CCR5-Δ32 polymorphism-a possible protective factor from gait impairment amongst post-stroke patients.
European journal of neurology | 2023-03-01 | PMID 36380716
Molad Jeremy, Hallevi Hen, Seyman Estelle and 7 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 9045 of 10600
Somatic mutations of activating signalling, transcription factor, and tumour suppressor are a precondition for leukaemia transformation in myelodysplastic syndromes.
Journal of cellular and molecular medicine | 2022-12-01 | PMID 36380727
Xu Feng, Wu Lin-Yun, Guo Juan and 3 more
α-Synuclein Disrupts Vesicle Fusion by Two Mutant-Specific Mechanisms.
Molecules and cells | 2022-11-30 | PMID 36380732
Yoo Gyeongji, An Hyeong Jeon, Yeou Sanghun and 1 more
Anti-cancer effect of targeting fibroblast activation protein alpha in glioblastoma through remodeling macrophage phenotype and suppressing tumor progression.
CNS neuroscience & therapeutics | 2023-03-01 | PMID 36382346
Miao Yazhou, Deng Yuxuan, Liu Jinqiu and 13 more
In silico versus functional characterization of genetic variants: lessons from muscle channelopathies.
Brain : a journal of neurology | 2023-04-19 | PMID 36382348
Vivekanandam Vinojini, Ellmers Rebecca, Jayaseelan Dipa and 3 more
Lipoprotein(a) levels in children with suspected familial hypercholesterolaemia: a cross-sectional study.
European heart journal | 2023-04-21 | PMID 36382390
de Boer Lotte M, Hutten Barbara A, Zwinderman Aeilko H and 1 more
Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumors.
Molecular genetics & genomic medicine | 2023-02-01 | PMID 36382415
van de Beek Irma, Glykofridis Iris E, Wagner Anja and 9 more
Activating de novo monoallelic variants causing inborn errors of immunity in two unrelated children born of HIV-seroconcordant couples.
AIDS (London, England) | 2022-12-01 | PMID 36382434
Lugo Reyes Saul O, Solórzano Suárez Andrea, Scheffler Mendoza Selma C and 10 more
Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease-causing variants.
Molecular genetics & genomic medicine | 2022-12-01 | PMID 36382472
Sadat Fatemi Seyedeh Helia, Eshraghi Peyman, Ghanei Mahmoud and 1 more
Presentation of cryopyrin-associated periodic fever syndrome as chronic, afebrile urticaria in a 12-month-old female.
Pediatric dermatology | 2000-01-01 | PMID 36382474
Fitzgerald Lauren A, Drissi Madeeha, Sepulveda Kirstin and 3 more
Thyroid carcinoma metastases to central nervous system and vertebrae.
Folia neuropathologica | 2022-01-01 | PMID 36382481
Kleinschmidt-DeMasters Bette, Marshall Carrie
The mutational spectrum of SARS-CoV-2 genomic and antigenomic RNA.
Proceedings. Biological sciences | 2022-11-30 | PMID 36382519
Zhao Lele, Hall Matthew, de Cesare Mariateresa and 6 more
Functional space expansion driven by transitions between energetically advantageous traits in the deep sea.
Proceedings. Biological sciences | 2022-11-30 | PMID 36382521
Bryant S River D, McClain Craig R
Female dewlap ornaments are evolutionarily labile and associated with increased diversification rates in Anolis lizards.
Proceedings. Biological sciences | 2022-11-30 | PMID 36382524
Yuan Michael L, Westeen Erin P, Wogan Guinevere O U and 1 more
Absence of copy number gain of EGFR: A possible predictive marker of long-term response to afatinib.
Cancer science | 2023-03-01 | PMID 36382532
Nakamura Tomomi, Sato Akemi, Nakashima Chiho and 5 more
Genes: EGFR
Random variations, gradualism and the role of natural selection.
Theoretical biology forum | 2021-07-01 | PMID 36382547
Saunders Peter
Association of genetic variants and survival in patients with acute myeloid leukemia in rural Appalachia.
Cancer reports (Hoboken, N.J.) | 2023-03-01 | PMID 36382570
Shultz Carl, Gates Christopher, Petros William and 8 more
The novel HLA-B*15:644 allele, identified by Sanger dideoxy nucleotide sequencing in a Chinese individual.
HLA | 2023-03-01 | PMID 36382584
Shi Zhuo-Yue, Zheng Zhong-Zheng, Du Ke-Ming and 2 more
Genomic sequence of the HLA-A*02:01:209 allele identified in a solid organ recipient.
HLA | 2023-03-01 | PMID 36382586
Thakker Nirali C, Buch Hiteshree, Chaudhary Akshay and 2 more
Gene detection in a family with monilethrix and treatment with 5% topical minoxidil.
Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) | 2023-01-01 | PMID 36382623
Shen Qingli, Fu Zhonghua, Du Pengqiang and 1 more
The Association of HLA Alleles and Haplotypes with Age of Disease Onset in Pakistani Psoriatic Patients.
International archives of allergy and immunology | 2023-01-01 | PMID 36382644
Munir Saeeda, Rahman Simeen Ber, Rehman Sadia and 3 more
Pharmacokinetics of a single dose of Aficamten (CK-274) on cardiac contractility in a A31P MYBPC3 hypertrophic cardiomyopathy cat model.
Journal of veterinary pharmacology and therapeutics | 2023-01-01 | PMID 36382714
Sharpe Ashley N, Oldach Maureen S, Kaplan Joanna L and 7 more
Anti-hsa-miR-59 alleviates premature senescence associated with Hutchinson-Gilford progeria syndrome in mice.
The EMBO journal | 2023-01-04 | PMID 36382717
Hu Qianying, Zhang Na, Sui Tingting and 8 more
Genetic polymorphism of fatty acid binding protein-2 in hyperlipidemic Asian Indians in North India.
American journal of human biology : the official journal of the Human Biology Council | 2023-03-01 | PMID 36382874
Meena Kiran, Misra Anoop, Vikram Naval and 3 more
ABCG2 and SLCO1B1 gene polymorphisms in the Croatian population.
Annals of human biology | 2022-12-01 | PMID 36382878
Božina Tamara, Ganoci Lana, Karačić Ena and 6 more
Ter-Seq: A high-throughput method to stabilize transient ternary complexes and measure associated kinetics.
Protein science : a publication of the Protein Society | 2023-01-01 | PMID 36382921
Chattopadhyay Gopinath, Ahmed Shahbaz, Srilatha Nonavinakere Seetharam and 2 more
Upgrading the genome of an elite japonica rice variety Kongyu 131 for lodging resistance improvement.
Plant biotechnology journal | 2023-02-01 | PMID 36382925
Wang Chen, Feng Xiaomin, Yuan Qingbo and 11 more
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD alleles.
Transfusion | 2023-02-01 | PMID 36382965
Wen Jizhi, Jia Shuangshuang, Wang Zhen and 7 more
[Alpha-1 antitrypsin deficiency].
Revue medicale suisse | 2022-11-16 | PMID 36382978
Marando Marco, Rayroux Caroline, Bergeron Anne
The O-GlcNAc cycling in neurodevelopment and associated diseases.
Biochemical Society transactions | 2022-12-16 | PMID 36383066
Wenzel Dawn M, Olivier-Van Stichelen Stephanie
KRAS inhibitors: going noncovalent.
Molecular oncology | 2022-12-01 | PMID 36383067
Drosten Matthias, Barbacid Mariano
Genetic architecture of natural variation of cardiac performance from flies to humans.
eLife | 2022-11-16 | PMID 36383075
Saha Saswati, Spinelli Lionel, Castro Mondragon Jaime A and 12 more
Genes: EGR2, PAX9
Capitalizing on paradoxical activation of the mitogen-activated protein kinase pathway for treatment of Imatinib-resistant mast cell leukemia.
Hematological oncology | 2023-08-01 | PMID 36383121
Wilhelm Thomas, Toledo Marcelo A S, Simons Ilka and 12 more
Robust genetic model-based SNP-set association test using CauchyGM.
Bioinformatics (Oxford, England) | 2023-01-01 | PMID 36383169
Kim Yeonil, Chi Yueh-Yun, Shen Judong and 1 more
Genes: MAF
Contraceptives and cancer risks in BRCA1/2 pathogenic variant carriers: a systematic review and meta-analysis.
Human reproduction update | 2023-03-01 | PMID 36383189
van Bommel Majke H D, IntHout Joanna, Veldmate Guus and 4 more
Hearing of Otof-deficient mice restored by trans-splicing of N- and C-terminal otoferlin.
Human genetics | 2023-02-01 | PMID 36383253
Tang Honghai, Wang Hui, Wang Shengyi and 10 more
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development.
Human genetics | 2023-08-01 | PMID 36383254
Safizadeh Shabestari Seyed Ali, Nassir Nasna, Sopariwala Samana and 7 more
Neighborhood disadvantage is associated with KRAS-mutated non-small cell lung cancer risk.
Journal of cancer research and clinical oncology | 2023-07-01 | PMID 36383274
Wing Sam E, Jankowska Marta M, Zou Xiaoke and 8 more
Genes: KRAS
Variations in the NSP4 gene of the type 2 porcine reproductive and respiratory syndrome virus isolated in China from 1996 to 2021.
Virus genes | 2023-02-01 | PMID 36383275
Sha Huiyang, Zhang Hang, Luo Qin and 7 more
Virtual screening and zebrafish models in tandem, for drug discovery and development.
Expert opinion on drug discovery | 2000-01-01 | PMID 36383405
Hernández-Silva David, Alcaraz-Pérez Francisca, Pérez-Sánchez Horacio and 1 more
Tracking the distribution, genetic diversity and lineage of Brucella melitensis recovered from humans and animals in Egypt based on core-genome SNP analysis and in silico MLVA-16.
Transboundary and emerging diseases | 2022-11-01 | PMID 36383491
Holzer Katharina, Wareth Gamal, El-Diasty Mohamed and 11 more
Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.
PloS one | 2022-01-01 | PMID 36383556
Effraimidis Grigoris, Rasmussen Åse Krogh, Dunoe Morten and 20 more
Genetic ablation of metabotropic glutamate receptor 5 in rats results in an autism-like behavioral phenotype.
PloS one | 2022-01-01 | PMID 36383609
Eshraghi Adrien A, Memis Idil, Wang Florence and 6 more
A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables.
PLoS genetics | 2022-11-01 | PMID 36383614
Hecker Julian, Prokopenko Dmitry, Moll Matthew and 13 more
An effective preselection criterion for MODY with an increasingly positive genetic testing rate by NGS: results from two cohorts of Chinese children.
American journal of physiology. Endocrinology and metabolism | 2022-12-01 | PMID 36383636
Cao Bingyan, Liu Meijuan, Zhang Yingxian and 11 more
The translocated virulence protein VirD5 causes DNA damage and mutation during Agrobacterium-mediated transformation of yeast.
Science advances | 2022-11-18 | PMID 36383666
Zhang Xiaorong, Hooykaas Marjolein J G, van Heusden G Paul and 1 more
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes.
Science advances | 2022-11-18 | PMID 36383675
Nag Abhishek, Dhindsa Ryan S, Mitchell Jonathan and 26 more
APOE ε4 genotype, amyloid-β, and sex interact to predict tau in regions of high APOE mRNA expression.
Science translational medicine | 2022-11-16 | PMID 36383681
Dincer Aylin, Chen Charles D, McKay Nicole S and 15 more
Multimodal Genotype and Phenotype Data Integration to Improve Partial Data-Based Longitudinal Prediction.
Journal of computational biology : a journal of computational molecular cell biology | 2022-12-01 | PMID 36383766
Ganjdanesh Alireza, Zhang Jipeng, Yan Sarah and 2 more
Genetic diversity of Trypanosoma cruzi strains isolated from chronic chagasic patients and non-human hosts in the state of São Paulo, Brazil.
Memorias do Instituto Oswaldo Cruz | 2022-01-01 | PMID 36383785
Souza Thiago Kury Moreno de, Westphalen Elizabeth Visone Nunes, Westphalen Sansão da Rocha and 15 more
Prevalence of human cryptosporidiosis in the Americas: systematic review and meta-analysis.
Revista do Instituto de Medicina Tropical de Sao Paulo | 2022-01-01 | PMID 36383892
Jann Higor Wilson, Cabral-Castro Mauro Jorge, Costa João Victor Barreto and 3 more
Next-generation Sequencing as a Potential Diagnostic Adjunct in Distinguishing Between Desmoplastic Melanocytic Neoplasms.
The American journal of surgical pathology | 2023-03-01 | PMID 36383901
Roth Andrew, Boutko Anastasiya, Lampley Nathaniel and 8 more
Molecular Dynamics Simulations of the Cardiac Ryanodine Receptor Type 2 (RyR2) Gating Mechanism.
The journal of physical chemistry. B | 2022-12-01 | PMID 36384028
Greene D'Artagnan, Barton Michael, Luchko Tyler and 1 more
Targeted in vivo mutagenesis of a sensor histidine kinase playing an essential role in ABA signaling of the moss Physcomitrium patens.
Biochemical and biophysical research communications | 2022-12-31 | PMID 36384069
Sk Rahul, Miyabe Marcos Takeshi, Takezawa Daisuke and 4 more
Privacy-aware estimation of relatedness in admixed populations.
Briefings in bioinformatics | 2022-11-19 | PMID 36384083
Wang Su, Kim Miran, Li Wentao and 3 more
Identifying inflammatory phenotypes to target mechanism-specific treatments in sepsis.
Cell reports. Medicine | 2022-11-15 | PMID 36384087
Gómez Hernando, Anderko Renee R, Carcillo Joseph A
Switching to coformulated bictegravir, emtricitabine, and tenofovir alafenamide maintained viral suppression in adults with historical virological failures and K65N/R mutation.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases | 2023-01-01 | PMID 36384186
Tsai Mao-Song, Sun Hsin-Yun, Chen Cheng-Pin and 10 more
Rare multiple congenital anomalies-hypotonia-seizures syndrome type 1 (MCAHS1) - the clinical and molecular summary.
European journal of medical genetics | 2023-01-01 | PMID 36384198
Bukowska-Olech Ewelina, Glista Filip, Dinwiddie April and 2 more
Genetic Predisposition of Both Waist Circumference and Hip Circumference Increased the Risk of Venous Thromboembolism.
Thrombosis and haemostasis | 2023-03-01 | PMID 36384228
Wang Jiayu, Tan Jiangshan, Hua Lu and 3 more
Animal models of Diamond-Blackfan anemia: updates and challenges.
Haematologica | 2023-05-01 | PMID 36384250
Liu Y Lucy, Shibuya Aya, Glader Bert and 3 more
ApoA-I Nanotherapy Rescues Postischemic Vascular Maladaptation by Modulating Endothelial Cell and Macrophage Phenotypes in Type 2 Diabetic Mice.
Arteriosclerosis, thrombosis, and vascular biology | 2023-01-01 | PMID 36384268
Babu Mohan, Devi Durga, Mäkinen Petri and 4 more
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association | 2024-04-01 | PMID 36384317
Awotoye Waheed, Mossey Peter A, Hetmanski Jacqueline B and 38 more
Facial features of lysosomal storage disorders.
Expert review of endocrinology & metabolism | 2022-11-01 | PMID 36384353
D'Souza Andrea, Ryan Emory, Sidransky Ellen
Polymorphism in ovine ADCY8 gene and its association with residual feed intake in Hu sheep.
Animal biotechnology | 2023-12-01 | PMID 36384395
Yang Xiaobin, Wang Weimin, Wang Xiaojuan and 17 more
Genes: ADCY8
Signatures of selection in riverine buffalo populations revealed by genome-wide SNP data.
Animal biotechnology | 2023-12-01 | PMID 36384399
Saravanan K A, Rajawat Divya, Kumar Harshit and 4 more
Genes: FST
Impact of GTF2H1 and RAD54L2 polymorphisms on the risk of lung cancer in the Chinese Han population.
BMC cancer | 2022-11-16 | PMID 36384536
Geng Tingting, Li Miao, Chen Rong and 4 more
Inflammatory Diseases, Inflammatory Biomarkers, and Alzheimer Disease: An Observational Analysis and Mendelian Randomization.
Neurology | 2023-02-07 | PMID 36384659
Huang Jian, Su Bowen, Karhunen Ville and 18 more
Genetic mechanism of adaptive evolution: the example of adaptation to high altitudes.
Yi chuan = Hereditas | 2022-08-20 | PMID 36384664
Hao Yan, Lei Fu-Min
Genetic predisposition in patients with severe COVID-19.
Yi chuan = Hereditas | 2022-08-20 | PMID 36384666
Liu Wen-Bing, Liu Dan, Yan Jin and 2 more
Advances in genetic mechanisms of hypothalamic dysfunction in Prader-Willi syndrome.
Yi chuan = Hereditas | 2022-10-20 | PMID 36384726
Wang Xin-Yuan, Sun Rui, Gao Yuan-Qing
Advances in lipodystrophy syndrome caused by LMNA gene mutation.
Yi chuan = Hereditas | 2022-10-20 | PMID 36384727
Xiao Cheng, Liu Jie-Ying, Yang Chun-Ru and 1 more
A study of congenital generalized lipodystrophy (CGL) caused by BSCL2 gene mutation.
Yi chuan = Hereditas | 2022-10-20 | PMID 36384728
Ye Jing-Ya, Huang Ai-Jie, Fu Zhen-Zhen and 3 more
Research on the variants of FGFR1 and CEP290 genes in idiopathic hypogonadotropin hypogonadism.
Yi chuan = Hereditas | 2022-10-20 | PMID 36384729
Wang Shan-Shan, Zhao Wan-Yi, Wu Hui-Xiao and 4 more
Diagnosis and genetic analysis of a case with Bardet-Biedl syndrome caused by compound heterozygous mutations in the BBS12 gene.
Yi chuan = Hereditas | 2022-10-20 | PMID 36384733
Shen Yan-Ting, Ling Yan, Lu Zhi-Qiang and 8 more
Influence of single nucleotide polymorphism in the IGF-1 gene on performance and conformation traits in Munjal sheep.
Zygote (Cambridge, England) | 2023-02-01 | PMID 36384917
Kumar Sandeep, Dahiya S P, Magotra Ankit and 2 more
Diagnosis, treatment and genetic analysis of a case of hypoglycemia caused by glucokinase gene mutation.
Yi chuan = Hereditas | 2022-09-20 | PMID 36384957
Li Lu-Yang, Liu Sun-Qiang, Shi Yun and 3 more
Functional Assessment of Cancer-Linked Mutations in Sensitive Regions of Regulators of G Protein Signaling Predicted by Three-Dimensional Missense Tolerance Ratio Analysis.
Molecular pharmacology | 2023-01-01 | PMID 36384958
Montañez-Miranda Carolina, Perszyk Riley E, Harbin Nicholas H and 4 more
Progress on genomics and locus of important agronomic traits in Chenopodium quinoa.
Yi chuan = Hereditas | 2022-11-20 | PMID 36384994
Li Ling-Hong, Gou Tong, Ren Ai-Xia and 5 more
Diagnosis, treatment and genetic analysis of two cases of congenital hyperinsulinemic hypoglycemia caused by GCK gene mutation.
Yi chuan = Hereditas | 2022-11-20 | PMID 36384997
Jiajue Rui-Zhi, Xiao Cheng, Liu Yi-Wen and 3 more
Diagnosis and genetic analysis of a case with glycogen storage disease type V caused by compound heterozygous mutations in the PYGM gene.
Yi chuan = Hereditas | 2022-11-20 | PMID 36384998
Jiang Wan-Zi, Xu Yi-Wen, Wang Yi-Wen and 4 more
Diagnosis, treatment and genetic analysis of a case of familial aldosteronism type II with WFS1 gene mutation.
Yi chuan = Hereditas | 2022-11-20 | PMID 36384999
Sun Zhi-Lian, He Jun-Ying, Cheng Xiao-Ling and 2 more
Diagnosis, treatment and genetic analysis of a case with fibrocalculous pancreatic diabetes.
Yi chuan = Hereditas | 2022-11-20 | PMID 36385000
Shen Min, Gu Yong, Ying Chang-Jiang and 3 more
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder.
Nature communications | 2022-11-16 | PMID 36385105
de Thonel Aurélie, Ahlskog Johanna K, Daupin Kevin and 35 more
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors.
European journal of human genetics : EJHG | 2023-03-01 | PMID 36385154
Klimentidis Yann C, Chen Zhao, Gonzalez-Garay Manuel L and 5 more
Integrative network analysis interweaves the missing links in cardiomyopathy diseasome.
Scientific reports | 2022-11-16 | PMID 36385157
Chauhan Pankaj Kumar, Sowdhamini Ramanathan
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
Molecular psychiatry | 2023-02-01 | PMID 36385166
Palmer Elizabeth E, Pusch Michael, Picollo Alessandra and 96 more
Genetic nurture versus genetic transmission of risk for ADHD traits in the Norwegian Mother, Father and Child Cohort Study.
Molecular psychiatry | 2023-04-01 | PMID 36385167
Pingault Jean-Baptiste, Barkhuizen Wikus, Wang Biyao and 13 more
Motor symptoms in genetic frontotemporal dementia: developing a new module for clinical rating scales.
Journal of neurology | 2023-03-01 | PMID 36385202
Samra Kiran, MacDougall Amy M, Peakman Georgia and 33 more
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation.
Acta neuropathologica | 2023-01-01 | PMID 36385230
Forsberg Karin M, Graffmo Karin S, Stenvall Erica and 4 more
First detection of Cryptosporidium proventriculi from wild birds in Cyprus.
Parasitology research | 2023-01-01 | PMID 36385306
Hasapis Kyriacos A, Charalambidou Iris, Tsouma Eleni and 4 more
The effect of caffeine on exercise performance is not influenced by ADORA2A genotypes, alone or pooled with CYP1A2 genotypes, in adolescent athletes.
European journal of nutrition | 2023-03-01 | PMID 36385314
Dos Santos Maryssa P Pinto, Spineli Higor, Dos Santos Bruna P and 4 more
Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan.
Journal of clinical immunology | 2023-04-01 | PMID 36385359
Inoue Kento, Miyamoto Satoshi, Tomomasa Dan and 16 more
Breaking down the components of the competition-colonization trade-off: New insights into its role in diverse systems.
The Journal of animal ecology | 2023-02-01 | PMID 36385373
Ferzoco Ilia Maria C, McCauley Shannon J
The need for evolutionary theory in cancer research.
European journal of epidemiology | 2023-12-01 | PMID 36385398
Boddy Amy M
A new enrichment approach for candidate gene detection in unexplained recurrent pregnancy loss and implantation failure.
Molecular genetics and genomics : MGG | 2023-01-01 | PMID 36385415
Berkay Ezgi Gizem, Şoroğlu Can Veysel, Kalaycı Tuğba and 3 more
Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.
International journal of cancer | 2023-03-15 | PMID 36385461
Qin Zixin, Li Jiaheng, Tam Benjamin and 15 more
Understanding Mendelian errors in SNP arrays data using a Gochu Asturcelta pig pedigree: genomic alterations, family size and calling errors.
Scientific reports | 2022-11-16 | PMID 36385499
Arias Katherine D, Álvarez Isabel, Gutiérrez Juan Pablo and 4 more
KITD816V mutation in blood for the diagnostic screening of systemic mastocytosis and mast cell activation syndromes.
Allergy | 2023-05-01 | PMID 36385619
Navarro-Navarro Paula, Álvarez-Twose Iván, Pérez-Pons Alba and 9 more
ABE8e adenine base editor precisely and efficiently corrects a recurrent COL7A1 nonsense mutation.
Scientific reports | 2022-11-16 | PMID 36385635
Sheriff Adam, Guri Ina, Zebrowska Paulina and 16 more
Lactoferrin gene polymorphisms associated with clinical mastitis in Honduran Holstein inheritance cows.
Molecular biology reports | 2023-02-01 | PMID 36385664
Moncada-Laínez M, Valladares-Medina P A, Castillo R and 5 more