Bispecific T cell engagers kill resistant cells during KRAS-G12C blockade therapy.
Oncoimmunology | 2022-01-01 | PMID 36338145
Song Xinxin, Zhou Zhuan, Kang Rui and 1 more
Genes: KRAS
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 9037 of 10600
Association of IGF1 polymorphisms with exotropia in a Pakistani cohort.
Molecular vision | 2022-01-01 | PMID 36338665
Zehra Zainab, Khan Netasha, Nadeem Minhal and 4 more
Clinical and genetic studies of 17 Han Chinese pedigrees and 31 sporadic patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
Molecular vision | 2022-01-01 | PMID 36338666
Wang Yuan, Wu Qian, Cao Wenhong and 4 more
Structural and functional analysis of SNP rs76740365 G>A in exon-3 of the alpha A-crystallin gene in lens epithelial cells.
Molecular vision | 2022-01-01 | PMID 36338667
Zhao Zhennan, Sun Yang, Fan Qi and 2 more
Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene.
Molecular vision | 2022-01-01 | PMID 36338669
Ali-Nasser Tahleel, Zayit-Soudry Shiri, Banin Eyal and 2 more
A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes.
Molecular vision | 2022-01-01 | PMID 36338671
Kjellström Ulrika, Andréasson Sten
Association of CYP2D6*4 Polymorphism with the Steady-State Concentration of Haloperidol in Patients with Alcohol-Induced Psychotic Disorders.
Psychopharmacology bulletin | 2022-10-27 | PMID 36339274
Parkhomenko A A, Zastrozhin M S, Pozdnyakov S A and 8 more
A novel STAT1 loss-of-function mutation associated with Mendelian susceptibility to mycobacterial disease.
Frontiers in cellular and infection microbiology | 2022-01-01 | PMID 36339330
Ye Fanghua, Zhang Wen, Dong Jiajia and 5 more
NGS in the clinical microbiology settings.
Frontiers in cellular and infection microbiology | 2022-01-01 | PMID 36339334
Pitashny Milena, Kadry Balqees, Shalaginov Raya and 5 more
Cardiovascular abnormalities and its correlation with genotypes of children with osteogenesis imperfecta.
Frontiers in endocrinology | 2022-01-01 | PMID 36339400
Zhao Dichen, Liu Yongtai, Liu Jidong and 7 more
Genetic risk score to improve prediction and treatment in gestational diabetes mellitus.
Frontiers in endocrinology | 2022-01-01 | PMID 36339414
Tian Yumeng, Li Ping
An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature.
Frontiers in endocrinology | 2022-01-01 | PMID 36339422
Liao Qian, Shen Rufei, Liao Mingyu and 7 more
Causal relationship between osteoporosis and osteoarthritis: A two-sample Mendelian randomized study.
Frontiers in endocrinology | 2022-01-01 | PMID 36339427
Lin Liu, Luo Pan, Yang Mingyi and 3 more
Betaine Inhibits NLRP3 Inflammasome Hyperactivation and Regulates Microglial M1/M2 Phenotypic Differentiation, Thereby Attenuating Lipopolysaccharide-Induced Depression-Like Behavior.
Journal of immunology research | 2022-01-01 | PMID 36339940
Zhang Man, Wang Xiao-Long, Shi Hui and 5 more
Genes: NLRP3, TNF, TST
A synonymous mutation in PI4KA impacts the transcription and translation process of gene expression.
Frontiers in immunology | 2022-01-01 | PMID 36341355
Zhang Kaihui, Kang Lili, Zhang Haozheng and 12 more
The immune factors have complex causal regulation effects on bone mineral density.
Frontiers in immunology | 2022-01-01 | PMID 36341399
Cao Rong-Rong, Yu Xing-Hao, Xiong Meng-Fei and 3 more
Association of smoking status with non-small cell lung cancer patients harboring uncommon epidermal growth factor receptor mutation.
Frontiers in immunology | 2022-01-01 | PMID 36341427
Ko How-Wen, Shie Shian-Sen, Wang Chih-Wei and 10 more
Case report: ETS1 gene deletion associated with a low number of recent thymic emigrants in three patients with Jacobsen syndrome.
Frontiers in immunology | 2022-01-01 | PMID 36341443
Trachsel Tina, Prader Seraina, Steindl Katharina and 1 more
IL7RA single nucleotide polymorphisms are associated with the size and function of the MAIT cell population in treated HIV-1 infection.
Frontiers in immunology | 2022-01-01 | PMID 36341446
Han Fei, Gulam Muhammad Yaaseen, Zheng Yichao and 14 more
T cell-inflamed gene expression profile is associated with favorable disease-specific survival in non-hypermutated microsatellite-stable colorectal cancer patients.
Cancer medicine | 2023-03-01 | PMID 36341526
Yin Hang, Harrison Tabitha A, Thomas Sushma S and 11 more
Genes: APC, AREG, EPCAM, ITGA6, RPL23, RYR1
Association of Gene Polymorphisms in CXC Chemokine Receptor 5 with Rheumatoid Arthritis Susceptibility.
Iranian journal of allergy, asthma, and immunology | 2022-10-26 | PMID 36341562
Su Zhenzhen, Chen Lin, Niu Qian and 2 more
A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants.
Ophthalmic genetics | 2023-10-01 | PMID 36341712
Hikoya Akiko, Hosono Katsuhiro, Ono Kaoru and 8 more
Identification of RP1 as the genetic cause of retinitis pigmentosa in a multi-generational pedigree using Extremely Low-Coverage Whole Genome Sequencing (XLC-WGS).
Gene | 2023-01-30 | PMID 36341727
Lázaro-Guevara José M, Flores-Robles Bryan-Josué, Garrido-Lopez Karen M and 10 more
Mercaptopurine induced myelosuppression in a child with a NUDT15 rs116855232 homozygous variant.
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners | 2023-06-01 | PMID 36341754
Gupta Navya, Magatha Latha Sneha, Jayaraman Dhaarani and 3 more
Gene drive by Fusarium SKC1 is dependent on its competing allele.
Fungal genetics and biology : FG & B | 2022-11-01 | PMID 36341840
Lohmar Jessica M, Rhoades Nicholas A, Hammond Thomas M and 1 more
Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A.
European journal of medical genetics | 2022-12-01 | PMID 36341869
Zhang Bo, Ding Ying, Ren Xianqing and 4 more
Knockdown and mutation of Pou4f3 gene mutation promotes pyroptosis of cochleae in cisplatin-induced deafness mice by NLRP3/caspase-3/GSDME pathway.
Toxicology | 2022-12-01 | PMID 36341876
Yu Rong, Wang Kai, Luo Wugen and 1 more
Right anterior theta connectivity predicts autistic social traits in typically developing children.
Biological psychology | 2022-11-01 | PMID 36341882
Hill Aron T, Van Der Elst Jodie, Bigelow Felicity J and 2 more
A pituitary gene network linking vgll3 to regulators of sexual maturation in male Atlantic salmon.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology | 2023-01-01 | PMID 36341967
Ahi Ehsan Pashay, Sinclair-Waters Marion, Donner Iikki and 1 more
RAS: Circuitry and therapeutic targeting.
Cellular signalling | 2023-01-01 | PMID 36341985
Singh Gagandeep, Thakur Neelam, Kumar Umesh
Sequence-based Prediction of the Cellular Toxicity Associated with Amyloid Aggregation within Protein Condensates.
Biochemistry | 2022-11-15 | PMID 36341999
Horvath Attila, Vendruscolo Michele, Fuxreiter Monika
Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole-exome sequencing.
Molecular genetics & genomic medicine | 2022-12-01 | PMID 36342087
Xu Yan, Zhao Rui, Wang Min and 6 more
Chromosome 6p amplification detected in blood cell-free DNA in advanced intraocular retinoblastoma.
Ophthalmic genetics | 2022-12-01 | PMID 36342106
Sirivolu Shreya, Xu Liya, Warren Mikako and 5 more
Defining Composition and Function of the Rhizosphere Microbiota of Barley Genotypes Exposed to Growth-Limiting Nitrogen Supplies.
mSystems | 2022-12-20 | PMID 36342125
Alegria Terrazas Rodrigo, Robertson-Albertyn Senga, Corral Aileen Mary and 11 more
A refreshed approach to homology-Prioritizing epistemology over metaphysics.
Journal of morphology | 2023-01-01 | PMID 36342140
Minelli Alessandro
Identification of the novel HLA-DPA1*01:03:43 allele resulting from an intralocus recombination involving the DPA1*04:01:01:03 and DPA1*01:03:01:27 alleles sequenced by Next Generation Sequencing (NGS).
International journal of immunogenetics | 2023-02-01 | PMID 36342183
Hannah Turnbull, Gemma Brewin, Sarah Peacock
Identification of a Functional Susceptibility Variant for Adolescent Idiopathic Scoliosis that Upregulates Early Growth Response 1 (EGR1)-Mediated UNCX Expression.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2023-01-01 | PMID 36342191
Yonezawa Yoshiro, Guo Long, Kakinuma Hisaya and 46 more
Gene-by-environment interactions in plants: Molecular mechanisms, environmental drivers, and adaptive plasticity.
The Plant cell | 2023-01-02 | PMID 36342220
Napier Joseph D, Heckman Robert W, Juenger Thomas E
ViMRT: a text-mining tool and search engine for automated virus mutation recognition.
Bioinformatics (Oxford, England) | 2023-01-01 | PMID 36342236
Tong Yuantao, Tan Fanglin, Huang Honglian and 10 more
Parallel Evolution of Pseudomonas aeruginosa during a Prolonged ICU-Infection Outbreak.
Microbiology spectrum | 2022-12-21 | PMID 36342287
Cameron David R, Pitton Melissa, Oberhaensli Simone and 5 more
Implementing High Dimensional Reduction Analysis on Histocytometric Data.
Current protocols | 2022-11-01 | PMID 36342306
Munoz-Erazo Luis, Shinko Diana, Schmidt Alfonso J and 1 more
Dorzagliatin, a Dual-Acting Glucokinase Activator, Increases Insulin Secretion and Glucose Sensitivity in Glucokinase Maturity-Onset Diabetes of the Young and Recent-Onset Type 2 Diabetes.
Diabetes | 2023-02-01 | PMID 36342518
Chow Elaine, Wang Ke, Lim Cadmon K P and 9 more
On- and Off-Target Analyses of CRISPR-Cas12b Genome Editing Systems in Rice.
The CRISPR journal | 2023-02-01 | PMID 36342783
Gurel Filiz, Wu Yuechao, Pan Changtian and 4 more
Neonatal kaempferol exposure attenuates gait and strength deficits and prevents altered muscle phenotype in a rat model of cerebral palsy.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience | 2023-02-01 | PMID 36342836
Visco Diego Bulcão, Manhães de Castro Raul, da Silva Márcia Maria and 8 more
Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations.
PLoS genetics | 2022-11-01 | PMID 36342933
Taraszka Kodi, Zaitlen Noah, Eskin Eleazar
The OPRM1 gene and interactions with the 5-HT1a gene regulate conditioned pain modulation in fibromyalgia patients and healthy controls.
PloS one | 2022-01-01 | PMID 36342939
Tour Jeanette, Sandström Angelica, Kadetoff Diana and 2 more
Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype.
Annals of the American Thoracic Society | 2023-03-01 | PMID 36342963
Barber Andrew T, Shapiro Adam J, Davis Stephanie D and 14 more
Cryo-EM of prion strains from the same genotype of host identifies conformational determinants.
PLoS pathogens | 2022-11-01 | PMID 36342968
Hoyt Forrest, Alam Parvez, Artikis Efrosini and 8 more
Mosaic patterns of selection in genomic regions associated with diverse human traits.
PLoS genetics | 2022-11-01 | PMID 36342969
Abraham Abin, LaBella Abigail L, Capra John A and 1 more
Transcriptional licensing is required for Pyrin inflammasome activation in human macrophages and bypassed by mutations causing familial Mediterranean fever.
PLoS biology | 2022-11-01 | PMID 36342970
Mangan Matthew S J, Gorki Friederike, Krause Karoline and 10 more
Polygenic risk scores for prediction of breast cancer in Korean women.
International journal of epidemiology | 2023-06-06 | PMID 36343017
Jee Yon Ho, Ho Weang-Kee, Park Sohee and 4 more
Poziotinib in non-small-cell lung cancer patients with HER2 exon 20 mutations: A pooled analysis of randomized clinical trials.
Medicine | 2022-11-04 | PMID 36343036
Wang Bi-Cheng, Kuang Bo-Hua, Liu Xin-Xiu and 1 more
Severe congenital neutropenia caused by ELANE gene mutation: A case report and literature review.
Medicine | 2022-11-04 | PMID 36343040
Wang Jing, Zhang Haitao, Wang Yu and 2 more
Inherited antithrombin deficiency caused by a mutation in the SERPINC1 gene: A case report.
Medicine | 2022-11-04 | PMID 36343066
Hou Xinwei, Zhang Kairu, Wu Qian and 3 more
Cryo-EM structures of cancer-specific helical and kinase domain mutations of PI3Kα.
Proceedings of the National Academy of Sciences of the United States of America | 2022-11-16 | PMID 36343266
Liu Xiao, Zhou Qingtong, Hart Jonathan R and 5 more
Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition.
Journal of pediatric endocrinology & metabolism : JPEM | 2023-01-27 | PMID 36343308
Yilmaz Uğur Cem, Evin Ferda, Onay Huseyin and 3 more
Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis | 2023-06-01 | PMID 36343383
de Frutos Fernando, Ochoa Juan Pablo, Gómez-González Cristina and 13 more
An investigation of the sleep macrostructure of girls with Rett syndrome.
Sleep medicine | 2023-01-01 | PMID 36343395
Zhang Xinyan, Smits Marcel, Curfs Leopold and 1 more
Non-kin selection enhances complexity in cooperation: A unified quantitative law.
Computational biology and chemistry | 2022-12-01 | PMID 36343483
Wang Xiaoliang, Harrison Andrew
Silencing LINC01234 represses pancreatic cancer progression by inhibiting the malignant phenotypes of pancreatic cancer cells.
Immunobiology | 2022-11-01 | PMID 36343541
Song YuBao, Gao ZeFeng, Zheng CaiHong
Inferring bio-geographical ancestry with 35 microhaplotypes.
Forensic science international | 2022-12-01 | PMID 36343584
Huang Shuainan, Sheng Mingchen, Li Zheng and 13 more
Prevalence of polycystic ovary syndrome in European countries and USA: A systematic review and meta-analysis.
European journal of obstetrics, gynecology, and reproductive biology | 2022-12-01 | PMID 36343588
Chiaffarino Francesca, Cipriani Sonia, Dalmartello Michela and 6 more
Evolutionary dynamics under partner preferences.
Journal of theoretical biology | 2023-01-21 | PMID 36343667
Zhang Feipeng, Wang Xiaofeng, Wu Te and 1 more
Depression-related phenotypes at early stages of Aβ and tau accumulation in inducible Alzheimer's disease mouse model: Task-oriented and concept-driven interpretations.
Behavioural brain research | 2023-02-13 | PMID 36343696
Leyder Erica, Suresh Prakul, Jun Rachel and 4 more
Geographical distribution of host's specific SARS-CoV-2 mutations in the early phase of the COVID-19 pandemic.
Gene | 2023-01-30 | PMID 36343703
Khalid Mohammad, Murphy David, Shoai Maryam and 2 more
IRF5 knockdown reverses TDP-related phenotypes partially by increasing TBK1 expression.
Brain research | 2023-01-01 | PMID 36343723
Li Yuanyuan, Yu Lishuang, Liu Chang and 8 more
Establishment of fibroblast and myofibroblast phenotypes for use in in vitro co-culture models.
Biochimie | 2023-04-01 | PMID 36343754
Ramklowan D S H, Snyman C, van de Vyver M and 1 more
Diagnostic yield of next generation sequencing gene panel assays for early-onset glaucoma in an ethnically diverse population.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus | 2022-12-01 | PMID 36343799
Villalba Maria Fernanda, Grajewski Alana L, Tekin Mustafa and 2 more
Pathogenicity of Intronic and Synonymous Variants of ATP7B in Wilson Disease.
The Journal of molecular diagnostics : JMD | 2023-01-01 | PMID 36343861
Xu Wan-Qing, Wang Rou-Min, Dong Yi and 1 more
Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor.
European journal of medical genetics | 2022-12-01 | PMID 36343887
Aycan Zehra, Keskin Melikşah, Lafcı Naz Güleray and 14 more
Influence of tumor cell-derived TGF-β on macrophage phenotype and macrophage-mediated tumor cell invasion.
The international journal of biochemistry & cell biology | 2022-12-01 | PMID 36343916
Maldonado Laura Andrea González, Nascimento Camyla Rodrigues, Rodrigues Fernandes Natalie Aparecida and 3 more
SLC4A2, another gene involved in acid-base balancing machinery of osteoclasts, causes osteopetrosis.
Bone | 2023-02-01 | PMID 36343920
Xue Jing-Yi, Ikegawa Shiro, Guo Long
[RFC1 CANVAS/Spectrum Disorder: Historical Details and Clinical Diversity].
Brain and nerve = Shinkei kenkyu no shinpo | 2022-11-01 | PMID 36343927
Yoshida Kunihiro
Macular neovascularisation in a patient with osteogenesis imperfecta exhibiting a novel COL1A1 mutation.
BMJ case reports | 2022-11-07 | PMID 36343986
Sato Yoshiki, Kimoto Kenichi, Takaki Yasuhiro and 1 more
Toward a Broader Understanding of Cystic Fibrosis Epidemiology and Its Impact on Clinical Manifestations.
Clinics in chest medicine | 2022-12-01 | PMID 36344067
McBennett Kimberly A, Davis Pamela B
Genetics of Cystic Fibrosis: Clinical Implications.
Clinics in chest medicine | 2022-12-01 | PMID 36344068
Joynt Anya T, Cutting Garry R, Sharma Neeraj
Novel Applications of Biomarkers and Personalized Medicine in Cystic Fibrosis.
Clinics in chest medicine | 2022-12-01 | PMID 36344070
Guimbellot Jennifer S, Nichols David P, Brewington John J
The Impact of Highly Effective Modulator Therapy on Cystic Fibrosis Microbiology and Inflammation.
Clinics in chest medicine | 2022-12-01 | PMID 36344072
Caverly Lindsay J, Riquelme Sebastián A, Hisert Katherine B
Update on Clinical Outcomes of Highly Effective Modulator Therapy.
Clinics in chest medicine | 2022-12-01 | PMID 36344074
Gifford Alex H, Taylor-Cousar Jennifer L, Davies Jane C and 1 more
Non-Modulator Therapies: Developing a Therapy for Every Cystic Fibrosis Patient.
Clinics in chest medicine | 2022-12-01 | PMID 36344076
Egan Marie E
Updates in Nutrition Management of Cystic Fibrosis in the Highly Effective Modulator Era.
Clinics in chest medicine | 2022-12-01 | PMID 36344077
Wilson Alexandra, Altman Kimberly, Schindler Terri and 1 more
D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis.
Neurology | 2022-11-08 | PMID 36344272
Palaiodimou Lina, Stefanou Maria-Ioanna, Bakola Eleni and 14 more
Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing.
Nature communications | 2022-11-07 | PMID 36344503
Macken William L, Falabella Micol, McKittrick Caroline and 19 more
Discerning asthma endotypes through comorbidity mapping.
Nature communications | 2022-11-07 | PMID 36344522
Jia Gengjie, Zhong Xue, Im Hae Kyung and 16 more
The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.
Scientific reports | 2022-11-07 | PMID 36344539
Al-Kasbi Ghalia, Al-Murshedi Fathiya, Al-Kindi Adila and 12 more
Analysis of matched primary and recurrent BRCA1/2 mutation-associated tumors identifies recurrence-specific drivers.
Nature communications | 2022-11-07 | PMID 36344544
Shah Jennifer B, Pueschl Dana, Wubbenhorst Bradley and 17 more
MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children.
Scientific reports | 2022-11-07 | PMID 36344553
Saad Entsar A, Elsaid Afaf M, Shoaib Rasha M S and 2 more
Machine learning based personalized drug response prediction for lung cancer patients.
Scientific reports | 2022-11-07 | PMID 36344580
Qureshi Rizwan, Basit Syed Abdullah, Shamsi Jawwad A and 4 more
A bioinformatics approach to the identification of novel deleterious mutations of human TPMT through validated screening and molecular dynamics.
Scientific reports | 2022-11-07 | PMID 36344599
Saxena Sidharth, Krishna Murthy T P, Chandrashekhar C R and 7 more
Association studies between chromosomal regions 1q21.3, 5q21.3, 14q21.2 and 17q21.31 and numbers of children in Poland.
Scientific reports | 2022-11-07 | PMID 36344606
Clark Jeremy S C, van de Wetering Thierry, Marciniak Błażej and 7 more
Incidence of antibiotic resistance genotypes of Vibrio species recovered from selected freshwaters in Southwest Nigeria.
Scientific reports | 2022-11-07 | PMID 36344620
Adesiyan Ibukun M, Bisi-Johnson Mary A, Okoh Anthony I
Dissociable brain structural asymmetry patterns reveal unique phenome-wide profiles.
Nature human behaviour | 2023-02-01 | PMID 36344655
Saltoun Karin, Adolphs Ralph, Paul Lynn K and 4 more
Genetic diversity and population structure of Saccharomyces cerevisiae isolated from Turkish sourdough by iPBS-retrotransposons markers.
Archives of microbiology | 2022-11-08 | PMID 36344755
Aydın Furkan, Özer Göksel, Alkan Mehtap and 1 more
Habenula as a Possible Target for Treatment-Resistant Depression Phenotype in Wistar Kyoto Rats.
Molecular neurobiology | 2023-02-01 | PMID 36344870
Korlatowicz Agata, Pabian Paulina, Solich Joanna and 4 more
Duet: SNP-assisted structural variant calling and phasing using Oxford nanopore sequencing.
BMC bioinformatics | 2022-11-07 | PMID 36344913
Zhou Yekai, Leung Amy Wing-Sze, Ahmed Syed Shakeel and 2 more
Unveiling a hotspot of genetic diversity in southern Italy for the endangered Hermann's tortoise Testudo hermanni.
BMC ecology and evolution | 2022-11-07 | PMID 36344915
Chiocchio Andrea, Zampiglia Mauro, Biaggini Marta and 8 more
Unlocking the molecular basis of wheat straw composition and morphological traits through multi-locus GWAS.
BMC plant biology | 2022-11-08 | PMID 36344939
Esposito Salvatore, Taranto Francesca, Vitale Paolo and 4 more
Prevalence and patterns of mutations in RAS/RAF/MEK/ERK/MAPK signaling pathway in colorectal cancer in North Africa.
BMC cancer | 2022-11-07 | PMID 36344948
Jafari Meryem, Laraqui Abdelilah, Baba Walid and 19 more
A genome-wide association study of mammographic texture variation.
Breast cancer research : BCR | 2022-11-07 | PMID 36344993
Liu Yuxi, Chen Hongjie, Heine John and 8 more
Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.
Orphanet journal of rare diseases | 2022-11-07 | PMID 36345033
Yang Xunzhe, Sun Xiaohai, Liu Qing and 10 more