pathway-Based Gene Signatures of Druggable Gene Mutations in Melanoma, Breast, Lung, and Thyroid Cancers.
Biochemistry. Biokhimiia | 2021-11-01 | PMID 34906047
Raevskiy Mikhail, Sorokin Maxim, Vladimirova Uliana and 8 more
OTC intron 4 variations mediate pathogenic splicing patterns caused by the c.386G>A mutation in humans and spfash mice, and govern susceptibility to RNA-based therapies.
Molecular medicine (Cambridge, Mass.) | 2021-12-14 | PMID 34906067
Sacchetto Claudia, Peretto Laura, Baralle Francisco and 7 more
Risk of gallstones based on ABCG8 rs11887534 single nucleotide polymorphism among Taiwanese men and women.
BMC gastroenterology | 2021-12-14 | PMID 34906072
Liang Keng-Wei, Huang Hsin-Hui, Wang Lee and 7 more
gcMECM: graph clustering of mutual exclusivity of cancer mutations.
BMC bioinformatics | 2021-12-14 | PMID 34906079
Hu Ying, Yan Chunhua, Chen Qingrong and 1 more
Identification and validation of a regulatory mutation upstream of the BMP2 gene associated with carcass length in pigs.
Genetics, selection, evolution : GSE | 2021-12-14 | PMID 34906088
Li Jing, Peng Song, Zhong Liepeng and 5 more
Causal role of high body mass index in multiple chronic diseases: a systematic review and meta-analysis of Mendelian randomization studies.
BMC medicine | 2021-12-15 | PMID 34906131
Larsson Susanna C, Burgess Stephen
Dynamic changes in genetic diversity, drug resistance mutations, and treatment outcomes of falciparum malaria from the low-transmission to the pre-elimination phase on the islands of São Tomé and Príncipe.
Malaria journal | 2021-12-14 | PMID 34906134
Chen Ying-An, Shiu Tsen-Ju, Tseng Lien-Fen and 4 more
Temporal evolution of the resistance genotypes of Plasmodium falciparum in isolates from Equatorial Guinea during 20 years (1999 to 2019).
Malaria journal | 2021-12-14 | PMID 34906159
Berzosa Pedro, Molina de la Fuente Irene, Ta-Tang Thuy-Huong and 9 more
Genetic testing and diagnosis of inherited retinal diseases.
Orphanet journal of rare diseases | 2021-12-14 | PMID 34906171
Lam Byron L, Leroy Bart P, Black Graeme and 3 more
Leukocyte telomere length and amyotrophic lateral sclerosis: a Mendelian randomization study.
Orphanet journal of rare diseases | 2021-12-14 | PMID 34906191
Xia Kailin, Zhang Linjing, Zhang Gan and 3 more
Novel LTBP3 mutations associated with thoracic aortic aneurysms and dissections.
Orphanet journal of rare diseases | 2021-12-14 | PMID 34906192
Zhu Guoyan, Luo Mingyao, Chen Qianlong and 6 more
Driving mosaicism: somatic variants in reference population databases and effect on variant interpretation in rare genetic disease.
Human genomics | 2021-12-14 | PMID 34906245
Avramović Vladimir, Frederiksen Simona Denise, Brkić Marjana and 1 more
Dural Venous Sinus Thrombosis and Papilledema Related to JAK2 Mutation: A Case Series.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques | 2023-03-01 | PMID 34906267
Donaldson Laura, Dhoot Arjan S, Margolin Edward
Estrogen receptor alpha and NFATc1 bind to a bone mineral density-associated SNP to repress WNT5B in osteoblasts.
American journal of human genetics | 2022-01-06 | PMID 34906330
Suthon Sarocha, Lin Jianjian, Perkins Rachel S and 3 more
A single-nucleotide mutation within the TBX3 enhancer increased body size in Chinese horses.
Current biology : CB | 2022-01-24 | PMID 34906355
Liu Xuexue, Zhang Yanli, Liu Wujun and 7 more
Prognostic markers in invasive bladder cancer: FGFR3 mutation status versus P53 and KI-67 expression: a multi-center, multi-laboratory analysis in 1058 radical cystectomy patients.
Urologic oncology | 2022-03-01 | PMID 34906411
Mertens Laura S, Claps Francesco, Mayr Roman and 32 more
The influence of CYP2R1 polymorphisms and gene-obesity interaction with hypertension risk in a Chinese rural population.
Nutrition, metabolism, and cardiovascular diseases : NMCD | 2022-01-01 | PMID 34906413
Xu Z, Zhang D, Lin J and 11 more
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906446
Akin Leyla, Rizzoti Karine, Gregory Louise C and 27 more
KDM1A inactivation causes hereditary food-dependent Cushing syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906447
Vaczlavik Anna, Bouys Lucas, Violon Florian and 28 more
Risk of cancer in heterozygous relatives of patients with Fanconi anemia.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906449
McReynolds Lisa J, Giri Neelam, Leathwood Lisa and 3 more
Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906453
Loong Lucy, Cubuk Cankut, Choi Subin and 17 more
The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906454
Chora Joana R, Iacocca Michael A, Tichý Lukáš and 25 more
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906456
Isidor Bertrand, Ebstein Frédéric, Hurst Anna and 48 more
Quantifying evidence toward pathogenicity for rare phenotypes: The case of succinate dehydrogenase genes, SDHB and SDHD.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906457
Garrett Alice, Loveday Chey, King Laura and 30 more
The ACMG SF v3.0 gene list increases returnable variant detection by 22% when compared with v2.0 in the ClinSeq cohort.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906458
Johnston Jennifer J, Brennan Marie-Luise, Radenbaugh Bailey and 6 more
Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906464
Gonzales Patrick R, Andersen Erica F, Brown Teneille R and 7 more
Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906465
Osmond Matthew, Hartley Taila, Dyment David A and 5 more
Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humans.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906466
Qi Cai, Feng Irena, Costa Ana Rita and 23 more
Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906469
Hassanin Emadeldin, May Patrick, Aldisi Rana and 7 more
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906471
Duenas Devan M, Shipman Kelly J, Porter Kathryn M and 8 more
Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906479
Li Hongyan, Engel Christoph, de la Hoya Miguel and 58 more
Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disorders.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906484
Dingemans Alexander J M, Hinne Max, Jansen Sandra and 10 more
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906488
Fasham James, Lin Siying, Ghosh Promita and 37 more
Performance of polygenic risk scores for cancer prediction in a racially diverse academic biobank.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906489
Wang Louise, Desai Heena, Verma Shefali S and 12 more
Targeted BRCA1/2 population screening among Ashkenazi Jewish individuals using a web-enabled medical model: An observational cohort study.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906490
Morgan Kelly M, Hamilton Jada G, Symecko Heather and 25 more
Structural mapping of GABRB3 variants reveals genotype-phenotype correlations.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906499
Johannesen Katrine M, Iqbal Sumaiya, Guazzi Milena and 44 more
Identification and quantification of oligogenic loss-of-function disorders.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906500
Stefanski Arthur, Pérez-Palma Eduardo, Mrdjen Marko and 3 more
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906502
Bournazos Adam M, Riley Lisa G, Bommireddipalli Shobhana and 106 more
Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-01-01 | PMID 34906508
Yang Muyi, Johnsson Per, Bräutigam Lars and 17 more
Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906510
Zouk Hana, Yu Wanfeng, Oza Andrea and 14 more
Suspected clonal hematopoiesis as a natural functional assay of TP53 germline variant pathogenicity.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906512
Fortuno Cristina, McGoldrick Kelly, Pesaran Tina and 7 more
Polygenic risk scores for prediction of breast cancer risk in Asian populations.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-03-01 | PMID 34906514
Ho Weang-Kee, Tai Mei-Chee, Dennis Joe and 70 more
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-02-01 | PMID 34906515
Seltzsam Steve, Wang Chunyan, Zheng Bixia and 42 more
Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings.
Clinica chimica acta; international journal of clinical chemistry | 2022-01-15 | PMID 34906559
Liu Bei, Chen Mengjia, Yang Yanmei and 3 more
Effect of long-term chronic hyperhomocysteinemia on retinal structure and function in the cystathionine-β-synthase mutant mouse.
Experimental eye research | 2022-01-01 | PMID 34906600
Xiao Haiyan, Wang Jing, Barwick Shannon R and 2 more
The GG genotype of the serotonin 4 receptor genetic polymorphism, rs1345697, is associated with lower remission rates after antidepressant treatment: Findings from the METADAP cohort.
Journal of affective disorders | 2022-02-15 | PMID 34906639
Poinsignon Vianney, Colle Romain, Asmar Khalil El and 10 more
Description of PTPRG genetic variants identified in a cohort of Chronic Myeloid Leukemia patients and their ability to influence response to Tyrosine kinase Inhibitors.
Gene | 2022-03-01 | PMID 34906644
Ismail Mohamed A, Nasrallah Gheyath K, Monne Maria and 8 more
Whole exome sequencing identifies the potential role of genes involved in p53 pathway in Nasopharyngeal Carcinoma from Northeast India.
Gene | 2022-02-20 | PMID 34906645
Laskar Shaheen, Das Raima, Kundu Sharbadeb and 4 more
Gene migration of giardiasis in Iran; a microevolutionary scale for reflecting transmission patterns of Giardia lamblia assemblages in symptomatic patients.
Microbial pathogenesis | 2022-01-01 | PMID 34906658
Spotin Adel, Mohammadi-Ghalehbin Behnam, Mahami-Oskouei Mahmoud and 1 more
Efficacy of mRNA, adenoviral vector, and perfusion protein COVID-19 vaccines.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie | 2022-02-01 | PMID 34906769
Zinatizadeh Mohammad Reza, Zarandi Peyman Kheirandish, Zinatizadeh Maryam and 3 more
Characterization of a novel Lbx1 mouse loss of function strain.
Differentiation; research in biological diversity | 2000-01-01 | PMID 34906895
Decourtye Lyvianne, McCallum-Loudeac Jeremy A, Zellhuber-McMillan Sylvia and 3 more
Variant Identification in BARD1, PRDM9, RCC1, and RECQL in Patients with Ovarian Cancer by Targeted Next-generation Sequencing of DNA Pools.
Cancer prevention research (Philadelphia, Pa.) | 2022-03-01 | PMID 34906988
Suszynska Malwina, Ratajska Magdalena, Galka-Marciniak Paulina and 7 more
Senolytic-Mediated Elimination of Head and Neck Tumor Cells Induced Into Senescence by Cisplatin.
Molecular pharmacology | 2022-03-01 | PMID 34907000
Ahmadinejad Fereshteh, Bos Tasia, Hu Bin and 7 more
Oxidative regulation of chloroplast enzymes by thioredoxin and thioredoxin-like proteins in Arabidopsis thaliana.
Proceedings of the National Academy of Sciences of the United States of America | 2021-12-21 | PMID 34907017
Yokochi Yuichi, Fukushi Yuka, Wakabayashi Ken-Ichi and 2 more
Photosynthetic reaction center variants made via genetic code expansion show Tyr at M210 tunes the initial electron transfer mechanism.
Proceedings of the National Academy of Sciences of the United States of America | 2021-12-21 | PMID 34907018
Weaver Jared Bryce, Lin Chi-Yun, Faries Kaitlyn M and 5 more
Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome.
RMD open | 2021-12-01 | PMID 34907023
Norheim Katrine Brække, Imgenberg-Kreuz Juliana, Alexsson Andrei and 13 more
BAP1-deficient meningioma presenting with trabecular architecture and cytokeratin expression: a report of two cases and review of the literature.
Journal of clinical pathology | 2023-05-01 | PMID 34907091
Landry Alexander P, Wang Justin Z, Nassiri Farshad and 3 more
Metabolic drug survey highlights cancer cell dependencies and vulnerabilities.
Nature communications | 2021-12-14 | PMID 34907165
Pemovska Tea, Bigenzahn Johannes W, Srndic Ismet and 8 more
Social stratification without genetic differentiation at the site of Kulubnarti in Christian Period Nubia.
Nature communications | 2021-12-14 | PMID 34907168
Sirak Kendra A, Fernandes Daniel M, Lipson Mark and 22 more
Estimating the strength of selection for new SARS-CoV-2 variants.
Nature communications | 2021-12-14 | PMID 34907182
Dorp Christiaan H van, Goldberg Emma E, Hengartner Nick and 2 more
Competitive endogenous RNA network and pathway-based analysis of LncRNA single-nucleotide polymorphism in myasthenia gravis.
Scientific reports | 2021-12-14 | PMID 34907261
Wang Tianfeng, Xu Si, Zhang Huixue and 9 more
The minor T allele of the MUC5B promoter rs35705950 associated with susceptibility to idiopathic pulmonary fibrosis: a meta-analysis.
Scientific reports | 2021-12-14 | PMID 34907291
Wu Xiaozheng, Li Wen, Luo Zhenliang and 1 more
Distal mutation V486M disrupts the catalytic activity of DPP4 by affecting the flap of the propeller domain.
Acta pharmacologica Sinica | 2022-08-01 | PMID 34907358
Li Teng-Teng, Peng Cheng, Wang Ji-Qiu and 5 more
Genetic basis to structural grey matter associations with chronic pain.
Brain : a journal of neurology | 2021-12-31 | PMID 34907416
Farrell Scott F, Campos Adrián I, Kho Pik-Fang and 5 more
Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males.
Human genetics | 2022-02-01 | PMID 34907471
Kreienkamp Hans-Jürgen, Wagner Matias, Weigand Heike and 16 more
Anhedonia in Posttraumatic Stress Disorder: Prevalence, Phenotypes, and Neural Circuitry.
Current topics in behavioral neurosciences | 2022-01-01 | PMID 34907507
Vinograd Meghan, Stout Daniel M, Risbrough Victoria B
Evaluation of genetic divergence of coffee genotypes using the volatile compounds and sensory attributes profile.
Journal of food science | 2022-01-01 | PMID 34907528
Machado Jéssica Louzada, Tomaz Marcelo Antonio, da Luz José Maria Rodrigues and 5 more
Prenatal diagnosis of a likely pathogenic variant in ZBTB18: Natural evolution of fetal phenotype including the long bones and corpus callosum.
American journal of medical genetics. Part A | 2022-03-01 | PMID 34907638
Birnbaum Roee, Markovitch Ofer, Biron-Shental Tal and 4 more
Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.
American journal of medical genetics. Part A | 2022-04-01 | PMID 34907639
Schwarz Martin, Ryba Lukáš, Křepelová Anna and 8 more
Who are you? A framework to identify and report genetic sample mix-ups.
Molecular ecology resources | 2022-07-01 | PMID 34907643
Duntsch Laura, Brekke Patricia, Ewen John G and 1 more
The NF-κB pathway is critically implicated in the oncogenic phenotype of human osteosarcoma cells.
Journal of applied biomedicine | 2021-12-01 | PMID 34907738
Tan Bingyi, Yuan Zenong, Zhang Qingyu and 2 more
Genetic studies of nephrotic syndrome in Egyptian children.
Journal of applied biomedicine | 2021-12-01 | PMID 34907742
Elmougy Rehab
Genetic Diversity and Aggressiveness of Fusarium virguliforme Isolates Across the Midwestern United States.
Phytopathology | 2022-06-01 | PMID 34907789
Olarte Rodrigo A, Hall Rebecca, Tabima Javier F and 2 more
Mannose-binding lectin serum levels and (Gly54asp) gene polymorphism in recurrent aphthous stomatitis: A case-control study.
International journal of immunopathology and pharmacology | 2000-01-01 | PMID 34907799
Baioumy Shereen A, Fouad Shaimaa H, Abdalgeleel Shaimaa A and 3 more
Polymorphisms in vitamin B12 and folate metabolising genes and their association with adverse pregnancy outcome: secondary analysis of a population based case control study.
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology | 2022-07-01 | PMID 34907829
Dhiman Pooja, Bharadwaj Balaji, Veena P and 1 more
A Cluster-based Method to Quantify Individual Heterogeneity in Tuberculosis Transmission.
Epidemiology (Cambridge, Mass.) | 2022-03-01 | PMID 34907974
Smith Jonathan P, Gandhi Neel R, Silk Benjamin J and 8 more
A Multiplex SNaPshot Assay is a Rapid and Cost-Effective Method for Detecting POLE Exonuclease Domain Mutations in Endometrial Carcinoma.
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists | 2022-11-01 | PMID 34907997
Devereaux Kelly A, Steiner David F, Ho Chandler and 6 more
Correlation of epidermal growth factor receptor mutation status and PD-L1 expression with [18F]FDG PET using volume-based parameters in non-small cell lung cancer.
Nuclear medicine communications | 2022-03-01 | PMID 34908022
Ishimura Mariko, Norikane Takashi, Mitamura Katsuya and 6 more
CLOCK Genetic Variations Are Associated With Age-Related Changes in Sleep Duration and Brain Volume.
The journals of gerontology. Series A, Biological sciences and medical sciences | 2022-09-01 | PMID 34908110
Kim Song E, Kim Soriul, Kim Hyeon-Jin and 4 more
Circular RNAs in stem cells: from basic research to clinical implications.
Bioscience reports | 2022-01-28 | PMID 34908111
Lu Hui-Juan, Li Juan, Yang Guodong and 4 more
Chromosomal Fusions Facilitate Adaptation to Divergent Environments in Threespine Stickleback.
Molecular biology and evolution | 2022-02-03 | PMID 34908155
Liu Zuyao, Roesti Marius, Marques David and 3 more