SPERM FACTORS AND EGG ACTIVATION: The phenotype of PLCZ1-deficient mice.
Reproduction (Cambridge, England) | 2022-05-23 | PMID 35239501
Satouh Yuhkoh
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 8853 of 10600
Bilateral Sudden Sensorineural Hearing Loss: A Distinct Phenotype Entity.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology | 2022-04-01 | PMID 35239621
Elias Thaís Gomes Abrahão, Monsanto Rafael da Costa, Jean Line-Dore Saint and 2 more
Proteome-wide Mendelian randomization identifies causal links between blood proteins and severe COVID-19.
PLoS genetics | 2022-03-01 | PMID 35239653
Palmos Alish B, Millischer Vincent, Menon David K and 7 more
TNF-α levels and presence of SNP-308G/A of TNF-α gene in temporomandibular disorder patients.
Dental press journal of orthodontics | 2022-01-01 | PMID 35239943
Campello Camilla Porto, Lima Elker Lene Santos de, Fernandes Renata Silva Melo and 2 more
Fisher's historic 1922 paper On the dominance ratio.
Genetics | 2022-03-03 | PMID 35239967
Charlesworth Brian
Lack of association between 11 gene polymorphisms on weight loss 1 year after Roux-en-y gastric bypass surgery in woman.
Journal of human nutrition and dietetics : the official journal of the British Dietetic Association | 2022-08-01 | PMID 35239993
Novais Patrícia Fatima Sousa, Crisp Alex Harley, Leandro-Merhi Vania Aparecida and 3 more
Circulating Tumor DNA-Based Genotyping and Monitoring for Predicting Disease Relapses of Patients with Peripheral T-Cell Lymphomas.
Cancer research and treatment | 2023-01-01 | PMID 35240014
Kim Seok Jin, Kim Yeon Jeong, Yoon Sang Eun and 9 more
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures.
American journal of human genetics | 2022-04-07 | PMID 35240055
Lu Shenzhao, Hernan Rebecca, Marcogliese Paul C and 15 more
The individual and global impact of copy-number variants on complex human traits.
American journal of human genetics | 2022-04-07 | PMID 35240056
Auwerx Chiara, Lepamets Maarja, Sadler Marie C and 7 more
SARS-CoV-2 Nucleocapsid Protein Targets a Conserved Surface Groove of the NTF2-like Domain of G3BP1.
Journal of molecular biology | 2022-05-15 | PMID 35240128
Biswal Mahamaya, Lu Jiuwei, Song Jikui
Zinc alters behavioral phenotypes, neurotransmitter signatures, and immune homeostasis in male zebrafish (Danio rerio).
The Science of the total environment | 2022-07-01 | PMID 35240190
Yu Fan, Hou Zhi-Shuai, Luo Hong-Rui and 11 more
Evidence for a phenotypic switch in corneal afferents after lacrimal gland excision.
Experimental eye research | 2022-05-01 | PMID 35240196
Sullivan Cara, Lee Jun, Bushey William and 5 more
The Phenotypic Course of Age-Related Macular Degeneration for ARMS2/HTRA1: The EYE-RISK Consortium.
Ophthalmology | 2022-07-01 | PMID 35240203
Thee Eric F, Colijn Johanna M, Cougnard-Grégoire Audrey and 11 more
The influence of SLC22A3 rs543159 and rs1317652 genetic variants on metformin therapeutic efficacy in newly diagnosed patients with type 2 diabetes mellitus: 25 weeks follow-up study.
Gene | 2022-05-20 | PMID 35240257
Taheri Rana, Kazerouni Faranak, Mirfakhraei Reza and 3 more
A high prevalence of myeloid malignancies in progeria with Werner syndrome is associated with p53 insufficiency.
Experimental hematology | 2022-05-01 | PMID 35240258
Kato Hisaya, Maezawa Yoshiro, Nishijima Dai and 23 more
Combinations of Preoperative Patient-Reported Outcome Measure Phenotype (Pain, Function, and Mental Health) Predict Outcome After Total Knee Arthroplasty.
The Journal of arthroplasty | 2022-06-01 | PMID 35240283
Orr Melissa N, Klika Alison K, Emara Ahmed K and 1 more
Old and new perspectives on Neurofibromatosis type 1: Clinical and molecular characterization of 832 patients from a single centre over 16 years.
European journal of medical genetics | 2022-04-01 | PMID 35240321
Ho Stephanie Kl, Luk Ho-Ming, Ng Samuel Yl and 6 more
Further evidence for attenuated phenotype with variants in the BMPER gene causing DSD: Case report and literature review.
European journal of medical genetics | 2022-04-01 | PMID 35240322
Batey Natalie, Spiller Michael, Balasubramanian Meena
TUBB4B gene mutation in Leber phenotype of congenital amaurosis syndrome associated with early-onset deafness.
European journal of medical genetics | 2022-04-01 | PMID 35240325
Maasz Anita, Hadzsiev Kinga, Ripszam Reka and 9 more
Adaptations and counter-adaptations in Drosophila host-parasitoid interactions: advances in the molecular mechanisms.
Current opinion in insect science | 2022-06-01 | PMID 35240335
Wertheim Bregje
Extensive genetic diversity and recombination events identified in goose circoviruses circulating in partial areas of Guangdong province, Southern China.
Poultry science | 2022-04-01 | PMID 35240356
Yao Xin-Yan, Yang Jia-Chun, Yuan Sheng and 7 more
Induced pluripotent stem cell line from a mouse model of human azoospermia with a frameshift mutation Tex11_1260Ins(TT).
Stem cell research | 2022-04-01 | PMID 35240466
Tran Kien T D, Sheng Yi, Doungkamchan Chatchanan and 2 more
ANXA1 and the risk for early-onset Parkinson's disease.
Neurobiology of aging | 2022-04-01 | PMID 35240489
Li Chunyu, Ou Ruwei, Gu Xiaojing and 12 more
High glucose stimulating ECM remodeling and an inflammatory phenotype in the IPFP via upregulation of MFAP5 expression.
Biochemical and biophysical research communications | 2022-04-23 | PMID 35240498
Dong Xiao-Ying, Yin Jing-Xia, Zhang Hao and 1 more
Characterization of embB mutations involved in ethambutol resistance in multi-drug resistant Mycobacterium tuberculosis isolates in Zambia.
Tuberculosis (Edinburgh, Scotland) | 2022-03-01 | PMID 35240539
Bwalya Precious, Solo Eddie S, Chizimu Joseph Y and 5 more
Genetic variation of 17 autosomal STR loci in the Lahu population from Yunnan and phylogenetic structure exploration among 28 populations.
Legal medicine (Tokyo, Japan) | 2022-05-01 | PMID 35240543
Zhang Xiufeng, Li Jing, Wen Jingtao
The mutational landscape of upper gastrointestinal adenocarcinomas- A study of similarities and differences.
Pathology, research and practice | 2022-04-01 | PMID 35240548
Krishnamurthy Kritika, Urioste Sophia Navajas, Cusnir Mike and 4 more
DTSMA: Dominant Swarm with Adaptive T-distribution Mutation-based Slime Mould Algorithm.
Mathematical biosciences and engineering : MBE | 2022-01-04 | PMID 35240784
Yin Shihong, Luo Qifang, Du Yanlian and 1 more
Estimating the transmissibility of SARS-CoV-2 VOC 202012/01 in Japan using travel history information.
Mathematical biosciences and engineering : MBE | 2022-01-12 | PMID 35240804
Kayano Taishi, Nishiura Hiroshi
A novel frameshift variant in CEP78 associated with nonsyndromic retinitis pigmentosa, and a review of CEP78-related phenotypes.
Ophthalmic genetics | 2022-04-01 | PMID 35240912
Lähteenoja Laura, Häkli Sanna, Tuupanen Sari and 4 more
Rotavirus genotypes and clinical outcome of natural infection based on vaccination status in the post-vaccine era.
Human vaccines & immunotherapeutics | 2022-12-31 | PMID 35240934
Kozawa Kei, Higashimoto Yuki, Kawamura Yoshiki and 7 more
Deciphering the Significance of Plasma Chemokines as Prognostic Biomarkers in Pegylated IFN-Α-2a /Ribavirin-Treated Chronic Hepatitis C Genotype 4 Patients.
Infectious disorders drug targets | 2022-01-01 | PMID 35240967
Hamed M Haroon, Pushparaj Peter Natesan, Rehman Shafiqur and 3 more
Integrase Strand Transfer Inhibitor (INSTI) Genotypic Resistance Analysis in Treatment-Naive, INSTI Free Antiretroviral-Experienced and INSTI-Experienced Turkish Patients Infected with HIV-1.
Current HIV research | 2022-08-12 | PMID 35240975
Sayan Murat, Yildirim Figen Sarigul, Akhan Sila and 2 more
Expanding the phenotype associated with SMARCC2 variants: a fetus with tetralogy of Fallot.
BMC medical genomics | 2022-03-03 | PMID 35241061
Sun Hairui, Zhang Siyao, Wang Jingyi and 4 more
Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene.
BMC medical genomics | 2022-03-03 | PMID 35241069
Dessay Mariam, Couture Emile, Maaroufi Halim and 5 more
Genetic polymorphisms in genes associated with drug resistance in Plasmodium vivax parasites from northeastern Myanmar.
Malaria journal | 2022-03-03 | PMID 35241080
Huang Fang, Li Shigang, Tian Peng and 5 more
Survival prediction in acute myeloid leukemia using gene expression profiling.
BMC medical informatics and decision making | 2022-03-03 | PMID 35241089
Lai Binbin, Lai Yanli, Zhang Yanli and 2 more
Strategies to overcome the main challenges of the use of CRISPR/Cas9 as a replacement for cancer therapy.
Molecular cancer | 2022-03-03 | PMID 35241090
Rasul Mohammed Fatih, Hussen Bashdar Mahmud, Salihi Abbas and 8 more
LPL, FNDC5 and PPARγ gene polymorphisms related to body composition parameters and lipid metabolic profile in adolescents from Southern Italy.
Journal of translational medicine | 2022-03-03 | PMID 35241092
Perrone Benedetta, Ruffo Paola, Zelasco Samanta and 10 more
Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome.
Orphanet journal of rare diseases | 2022-03-03 | PMID 35241111
Rad Aboulfazl, Najafi Maryam, Suri Fatemeh and 13 more
Association of COL5A1 gene polymorphisms and musculoskeletal soft tissue injuries: a meta-analysis based on 21 observational studies.
Journal of orthopaedic surgery and research | 2022-03-03 | PMID 35241120
Guo Rui, Ji Zhe, Gao Shutao and 4 more
Towards accurate and reliable resolution of structural variants for clinical diagnosis.
Genome biology | 2022-03-03 | PMID 35241127
Liu Zhichao, Roberts Ruth, Mercer Timothy R and 3 more
Endemicity and genetic diversity of Hepatitis delta virus among Pygmies in Cameroon, Central Africa.
BMC research notes | 2022-03-03 | PMID 35241131
Foupouapouognigni Yacouba, Mfonkou Jacques Delors Toumansie, Boyomo Onana and 2 more
A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report.
Journal of medical case reports | 2022-03-04 | PMID 35241161
Wei Xin, Li Juan, Zhan Xiaojiang and 3 more
Importance of the determination of enzymatic activity in the diagnosis of deficiency of adenosine deaminase 2 (DADA2).
Medicina clinica | 2022-09-23 | PMID 35241284
Abbasi Adrián, Batllori Marta, Gil-Sáez Francisco Jose and 3 more
Addressing the challenges of accelerated and blast phase myeloproliferative neoplasms in 2022 and beyond.
Blood reviews | 2022-09-01 | PMID 35241294
Saha Chandan, Attwell Luke, Harrison Claire N and 1 more
Heart failure and catheter ablation of atrial fibrillation: Navigating the difficult waters of heart failure phenotypes.
European journal of internal medicine | 2022-05-01 | PMID 35241349
Tavazzi Luigi, Maggioni Aldo P, Rapezzi Claudio and 1 more
Randomised, open-label, multicentric phase III trial to evaluate the safety and efficacy of palbociclib in combination with endocrine therapy, guided by ESR1 mutation monitoring in oestrogen receptor-positive, HER2-negative metastatic breast cancer patients: study design of PADA-1.
BMJ open | 2022-03-03 | PMID 35241469
Berger Frédérique, Marce Margaux, Delaloge Suzette and 12 more
Antibody escape and global spread of SARS-CoV-2 lineage A.27.
Nature communications | 2022-03-03 | PMID 35241661
Kaleta Tamara, Kern Lisa, Hong Samuel Leandro and 30 more
Cryo-EM structure of a SARS-CoV-2 omicron spike protein ectodomain.
Nature communications | 2022-03-03 | PMID 35241675
Ye Gang, Liu Bin, Li Fang
High-content analysis of microRNAs involved in the phenotype regulation of vascular smooth muscle cells.
Scientific reports | 2022-03-03 | PMID 35241704
Zhang Jian, Starkuviene Vytaute, Erfle Holger and 7 more
Gene-based association tests using GWAS summary statistics and incorporating eQTL.
Scientific reports | 2022-03-03 | PMID 35241742
Cao Xuewei, Wang Xuexia, Zhang Shuanglin and 1 more
LIM domain-wide comprehensive virtual mutagenesis provides structural rationale for cardiomyopathy mutations in CSRP3.
Scientific reports | 2022-03-03 | PMID 35241752
Chauhan Pankaj Kumar, Sowdhamini Ramanathan
Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits.
Molecular psychiatry | 2022-03-01 | PMID 35241783
Pathak Gita A, Singh Kritika, Wendt Frank R and 19 more
Chromosome-scale Echinococcus granulosus (genotype G1) genome reveals the Eg95 gene family and conservation of the EG95-vaccine molecule.
Communications biology | 2022-03-03 | PMID 35241789
Korhonen Pasi K, Kinkar Liina, Young Neil D and 32 more
Chromosome-scale and haplotype-resolved genome assembly of a tetraploid potato cultivar.
Nature genetics | 2022-03-01 | PMID 35241824
Sun Hequan, Jiao Wen-Biao, Krause Kristin and 6 more
Synthetic introns enable splicing factor mutation-dependent targeting of cancer cells.
Nature biotechnology | 2022-07-01 | PMID 35241838
North Khrystyna, Benbarche Salima, Liu Bo and 17 more
Genes: SF3B1
Homozygous Mutation of gsdf Causes Infertility in Female Nile Tilapia (Oreochromis niloticus).
Frontiers in endocrinology | 2022-01-01 | PMID 35242110
Jiang Dong-Neng, Peng You-Xing, Liu Xing-Yong and 6 more
The Predictive Value of PAK7 Mutation for Immune Checkpoint Inhibitors Therapy in Non-Small Cell Cancer.
Frontiers in immunology | 2022-01-01 | PMID 35242138
Zeng Hao, Tong Fan, Bin Yawen and 5 more
A Pyroptosis-Related Gene Signature to Predict Patients' Prognosis and Immune Landscape in Liver Hepatocellular Carcinoma.
Computational and mathematical methods in medicine | 2022-01-01 | PMID 35242200
Wang Jiakun, Huang Zhihao, Lu Hongcheng and 3 more
Prognosis of Tumor Microenvironment in Luminal B-Type Breast Cancer.
Disease markers | 2022-01-01 | PMID 35242245
Lv Ji, Ren Jia, Zheng Jie and 2 more
Machine Learning Identifies Pan-Cancer Landscape of Nrf2 Oxidative Stress Response Pathway-Related Genes.
Oxidative medicine and cellular longevity | 2022-01-01 | PMID 35242279
Li Na, Zhan Xianquan
Vitamin D Receptor Genetic Variations May Associate with the Risk of Developing Late Fracture-Related Infection in the Chinese Han Population.
Journal of immunology research | 2022-01-01 | PMID 35242885
Zhao Xing-Qi, Chen Kun, Wan Hao-Yang and 4 more
Protocol to identify and monitor key mutations of broadly neutralizing antibody lineages following sequential immunization of Ig-humanized mice.
STAR protocols | 2022-03-18 | PMID 35243372
Chen Xuejun, Schmidt Stephen D, Duan Hongying and 2 more
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability.
Cell reports. Medicine | 2022-02-15 | PMID 35243414
Teekakirikul Polakit, Zhu Wenjuan, Xu Xinxiu and 34 more
Rare Case of Accelerated-Phase Chronic Myeloid Leukemia Diagnosed During Treatment for JAK2 V617F-Positive Primary Myelofibrosis.
Laboratory medicine | 2022-11-03 | PMID 35243502
Ryu Jeayeon, Chu Daehyun, Park Bosung and 7 more
Carcinosarcoma of the stomach: four cases that expand the morphologic spectrum of gastric cancer with a primitive phenotype.
Virchows Archiv : an international journal of pathology | 2022-05-01 | PMID 35243539
Yamazawa Sho, Ushiku Tetsuo
The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta.
Clinical oral investigations | 2022-06-01 | PMID 35243551
Choi Hyejin, Lee Kwanghwan, Kim Donghyo and 2 more
First cases of infection with the 21L/BA.2 Omicron variant in Marseille, France.
Journal of medical virology | 2022-07-01 | PMID 35243660
Colson Philippe, Delerce Jérémy, Beye Mamadou and 10 more
Single-cell profiling of human CD127+ innate lymphoid cells reveals diverse immune phenotypes in hepatocellular carcinoma.
Hepatology (Baltimore, Md.) | 2022-10-01 | PMID 35243668
He Yuanlin, Luo Jiajing, Zhang Guannan and 8 more
Delineating the epilepsy phenotype of NGLY1 deficiency.
Journal of inherited metabolic disease | 2022-05-01 | PMID 35243670
Levy Rebecca J, Frater Christina H, Gallentine William B and 2 more
Genes and compounds that increase type VII collagen expression as potential treatments for dystrophic epidermolysis bullosa.
Experimental dermatology | 2022-07-01 | PMID 35243691
Thompson Elizabeth L, Pickett-Leonard Michael, Riddle Megan J and 3 more
A novel pathogenic variant at the C-terminal propeptide cleavage site of COL1A1, causing osteogenesis imperfecta with intrafamilial variability.
American journal of medical genetics. Part A | 2022-06-01 | PMID 35243755
Lang Steven H, Gallo Ryan A, Forghani Irman
BRPF1-associated syndrome: A patient with congenital ptosis, neurological findings, and normal intellectual development.
American journal of medical genetics. Part A | 2022-06-01 | PMID 35243762
Souza Josiane, do Valle Daniel Almeida, Santos Mara Lucia Schmidt Ferreira and 4 more
A mutant allele of glycoprotein M6-B (Gpm6b) facilitates behavioral flexibility but increases delay discounting.
Genes, brain, and behavior | 2022-04-01 | PMID 35243767
Sanchez-Roige Sandra, Barnes Samuel A, Mallari Jazlene and 3 more
Forensic Application of ForenSeqTM DNA Signature Prep Kit in Zhengjiang She Ethnic Group.
Fa yi xue za zhi | 2021-12-25 | PMID 35243847
Qu Yi-Ling, Lin Yuan, Yang Zi-Hao and 10 more
Application of ITO Method in Determination of Special Half-Sibling Relationship.
Fa yi xue za zhi | 2021-12-25 | PMID 35243850
Shao Cheng-Chen, Yao Yi-Ning, Zhou Yue-Qin and 4 more
The prevalence and outcomes of α- and β-thalassemia among pregnant women in Hubei Province, Central China: An observational study.
Medicine | 2022-03-04 | PMID 35244037
Cheng Yao, Chen Miaomiao, Ye Jiazhi and 10 more
Transgene-design: a web application for the design of mammalian transgenes.
Bioinformatics (Oxford, England) | 2022-04-28 | PMID 35244144
Mühlhausen Stefanie, Hurst Laurence D
A dog model for centronuclear myopathy carrying the most common DNM2 mutation.
Disease models & mechanisms | 2022-04-01 | PMID 35244154
Böhm Johann, Barthélémy Inès, Landwerlin Charlène and 5 more
Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.
International journal of molecular medicine | 2022-05-01 | PMID 35244186
Chevrier Sandy, Brasselet Astrid, Carnet Marion and 13 more
Habitat effects on reproductive phenotype, pollinator behavior, fecundity, and mating outcomes of a bumble bee-pollinated herb.
American journal of botany | 2022-03-01 | PMID 35244204
Tian Hao, Harder Lawrence D, Wang Ai-Ying and 2 more
Attention to audiovisual speech does not facilitate language acquisition in infants with familial history of autism.
Journal of child psychology and psychiatry, and allied disciplines | 2022-12-01 | PMID 35244219
Chawarska Katarzyna, Lewkowicz David, Feiner Hannah and 2 more
The Detection of Toxoplasma gondii in Wild Rats (Rattus norvegicus) on Mink Farms in Shandong Province, Eastern China.
Vector borne and zoonotic diseases (Larchmont, N.Y.) | 2022-03-01 | PMID 35244455
Zou Yang, Geng Hong-Li, Jia Hong-Lin and 4 more
Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy.
Genetic testing and molecular biomarkers | 2022-03-01 | PMID 35244470
Wang Yuze, Zhao Rulian, Dai Erkuan and 4 more
Detection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis using aneuploidy and mutation identification in plasma.
eLife | 2022-03-04 | PMID 35244537
Mattox Austin K, Douville Christopher, Silliman Natalie and 13 more
Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial.
JAMA network open | 2022-03-01 | PMID 35244702
Nadkarni Girish N, Fei Kezhen, Ramos Michelle A and 12 more
Childhood Height Growth Rate Association With the Risk of Islet Autoimmunity and Development of Type 1 Diabetes.
The Journal of clinical endocrinology and metabolism | 2022-05-17 | PMID 35244713
Li Zhiguo, Veijola Riitta, Koski Eileen and 10 more
Genotyping-by-sequencing and genome-wide association study reveal genetic diversity and loci controlling agronomic traits in triticale.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2022-05-01 | PMID 35244733
Cao Dong, Wang Dongxia, Li Shiming and 3 more
Genetic mapping of powdery mildew resistance genes in wheat landrace Guizi 1 via genotyping by sequencing.
Molecular biology reports | 2022-06-01 | PMID 35244868
Li Luhua, Yang Xicui, Wang Zhongni and 4 more
Characterization of a novel variant allele, HLA-C*03:587, identified in a Chinese Han individual.
HLA | 2022-07-01 | PMID 35244979
He Liu-Mei, Yang Xiao-Ke, Zou Hong-Yan
Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing.
Science advances | 2022-03-04 | PMID 35245110
Stevanovski Igor, Chintalaphani Sanjog R, Gamaarachchi Hasindu and 18 more
Selective requirement for polycomb repressor complex 2 in the generation of specific hypothalamic neuronal subtypes.
Development (Cambridge, England) | 2022-03-01 | PMID 35245348
Yaghmaeian Salmani Behzad, Balderson Brad, Bauer Susanne and 6 more
KIT D816V is dimerization-independent and activates downstream pathways frequently perturbed in mastocytosis.
British journal of haematology | 2023-09-01 | PMID 35245395
Rajan Vinothkumar, Prykhozhij Sergey V, Pandey Aditya and 3 more
Personalized Risk Model and Leveraging of Magnetic Resonance Imaging-Based Structural Phenotypes and Clinical Factors to Predict Incidence of Radiographic Osteoarthritis.
Arthritis care & research | 2023-03-01 | PMID 35245407
Lee Jinhee J, Namiri Nikan K, Astuto Bruno and 3 more
Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemia.
Clinica chimica acta; international journal of clinical chemistry | 2022-06-01 | PMID 35245483
Zhou Qimin, Teng Yanling, Pan Jianyan and 6 more
Neuroectodermal elements are part of the morphological spectrum of DICER1-associated neoplasms.
Human pathology | 2022-05-01 | PMID 35245609
McCluggage W Glenn, Stewart Colin J R, Belcijan Neza Lebic and 6 more
Next step in molecular genetics of hereditary breast/ovarian cancer: Multigene panel testing in clinical actionably genes and prioritization algorithms in the study of variants of uncertain significance.
European journal of medical genetics | 2022-04-01 | PMID 35245693
Castillo-Guardiola Verónica, Rosado-Jiménez Laura, Sarabia-Meseguer María Desamparados and 12 more
Single nucleotide polymorphism array versus karyotype for prenatal diagnosis in fetuses with abnormal ultrasound: A systematic review and meta-analysis.
European journal of obstetrics, gynecology, and reproductive biology | 2022-04-01 | PMID 35245714
Kamath Vandana, Purna Chacko Mary, Kirubakaran Richard and 2 more
The stalk domain of SARS-CoV-2 NSP13 is essential for its helicase activity.
Biochemical and biophysical research communications | 2022-04-23 | PMID 35245742
Yue Kun, Yao Bin, Shi Yingchao and 4 more