EGFR-TKI-induced Factor V deficiency in a patient with advanced non-small cell lung cancer: The first case report.
Lung cancer (Amsterdam, Netherlands) | 2024-08-01 | PMID 38970909
Yoshizaki Chinatsu, Yoshida Yuki, Nohmi Shiho and 6 more
Genes: EGFR
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 9517 of 10600
Potential clinical applications of advanced genomic analysis in cerebral palsy.
EBioMedicine | 2024-08-01 | PMID 38970919
Lewis Sara A, Ruttenberg Andrew, Iyiyol Tuğçe and 3 more
Genes: CP
Polygenic inheritance and its interplay with smoking history in predicting lung cancer diagnosis: a French-Canadian case-control cohort.
EBioMedicine | 2024-08-01 | PMID 38970920
Boumtje Véronique, Manikpurage Hasanga D, Li Zhonglin and 21 more
The potential benefits of PGC-1α in treating Alzheimer's disease are dependent on the integrity of the LLKYL L3 motif: Effect of regulating mitochondrial axonal transportation.
Experimental gerontology | 2024-09-01 | PMID 38971132
Shi Hou-Zhen, Wang Yi-Jie, Wang Yu-Xin and 4 more
The Role of DNA Methylation in Gastrointestinal Disease: An Expanded Review of Malignant and Nonmalignant Gastrointestinal Diseases.
Gastroenterology | 2025-02-01 | PMID 38971197
Kalra Andrew, Meltzer Stephen J
Residues in the fructose-binding pocket are required for ketohexokinase-A activity.
The Journal of biological chemistry | 2024-08-01 | PMID 38971308
Ferreira Juliana C, Villanueva Adrian J, Fadl Samar and 8 more
Bioelectric pharmacology of cancer: A systematic review of ion channel drugs affecting the cancer phenotype.
Progress in biophysics and molecular biology | 2024-09-01 | PMID 38971325
Kofman Karina, Levin Michael
Clinicopathologic features and outcomes of acute leukemia harboring PICALM::MLLT10 fusion.
Human pathology | 2024-09-01 | PMID 38971327
Wang Jeffrey, Zhang Weiwei, Xu Xinjie and 13 more
DUSP22-rearranged primary cutaneous CD30-positive T-cell lymphoproliferative disorders and adult T-cell leukemia/lymphoma frequently share the LEF1+/TIA1- immunophenotype.
Human pathology | 2024-08-01 | PMID 38971328
Chen Bo-Jung, Hsieh Shu-Min, Hsieh Tsung-Han and 2 more
Comparison of strain specific pathogenicity of Herpes Simplex Virus Type 1 by high-throughput sequencing.
Journal of virological methods | 2024-09-01 | PMID 38971379
Demir Sevda, Tastan Cihan, Ulu Zehra Omeroglu and 3 more
fMRI and gene therapy in adults with CNGB3 mutation.
Brain research bulletin | 2024-09-01 | PMID 38971478
Anderson Elaine J, Dekker Tessa M, Farahbakhsh Mahtab and 4 more
Reducing the lipase LIPE in mutant α-synuclein mice improves Parkinson-like deficits and reveals sex differences in fatty acid metabolism.
Neurobiology of disease | 2024-09-01 | PMID 38971480
Adom M A, Hahn W N, McCaffery T D and 6 more
A novel mutation alters GNE bifunctional enzyme activity and leads to familial inherited GNE diseases.
Gene | 2024-11-15 | PMID 38971548
Li Yufei, Li Wenwu, Fan Baitong and 7 more
Targeted Therapy Innovations for Melanoma.
Hematology/oncology clinics of North America | 2024-10-01 | PMID 38971651
Amarillo Dahiana, Flaherty Keith T, Sullivan Ryan J
The Benefit of a National Genomic Testing Scheme.
The Veterinary clinics of North America. Food animal practice | 2024-11-01 | PMID 38971688
Berry Donagh P, Spangler Matthew L
Genetics of osteoarthritis.
Best practice & research. Clinical rheumatology | 2024-12-01 | PMID 38971692
Zhai Guangju, Huang Jingyi
Targeting epigenetic dysregulation in autism spectrum disorders.
Trends in molecular medicine | 2024-11-01 | PMID 38971705
Herrera Macarena L, Paraíso-Luna Juan, Bustos-Martínez Isabel and 1 more
Comparative genomics of quinolone-resistant Escherichia coli from broilers and humans in Norway.
BMC microbiology | 2024-07-06 | PMID 38971718
Slettemeås Jannice Schau, Sekse Camilla, Sunde Marianne and 7 more
Simulated complexes formed from a set of postsynaptic proteins suggest a localised effect of a hypomorphic Shank mutation.
BMC neuroscience | 2024-07-06 | PMID 38971749
Miski Marcell, Weber Áron, Fekete-Molnár Krisztina and 3 more
Obesity, abdominal obesity, metabolic obesity phenotypes, and Helicobacter pylori infection: results from NHANES 1999-2000.
BMC infectious diseases | 2024-07-06 | PMID 38971751
Chen Danni, Wang Shiling, Yang Wei and 2 more
The human VGLUT3-pT8I mutation elicits uneven striatal DA signaling, food or drug maladaptive consumption in male mice.
Nature communications | 2024-07-07 | PMID 38971801
Favier Mathieu, Martin Garcia Elena, Icick Romain and 25 more
The loci of environmental adaptation in a model eukaryote.
Nature communications | 2024-07-06 | PMID 38971805
Chen Piaopiao, Zhang Jianzhi
Emergence of genetic diversity and multi-drug resistant Clostridium perfringens from wild birds.
BMC veterinary research | 2024-07-06 | PMID 38971814
Song Xinglong, Zhong Zhenyu, Bai Jiade and 6 more
Erythroid-intrinsic activation of TLR8 impairs erythropoiesis in inherited anemia.
Nature communications | 2024-07-06 | PMID 38971858
Liang Jing, Wan Yang, Gao Jie and 23 more
Genes: TLR8, ANXA2, CD34, EPO, RPS19
New Variants Identified by Next-Generation Sequencing in Polycystic Kidney Disease Patients.
Biochemical genetics | 2024-12-01 | PMID 38971859
Ozyavuz Cubuk Pelin, Akin Duman Tugba
Genomic sequencing reveals convergent adaptation during experimental evolution in two budding yeast species.
Communications biology | 2024-07-07 | PMID 38971878
Wang Pu, Driscoll William W, Travisano Michael
Novel genomic variants related to visceral adiposity index (VAI) and body adiposity index (BAI) in Indian sib-pairs.
International journal of obesity (2005) | 2024-11-01 | PMID 38971891
Agarwal Tripti, Lyngdoh Tanica, Khadgawat Rajesh and 9 more
Comparative Fitness of Monilinia fructicola Isolates with Multiple Fungicide-Resistant Phenotypes.
Plant disease | 2024-11-01 | PMID 38971961
Dutra Pamela S S, Carraro Thiago A, Nesi Cristiano N and 2 more
Molecular mechanisms of precise timing in cell lysis.
Biophysical journal | 2024-09-17 | PMID 38971973
Mondal Anupam, Teimouri Hamid, Kolomeisky Anatoly B
Enhanced cancer cell proliferation and aggressive phenotype counterbalance in breast cancer with high BRCA1 gene expression.
Breast cancer research and treatment | 2024-11-01 | PMID 38972017
Chida Kohei, Oshi Masanori, Roy Arya Mariam and 6 more
GWAS elucidated grain yield genetics in Indian spring wheat under diverse water conditions.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2024-07-07 | PMID 38972024
Gaur Arpit, Jindal Yogesh, Singh Vikram and 7 more
Unveiling novel genetic variants in 370 challenging medically relevant genes using the long read sequencing data of 41 samples from 19 global populations.
Molecular genetics and genomics : MGG | 2024-07-07 | PMID 38972030
Ji Yanfeng, Zhao Junfan, Gong Jiao and 2 more
Artificial sweetener and respiratory system cancer: A Mendelian randomization analysis.
Clinical nutrition ESPEN | 2024-10-01 | PMID 38972036
Zhang Jiaqi, Fan Rencai, Mao Chenkai and 4 more
Placental somatic mutation in human stillbirth and live birth: A pilot case-control study of paired placental, fetal, and maternal whole genomes.
Placenta | 2024-09-02 | PMID 38972082
Wallace Amelia D, Blue Nathan R, Morgan Terry and 3 more
Pro-fibrotic effect of the susceptible gene PCSK5 in vascular fibrosis of Takayasu arteritis via TGF-β and SMAD3 signaling pathway activation.
Journal of autoimmunity | 2024-09-01 | PMID 38972101
Wang Jinghua, Sun Ying, Chen Rongyi and 4 more
Impact of coding risk variant IFNGR2 on the B cell-intrinsic IFN-γ signaling pathway in multiple sclerosis.
Journal of autoimmunity | 2024-09-01 | PMID 38972102
Bogers Laurens, Rip Jasper, Rijvers Liza and 9 more
Therapeutic implications of the metabolic changes associated with BRAF inhibition in melanoma.
Cancer treatment reviews | 2024-09-01 | PMID 38972133
Loftus Alexander W, Zarei Mehrdad, Kakish Hanna and 8 more
Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene.
Stem cell research | 2024-09-01 | PMID 38972232
Ning Jiaying, Zhou Tiancheng, Luo Xianqiong and 4 more
Cryo-EM structure and biochemical analyses of the nucleosome containing the cancer-associated histone H3 mutation E97K.
Genes to cells : devoted to molecular & cellular mechanisms | 2024-09-01 | PMID 38972377
Kimura Tomoaki, Hirai Seiya, Kujirai Tomoya and 6 more
Symptomatic Heart Failure and Clonal Hematopoiesis-Related Mutations in Patients With Acute Myeloid Leukemia.
The American journal of cardiology | 2024-09-01 | PMID 38972534
Kang Yu, Lefebvre Benedicte, Pamies Ingrid Marti and 8 more
Genes: DNMT3A, ASXL1, TET2
Cluster analysis of clinical manifestations assigns systemic lupus erythematosus-phenotype subgroups: A multicentre study on 440 patients.
Joint bone spine | 2024-12-01 | PMID 38972539
Mariette Fanny, Le Guern Véronique, Nguyen Yann and 8 more
Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular Phenotypes.
The Journal of pediatrics | 2024-11-01 | PMID 38972567
Kobayashi Erica Sanford, Lotan Nava Shaul, Schejter Yael Dinur and 11 more
Genes: SENP7
Validation and Implementation of a Somatic-Only Tumor Exome for Routine Clinical Application.
The Journal of molecular diagnostics : JMD | 2024-09-01 | PMID 38972591
Shah Parth S, Hughes Edward G, Sukhadia Shrey S and 4 more
Assessing the Risk Stratification of Breast Cancer Polygenic Risk Scores in a Brazilian Cohort.
The Journal of molecular diagnostics : JMD | 2024-09-01 | PMID 38972593
Barreiro Rodrigo A S, de Almeida Tatiana F, Gomes Catarina and 15 more
Development, Validation, and Implementation of an Augmented Multiwell, Multitarget Quantitative PCR for the Analysis of Human Papillomavirus Genotyping through Software Automation, Data Science, and Artificial Intelligence.
The Journal of molecular diagnostics : JMD | 2024-09-01 | PMID 38972594
Pereira A Rita, Redzic Nina, Van Vooren Steven and 10 more
Four amino acids play an important role in the allergenicity of hemocyanin allergen.
International journal of biological macromolecules | 2024-08-01 | PMID 38972655
Luan Hongwei, Lu Jiada, Shi Wenzheng and 1 more
Characterization of senescent mesenchymal stem/stromal cells derived from equine bone marrow and the effects of NANOG on the senescent phenotypes.
The Journal of veterinary medical science | 2024-09-01 | PMID 38972751
Kushida Chiho, Tamura Norihisa, Kasashima Yoshinori and 2 more
Ubiquitin system mutations in neurological diseases.
Trends in biochemical sciences | 2024-10-01 | PMID 38972780
Zenge Colin, Ordureau Alban
Genetic diversity, determinants, and dissemination of Burkholderia pseudomallei lineages implicated in melioidosis in Northeast Thailand.
Nature communications | 2024-07-07 | PMID 38972886
Seng Rathanin, Chomkatekaew Chalita, Tandhavanant Sarunporn and 11 more
Tracking the hologenome dynamics in aquatic invertebrates by the holo-2bRAD approach.
Communications biology | 2024-07-07 | PMID 38972908
Ma Cen, Xu Chang, Zhang Tianqi and 14 more
Survey on Interaction Between Nutrient Status and Selected Polymorphisms in Association with Weight Loss of Patients with Severe Obesity Underwent Bariatric Surgery.
Obesity surgery | 2024-08-01 | PMID 38972938
Cheraghi Sara, Taheri Golmehr, Safari Saeed and 4 more
Genes: UCP2, FTO, GHRL, LEPR, NPY
The risks for major psychiatric disorders in the siblings of probands with major depressive disorder.
Molecular psychiatry | 2025-01-01 | PMID 38972942
Rhee Sang Jin, Abrahamsson Linda, Sundquist Jan and 2 more
Spinal muscular atrophy caused by compound heterozygous SMN1 mutations: two cases and literature review.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2024-12-01 | PMID 38972959
Chi Yuewei, Qiao Yue, Ma Ying
Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome.
European journal of human genetics : EJHG | 2024-09-01 | PMID 38972963
Starosta Rodrigo Tzovenos, Jensen Nathaniel, Couteranis Sophia and 11 more
Genes: FREM1
Genetic diversity of astroviruses detected in wild aquatic birds in Hong Kong.
Virology journal | 2024-07-07 | PMID 38972989
Ng Daisy Y M, Sun Wanying, Sit Thomas H C and 11 more
[Clinical phenotypic and genetic analysis of syndrome families with EYA1 gene variants].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery | 2024-07-01 | PMID 38973045
Shao Hua, Li Yonghua, Zhao Heng and 4 more
Maize zinc uptake is influenced by arbuscular mycorrhizal symbiosis under various soil phosphorus availabilities.
The New phytologist | 2024-09-01 | PMID 38973063
Yu Baogang, Zhou Chengxiang, Wang Zhonghua and 7 more
Combined Treatment of Severe Acute Respiratory Syndrome Coronavirus 2 Reduces Molnupiravir-Induced Mutagenicity and Prevents Selection for Nirmatrelvir/Ritonavir Resistance Mutations.
The Journal of infectious diseases | 2024-12-16 | PMID 38973065
Zhou Shuntai, Long Nathan, Rosenke Kyle and 3 more
A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.
Movement disorders : official journal of the Movement Disorder Society | 2024-09-01 | PMID 38973070
van Prooije Teije H, Pennings Maartje, Dorresteijn Lucille and 8 more
Genetic Variants in the Fat Mass and Obesity-Associated Gene and Risk of Obesity/Overweight in Children and Adolescents: A Systematic Review and Meta-Analysis.
Endocrinology, diabetes & metabolism | 2024-07-01 | PMID 38973101
Eghbali Maryam, Mottaghi Azadeh, Taghizadeh Sara and 1 more
Genes: FTO
Exploring the potential causal effects of food preferences on irritable bowel syndrome risk: A two-sample Mendelian randomization study.
Journal of digestive diseases | 2024-05-01 | PMID 38973137
Zhang Tao, Li Xiao Ang, Duan Li Ping
Body-wide chimerism and mosaicism are predominant causes of naturally occurring ABO discrepancies.
British journal of haematology | 2024-09-01 | PMID 38973155
Dauber Eva-Maria, Haas Oskar A, Nebral Karin and 10 more
Early blood immune molecular alterations in cynomolgus monkeys with a PSEN1 mutation causing familial Alzheimer's disease.
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2024-08-01 | PMID 38973166
Li Mengqi, Guan Mingfeng, Lin Jianbang and 19 more
SRY-positive 45,X/46,XY karyotype in a phenotypically Turner-like Chinese adolescent female with ovarian dysgerminoma and gonadoblastoma.
Journal of pediatric endocrinology & metabolism : JPEM | 2024-08-27 | PMID 38973169
Zhou Jiahong, Zhan Ping, Cheng Yang and 5 more
Adult presentation of a rare mitochondrial tRNA Val gene mutation-an expanding clinical phenotype.
European journal of neurology | 2024-10-01 | PMID 38973423
Joyce Eimear, Ali Mohib, Richard Georgia and 6 more
The DEFB1 gene rs11362 A/G genetic variant is associated with risk of developing CAD: a case-control study.
Acta cardiologica | 2024-08-01 | PMID 38973431
Vargas-Alarcón Gilberto, Pérez-Méndez Óscar, Martínez-Ríos Marco Antonio and 6 more
Autophagy is suppressed by low temperatures and is dispensable for cold acclimation in Arabidopsis.
Physiologia plantarum | 2000-01-01 | PMID 38973450
Sato Akito, Inayoshi Sena, Kitawaki Kohei and 4 more
Deciphering the role of cuproptosis-related lncRNAs in shaping the lung cancer immune microenvironment: A comprehensive prognostic model.
Journal of cellular and molecular medicine | 2024-07-01 | PMID 38973477
Huang Hai, Chen Guoxi, Zhang Zongqi and 7 more
Genes: SND1, TMPO
Association of dietary intake and serum concentration of omega-3 fatty acids on celiac disease: evidence from observational study and Mendelian randomization.
European journal of gastroenterology & hepatology | 2024-09-01 | PMID 38973512
Bai Tongtong, Peng Juanjuan, Wu Chengyu
Causal relationships between psychological disorders and functional gastrointestinal disorders: a bidirectional two-sample Mendelian randomization study.
European journal of gastroenterology & hepatology | 2024-11-01 | PMID 38973539
Liu Tangyi, Wang Zeyu, Kang Xiaoyu and 9 more
Genetically Proxied Interleukin-13 Inhibition Is Associated With Risk of Psoriatic Disease: A Mendelian Randomization Study.
Arthritis & rheumatology (Hoboken, N.J.) | 2024-11-01 | PMID 38973570
Zhao Sizheng Steven, Hyrich Kimme, Yiu Zenas and 2 more
Long-term outcomes and patterns of relapse in patients with bilateral Wilms tumor or bilaterally predisposed unilateral Wilms tumor, a report from the COG AREN0534 study.
International journal of cancer | 2024-11-15 | PMID 38973574
Murphy Andrew J, Brzezinski Jack, Renfro Lindsay A and 17 more
Genes: EFS
New variants expand the neurological phenotype of COQ7 deficiency.
Journal of inherited metabolic disease | 2024-09-01 | PMID 38973597
Fabra María Alcázar, Paredes-Fuentes Abraham J, Torralba Carnerero Manuel and 31 more
A Genome-Wide Association Study Suggests New Susceptibility Loci for Primary Antiphospholipid Syndrome.
Arthritis & rheumatology (Hoboken, N.J.) | 2024-11-01 | PMID 38973605
Casares-Marfil Desiré, Martínez-Bueno Manuel, Borghi Maria Orietta and 15 more
Distinct transcriptional and prognostic impacts of TERT promoter mutations C228T and C250T in papillary thyroid carcinoma.
Endocrine-related cancer | 2024-09-01 | PMID 38973620
Marczyk Vicente Rodrigues, Maia Ana Luiza, Goemann Iuri Martin
Labetalol Dosing in Pregnancy: PBPK/PD and CYP2C19 Polymorphisms.
Journal of clinical pharmacology | 2024-11-01 | PMID 38973651
Liu Xiaomei I, Green Dionna J, van den Anker John and 4 more
Genes: CYP2C19
Phenotypic and cytogenetic variability of patau syndrome in Morocco.
African health sciences | 2023-12-01 | PMID 38974285
Hammou Hanane Ait, Sennaoui Mariam, Bouzid Fatimazahra and 7 more
Maternal inherited thrombophilia and recurrent pregnancy loss: a Tunisian study and review of literature.
African health sciences | 2023-12-01 | PMID 38974294
Frikha Rim, Turki Fatma, Abdelmoula Nouha and 1 more
Conditioned culture medium of bone marrow mesenchymal stem cells promotes phenotypic transformation of microglia by regulating mitochondrial autophagy.
PeerJ | 2024-01-01 | PMID 38974415
Ji Hangyu, Chu Weiming, Yang Yong and 2 more
Case report: Nerve fiber regeneration in children with melanocortin 4 receptor gene mutation related obesity treated with semaglutide.
Frontiers in endocrinology | 2024-01-01 | PMID 38974580
Gad Hoda, Mohammed Idris, Dauleh Hajar and 4 more
De novo p.Glu61Ter mutation in GCH1 in a Moroccan patient with dopa-responsive dystonia: a case report.
The Pan African medical journal | 2024-01-01 | PMID 38974698
Bouhouche Ahmed, Tamaoui Leila, Birouk Nazha
Lung Hyperinflation as Treatable Trait in Chronic Obstructive Pulmonary Disease: A Narrative Review.
International journal of chronic obstructive pulmonary disease | 2024-01-01 | PMID 38974815
Koopman Maud, Posthuma Rein, Vanfleteren Lowie E G W and 2 more
Attenuated mutants of Salmonella enterica Typhimurium mediate melanoma regression via an immune response.
Experimental biology and medicine (Maywood, N.J.) | 2024-01-01 | PMID 38974834
Pérez Jorge Genesy, Gontijo Marco, Silva Marina Flóro E and 6 more
Genomic and phenotypic inconsistencies in Pseudomonas aeruginosa resistome among intensive care patients.
Frontiers in cellular and infection microbiology | 2024-01-01 | PMID 38975326
Dolgusevs Mihails, Jain Nityanand, Savicka Oksana and 7 more
Mitochondrial dysfunction and metabolic reprogramming induce macrophage pro-inflammatory phenotype switch and atherosclerosis progression in aging.
Frontiers in immunology | 2024-01-01 | PMID 38975335
Vendrov Aleksandr E, Lozhkin Andrey, Hayami Takayuki and 5 more
Genes: NOX4, CD38, EGR2, CD163, CD80, CD68, IL4
Generation of functionally active resident macrophages from adipose tissue by 3D cultures.
Frontiers in immunology | 2024-01-01 | PMID 38975341
Arlat Adèle, Renoud Marie-Laure, Nakhle Jean and 10 more
Adolescent sleep patterns, genetic predisposition, and risk of multiple sclerosis.
Sleep | 2024-10-11 | PMID 38975699
Johansson Eva, Olsson Tomas, Strid Pernilla and 3 more
Are SCN2A-related BFNISs also responsible for seizures in adulthood? A case report opens new scenarios.
American journal of medical genetics. Part A | 2024-11-01 | PMID 38975734
Brunetti Sara, Muda Alice, Conti Chiara and 3 more
Genes: SCN2A
Partial atrioventricular canal defect and aortic coarctation associated with variants in GDF1 and NOTCH1 genes: A case report.
Birth defects research | 2024-07-01 | PMID 38975735
Putotto Carolina, Masci Marco, Magliozzi Monia and 4 more
Genes: GDF1, NOTCH1
Cohesin composition and dosage independently affect early development in zebrafish.
Development (Cambridge, England) | 2024-08-01 | PMID 38975838
Labudina Anastasia A, Meier Michael, Gimenez Gregory and 6 more
Mechanisms of Resistance to Oncogenic KRAS Inhibition in Pancreatic Cancer.
Cancer discovery | 2024-11-01 | PMID 38975874
Dilly Julien, Hoffman Megan T, Abbassi Laleh and 52 more
Genes: KRAS, CDK6, EGFR, MET, MYC, PIK3CA
Mechanisms of Response and Tolerance to Active RAS Inhibition in KRAS-Mutant Non-Small Cell Lung Cancer.
Cancer discovery | 2024-11-01 | PMID 38975897
Araujo Haniel A, Pechuan-Jorge Ximo, Zhou Teng and 24 more
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy.
Journal of neurogenetics | 2024-06-01 | PMID 38975939
Sharma Shivani, Mahadevan Anita, Narayanappa Gayathri and 10 more
F2c.*C20209T mutation in patients with a history of thrombosis: A case report, retrospective 2 site-results and review of the literature.
International journal of laboratory hematology | 2024-10-01 | PMID 38975952
Jambou Didier, Saut Noemie, Queyrel Viviane and 5 more
SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause.
Journal of neurogenetics | 2024-06-01 | PMID 38975976
Arlt Annabelle, Akova-Öztürk Esra, Schirmacher Anja and 5 more
Genes: SORD
Fertility-sparing strategy in a rare case of highly malignant Dicer-1-associated sarcoma of the cervix.
Archives of gynecology and obstetrics | 2024-11-01 | PMID 38976022
Altmann J, Kubiak K, Sehouli J and 1 more
Genes: DICER1
Plasminogen activator inhibitor-1 genotype 4G/5G associates with skin involvement in Armenian familial Mediterranean fever patients.
Rheumatology international | 2024-11-01 | PMID 38976029
Kriegshäuser Gernot, Hayrapetyan Hasmik, Oberkanins Christian and 1 more
Large-scale single-virus genomics uncovers hidden diversity of river water viruses and diversified gene profiles.
The ISME journal | 2024-01-08 | PMID 38976038
Nishikawa Yohei, Wagatsuma Ryota, Tsukada Yuko and 4 more
Tumor Mutational Load: A Novel Predictor for Clinical Benefit of Pembrolizumab.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2024-09-03 | PMID 38976040
Hsu Fang-Chi, Yen Yun
Similar genetic profile in early and late stage urothelial tract cancer.
Journal of cancer research and clinical oncology | 2024-07-08 | PMID 38976041
Stormoen Dag Rune, Rohrberg Kristoffer Staal, Mouw Kent William and 5 more