The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network.
Yonsei medical journal | 2022-08-01 | PMID 35914754
Kim Yun Joong, Kim Kiyong, Lee Heonwoo and 3 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 8966 of 10600
Pharmacogenetics of Antiplatelet Therapy.
Annual review of pharmacology and toxicology | 2023-01-20 | PMID 35914768
Castrichini Matteo, Luzum Jasmine A, Pereira Naveen
The differences of hemogram, myelogram, and driver gene mutations in classic myeloproliferative neoplasms.
Blood cells, molecules & diseases | 2022-11-01 | PMID 35914897
Wang Jin, Zhang Jin, Huang Jinjin and 2 more
New design and optimization of an in-house quantitative TaqMan Real-Time PCR-based assay for the detection and monitoring of occult hepatitis B virus (genotype A-J) infection.
Indian journal of medical microbiology | 2000-01-01 | PMID 35914958
Ghorbani Mohammad, Shokri Rahman, Kia Vahid and 3 more
Functional genomic tools for emerging model species.
Trends in ecology & evolution | 2022-12-01 | PMID 35914975
Gudmunds Erik, Wheat Christopher W, Khila Abderrahman and 1 more
Study of the genetic diversity of Moraxella spp. isolates obtained from corneal abscesses.
Revista Argentina de microbiologia | 2000-01-01 | PMID 35915013
Roitman Karina L, Cipolla Lucía, Minervini Patricia and 1 more
Tubulin mutations in human neurodevelopmental disorders.
Seminars in cell & developmental biology | 2023-03-15 | PMID 35915025
Maillard Camille, Roux Charles Joris, Charbit-Henrion Fabienne and 4 more
Impact of highly effective CFTR modulator therapy on digital clubbing in patients with cystic fibrosis.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society | 2022-09-01 | PMID 35915048
Mahlen Tsaina, Barton Lottie, Roberts Dion
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.
Nature medicine | 2022-08-01 | PMID 35915156
Tcheandjieu Catherine, Zhu Xiang, Hilliard Austin T and 79 more
Genes: CAD
Circulating tumor DNA to guide rechallenge with panitumumab in metastatic colorectal cancer: the phase 2 CHRONOS trial.
Nature medicine | 2022-08-01 | PMID 35915157
Sartore-Bianchi Andrea, Pietrantonio Filippo, Lonardi Sara and 22 more
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.
Nature genetics | 2022-08-01 | PMID 35915169
Byun Jinyoung, Han Younghun, Li Yafang and 82 more
Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders.
Nature neuroscience | 2022-08-01 | PMID 35915177
Bryois Julien, Calini Daniela, Macnair Will and 13 more
The histone deacetylase SIRT6 promotes glycolysis through the HIF-1α/HK2 signaling axis and induces erlotinib resistance in non-small cell lung cancer.
Apoptosis : an international journal on programmed cell death | 2022-12-01 | PMID 35915188
You Qiai, Wang Jianmin, Yu Yongxin and 8 more
Thyroid gland dysfunction and vitamin D receptor gene polymorphism in keratoconus.
Eye (London, England) | 2023-06-01 | PMID 35915233
Awad Eman A, Torky Magda A, Bassiouny Rania M and 3 more
Genetic networks underlying salinity tolerance in wheat uncovered with genome-wide analyses and selective sweeps.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2022-09-01 | PMID 35915266
Shan Danting, Ali Mohsin, Shahid Mohammed and 10 more
SSR marker-based genetic characterization of Turkish oriental tobaccos.
Molecular biology reports | 2022-12-01 | PMID 35915362
Saygili Ibrahim, Kandemir Nejdet, Kinay Ahmet and 2 more
Sex-Based Clinicopathologic and Survival Differences Among Patients with Pancreatic Neuroendocrine Tumors.
Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract | 2022-11-01 | PMID 35915373
Greenberg Jacques A, Ivanov Nikolay A, Egan Caitlin E and 5 more
Identifying genetic markers enriched by brain imaging endophenotypes in Alzheimer's disease.
BMC medical genomics | 2022-08-01 | PMID 35915443
Kim Mansu, Wu Ruiming, Yao Xiaohui and 3 more
Characterization of compliance phenotypes in COVID-19 acute respiratory distress syndrome.
BMC pulmonary medicine | 2022-08-01 | PMID 35915487
Zacchetti Lucia, Longhi Luca, Bianchi Isabella and 14 more
Testicular exosomes disturb the immunosuppressive phenotype of testicular macrophages mediated by miR-155-5p in uropathogenic Escherichia coli-induced orchitis.
Asian journal of andrology | 2000-01-01 | PMID 35915541
Xu Jia, He Chao, Fang Yi-Wei and 7 more
Case report of mild TCIRG1-associated autosomal recessive osteopetrosis in Vietnam.
American journal of medical genetics. Part A | 2022-10-01 | PMID 35915932
Luong Long Hoang, Nguyen Hieu Dinh, Trung Tuyen Nguyen and 5 more
[Association of RAAS gene polymorphisms with susceptibility to essential hypertension in military secret service personnel].
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases | 2022-07-20 | PMID 35915940
Cao Y H, Li X, Liu M H and 3 more
Ethical implications of early genetic diagnosis in an infant with Lesch-Nyhan syndrome.
Journal of genetic counseling | 2022-12-01 | PMID 35916015
Zhang Tian, Briere Julie M, Leeman Kristen T and 2 more
Selenoprotein I deficiency in T cells promotes differentiation into tolerant phenotypes while decreasing Th17 pathology.
Journal of leukocyte biology | 2022-12-01 | PMID 35916034
Ma Chi, Hoffmann FuKun W, Nunes Lance G and 5 more
Neutrophil functional heterogeneity is a fixed phenotype and is associated with distinct gene expression profiles.
Journal of leukocyte biology | 2022-12-01 | PMID 35916035
Maskarinec Stacey A, McKelvy Margaret, Boyle Kimberly and 7 more
Phenotype of Asthma-COPD Overlap in COPD and Severe Asthma Cohorts.
Journal of Korean medical science | 2022-08-01 | PMID 35916048
Joo Hyonsoo, Park So-Young, Park So Young and 6 more
Phenotypic and genotypic analysis of Edwardsiella isolates from Taiwan indicates wide variation with a particular reference to Edwardsiella tarda and Edwardsiella anguillarum.
Journal of fish diseases | 2022-11-01 | PMID 35916068
Rahmawaty Atiek, Chen Mei-Yun, Byadgi Omkar Vijay and 2 more
Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non-syndromic retinitis pigmentosa.
Clinical genetics | 2022-12-01 | PMID 35916082
Dvaladze Anna, Tavares Erika, Di Scipio Matteo and 15 more
XDH genotypes through gene-gene interactions with NUDT15 affect azathioprine-induced leukopenia in Chinese patients.
Pharmacogenomics | 2022-08-01 | PMID 35916133
Liu Jiquan, Wen Zhiyong, Huang Sichao and 3 more
Anthropometric fluctuating asymmetries in living humans through the eyes of an anthropologist.
Emerging topics in life sciences | 2022-09-09 | PMID 35916213
Özener Barış
Anti-Müllerian hormone as an endocrine biomarker of reproductive longevity and assessment of single nucleotide polymorphisms in AMH gene of Bos indicus breeds of cattle.
Reproduction in domestic animals = Zuchthygiene | 2022-11-01 | PMID 35916244
Ramesha Kerekoppa P, Jeyakumar Sakthivel, Mall Shweta and 7 more
Frequency and distribution of HLA-DQB1 alleles from 2076 cord blood samples of the Vietnamese cohort.
International journal of immunogenetics | 2022-10-01 | PMID 35916345
Que Tran Ngoc, Khanh Nguyen Ba, Tung Pham Dinh and 3 more
Artificial selection methods from evolutionary computing show promise for directed evolution of microbes.
eLife | 2022-08-02 | PMID 35916365
Lalejini Alexander, Dolson Emily, Vostinar Anya E and 1 more
A paternal bias in germline mutation is widespread in amniotes and can arise independently of cell division numbers.
eLife | 2022-08-02 | PMID 35916372
de Manuel Marc, Wu Felix L, Przeworski Molly
A Variant Allele in Varicella-Zoster Virus Glycoprotein B Selected during Production of the Varicella Vaccine Contributes to Its Attenuation.
mBio | 2022-08-30 | PMID 35916400
Sadaoka Tomohiko, Depledge Daniel P, Rajbhandari Labchan and 3 more
Immune Escape Adaptive Mutations in Hemagglutinin Are Responsible for the Antigenic Drift of Eurasian Avian-Like H1N1 Swine Influenza Viruses.
Journal of virology | 2022-08-24 | PMID 35916512
Xu Chengzhi, Zhang Naixin, Yang Yuying and 9 more
Investigation of pharmacologic interactions between omeprazole and tacrolimus in a membranous nephropathy patient with CYP3A5 nonexpresser: a case report.
Pharmacogenetics and genomics | 2022-09-01 | PMID 35916550
Li Yanli, Liu Yi, Sun Zengxian
The -α3.7III subtype of α+-thalassemia was identified in China.
Hematology (Amsterdam, Netherlands) | 2022-12-01 | PMID 35916627
Bao Xiuqin, Wang Jicheng, Qin Danqing and 5 more
Discovery of the novel HLA-B*52:109 allele in a Taiwanese individual.
HLA | 2022-11-01 | PMID 35916638
Yang Kuo-Liang, Lin Py-Yu
Identification of NS5B resistance against SOFOSBUVIR in hepatitis C virus genotype 3a, naive and treated patients.
Journal of applied microbiology | 2022-11-01 | PMID 35916643
Younas Saima, Sumrin Aleena, Hussain Nazim and 1 more
Genetic variants of TORC1 gene promoter and their association with carcass quality and body measurement traits in Qinchuan beef cattle.
Animal biotechnology | 2023-12-01 | PMID 35916659
Zhao Xianlin, Khan Rajwali, Hongfang Guo and 8 more
Identifying cellular cancer mechanisms through pathway-driven data integration.
Bioinformatics (Oxford, England) | 2022-09-15 | PMID 35916710
Windels Sam F L, Malod-Dognin Noël, Pržulj Nataša
Construction of prediction models for growth traits of soybean cultivars based on phenotyping in diverse genotype and environment combinations.
DNA research : an international journal for rapid publication of reports on genes and genomes | 2022-06-25 | PMID 35916715
Manggabarani Andi Madihah, Hashiguchi Takuyu, Hashiguchi Masatsugu and 11 more
Multisite chronic pain as a causal risk factor for coronary artery disease: findings from Mendelian randomization.
Pain | 2023-03-01 | PMID 35916731
Zhu Jiahao, Wang Nini, Liu Houpu and 4 more
Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndrome.
European review for medical and pharmacological sciences | 2022-07-01 | PMID 35916809
Ramírez-Hernández M A, Figuera L E, Rizo-de la Torre L C and 7 more
Bone Deformities and Kidney Failure: Coincidence of PHEX-Related Hypophosphatemic Rickets and m.3243A>G Mitochondrial Disease.
Calcified tissue international | 2022-12-01 | PMID 35916905
Nielsen Simone Rask, Hansen Stinus Gadegaard, Bistrup Claus and 2 more
Polygene control and trait dominance in death-feigning syndrome in the red flour beetle Tribolium castaneum.
Behavior genetics | 2022-09-01 | PMID 35916953
Matsumura Kentarou, Miyatake Takahisa
Juvenile patients with the homozygous MTHFR C677T genotype develop ischemic stroke 5 years earlier than wild type.
Journal of thrombosis and thrombolysis | 2022-08-01 | PMID 35917096
Ames Paul R J, D'Andrea Giovanna, Marottoli Vincenzo and 4 more
GIGYF1 disruption associates with autism and impaired IGF-1R signaling.
The Journal of clinical investigation | 2022-10-03 | PMID 35917186
Chen Guodong, Yu Bin, Tan Senwei and 31 more
A CRISPR-Cas12a-based diagnostic method for multiple genotypes of severe fever with thrombocytopenia syndrome virus.
PLoS neglected tropical diseases | 2022-08-01 | PMID 35917293
Park Bum Ju, Yoo Jeong Rae, Heo Sang Taek and 3 more
De novo mutations in KIF1A-associated neuronal disorder (KAND) dominant-negatively inhibit motor activity and axonal transport of synaptic vesicle precursors.
Proceedings of the National Academy of Sciences of the United States of America | 2022-08-09 | PMID 35917346
Anazawa Yuzu, Kita Tomoki, Iguchi Rei and 2 more
Cediranib in Combination with Olaparib in Patients without a Germline BRCA1/2 Mutation and with Recurrent Platinum-Resistant Ovarian Cancer: Phase IIb CONCERTO Trial.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2022-10-03 | PMID 35917514
Lee Jung-Min, Moore Richard G, Ghamande Sharad and 12 more
Study of pyrethroid resistance mutations in populations of Varroa destructor across Spain.
Research in veterinary science | 2022-12-20 | PMID 35917591
Benito-Murcia M, Martín-Hernández R, Meana A and 2 more
Hormones do not maketh the mole-rat: No steroid hormone signatures of subordinate behavioral phenotypes.
Hormones and behavior | 2022-09-01 | PMID 35917594
Toor Ilapreet, Faykoo-Martinez Mariela, Edwards Phoebe D and 2 more
An induced pluripotent stem cell line (YCMi006-A) generated from a patient with hypertrophic cardiomyopathy who carries the ACTA1 mutation p.Ile343Met.
Stem cell research | 2022-08-01 | PMID 35917599
Kim Hyoeun, Kim Hyeong-Jin, Oh Jaewon and 10 more
Generation of a heterozygous TPM1-E192K knock-in human induced pluripotent stem cell line using CRISPR/Cas9 system.
Stem cell research | 2022-08-01 | PMID 35917600
Kang Ji-Young, Mun Dasom, Chun Yumin and 4 more
Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort.
Parkinsonism & related disorders | 2022-09-01 | PMID 35917738
Loesch Douglas P, Horimoto Andrea R V R, Sarihan Elif Irem and 32 more
Population structure, susceptibility profile, phenotypic and mating properties of Candida tropicalis isolated from pediatric patients.
Microbial pathogenesis | 2022-09-01 | PMID 35917988
Jafarian Hadis, Hardani Amir Kamal, Asnafi Ali Amin and 1 more
EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia.
European journal of medical genetics | 2022-10-01 | PMID 35918037
Courdier Cécile, Gemahling Anna, Guindolet Damien and 7 more
Traboulsi syndrome caused by mutations in ASPH: An autosomal recessive disorder with overlapping features of Marfan syndrome.
European journal of medical genetics | 2022-10-01 | PMID 35918038
Jones Gabriela, Johnson Katie, Eason Jacqueline and 5 more
De novo SCN3A missense variant associated with self-limiting generalized epilepsy with fever sensitivity.
European journal of medical genetics | 2022-10-01 | PMID 35918039
Johannesen Katrine M, Gardella Elena, Ahring Philip K and 1 more
Genotype/phenotype correlation in 123 Chinese patients with Tuberous Sclerosis Complex.
European journal of medical genetics | 2022-10-01 | PMID 35918040
Ng Samuel Yl, Luk Ho-Ming, Hau Edgar Wl and 5 more
Inactivated genotype 1a, 2a and 3a HCV vaccine candidates induced broadly neutralising antibodies in mice.
Gut | 2023-03-01 | PMID 35918103
Alzua Garazi Pena, Pihl Anne Finne, Offersgaard Anna and 11 more
Association of Vitamin D Receptor Genetic Polymorphisms With Nephrolithiasis and End-Stage Renal Disease: A Meta-Analysis.
Transplantation proceedings | 2022-09-01 | PMID 35918192
Xu Ning, Yang Maoquan, Liu Jie and 1 more
The role of timing in intraspecific trait ecology.
Trends in ecology & evolution | 2022-11-01 | PMID 35918208
Cope Olivia L, Burkle Laura A, Croy Jordan R and 3 more
Genetic Variations in IFNGR1, BDNF and IL-10 May Predict the Susceptibility to Depression and Anxiety in Chinese Women With Breast Cancer.
Clinical breast cancer | 2022-10-01 | PMID 35918221
Lan Bo, Lv Dan, Sun Xiaoying and 3 more
A common deletion at BAK1 reduces enhancer activity and confers risk of intracranial germ cell tumors.
Nature communications | 2022-08-02 | PMID 35918310
Sonehara Kyuto, Kimura Yui, Nakano Yoshiko and 25 more
Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity.
Nature communications | 2022-08-02 | PMID 35918329
Möhrmann Lino, Werner Maximilian, Oleś Małgorzata and 41 more
Systematic strategies for developing phage resistant Escherichia coli strains.
Nature communications | 2022-08-02 | PMID 35918338
Zou Xuan, Xiao Xiaohong, Mo Ziran and 8 more
Exploring synthetic lethal network for the precision treatment of clear cell renal cell carcinoma.
Scientific reports | 2022-08-02 | PMID 35918352
Liu Zhicheng, Lin Dongxu, Zhou Yi and 10 more
ExAgBov: A public database of annotated variations from hundreds of bovine whole-exome sequencing samples.
Scientific data | 2022-08-02 | PMID 35918364
Raz Rotem, Roth Zvi, Gershoni Moran
PILRA polymorphism modifies the effect of APOE4 and GM17 on Alzheimer's disease risk.
Scientific reports | 2022-08-02 | PMID 35918447
Lopatko Lindman Karin, Jonsson Caroline, Weidung Bodil and 8 more
Demographic history and population genetic structure of Anisakis pegreffii in the cutlassfish Trichiurus japonicus along the coast of mainland China and Taiwan.
Parasitology research | 2022-10-01 | PMID 35918454
Ding Fang, Gu Sui, Yi Mu-Rong and 3 more
Elucidating the genetic architecture controlling antioxidant status and ionic balance in barley under salt stress.
Plant molecular biology | 2022-10-01 | PMID 35918559
Thabet Samar G, Alomari Dalia Z, Börner Andreas and 2 more
Molecular characterization of Infectious Bursal Disease Virus isolated in Chile reveals several mutations in VP2 coding region and a reassortment in its genome.
Veterinary research communications | 2022-12-01 | PMID 35918572
Guzmán Miguel, Cádiz Leandro, Guerrero-Moncayo Alejandra and 5 more
Bias and inconsistency in the estimation of tumour mutation burden.
BMC cancer | 2022-08-02 | PMID 35918650
Makrooni Mohammad A, O'Sullivan Brian, Seoighe Cathal
Genetic diversity and population structure of 93 rice cultivars (lines) (Oryza sativa Xian group) in Qinba in China by 3 types of genetic markers.
BMC genomics | 2022-08-02 | PMID 35918653
Zhang Yu, He Qiaoqiao, Zhou Xixi and 4 more
Sleep duration, genetic susceptibility, and Alzheimer's disease: a longitudinal UK Biobank-based study.
BMC geriatrics | 2022-08-02 | PMID 35918656
Yuan Shiqi, Ma Wen, Yang Rui and 6 more
Germline variants profiling of BRCA1 and BRCA2 in Chinese Hakka breast and ovarian cancer patients.
BMC cancer | 2022-08-02 | PMID 35918668
Zhang Yunuo, Wu Heming, Yu Zhikang and 4 more
Long-term clinical prognosis of 335 infant single-gene positive FEVR cases.
BMC ophthalmology | 2022-08-02 | PMID 35918671
Chen Chunli, Cheng Yizhe, Zhang Zhihan and 4 more
Cluster analysis unveils a severe persistent respiratory impairment phenotype 3-months after severe COVID-19.
Respiratory research | 2022-08-02 | PMID 35918719
Perotin Jeanne-Marie, Gierski Fabien, Bolko Lois and 17 more
Fatal systemic disorder caused by biallelic variants in FARSA.
Orphanet journal of rare diseases | 2022-08-02 | PMID 35918773
Kim Soo Yeon, Ko Saebom, Kang Hyunook and 7 more
Hyperuricemia is Associated with the Presence of Metabolically Obese Normal-Weight and Metabolically Healthy Obese Phenotypes.
Endocrine research | 2000-01-01 | PMID 35918814
Guerrero-Romero Fernando, Simental-Mendía Luis E
Functional significance of the rare rs35667974 IFIH1 gene polymorphism, associated with multiple autoimmune diseases, using a structural biological approach.
Autoimmunity | 2022-11-01 | PMID 35918839
Zervou Maria I, Andreou Athena C, Eliopoulos Elias E and 1 more
Carboxylic Acid Amide but Not Quinone Outside Inhibitor Fungicide Resistance Mutations Show Clade-Specific Occurrence in Pseudoperonospora cubensis Causing Downy Mildew in Commercial and Wild Cucurbits.
Phytopathology | 2023-01-01 | PMID 35918851
D'Arcangelo K N, Wallace E C, Miles T D and 1 more
Clonal Expansion and Dispersal Pathways of Puccinia polysora in China.
Phytopathology | 2023-01-01 | PMID 35918852
Sun Qiuyu, Liu Jie, Huang Chong and 5 more
Macrophages as a therapeutic target to promote diabetic wound healing.
Molecular therapy : the journal of the American Society of Gene Therapy | 2022-09-07 | PMID 35918892
Sharifiaghdam Maryam, Shaabani Elnaz, Faridi-Majidi Reza and 3 more
Association of the Interleukin-10-592C/A Polymorphism and Cervical Cancer Risk: A Meta-Analysis.
Genetics research | 2022-01-01 | PMID 35919032
Diakite Brehima, Kassogue Yaya, Maiga Mamoudou and 13 more
Genotype-Phenotype Correlation Reanalysis in 83 Chinese Cases with OCRL Mutations.
Genetics research | 2022-01-01 | PMID 35919034
Zhang Lingxia, Wang Shugang, Mao Ruoque and 10 more
Impaired Function of a Rare Mutation in the MMUT Gene Causes Methylmalonic Acidemia in a Chinese Patient.
Genetics research | 2022-01-01 | PMID 35919035
Dai Siyu, Yang Yanting, Li Yaqian and 1 more
[Pcr-rflp genotyping of pfcrt and pfmdr1 in plasmodium falciparum isolates from children in Vatomandry, Madagascar].
Medecine tropicale et sante internationale | 2022-06-30 | PMID 35919251
Ravaoarisoa Élisabeth, Andrianaranjaka Voahangy Hanitriniaina Isabelle, Ramanantsahala Aina David and 7 more
Drug resistant Mycobacterium tuberculosis in Oman: resistance-conferring mutations and lineage diversity.
PeerJ | 2022-01-01 | PMID 35919400
Al Mahrouqi Sara, Gadalla Amal, Al Azri Saleh and 8 more
Population structure and genomic footprints of selection in five major Iranian horse breeds.
Animal genetics | 2022-10-01 | PMID 35919961
Salek Ardestani Siavash, Zandi Mohammad Bagher, Vahedi Seyed Milad and 1 more
A tale of two plasmids: contributions of plasmid associated phenotypes to epidemiological success among Shigella.
Proceedings. Biological sciences | 2022-08-10 | PMID 35919999
Malaka De Silva P, Stenhouse George E, Blackwell Grace A and 4 more
Genetic diversity of honeybee colonies predicts gut bacterial diversity of individual colony members.
Environmental microbiology | 2022-12-01 | PMID 35920034
Bridson Calum, Vellaniparambil Latha, Antwis Rachel E and 3 more
Modulating streptococcal phenotypes using signal peptide analogues.
Open biology | 2022-08-01 | PMID 35920042
Brennan Alec A, Mehrani Mona, Tal-Gan Yftah
Efficacy of genotype-matched Newcastle disease virus vaccine formulated in carboxymethyl sago starch acid hydrogel in chickens vaccinated via different routes.
Journal of veterinary science | 2022-07-01 | PMID 35920119
Mahamud Siti Nor Azizah, Bello Muhammad Bashir, Ideris Aini and 1 more
Epidemiological investigation and phylogenetic analysis of Classical Swine Fever virus in Yunnan province from 2015 to 2021.
Journal of veterinary science | 2022-07-01 | PMID 35920121
Yao Jun, Su Linlin, Wang Qiaoping and 8 more
Novel splice‑site variants c.393G>A, c.278_2A>G in exon 2 and Q705K variant in exon 3 of NLRP3 gene are associated with bipolar I disorder.
Molecular medicine reports | 2022-09-01 | PMID 35920179
Öztürk Kuyaş Heki̇mler, Ünal Güli̇n Özdamar
Mcm2 hypomorph leads to acute leukemia or hematopoietic stem cell failure, dependent on genetic context.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2022-09-01 | PMID 35920299
Matsukawa Toshihiro, Yin Mianmian, Baslan Timour and 10 more