The Pattern of Haemoglobin Phenotypes and the Clinical Identity of Clients Tested at a Private Diagnostic Center in South-West Nigeria.
West African journal of medicine | 2021-12-30 | PMID 35037737
Alagbe A E, Adewoyin A S, Alagbe O A and 2 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 8811 of 10600
Osimertinib induced cardiac failure and QT-prolongation in a patient with advanced pulmonary adenocarcinoma.
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners | 2022-06-01 | PMID 35037771
Bardaro Floriana, Stirpe Emanuele
Association of human Hedgehog interacting protein gene polymorphisms with the risk of chronic obstructive pulmonary disease: a meta-analysis.
Expert review of respiratory medicine | 2022-04-01 | PMID 35037818
Liao Yi, Liao Yue, Wen Fuqiang
In silico assessment of DNA damage response gene variants associated with head and neck cancer.
Journal of biomolecular structure & dynamics | 2023-04-01 | PMID 35037836
Das Raima, Kundu Sharbadeb, Laskar Shaheen and 2 more
Repeated origins, widespread gene flow, and allelic interactions of target-site herbicide resistance mutations.
eLife | 2022-01-17 | PMID 35037853
Kreiner Julia M, Sandler George, Stern Aaron J and 4 more
Surveillance Improves Outcomes for Carriers of SDHB Pathogenic Variants: A Multicenter Study.
The Journal of clinical endocrinology and metabolism | 2022-04-19 | PMID 35037935
Davidoff Dahlia F, Benn Diana E, Field Michael and 6 more
[Spinal muscular atrophy].
Der Nervenarzt | 2022-02-01 | PMID 35037967
Martin Pascal, Horber Veronka, Park Joohyun and 2 more
Association of the MAOA-uVNTR polymorphism with psychopathic traits may change from childhood to adolescence.
European archives of psychiatry and clinical neuroscience | 2022-12-01 | PMID 35038001
Kant Tuana, Koyama Emiko, Zai Clement C and 2 more
Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations.
Cellular and molecular life sciences : CMLS | 2022-01-17 | PMID 35038030
Medina-Carbonero Marta, Sanz-Alcázar Arabela, Britti Elena and 4 more
Genetic control of source-sink relationships in grain sorghum.
Planta | 2022-01-17 | PMID 35038036
Chiluwal Anuj, Perumal Ramasamy, Poudel Hari P and 11 more
Whole-exome sequencing analysis to identify novel potential pathogenetic NPC1 mutations in two Chinese families with Niemann-Pick disease type C.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2022-06-01 | PMID 35038048
Guan Chengcheng, Gan Xinhui, Yang Chengqing and 3 more
Identifying Candidate Genes Associated with Sporadic Amyotrophic Lateral Sclerosis via Integrative Analysis of Transcriptome-Wide Association Study and Messenger RNA Expression Profile.
Cellular and molecular neurobiology | 2023-01-01 | PMID 35038056
Li Ping, Cheng Shiqiang, Wen Yan and 9 more
Real-world data of off-label drug use in patients with actionable genomic alterations on next-generation sequencing.
Investigational new drugs | 2022-06-01 | PMID 35038126
Roman Souza Gabriel, Abdalla Ahmed, Arora Sukeshi and 1 more
Prevalence of bladder cancer in Costello syndrome: New insights to drive clinical decision-making.
Clinical genetics | 2022-04-01 | PMID 35038173
Leoni Chiara, Paradiso Filomena Valentina, Foschi Nazario and 14 more
Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function.
Journal of inherited metabolic disease | 2022-05-01 | PMID 35038180
Ducich Nicole H, Mears Jason A, Bedoyan Jirair K
Whole-exome sequencing reveals rare genetic variations in ovarian granulosa cell tumor.
Bosnian journal of basic medical sciences | 2022-06-01 | PMID 35038288
Kim Seungyeon, Kim Songmi, Mun Seyoung and 4 more
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders.
European journal of endocrinology | 2022-02-04 | PMID 35038313
Canaff Lucie, Guarnieri Vito, Kim Yoojung and 11 more
Adult-Onset Diamond-Blackfan Anemia with RPL11 Gene Variation Case Report.
The American journal of case reports | 2022-01-17 | PMID 35038319
Mars-Holt Evida, Murdoch Alex, Frugoli Amanda and 2 more
PHILOPHTHALMUS HECHINGERI N. SP. (DIGENEA: PHILOPHTHALMIDAE), A HUMAN-INFECTING EYE FLUKE FROM THE ASIAN MUD SNAIL, BATILLARIA ATTRAMENTARIA.
The Journal of parasitology | 2022-01-01 | PMID 35038324
Sasaki Mizuki, Miura Osamu, Nakao Minoru
Signatures of natural selection in a foundation tree along Mediterranean climatic gradients.
Molecular ecology | 2022-03-01 | PMID 35038378
Filipe João Carlos, Rymer Paul D, Byrne Margaret and 3 more
A life cycle alteration can correct molting defects in Caenorhabditis elegans.
Developmental biology | 2022-03-01 | PMID 35038442
Binti Shaonil, Melinda Rosa V, Joseph Braveen B and 3 more
A tiered approach to investigate the inhalation toxicity of cobalt substances. Tier 2 b: Reactive cobalt substances induce oxidative stress in ToxTracker and activate hypoxia target genes.
Regulatory toxicology and pharmacology : RTP | 2022-03-01 | PMID 35038485
Derr Remco, Moelijker Nynke, Hendriks Giel and 1 more
High genetic differentiation and moderate genetic diversity of the degenerative branching coral Pocillopora verrucosa in the tropical South China Sea.
The Science of the total environment | 2022-05-01 | PMID 35038534
Li Ming, Huang Wen, Wu Qian and 8 more
Exosome-derived circTRPS1 promotes malignant phenotype and CD8+ T cell exhaustion in bladder cancer microenvironments.
Molecular therapy : the journal of the American Society of Gene Therapy | 2022-03-02 | PMID 35038580
Yang Chen, Wu Siqi, Mou Zezhong and 13 more
Synapsin III gene silencing redeems alpha-synuclein transgenic mice from Parkinson's disease-like phenotype.
Molecular therapy : the journal of the American Society of Gene Therapy | 2022-04-06 | PMID 35038583
Faustini Gaia, Longhena Francesca, Masato Anna and 12 more
High-Throughput Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis for Selective and Reliable Identification of Actionable FMR1 Genotypes.
The Journal of molecular diagnostics : JMD | 2022-03-01 | PMID 35038595
Rajan-Babu Indhu-Shree, Phang Gui-Ping, Law Hai-Yang and 2 more
Bidirectional Introgression between Mus musculus domesticus and Mus spretus.
Genome biology and evolution | 2022-01-04 | PMID 35038727
Banker Sarah E, Bonhomme François, Nachman Michael W
The Contribution of Deleterious Rare Alleles in ENPP1 and Osteomalacia Causative Genes to Atypical Femoral Fracture.
The Journal of clinical endocrinology and metabolism | 2022-04-19 | PMID 35038731
Furukawa Hiroshi, Oka Shomi, Kondo Naoki and 16 more
Fitness Effects of Mutations: An Assessment of PROVEAN Predictions Using Mutation Accumulation Data.
Genome biology and evolution | 2022-01-04 | PMID 35038732
Sandell Linnea, Sharp Nathaniel P
Associations of genetic variation in E3 SUMO-protein ligase CBX4 with noise-induced hearing loss.
Human molecular genetics | 2022-07-07 | PMID 35038734
Wang Boshen, Wan Liu, Sun Peng and 6 more
Canonical Thyroid Hormone Receptor β Action Stimulates Hepatocyte Proliferation in Male Mice.
Endocrinology | 2022-03-01 | PMID 35038735
Hönes Georg Sebastian, Kerp Helena, Hoppe Christoph and 5 more
The Emergence of SARS-CoV-2 Variants of Concern Is Driven by Acceleration of the Substitution Rate.
Molecular biology and evolution | 2022-02-03 | PMID 35038741
Tay John H, Porter Ashleigh F, Wirth Wytamma and 1 more
The prevalence of non-allergic rhinitis phenotypes in the general population: A cross-sectional study.
Allergy | 2022-07-01 | PMID 35038765
Avdeeva Klementina S, Fokkens Wytske J, Segboer Christine L and 1 more
Expected or unexpected clinical findings in liver glycogen storage disease type IX: distinct clinical and molecular variability.
Journal of pediatric endocrinology & metabolism : JPEM | 2022-04-26 | PMID 35038814
İnci Aslı, Kılıç Yıldırım Gonca, Cengiz Ergin Filiz Başak and 8 more
Assessment of Anti-tumor Efficacy of Osimertinib in Non-Small Cell Lung Cancer Patients by Liquid Biopsy Using Bronchoalveolar Lavage Fluid, Plasma, or Pleural Effusion.
Cancer research and treatment | 2022-10-01 | PMID 35038824
Kim Yeon Joo, Ji Won Jun, Lee Jae-Cheol and 2 more
Whole-Genome and Transcriptome Sequencing Identified NOTCH2 and HES1 as Potential Markers of Response to Imatinib in Desmoid Tumor (Aggressive Fibromatosis): A Phase II Trial Study.
Cancer research and treatment | 2022-10-01 | PMID 35038826
Kwon Joonha, Lee Jun Hyeong, Lee Young Han and 11 more
Breast reconstruction in patients with BRCA mutation and breast cancer - our approach.
Ceska gynekologie | 2021-01-01 | PMID 35038874
Ventruba Tomáš, Brančíková Dagmar, Ventruba Pavel and 3 more
Relationship between molecular characteristics of glioblastoma multiforme and the subventricular zone.
British journal of neurosurgery | 2024-10-01 | PMID 35038937
Ashraf Mohammad, Abdelsadg Mohamed, Grivas Athanasios
Molecular mechanism of mulberry response to drought stress revealed by complementary transcriptomic and iTRAQ analyses.
BMC plant biology | 2022-01-17 | PMID 35039015
Li Ruixue, Su Xueqiang, Zhou Rong and 2 more
Mitonuclear incompatibility as a hidden driver behind the genome ancestry of African admixed cattle.
BMC biology | 2022-01-17 | PMID 35039029
Kwon Taehyung, Kim Kwondo, Caetano-Anolles Kelsey and 5 more
Metabolic synthetic lethality by targeting NOP56 and mTOR in KRAS-mutant lung cancer.
Journal of experimental & clinical cancer research : CR | 2022-01-17 | PMID 35039048
Yang Zhang, Liang Shun-Qing, Zhao Liang and 11 more
The SF3B1R625H mutation promotes prolactinoma tumor progression through aberrant splicing of DLG1.
Journal of experimental & clinical cancer research : CR | 2022-01-17 | PMID 35039052
Guo Jing, Li Chuzhong, Fang Qiuyue and 5 more
ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines.
Genome medicine | 2022-01-18 | PMID 35039090
Preston Christine G, Wright Matt W, Madhavrao Rao and 32 more
Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA).
Clinical epigenetics | 2022-01-17 | PMID 35039093
Ammous Farah, Zhao Wei, Lin Lisha and 7 more
Genes: AHRR, GFI1
Progranulin as a therapeutic target in neurodegenerative diseases.
Trends in pharmacological sciences | 2022-08-01 | PMID 35039149
Rhinn Herve, Tatton Nadine, McCaughey Stella and 2 more
Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosis.
Neurobiology of aging | 2022-05-01 | PMID 35039179
Tohnai Genki, Nakamura Ryoichi, Atsuta Naoki and 30 more
Cumulative live birth rate after ovarian stimulation with freeze-all in women with polycystic ovaries: does the polycystic ovary syndrome phenotype have an impact?
Reproductive biomedicine online | 2022-03-01 | PMID 35039225
Mackens Shari, Drakopoulos Panagiotis, Moeykens Margot Fauve and 6 more
Clinical and laboratory relevance of JAK2 V617F and BCR-ABL co-existence in Philadelphia positive CML patients.
Pakistan journal of pharmaceutical sciences | 2021-11-01 | PMID 35039265
Ahmad Nasir, Qayum Saima, Jameel Abid and 4 more
The Idd2 Locus Confers Prominent Resistance to Autoimmune Diabetes.
Journal of immunology (Baltimore, Md. : 1950) | 2022-02-15 | PMID 35039332
Lombard-Vadnais Félix, Collin Roxanne, Daudelin Jean-François and 3 more
Novel CACNA1S mutation in hypokalaemic periodic paralysis.
BMJ case reports | 2022-01-17 | PMID 35039355
Luís Telma, Linhares Maria Inês, Silva Sónia Regina and 1 more
Unique correlation between GTF2I mutation and spindle cell morphology in thymomas (type A and AB thymomas).
Journal of clinical pathology | 2023-07-01 | PMID 35039450
Wells Kirsty, Lamrca Angela, Papaxoinis George and 4 more
POLE2 facilitates the malignant phenotypes of glioblastoma through promoting AURKA-mediated stabilization of FOXM1.
Cell death & disease | 2022-01-17 | PMID 35039475
Zhang Peng, Chen Xu, Zhang LingYun and 4 more
Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood.
Nature communications | 2022-01-17 | PMID 35039506
Wang Xiao-Hui, Gao Bo-Wen, Nakashima Yu and 15 more
Microbiome differential abundance methods produce different results across 38 datasets.
Nature communications | 2022-01-17 | PMID 35039521
Nearing Jacob T, Douglas Gavin M, Hayes Molly G and 8 more
Obligate mutualistic cooperation limits evolvability.
Nature communications | 2022-01-17 | PMID 35039522
Pauli Benedikt, Oña Leonardo, Hermann Marita and 1 more
Comparative transcriptome analysis of two contrasting resistant and susceptible Aegilops tauschii accessions to wheat leaf rust (Puccinia triticina) using RNA-sequencing.
Scientific reports | 2022-01-17 | PMID 35039525
Dorostkar Saeideh, Dadkhodaie Ali, Ebrahimie Esmaeil and 2 more
Phylogenetic relations and range history of jerboas of the Allactaginae subfamily (Dipodidae, Rodentia).
Scientific reports | 2022-01-17 | PMID 35039544
Lebedev Vladimir S, Shenbrot Georgy I, Krystufek Boris and 8 more
Germline sequence variants contributing to cancer susceptibility in South African breast cancer patients of African ancestry.
Scientific reports | 2022-01-17 | PMID 35039564
Eygelaar Dewald, van Rensburg Elizabeth J, Joubert Fourie
Mutated RAS-associating proteins and ERK activation in relapse/refractory diffuse large B cell lymphoma.
Scientific reports | 2022-01-17 | PMID 35039569
Benoit Alexandre, Bou-Petit Elisabeth, Chou Hsiang and 9 more
Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression.
Scientific reports | 2022-01-17 | PMID 35039573
Starikova Anna V, Skopenkova Victoria V, Polikarpova Anna V and 8 more
Serum-free cultures of C2C12 cells show different muscle phenotypes which can be estimated by metabolic profiling.
Scientific reports | 2022-01-17 | PMID 35039582
Jang Mi, Scheffold Jana, Røst Lisa Marie and 2 more
Comparative chloroplast genome analyses of cultivated spinach and two wild progenitors shed light on the phylogenetic relationships and variation.
Scientific reports | 2022-01-17 | PMID 35039603
She Hongbing, Liu Zhiyuan, Xu Zhaosheng and 5 more
Genomic interrogation of a MAGIC population highlights genetic factors controlling fiber quality traits in cotton.
Communications biology | 2022-01-17 | PMID 35039628
Wang Maojun, Qi Zhengyang, Thyssen Gregory N and 7 more
The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste.
Nature genetics | 2022-02-01 | PMID 35039640
Shelton Janie F, Shastri Anjali J, Fletez-Brant Kipper and 2 more
Subfertility, use of fertility treatments and BRCA mutation status and the risk of ovarian cancer.
Archives of gynecology and obstetrics | 2022-07-01 | PMID 35039881
Lerner-Geva Liat, Chetrit Angela, Farhi Adel and 2 more
Genetic diversity and population structure of rice (Oryza sativa L.) landraces from Kerala, India analyzed through genotyping-by-sequencing.
Molecular genetics and genomics : MGG | 2022-01-01 | PMID 35039933
Peringottillam Maya, Kunhiraman Vasumathy Smitha, Selvakumar Hari Krishna Kumar and 1 more
Plasminogen Activator Inhibitor-1 Polymorphisms and Risk of Coronary Artery Disease: Evidence From Meta-Analysis and Trial Sequential Analysis.
Biochemical genetics | 2022-10-01 | PMID 35039979
Tabaei Samira, Omraninava Melodi, Mehranfar Sahar and 2 more
Identification of putative genetic variants in major depressive disorder patients in Pakistan.
Molecular biology reports | 2022-03-01 | PMID 35040003
Qazi Sarah Rizwan, Irfan Muhammad, Ramzan Zoobia and 5 more
Cocktails of KLK5 Protease Inhibitors and Anti-TNFα Therapeutics: an Effective Treatment for Netherton Syndrome.
Journal of clinical immunology | 2022-04-01 | PMID 35040012
Zingkou Eleni, Pampalakis Georgios, Sotiropoulou Georgia
Genotype-phenotype correlations in alpha-sarcoglycanopathy: a systematic review.
Irish journal of medical science | 2022-12-01 | PMID 35040091
Carson Luke, Merrick Deborah
Evolution in small steps and giant leaps.
Evolution; international journal of organic evolution | 2022-02-01 | PMID 35040122
Whiteman Noah K
Characterization of RNF43 frameshift mutations that drive Wnt ligand- and R-spondin-dependent colon cancer.
The Journal of pathology | 2022-05-01 | PMID 35040131
Yamamoto Daisuke, Oshima Hiroko, Wang Dong and 11 more
A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep.
Animal genetics | 2022-04-01 | PMID 35040155
Zhao Yuhetian, Pu Yabin, Liang Benmeng and 4 more
Polymorphisms of acetaldehyde dehydrogenase 2 and alcohol dehydrogenase 1B on the malignant transformation of vocal cord leukoplakia: A Chinese cohort.
Molecular carcinogenesis | 2022-05-01 | PMID 35040215
Han Ping, Li Yixin, Liang Faya and 5 more
Do adverse childhood experiences and genetic obesity risk interact in relation to body mass index in young adulthood? Findings from the National Longitudinal Study of Adolescent to Adult Health.
Pediatric obesity | 2022-06-01 | PMID 35040268
Inoue Yosuke, Graff Mariaelisa, Howard Annie Green and 7 more
Epidemiological characteristics and genetic diversity of Bartonella species in rodents from southeastern China.
Zoonoses and public health | 2022-05-01 | PMID 35040279
Liu Haixin, Han Tengwei, Liu Weijun and 3 more
Characterization of the novel HLA-C*16:184 allele by next-generation sequencing.
HLA | 2022-06-01 | PMID 35040281
Gatouillat Grégory, Tabary Thierry, Tonye-Libyh Marcelle and 2 more
Racial and ethnic variation in multigene panel testing in a cohort of BRCA1/2-negative individuals who had genetic testing in a large urban comprehensive cancer center.
Cancer medicine | 2022-03-01 | PMID 35040284
Tatineni Sushma, Tarockoff Meri, Abdallah Nadine and 5 more
Genes: MSH2, CHEK2, MUTYH, BRCA1, MSH6, ATM, BRIP1, MLH1
Single Nucleotide Polymorphisms in Neonatal Necrotizing Enterocolitis.
Current pediatric reviews | 2022-01-01 | PMID 35040407
Donda Keyur T, Torres Benjamin A, Khashu Minesh and 1 more
Genetic variations in the long control region of human papillomavirus type 16 isolates from India: implications for cervical carcinogenesis.
Journal of medical microbiology | 2022-01-01 | PMID 35040427
Mane Arati, Limaye Sanket, Patil Linata and 1 more
Genetic basis and dual adaptive role of floral pigmentation in sunflowers.
eLife | 2022-01-18 | PMID 35040432
Todesco Marco, Bercovich Natalia, Kim Amy and 9 more
Data set and fitting dependencies when estimating protein mutant stability: Toward simple, balanced, and interpretable models.
Journal of computational chemistry | 2022-03-30 | PMID 35040492
Baek Kristoffer T, Kepp Kasper P
Near complete deletion of KMT2D in a college student.
American journal of medical genetics. Part A | 2022-05-01 | PMID 35040536
Gooch Catherine, Souder Jaclyn Paige, Tedder Matthew L and 6 more
Subthalamic deep brain stimulation in Parkinson's disease with SNCA mutations: Based on the follow-up to 10 years.
Brain and behavior | 2022-02-01 | PMID 35040589
Youn Jinyoung, Oyama Genko, Hattori Nobutaka and 8 more
Phosphorylation Regulation on the Homo-Dimeric Binding of Transactive Response DNA-Binding Protein.
Journal of chemical information and modeling | 2022-11-14 | PMID 35040651
Dong Wanqian, Zhou Rui, Chen Jiawen and 2 more
Neutralization of SARS-CoV-2 Omicron by BNT162b2 mRNA vaccine-elicited human sera.
Science (New York, N.Y.) | 2022-02-11 | PMID 35040667
Muik Alexander, Lui Bonny Gaby, Wallisch Ann-Kathrin and 14 more
XPXP: improving polygenic prediction by cross-population and cross-phenotype analysis.
Bioinformatics (Oxford, England) | 2022-03-28 | PMID 35040939
Xiao Jiashun, Cai Mingxuan, Hu Xianghong and 3 more
Characterising the age-dependent effects of risk factors on type 1 diabetes progression.
Diabetologia | 2022-04-01 | PMID 35041021
So Michelle, O'Rourke Colin, Ylescupidez Alyssa and 7 more
Methods for statistical fine-mapping and their applications to auto-immune diseases.
Seminars in immunopathology | 2022-01-01 | PMID 35041074
Wang Qingbo S, Huang Hailiang
A positive genetic selection for transmembrane domain mutations in HRD1 underscores the importance of Hrd1 complex integrity during ERAD.
Current genetics | 2022-04-01 | PMID 35041076
Nakatsukasa Kunio, Wigge Sylvia, Takano Yuki and 3 more
Interleukin 10 rs1800896 and interleukin 1B rs16944 polymorphisms and the risk of cervical cancer.
Wiener medizinische Wochenschrift (1946) | 2023-03-01 | PMID 35041104
Wagner Jasenka, Štibi Sanela, Selak Nikica and 7 more
A novel homozygous variant in RNF170 causes hereditary spastic paraplegia: a case report and review of the literature.
Neurogenetics | 2022-04-01 | PMID 35041108
Chouery Eliane, Mehawej Cybel, Megarbane Andre
Clinical phenotype and cytokine profile of adult IgA vasculitis with joint involvement.
Clinical rheumatology | 2022-05-01 | PMID 35041109
Delapierre Alice, Terrier Benjamin, Pillebout Evangéline and 20 more
Novel Mutations of TSPY1 Gene Associate Spermatogenic Failure Among Men.
Reproductive sciences (Thousand Oaks, Calif.) | 2022-04-01 | PMID 35041134
Paladhi Pranab, Dutta Saurav, Pal Samudra and 6 more
Hybridization despite elaborate courtship behavior and female choice in Neotropical tree frogs.
Integrative zoology | 2023-03-01 | PMID 35041294
Nali Renato C, Zamudio Kelly R, Prado Cynthia P A
[Spinocerebellar ataxia 17: full phenotype in a 42 CAG/CAA-repeats carrier].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 2021-01-01 | PMID 35041320
I D V, Proskokova T N, Sikora N V and 2 more
[Diversity of CACNA1A-related disorders].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 2021-01-01 | PMID 35041321
Rudenskaya G E, Sermyagina I G, Chukhrova A L and 3 more
Identification of 2 Chinese Primary Pancreatic Ductal Adenocarcinoma Cancer Cell Lines and Their Phenotypes.
Pancreas | 2000-01-01 | PMID 35041339
Wang Jianxin, Li Enliang, Chen Qi and 8 more
Adult Proinsulinomatosis Associated With a MAFA Germline Mutation as a Rare Cause of Recurrent Hypoglycemia.
Pancreas | 2000-01-01 | PMID 35041347
Mintziras Ioannis, Peer Katharina, Goerlach Jannis and 5 more
Molecular Characterization of Mycobacterium ulcerans DNA Gyrase and Identification of Mutations Reducing Susceptibility to Quinolones In Vitro.
Antimicrobial agents and chemotherapy | 2022-04-19 | PMID 35041504
Kim Hyun, Mori Shigetarou, Kenri Tsuyoshi and 1 more