Biomedical publications with connected research

The Mutation Portraits of Oncogenes and Tumor Supressor Genes in Predicting the Overall Survival in Pancreatic Cancer: A Bayesian Network Meta-Analysis.

Asian Pacific journal of cancer prevention : APJCP | 2023-08-01 | PMID 37642079

Aryanti Citra, Uwuratuw Julianus Aboyaman, Labeda Ibrahim and 7 more

Predicting EGFR Mutation in Lung Adenocarcinoma: Development and Validation of the EGFR Mutation Predictive Score (EMPS) in Bali, Indonesia.

Asian Pacific journal of cancer prevention : APJCP | 2023-08-01 | PMID 37642080

Njoto Edwin Nugroho, Jasminarti Dwi Kusumawardani Ida Ayu, Rai Ida Bagus Ngurah

MLH1 rs1800734 Pathogenic Variant among Patients with Colorectal Cancer in the Lower Northeastern Region of Thailand.

Asian Pacific journal of cancer prevention : APJCP | 2023-08-01 | PMID 37642081

Pongsavee Malinee, Wisuwan Kamol, Pongsavee Kritpipat

Genetic syndromes are prevalent in patients with comorbid neurodevelopmental disorders and catatonia.

American journal of medical genetics. Part A | 2023-11-01 | PMID 37642312

Shillington Amelle, Zappia Katherine J, White Lori and 4 more

Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani population.

The International journal of neuroscience | 2024-11-01 | PMID 37642370

Nasir Hashmi Aisha, Sabina Raja Merlyn, Taj Rizwan and 4 more

Venous Tortuosity in COL4A2-Associated Gould Syndrome.

Ophthalmic surgery, lasers & imaging retina | 2023-09-01 | PMID 37642429

Oh Jin Kyun, Levi Sarah R, de Carvalho Jose Ronaldo Lima and 4 more

Flagella-related gene mutations in Vibrio cholerae during extended cultivation in nutrient-limited media impair cell motility and prolong culturability.

mSystems | 2023-10-26 | PMID 37642466

Okada Kazuhisa, Roobthaisong Amonrattana, Hamada Shigeyuki

Case 320.

Radiology | 2023-08-01 | PMID 37642568

Abramson Zachary, Schechter Ann

Gene-Environment Analyses in a UK Biobank Skin Cancer Cohort Identifies Important SNPs in DNA Repair Genes That May Help Prognosticate Disease Risk.

Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology | 2023-11-01 | PMID 37642678

Jeremian Richie, Xie Pingxing, Fotovati Misha and 2 more

Genome-wide association and targeted transcriptomic analyses reveal loci and candidate genes regulating preharvest sprouting in barley.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2023-08-29 | PMID 37642745

Kaur Gurkamal, Toora Parneet K, Tuan Pham Anh and 4 more

Quality trait improvement in horticultural crops: OMICS and modern biotechnological approaches.

Molecular biology reports | 2023-10-01 | PMID 37642759

Bashir Tanzeel, Ul Haq Syed Anam, Masoom Salsabeel and 2 more

Clinical phenotypes and prognosis of IgG4-related diseases accompanied by deteriorated kidney function: a retrospective study.

Clinical rheumatology | 2024-01-01 | PMID 37642763

Guo Luying, Yang Zhenzhen, Cheng Yamei and 10 more

Investigating genetic polymorphism in E. histolytica isolates with distinct clinical phenotypes.

Parasitology research | 2023-11-01 | PMID 37642770

Sardar Sanjib K, Ghosal Ajanta, Haldar Tapas and 6 more

An early onset cone dystrophy due to CEP290 mutation: a case report.

Documenta ophthalmologica. Advances in ophthalmology | 2023-12-01 | PMID 37642804

Binder Anastasia, Kohl Susanne, Grasshoff Ute and 2 more

Targeted Mutagenesis of Mycobacterium Strains by Homologous Recombination.

Methods in molecular biology (Clifton, N.J.) | 2023-01-01 | PMID 37642839

Song Shikui, Su Zhengding

Roles of MT-ND1 in Cancer.

Current medical science | 2023-10-01 | PMID 37642864

Xu Yi-Chun, Su Jun, Zhou Jia-Jing and 2 more

Examining Phenotypical Heterogeneity and its Underlying Factors in Gesture Skills of Chinese Autistic Children: Clustering Analysis.

Journal of autism and developmental disorders | 2024-09-01 | PMID 37642873

Zhang Xin, Song Xue-Ke, So Wing-Chee

Vitamin B1 deficiency leads to high oxidative stress and mtDNA depletion caused by SLC19A3 mutation in consanguineous family with Leigh syndrome.

Metabolic brain disease | 2023-10-01 | PMID 37642897

Felhi Rahma, Sfaihi Lamia, Charif Majida and 5 more

Co-circulation of Hepatitis E Virus (HEV) Genotype 3 and Moose-HEV-Like Strains in Free-Ranging-Spotted Deer (Axis axis) in Uruguay.

Food and environmental virology | 2023-12-01 | PMID 37642917

Cancela Florencia, Cravino Alexandra, Icasuriaga Romina and 8 more

Mapping temperature-sensitive mutations at a genome scale to engineer growth switches in Escherichia coli.

Molecular systems biology | 2023-10-12 | PMID 37642940

Schramm Thorben, Lubrano Paul, Pahl Vanessa and 3 more

Cranio-cervical abnormalities in moderate-to-severe osteogenesis imperfecta - Genotypic and phenotypic determinants.

Orthodontics & craniofacial research | 2024-04-01 | PMID 37642979

Marulanda Juliana, Retrouvey Jean-Marc, Lee Brendan and 3 more

Predicting the changes in neutralizing antibody interaction with G protein derived from Bangladesh isolates of Nipah virus: molecular dynamics based approach.

Journal of biomolecular structure & dynamics | 2024-11-01 | PMID 37643003

Dsouza Norine, C Selvaa Kumar

Flavonoids as potential reactivators of structural mutation p53Y220C by computational and cell-based studies.

Journal of biomolecular structure & dynamics | 2024-11-01 | PMID 37643005

Malhotra Lakshay, Kaur Punit, Ethayathulla Abdul Samath

Acid-base homeostasis orchestrated by NHE1 defines the pancreatic stellate cell phenotype in pancreatic cancer.

JCI insight | 2023-10-09 | PMID 37643024

Pethő Zoltán, Najder Karolina, Beel Stephanie and 10 more

The Landscape of Alterations from 1407 Ultra-Rare Sarcomas from the AACR GENIE Database: Clinical Implications.

Clinical cancer research : an official journal of the American Association for Cancer Research | 2023-11-14 | PMID 37643131

Denu Ryan A, Moyers Justin T, Gouda Mohamed A and 3 more

Assessing the Genomic Landscape of Cervical Cancers: Clinical Opportunities and Therapeutic Targets.

Clinical cancer research : an official journal of the American Association for Cancer Research | 2023-11-14 | PMID 37643132

Friedman Claire F, Ravichandran Vignesh, Miller Kathryn and 19 more

Identification of MKI67, TPR , and TCHH Mutations as Prognostic Biomarkers for Patients With Defective Mismatch Repair Colon Cancer Stage II/III.

Diseases of the colon and rectum | 2023-11-01 | PMID 37643197

Lv Jingfang, Li Wenbin, Wang Xintong and 8 more

A Novel Pair of Compound Heterozygous Mutation of EYS in a Han Chinese Family with Retinitis Pigmentosa.

Genetic testing and molecular biomarkers | 2023-08-01 | PMID 37643323

Dai Chao, Ren Weiming, Wei Yao and 5 more

Phase II Trial of Dabrafenib Plus Trametinib in Relapsed/Refractory BRAF V600-Mutant Pediatric High-Grade Glioma.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2023-11-20 | PMID 37643378

Hargrave Darren R, Terashima Keita, Hara Junichi and 10 more

ProS-GNN: Predicting effects of mutations on protein stability using graph neural networks.

Computational biology and chemistry | 2023-12-01 | PMID 37643501

Wang Shuyu, Tang Hongzhou, Shan Peng and 2 more

Protomer selectivity of type II RAF inhibitors within the RAS/RAF complex.

Cell chemical biology | 2023-11-16 | PMID 37643616

Vasta James D, Michaud Ani, Zimprich Chad A and 7 more

Breast cancers arising in subjects with germline BRCA1 or BRCA2 mutations: Different biological and clinical entities with potentially diverse therapeutic opportunities.

Critical reviews in oncology/hematology | 2023-10-01 | PMID 37643668

Zattarin Emma, Taglialatela Ida, Lobefaro Riccardo and 13 more

Error-corrected next generation sequencing - Promises and challenges for genotoxicity and cancer risk assessment.

Mutation research. Reviews in mutation research | 2000-01-01 | PMID 37643677

Marchetti Francesco, Cardoso Renato, Chen Connie L and 17 more

Complete genome of an inhibitor-resistant blaTEM-30 encoding Escherichia coli sequence type 127 isolate identified in human saliva with a high genotypic virulence load.

Journal of global antimicrobial resistance | 2023-12-01 | PMID 37643688

McEvoy Niamh, O'Connor Andy, McDonagh Francesca and 7 more

A Bayesian method for estimating gene-level polygenicity under the framework of transcriptome-wide association study.

Statistics in medicine | 2023-11-20 | PMID 37643728

Majumdar Arunabha, Pasaniuc Bogdan

Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing.

Cancer genomics & proteomics | 2000-01-01 | PMID 37643779

Agiannitopoulos Konstantinos, Pepe Georgia, Tsaousis Georgios N and 32 more

CYBA as a Potential Biomarker for Renal Cell Carcinoma: Evidence from an Integrated Genetic Analysis.

Cancer genomics & proteomics | 2000-01-01 | PMID 37643785

Chang Chi-Fen, Huang Shu-Pin, Hsueh Yu-Mei and 5 more

Brain network structural connectome abnormalities among youth with attention-deficit/hyperactivity disorder at varying risk for bipolar I disorder: a cross-sectional graph-based magnetic resonance imaging study.

Journal of psychiatry & neuroscience : JPN | 2000-01-01 | PMID 37643802

Zhu Ziyu, Lei Du, Qin Kun and 10 more

Idiopathic CD4+ T-lymphocytopaenia with FLT1 mutation complicated by progressive multifocal leucoencephalopathy and EBV+ polymorphic lymphoproliferative disorder.

BMJ case reports | 2023-08-29 | PMID 37643816

Rippel Noa, Wong Joshua, Hussein Shafinaz and 1 more

Hypertriglyceridaemic waist phenotype and waist circumference triglyceride index are associated with higher incidence of acute pancreatitis: a nationwide population-based retrospective cohort study.

BMJ open | 2023-08-29 | PMID 37643853

Chung Kwang Hyun, Choi Young Hoon, Cho In Rae and 5 more

Long-term Natural History of Pediatric Dominant and Recessive RYR1-Related Myopathy.

Neurology | 2023-10-10 | PMID 37643885

Sarkozy Anna, Sa Mario, Ridout Deborah and 16 more

NEXMIF variants are associated with epilepsy with or without intellectual disability.

Seizure | 2024-03-01 | PMID 37643945

Ye Zi-Long, Yan Hong-Jun, Guo Qing-Hui and 10 more

[Analysis of phenotype and pathogenic variants in a Chinese pedigree affected with Multiple synostoses syndrome type 1].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2023-09-10 | PMID 37643958

Zhang Wenyuan, Mao Lu, Zhang Jinhui and 2 more

Clinical and genetic analysis of essential hypertension with CYB gene m.15024G>A mutation.

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences | 2023-08-25 | PMID 37643984

He Yunfan, Li Wenxu, Liu Zhen and 2 more

Global determinants of insect mitochondrial genetic diversity.

Nature communications | 2023-08-29 | PMID 37644003

French Connor M, Bertola Laura D, Carnaval Ana C and 9 more

Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families.

Nature communications | 2023-08-29 | PMID 37644014

AlAbdi Lama, Maddirevula Sateesh, Shamseldin Hanan E and 13 more

Effects of emotional content on social inhibition of gaze in live social and non-social situations.

Scientific reports | 2023-08-29 | PMID 37644088

Pasqualette Laura, Kulke Louisa

Clinicohistoradiological and surgical outcome in diffuse midline glioma.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery | 2024-01-01 | PMID 37644138

Kumar Suman Arvind, Bhattacharjee Suchanda, Uppin Megha S and 1 more

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

European journal of human genetics : EJHG | 2023-11-01 | PMID 37644171

Oppermann Henry, Marcos-Grañeda Elia, Weiss Linnea A and 52 more

Reduced ADP off-rate by the yeast CCT2 double mutation T394P/R510H which causes Leber congenital amaurosis in humans.

Communications biology | 2023-08-29 | PMID 37644231

Roy Mousam, Fleisher Rachel C, Alexandrov Alexander I and 1 more

Investigating the relationship between the VNTR variant of the interleukin-1 receptor antagonist gene and coronary in-stent restenosis.

Molecular biology reports | 2023-10-01 | PMID 37644369

Klashami Zeynab Nickhah, Mostafavi Atoosa, Roudbordeh Majid Gholamzadeh and 4 more

BRCA genes as candidates for colorectal cancer genetic testing panel: systematic review and meta-analysis.

BMC cancer | 2023-08-29 | PMID 37644384

Feng Zhewen, Yang Xiaobao, Tian Mingwei and 8 more

Anatomical observation and transcriptome analysis of branch-twisted mutations in Chinese jujube.

BMC genomics | 2023-08-29 | PMID 37644409

Luo Zhi, Gao Mengjiao, Zhao Xuan and 7 more

Genetic contribution of synapse-associated protein 97 to cerebellar functional connectivity changes in first-episode schizophrenia.

BMC psychiatry | 2023-08-29 | PMID 37644438

Xu Xusan, Luo Shucun, Wang Xiaoxia and 16 more

A knowledge graph approach to predict and interpret disease-causing gene interactions.

BMC bioinformatics | 2023-08-29 | PMID 37644440

Renaux Alexandre, Terwagne Chloé, Cochez Michael and 3 more

Meta-analysis of African ancestry genome-wide association studies identified novel locus and validates multiple loci associated with kidney function.

BMC genomics | 2023-08-29 | PMID 37644460

Kintu Christopher, Soremekun Opeyemi, Machipisa Tafadzwa and 6 more

Heritability and recursive influence of host genetics on the rumen microbiota drive body weight variance in male Hu sheep lambs.

Microbiome | 2023-08-29 | PMID 37644504

Wang Weimin, Zhang Yukun, Zhang Xiaoxue and 17 more

Association of integrin-β2 polymorphism and expression with the risk of rheumatoid arthritis and osteoarthritis in Egyptian patients.

BMC medical genomics | 2023-08-29 | PMID 37644537

Selim Aliaa M, Elsabagh Yumn A, El-Sawalhi Maha M and 2 more

Identification of two novel SALL1 mutations in chinese families with townes-brocks syndrome and literature review.

Orphanet journal of rare diseases | 2023-08-29 | PMID 37644569

Wang Zhendong, Sun Zhenfu, Diao Yujie and 5 more

Genes: SALL1

A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis.

Human genomics | 2023-08-29 | PMID 37644603

Jiang Yuan, Liu Qianwen, Alfredsson Lars and 3 more

Analysis of genetic factors associated with fatty liver disease-related hepatocellular carcinoma.

Cancer medicine | 2023-09-01 | PMID 37644826

Kogiso Tomomi, Ogasawara Yuri, Horiuchi Kentaro and 2 more

Genes: HSD17B13, PNPLA3, GC

A multivariate approach to understanding the genetic overlap between externalizing phenotypes and substance use disorders.

Addiction biology | 2023-09-01 | PMID 37644899

Poore Holly E, Hatoum Alexander, Mallard Travis T and 6 more

Machine learning-based radiomics for predicting BRAF-V600E mutations in ameloblastoma.

Frontiers in immunology | 2023-01-01 | PMID 37646022

Li Wen, Li Yang, Liu Xiaoling and 7 more

Discrepancy between recipient and donor rs4364254 heparanase single nucleotide polymorphism impacts graft-versus-host disease after allogeneic stem cell transplant.

International journal of laboratory hematology | 2023-12-01 | PMID 37646104

Metafuni Elisabetta, Giammarco Sabrina, Bellesi Silvia and 7 more

Is there a massive glacial-Holocene flora continuity in Central Europe?

Biological reviews of the Cambridge Philosophical Society | 2023-12-01 | PMID 37646107

Molnár Ábel Péter, Demeter László, Biró Marianna and 4 more

Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3.

British journal of haematology | 2023-11-01 | PMID 37646304

Novak Wolfgang, Berner Jakob, Svaton Michael and 13 more

Angioimmunoblastic T-cell lymphoma: Novel recurrent mutations and prognostic biomarkers by cell-free DNA profiling.

British journal of haematology | 2023-12-01 | PMID 37646306

Zhang Chunlan, Mou Biqin, Xu Juan and 6 more

Alzheimer's disease phenotype based upon the carrier status of the apolipoprotein E ɛ4 allele.

Brain pathology (Zurich, Switzerland) | 2024-01-01 | PMID 37646624

Ji Xiao-Yu, Peng Xin-Yuan, Tang Hai-Liang and 5 more

Structure-based virtual screening of natural compounds against wild and mutant (R1155K, A1156T and D1168A) NS3-4A protease of Hepatitis C virus.

Journal of biomolecular structure & dynamics | 2024-10-01 | PMID 37646701

Samantaray Mahesh, Pattabiraman Ramya, Murthy T P Krishna and 4 more

Autosomal recessive otospondylo-mega-epiphyseal dysplasia: comprehensive clinical review of a pediatric cohort.

Clinical dysmorphology | 2023-10-01 | PMID 37646720

Mutlu Hatice, Elçioğlu Nursel, Kiliç Esra

Phenotype Control techniques for Boolean gene regulatory networks.

Bulletin of mathematical biology | 2023-08-30 | PMID 37646851

Plaugher Daniel, Murrugarra David

Bioaccumulation of Chloropyrifos Organo-pesticide and Its Toxicogenic Association with Antioxidant GSTP1 in Pakistani Pest Control Workers.

Applied biochemistry and biotechnology | 2024-06-01 | PMID 37646887

Imran Iffat, Moin Syed Faraz, Saleem Saima and 2 more

Analysis of Rocky Mountain spotted fever cases in Northern Mexico reveals genetic variability of Rickettsia rickettsii and the different distribution of genotypes.

International microbiology : the official journal of the Spanish Society for Microbiology | 2024-06-01 | PMID 37646898

Brito-Lorán Carina Berenice, Araiza-Rodríguez Adnan, Garcés-Ayala Fabiola and 6 more

Generation of an induced pluripotent stem cell line from a patient with epileptic encephalopathy caused by the CYFIP2 R87C variant.

Human cell | 2023-11-01 | PMID 37646972

Silva Isabelle Leticia Zaboroski, Gomes-Júnior Rubens, da Silva Evelin Brandão and 4 more

Genes: CYFIP2

Longitudinal effects of FTO gene polymorphism on body composition, cardiorespiratory fitness, physical activity, inflammatory markers, and cardiovascular risk in children and adolescents. "The UP & DOWN study".

Scandinavian journal of medicine & science in sports | 2023-11-01 | PMID 37647022

Mier-Mota Julián, Ponce-González Jesús G, Perez-Bey Alejandro and 5 more

Genes: FTO

Association of single nucleotide variants in VEGFA and KDR with the risk and angiogenic features of diffuse large B-cell lymphoma.

Leukemia & lymphoma | 2023-12-01 | PMID 37647140

Assis-Mendonça Guilherme Rossi, Campos Letícia Goulart, Delamain Márcia Torresan and 6 more

Effect of vitamin D receptor gene BsmI polymorphism on hospitalization of SARS-CoV-2 positive patients.

Nucleosides, nucleotides & nucleic acids | 2024-01-01 | PMID 37647163

Aci Recai, Keskin Adem, Yigit Serbulent and 2 more

Evaluation of KIR3DL1/KIR3DS1 allelic polymorphisms in Kenyan children with endemic Burkitt lymphoma.

PloS one | 2023-01-01 | PMID 37647275

Muriuki Beatrice M, Forconi Catherine S, Kirwa Erastus K and 6 more

Sex differences in radioulnar contrasts of the finger ridge counts across 21 human population samples.

Annals of human biology | 2023-02-01 | PMID 37647353

Polcerová L, Jantz R L, Králík M and 2 more

Evolution of a fatty acyl-CoA elongase underlies desert adaptation in Drosophila.

Science advances | 2023-09-01 | PMID 37647401

Wang Zinan, Pu Jian, Richards Cole and 4 more

Leaf metabolic traits reveal hidden dimensions of plant form and function.

Science advances | 2023-09-01 | PMID 37647404

Walker Tom W N, Schrodt Franziska, Allard Pierre-Marie and 28 more

A new CECR1 mutation associated with severe hematological involvement in ADA2 deficiency.

Immunity, inflammation and disease | 2023-08-01 | PMID 37647436

Nicoară Delia, Niță Cristina, Stanilă Ana and 9 more

Whole-genome sequencing of diverse wheat accessions uncovers genetic changes during modern breeding in China and the United States.

The Plant cell | 2023-11-30 | PMID 37647532

Niu Jianqing, Ma Shengwei, Zheng Shusong and 23 more

A Genetic Lab-on-Phone Test for Point-of-Care Diagnostic of Lactose Intolerance near Patient and in less than 90 Minutes.

The journal of applied laboratory medicine | 2024-01-03 | PMID 37647590

Conceição Mariana, Assunção Hugo, Doria Gonçalo and 10 more

Arabidopsis thaliana Subclass I ACTIN DEPOLYMERIZING FACTORs Regulate Nuclear Organization and Gene Expression.

Plant & cell physiology | 2023-10-16 | PMID 37647615

Matsumoto Tomoko, Higaki Takumi, Takatsuka Hirotomo and 5 more

Extracorporeal Membrane Oxygenation-Dependent Fulminant Melioidosis From Caspase 4 Mutation Reversed by Interferon Gamma Therapy.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 2024-01-25 | PMID 37647624

Amali Aseervatham Anusha, Ravikumar Sharada, Chew Wei Leong and 6 more

diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype.

Bioinformatics (Oxford, England) | 2023-09-02 | PMID 37647638

Huang Daoyi, Jiang Jianping, Zhao Tingting and 10 more

HAPNEST: efficient, large-scale generation and evaluation of synthetic datasets for genotypes and phenotypes.

Bioinformatics (Oxford, England) | 2023-09-02 | PMID 37647640

Wharrie Sophie, Yang Zhiyu, Raj Vishnu and 10 more

Molecular MRD is strongly prognostic in patients with NPM1-mutated AML receiving venetoclax-based nonintensive therapy.

Blood | 2024-01-25 | PMID 37647641

Othman Jad, Tiong Ing S, O'Nions Jenny and 33 more

Correlations of receptor desensitization of gain-of-function GABRB3 variants with clinical severity.

Brain : a journal of neurology | 2024-01-04 | PMID 37647766

Lin Susan X N, Ahring Philip K, Keramidas Angelo and 4 more

Defining the phenotype of PGAP3-congenital disorder of glycosylation; a review of 65 cases.

Molecular genetics and metabolism | 2023-11-01 | PMID 37647829

Altassan Ruqaiah, Allers Michael M, De Graef Diederik and 5 more

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis.

Brain : a journal of neurology | 2023-12-01 | PMID 37647852

Stefanski Arthur, Pérez-Palma Eduardo, Brünger Tobias and 43 more

TP53 status and impact on AML prognosis within the ELN 2022 risk classification.

Blood | 2023-12-07 | PMID 37647854

Fleming Shaun, Tsai Xavier Cheng-Hong, Morris Rhiannon and 2 more

Differential patterns of within- and between-population genetically based trait variation in Lupinus angustifolius.

Annals of botany | 2023-11-23 | PMID 37647862

Poyatos Cristina, Sacristán-Bajo Sandra, Tabarés Pablo and 7 more

BRAF/MEK Inhibition as a Bridge to Immunotherapy for Symptomatic BRAF V600 Melanoma Brain Metastases: A Case Series.

Journal of the National Comprehensive Cancer Network : JNCCN | 2023-08-29 | PMID 37647938

Strelnikov Jacob, Zhou Alice, Butt Omar and 2 more

Mutation of aspartic acid 262 on estrogen receptor abrogates estradiol signaling pathway.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology | 2023-12-01 | PMID 37647939

Xu Xingyan, Yu Haowei, Zhu Shuihao and 7 more

SMAD4 and KCNQ3 alterations are associated with lymph node metastases in oesophageal adenocarcinoma.

Biochimica et biophysica acta. Molecular basis of disease | 2024-01-01 | PMID 37648039

Foley Kieran, Shorthouse David, Rahrmann Eric and 5 more

Genetic causes of sporadic and recurrent miscarriage.

Fertility and sterility | 2023-11-01 | PMID 37648143

Melo Pedro, Dhillon-Smith Rima, Islam Md Asiful and 2 more

Characterization of the novel HLA-A*26:233 allele by sequencing based typing.

HLA | 2023-11-01 | PMID 37648220

Liu Tongyuan, Chen Liting, Xiao Min and 2 more

NKG2A gene variant predicts outcome of immunotherapy in AML and modulates the repertoire and function of NK cells.

Journal for immunotherapy of cancer | 2023-08-01 | PMID 37648262

Hussein Brwa Ali, Kristenson Linnea, Pesce Silvia and 8 more