p16/Ki67 dual stain triage versus cytology in primary human papillomavirus-based cervical cancer screening with limited genotyping.
Journal of medical virology | 2023-11-01 | PMID 38009626
Trzeszcz Martyna, Mazurec Maciej, Jach Robert and 9 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 9320 of 10600
Sickle cell allele HBB-rs334(T) is associated with decreased risk of childhood Burkitt lymphoma in East Africa.
American journal of hematology | 2024-01-01 | PMID 38009642
Hong Hyokyoung G, Gouveia Mateus H, Ogwang Martin D and 45 more
Abnormal axonal development and severe epileptic phenotype in Dynamin-1 (DNM1) encephalopathy.
Epileptic disorders : international epilepsy journal with videotape | 2024-02-01 | PMID 38009673
Matsubara Kohei, Kuki Ichiro, Ishioka Risako and 8 more
Association of LOX gene G473A polymorphism with the occurrence of allergic rhinitis and efficacy of montelukast sodium in children.
Cell cycle (Georgetown, Tex.) | 2023-10-01 | PMID 38009683
Yao Xikun, Liu Yan, Jiao Hong and 2 more
An outbreak of a novel lineage of dengue virus 2 in Vietnam in 2022.
Journal of medical virology | 2023-11-01 | PMID 38009688
Nabeshima Takeshi, Ngwe Tun Mya Myat, Thuy Nguyen Thi Thu and 4 more
Autophagy related gene 5 polymorphism rs17587319 (C/G) in asthmatic patients in North Indian population.
The Journal of asthma : official journal of the Association for the Care of Asthma | 2024-05-01 | PMID 38009708
Kaur Sargeet, Arpna, Jha Durga and 5 more
UBE2R2-AS1, as a prognostic marker of gastric cancer, promotes the malignant phenotype of gastric cancer cells.
Histology and histopathology | 2024-06-01 | PMID 38009743
Xu Jie, Xiao Meiqin, Huang Zhijun and 2 more
ERBB3 deficiency causes a multisystemic syndrome in human patient and zebrafish.
Clinical genetics | 2024-03-01 | PMID 38009810
Liu Keqiang, Chen Ru, Zhang Minzhong and 3 more
Characterization of the novel, HLA-DRB1*07:147Q, identified by next-generation sequencing in a kidney donor.
HLA | 2024-01-01 | PMID 38009811
Nørgaard Maja, Drechsler Louise Ørnskov, Koefoed-Nielsen Pernille
The novel allele, HLA-B*15:627 was identified by next-generation sequencing in a Chinese cord blood donor.
HLA | 2024-01-01 | PMID 38009819
Tao Sudan, You Xuan, Wang Fang and 2 more
Differential sex-association between PCSK1 polymorphisms and obesity risk in Portuguese children.
American journal of human biology : the official journal of the Human Biology Council | 2024-05-01 | PMID 38009939
Manco Licínio, Albuquerque David, Aranda Beatriz and 3 more
Kristen rat sarcoma virus (KRAS) G12F-positive non-small cell lung cancer mimicking KRAS G12C positivity: A case report.
Thoracic cancer | 2024-01-01 | PMID 38010032
Oi Issei, Ito Takanori, Saito Zentaro and 5 more
EMERGENCE OF A TECHNOLOGY-DEPENDENT PHENOTYPE OF PEDIATRIC SEPSIS IN A LARGE CHILDREN'S HOSPITAL.
Shock (Augusta, Ga.) | 2024-01-01 | PMID 38010054
Aldewereld Zachary, Horvat Christopher, Carcillo Joseph A and 1 more
ALTERED PROFILES OF EXTRACELLULAR MITOCHONDRIAL DNA IN IMMUNOPARALYZED PEDIATRIC PATIENTS AFTER THERMAL INJURY.
Shock (Augusta, Ga.) | 2024-02-01 | PMID 38010095
Tetri Laura H, Penatzer Julia A, Tsegay Kaleb B and 5 more
Determining lineages between individuals with high-density mitochondrial and Y-chromosomal single-nucleotide polymorphisms.
Electrophoresis | 2024-05-01 | PMID 38010138
Chiao Austin, Ge Jianye
Using Polygenic Risk Scores to Aid Diagnosis of Patients With Early Inflammatory Arthritis: Results From the Norfolk Arthritis Register.
Arthritis & rheumatology (Hoboken, N.J.) | 2024-05-01 | PMID 38010198
Hum Ryan M, Sharma Seema D, Stadler Michael and 13 more
FDA Approval Summary: Ivosidenib in Combination with Azacitidine for Treatment of Patients with Newly Diagnosed Acute Myeloid Leukemia with an IDH1 Mutation.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2024-04-01 | PMID 38010220
Woods Ashley, Norsworthy Kelly J, Wang Xin and 9 more
Autosomic Dominant Tubulo Interstitial Kidney Disease: Case Report of a New Variant of the UMOD Gene.
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia | 2023-10-26 | PMID 38010247
Cárdenas Aguilera Juan Guillermo, Figueredo Rodriguez Lizeth Daniela, Chacón Acevedo Kelly Rocio and 2 more
Longitudinal Circulating Tumor DNA Modeling to Predict Disease Progression in First-Line Mutant Epidermal Growth Factor Receptor Non-Small Cell Lung Cancer.
Clinical pharmacology and therapeutics | 2024-02-01 | PMID 38010260
Johnson Martin, Serra Traynor Carlos, Vishwanathan Karthick and 8 more
DNA hydroxymethylation differences underlie phenotypic divergence of somatic growth in Nile tilapia reared in common garden.
Epigenetics | 2023-12-01 | PMID 38010265
Konstantinidis Ioannis, Sætrom Pål, Brieuc S O and 5 more
Assessment of runs of homozygosity, heterozygosity-rich regions and genomic inbreeding estimates in a subpopulation of Guzerá (Bos indicus) dual-purpose cattle.
Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie | 2024-03-01 | PMID 38010317
Carrara E R, Lopes P S, Veroneze R and 3 more
Completely Free from PAM Limitations: Asymmetric RPA with CRISPR/Cas12a for Nucleic Acid Assays.
ACS sensors | 2023-12-22 | PMID 38010352
Cao Gaihua, Yang Nannan, Xiong Yifan and 5 more
SNP array genomic analysis of matched pairs of brain and liver metastases in primary colorectal cancer.
Journal of cancer research and clinical oncology | 2023-12-01 | PMID 38010391
Brandt Vivian-Pascal, Holland Heidrun, Wallenborn Marco and 6 more
Methods for two nonstandard problems arising from the Luria-Delbrück experiment.
Genetica | 2023-12-01 | PMID 38010477
Zheng Qi
Role of Flow-Sensitive Endothelial Genes in Atherosclerosis and Antiatherogenic Therapeutics Development.
Journal of cardiovascular translational research | 2024-06-01 | PMID 38010480
Baek Kyung In, Ryu Kitae
Epidemiology and emm types among group A streptococcal pharyngitis in Finland: a prospective laboratory-based study.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2024-02-01 | PMID 38010594
Virolainen Mirva, Gröndahl-Yli-Hannuksela Kirsi, Rantakokko-Jalava Kaisu and 6 more
[The structure of pathogenic germline variants in colorectal cancer in Moscow patients].
Arkhiv patologii | 2023-01-01 | PMID 38010635
Semenova A B, Byakhova M M, Makarova M V and 8 more
EXTL3-Associated Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities: A Lethal Phenotype.
Pediatric allergy, immunology, and pulmonology | 2023-12-01 | PMID 38010729
Demir Engin, Adım Filiz, Döğen Mehmet Ercüment and 5 more
Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathway.
The Journal of pathology | 2024-02-01 | PMID 38010733
Saba Karim H, Difilippo Valeria, Kovac Michal and 15 more
High-Fidelity Identification of Single Nucleotide Polymorphism by Type V CRISPR Systems.
ACS sensors | 2023-12-22 | PMID 38010835
He Yawen, Shao Shengjie, Chen Juhong
Associations of genetic variations in the M3 receptor with salt sensitivity, longitudinal changes in blood pressure and the incidence of hypertension in Chinese adults.
Journal of clinical hypertension (Greenwich, Conn.) | 2024-01-01 | PMID 38010846
Zhang Xi, Yao Shi, Bao Peng and 20 more
Chrysanthemum coronarium L. Extract Attenuates Homocysteine-Induced Vascular Inflammation in Vascular Smooth Muscle Cells.
Journal of medicinal food | 2023-12-01 | PMID 38010869
Lee Ae Sin, Kim Yiseul, Hur Haeng Jeon and 2 more
The Exact Stochastic Process of the Haploid Multi-Allelic Wright-Fisher Mutation Model.
IEEE/ACM transactions on computational biology and bioinformatics | 2000-01-01 | PMID 38010931
Noland Jonas Kristiansen, Thorvaldsen Steinar
The future of HOXA- expressing leukemias: Menin inhibitor response and resistance.
Current opinion in hematology | 2024-03-01 | PMID 38010951
Wenge Daniela V, Armstrong Scott A
Infantile epileptic spasm syndrome as a new NR2F1 gene phenotype.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience | 2024-02-01 | PMID 38010976
Liang Yan, Wan Lin, Liu Xinting and 3 more
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss.
PLoS genetics | 2023-11-01 | PMID 38011198
Lewis Morag A, Schulte Jennifer, Matthews Lois and 6 more
Functional and evolutionary analysis of host Synaptogyrin-2 in porcine circovirus type 2 susceptibility.
PLoS genetics | 2023-11-01 | PMID 38011217
Walker Lianna R, Vu Hiep L, Montooth Kristi L and 1 more
Transfer learning with false negative control improves polygenic risk prediction.
PLoS genetics | 2023-11-01 | PMID 38011285
Jeng Xinge Jessie, Hu Yifei, Venkat Vaishnavi and 2 more
An allele-sharing, moment-based estimator of global, population-specific and population-pair FST under a general model of population structure.
PLoS genetics | 2023-11-01 | PMID 38011288
Goudet Jerome, Weir Bruce S
Single Nucleotide Polymorphisms Mutation of Tropoelastin Gene Affects Tropoelastin mRNA and Elastin Expressions in Human Aortic Smooth Muscle Cells.
DNA and cell biology | 2023-12-01 | PMID 38011321
Yue Jie, Qi You-Fei, Zhang Wen-Bo and 4 more
JAK2 V617F mutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes.
Blood advances | 2023-12-26 | PMID 38011490
Rafati Maryam, Brown Derek W, Zhou Weiyin and 15 more
High-throughput screening of glucocorticoid-induced enhancer activity reveals mechanisms of stress-related psychiatric disorders.
Proceedings of the National Academy of Sciences of the United States of America | 2023-12-05 | PMID 38011552
Penner-Goeke Signe, Bothe Melissa, Rek Nils and 20 more
SPA, a Stigma-style-transmitting tract Physical microenvironment Assay for investigating mechano-signaling in pollen tubes.
Proceedings of the National Academy of Sciences of the United States of America | 2023-12-05 | PMID 38011554
Zhou Xiang, Han Wenbo, Dai Jiawei and 5 more
A drug-resistant mutation in plant target of rapamycin validates the specificity of ATP-competitive TOR inhibitors in vivo.
The Plant journal : for cell and molecular biology | 2024-03-01 | PMID 38011587
Perdoux Romain, Barrada Adam, Boulaiz Manal and 5 more
Genes: RPS6
Genetic Diversity in Natural Populations of the Near-Threatened Species Lignobrycon myersi (Characiformes, Triportheidae): Implications for Species Conservation.
Zebrafish | 2023-12-01 | PMID 38011710
de Souza Oliveira Lisianne, de Araújo Bitencourt Jamille, Galdino José Henrique and 3 more
The Role of Platelets and von Willebrand Factor in the Procoagulant Phenotype of Inflammatory Bowel Disease.
Journal of Crohn's & colitis | 2024-05-31 | PMID 38011752
Schellenberg Célia, Lagrange Jérémy, Ahmed Muhammad Usman and 12 more
Generation of a gene-corrected isogenic iPSC cell line from an X-linked retinoschisis patient with a hemizygous mutation c.304C > T (p.R102W) in RS1 gene.
Stem cell research | 2023-12-01 | PMID 38011758
Mao Shengru, Sun Xihao, Duan Chunwen and 7 more
Complete F9 Gene Deletion, Duplication, and Triplication Rearrangements: Implications for Factor IX Expression and Clinical Phenotypes.
Thrombosis and haemostasis | 2024-04-01 | PMID 38011862
Ma YuXin, Li Yang, Sun Jie and 4 more
Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency.
Thrombosis and haemostasis | 2024-05-01 | PMID 38011863
Zhou Shijie, Wu Xi, Song Ying and 8 more
The functionality of a therapeutic antibody candidate restored by a single mutation from proline to threonine in the variable region.
Human vaccines & immunotherapeutics | 2023-12-15 | PMID 38012091
Hautiere Marie, Maffucci Irene, Costa Narciso and 4 more
Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations.
Pediatric transplantation | 2024-02-01 | PMID 38012111
Kadohisa Masashi, Okamoto Tatsuya, Yamamoto Miki and 12 more
Genes: POLG
SRSF2 mutation reduces polycythemia and impairs hematopoietic progenitor functions in JAK2V617F-driven myeloproliferative neoplasm.
Blood cancer journal | 2023-11-27 | PMID 38012156
Yang Yue, Abbas Salar, Sayem Mohammad A and 2 more
DNA polymerase ε harmonizes topological states and R-loops formation to maintain genome integrity in Arabidopsis.
Nature communications | 2023-11-27 | PMID 38012183
Li Qin, Zhou Jincong, Li Shuai and 5 more
A missense mutation in Lama3 causes androgen alopecia.
Scientific reports | 2023-11-27 | PMID 38012251
Ji Zhong-Hao, Ren Wen-Zhi, He Song and 4 more
Metabolic health status and renal disorders: a cross-sectional study.
Scientific reports | 2023-11-27 | PMID 38012254
Moeinzadeh Firouzeh, Rouhani Mohammad Hossein, Seirafian Shiva and 4 more
Single-molecule force stability of the SARS-CoV-2-ACE2 interface in variants-of-concern.
Nature nanotechnology | 2024-03-01 | PMID 38012274
Bauer Magnus S, Gruber Sophia, Hausch Adina and 7 more
Genes: ACE2
Infants' looking preferences for social versus non-social objects reflect genetic variation.
Nature human behaviour | 2024-01-01 | PMID 38012276
Portugal Ana Maria, Viktorsson Charlotte, Taylor Mark J and 4 more
A web-based genome-wide association study reveals the susceptibility loci of common adverse events following COVID-19 vaccination in the Japanese population.
Scientific reports | 2023-11-27 | PMID 38012279
Nogawa Shun, Kanamori Hajime, Tokuda Koichi and 4 more
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescue.
European journal of human genetics : EJHG | 2024-02-01 | PMID 38012313
Haque Bushra, Cheerie David, Birkadze Saba and 5 more
Changes in natural killer and T lymphocyte phenotypes in response to cardiovascular risk management.
Scientific reports | 2023-11-27 | PMID 38012327
Good Elin, Åkerman Linda, Nyström Sofia and 3 more
Predictive significance of circulating tumor DNA against patients with T790M-positive EGFR-mutant NSCLC receiving osimertinib.
Scientific reports | 2023-11-27 | PMID 38012343
Yamaguchi Ou, Kasahara Norimitsu, Soda Hiroshi and 17 more
Tumor heterogeneity and immune-evasive T follicular cell lymphoma phenotypes at single-cell resolution.
Leukemia | 2024-02-01 | PMID 38012392
Suma Sakurako, Suehara Yasuhito, Fujisawa Manabu and 19 more
Novel missense variants cause intermediate phenotypes in the phenotypic spectrum of SLC5A6-related disorders.
Journal of human genetics | 2024-02-01 | PMID 38012394
Utsuno Yasuhiro, Hamada Keisuke, Hamanaka Kohei and 16 more
Whole-brain in vivo base editing reverses behavioral changes in Mef2c-mutant mice.
Nature neuroscience | 2024-01-01 | PMID 38012399
Li Wei-Ke, Zhang Shu-Qian, Peng Wan-Ling and 15 more
Genetically Proxied Therapeutic Effect of Metformin Use, Blood Pressure, and Hypertension's Risk: a Drug Target-Based Mendelian Randomization Study.
Journal of cardiovascular translational research | 2024-06-01 | PMID 38012470
Jiang Junhong, Hu Di, Zhang Qi and 1 more
Multifaceted Roles of AFG3L2, a Mitochondrial ATPase in Relation to Neurological Disorders.
Molecular neurobiology | 2024-07-01 | PMID 38012514
Ghosh Dastidar Ranita, Banerjee Saradindu, Lal Piyush Behari and 1 more
Macrophage polarization toward M1 phenotype in T cell transfer colitis model.
BMC gastroenterology | 2023-11-27 | PMID 38012544
Ebihara Shin, Urashima Toshiki, Amano Wataru and 2 more
Phenotypic drug susceptibility characterization and clinical outcomes of tuberculosis strains with A-probe mutation by GeneXpert MTB/RIF.
BMC infectious diseases | 2023-11-27 | PMID 38012619
Nie Qi, Sun Dan, Zhu Muxin and 9 more
Relationship between PIWIL1 gene polymorphisms and epithelial ovarian cancer susceptibility among southern Chinese woman: a three-center case-control study.
BMC cancer | 2023-11-27 | PMID 38012622
Liu Shanshan, Yan Yaping, Cui Zhizhong and 6 more
Inhibition of microfold cells ameliorates early pathological phenotypes by modulating microglial functions in Alzheimer's disease mouse model.
Journal of neuroinflammation | 2023-11-27 | PMID 38012646
Kim Namkwon, Ju In Gyoung, Jeon Seung Ho and 8 more
Association between 14 candidate genes, PM2.5, and affective disorders: a study of the Taiwan Biobank.
BMC public health | 2023-11-27 | PMID 38012695
Ma Kai-Jie, Lin Yi-Ju, Liu Chiu-Shong and 4 more
Methylation-directed regulatory networks determine enhancing and silencing of mutation disease driver genes and explain inter-patient expression variation.
Genome biology | 2023-11-28 | PMID 38012713
Edrei Yifat, Levy Revital, Kaye Daniel and 3 more
Quartet DNA reference materials and datasets for comprehensively evaluating germline variant calling performance.
Genome biology | 2023-11-27 | PMID 38012772
Ren Luyao, Duan Xiaoke, Dong Lianhua and 31 more
Data of whole-genome sequencing of Karakul, Zel, and Kermani sheep breeds.
BMC research notes | 2023-11-27 | PMID 38012774
Saadatabadi Leila Mohammadipour, Mohammadabadi Mohammadreza, Ghanatsaman Zeinab Amiri and 7 more
Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma.
Acta neuropathologica communications | 2023-11-27 | PMID 38012788
Tateishi Kensuke, Miyake Yohei, Nakamura Taishi and 13 more
Investigation of the effects of oxidative stress, inflammation on the pathway of tryptophan/kynurenine in OCD.
Acta neuropsychiatrica | 2023-11-28 | PMID 38012854
Delen Elif, Kucukali Cem Ismail, Karaaslan Zerrin and 5 more
Genes: CYP1A1
Bioarchaeological and molecular evidence of tuberculosis in human skeletal remains from 18th-19th century orthodox cemeteries in Irkutsk, Eastern Siberia.
Tuberculosis (Edinburgh, Scotland) | 2023-12-01 | PMID 38012918
Kharlamova Natalia, Ogarkov Oleg, Berdnikov Ivan and 3 more
Towards a better understanding of the long-lasting evolutionary history of Mycobacterium tuberculosis.
Tuberculosis (Edinburgh, Scotland) | 2023-12-01 | PMID 38012920
Senelle Gaetan, Guyeux Christophe, Refrégier Guislaine and 1 more
Diagnostic utility, disease activity, and disease phenotype correlation of serum ASCA, pANCA, and PR3-ANCA in pediatric inflammatory bowel disease.
Jornal de pediatria | 2000-01-01 | PMID 38012956
Kim Jeong Min, Choi Young Min, Jung Seung A and 1 more
Increased expression of Mycobacterium tuberculosis Rv3737 gene associated with low-level amikacin resistance.
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy | 2024-03-01 | PMID 38012984
Li Qiong, Tian Peng, Xu Chao and 4 more
Real-World Efficacy and Safety of Amivantamab for EGFR-Mutant NSCLC.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2024-03-01 | PMID 38012986
Wang Kaiwen, Du Robyn, Myall Nathaniel J and 24 more
Characterization of Patient-Derived GNAQ Mutated Endothelial Cells from Capillary Malformations.
The Journal of investigative dermatology | 2024-06-01 | PMID 38013159
Langbroek Ginger Beau, Stor Merel L E, Janssen Vera and 7 more
Challenges for gene editing in common variable immunodeficiency disorders: Current and future prospects.
Clinical immunology (Orlando, Fla.) | 2024-01-01 | PMID 38013164
Ameratunga Rohan, Leung Euphemia, Woon See-Tarn and 7 more
LRP4 mutations, dental anomalies, and oral exostoses.
International journal of paediatric dentistry | 2024-07-01 | PMID 38013205
Kantaputra Piranit, Panichkul Weena, Sillapasorn Parisri and 10 more
A novel homozygous missense variant in LRP4 causing Cenani-Lenz syndactyly syndrome and literature review.
Molecular genetics & genomic medicine | 2024-01-01 | PMID 38013226
Fu Yadong, Zhou Yueyun, Zhang Qing'e and 4 more
Novel mutation in RPGRIP1L gene causing Joubert syndrome: A case report.
Medicine | 2023-11-24 | PMID 38013309
Duque-Cordoba Paola Andrea, Diaz-Ordoñez Lorena, Gutierrez-Medina Juan David and 1 more
Prolonged misdiagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: A case report.
Medicine | 2023-11-24 | PMID 38013338
Wang Yun, Zhang Weimin, Jiang Xuandong
Acute generalized exanthematous pustulosis caused by hydroxychloroquine in a patient with rheumatoid arthritis and CARD14 mutation: Case report.
Medicine | 2023-11-24 | PMID 38013380
Luo Feng, Yuan Xue-Mei, Xiong Hong and 3 more
Unlocking the link between haptoglobin polymorphism and noninfectious human diseases: insights and implications.
Critical reviews in clinical laboratory sciences | 2024-06-01 | PMID 38013410
Delanghe Joris R, Delrue Charlotte, Speeckaert Reinhart and 1 more
Usefulness Of Sofosbuvir And Daclatasvir Combination In The Treatment Of HCV Infection In Childhood Cancer Patients: Experience From A Tertiary Care Hospital.
JPMA. The Journal of the Pakistan Medical Association | 2023-11-01 | PMID 38013525
Imam Uzma, Parkash Arit, Daryani Nandlal and 1 more
Relationship Between Genetic Variant Of OXTR (Rs53576) And MTNR1B (Rs1387153) And Symptoms Of Psychological Stress In Females With Gestational Diabetes Mellitus.
JPMA. The Journal of the Pakistan Medical Association | 2023-11-01 | PMID 38013530
Abid Fatima, Ahmed Sadaf, Noushad Shamoon and 2 more
Optimizing selection strategy for enhancing reproduction efficiency in Indian crossbred goats using milk productivity as a selection criterion.
Reproduction in domestic animals = Zuchthygiene | 2024-01-01 | PMID 38013613
Upadhyay Amritanshu, Alex Rani, Sahoo Shweta and 5 more
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.
CNS neuroscience & therapeutics | 2024-04-01 | PMID 38013626
Wei Qiao, Yu Hao, Wang Pei-Shan and 4 more
Genes: COQ4
Gene polymorphism and prediction of toxicity to platinum-based chemotherapy in patients with gynecologic cancer.
Clinical and translational science | 2023-12-01 | PMID 38013655
Huang Xuan, Li Junmin, Pang Xiaoying and 4 more
The miRNA variants MIR196A2 (rs11614913) and MIR423 (rs6505162) contribute to an increase in the risk of myocardial infarction.
Molecular genetics & genomic medicine | 2024-01-01 | PMID 38013659
Uzair Muhammad, Haq Taqweem Ul, Ali Sajjad and 4 more
Body composition and risk of gestational diabetes mellitus: A univariable and multivariable Mendelian randomization study.
Journal of diabetes investigation | 2024-03-01 | PMID 38013660
Gao Yuan, Zhou Min, Xu Xuan and 2 more
Identification of the novel KIR3DP1*00604 allele in a Chinese individual.
HLA | 2024-01-01 | PMID 38014472
You Xuan, He Yizhen, Zhang Wei and 2 more
Novel IARS1 variants cause syndromic developmental disorder with epilepsy in a Chinese patient and the literature review.
Molecular genetics & genomic medicine | 2024-01-01 | PMID 38014478
Jiang Jinsong, Feng Yu, Tang Qiaoyin and 8 more
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.
Movement disorders : official journal of the Movement Disorder Society | 2024-01-01 | PMID 38014483
Lin Xiang, Jiang Jun-Yi, Hong Dao-Jun and 16 more
Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy.
Circulation. Genomic and precision medicine | 2023-12-01 | PMID 38014537
Curran Lara, de Marvao Antonio, Inglese Paolo and 25 more