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 8392 of 10600

Distinct phenotypes in COVID-19 may require distinct pulmonary rehabilitation strategies.
Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace | 2020-12-03 | PMID 33305555
De França Eduardo Eriko Tenório, Junior Ubirace Elihimas, Schwingel Paulo Adriano and 2 more
COVID-19 reinfection - An enigmatic public health threat.
Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace | 2020-11-30 | PMID 33305559
Iyengar Karthikeyan P, Jain Vijay Kumar, Ish Pranav
Case report: severe toxicity in an African-American patient receiving FOLFOX carrying uncommon allelic variants in DPYD.
Pharmacogenomics | 2021-01-01 | PMID 33305610
Sissung Tristan M, Cordes Lisa, Peer Cody J and 4 more
Guanine Nucleotide-Binding Protein-Like 1 (GNL1) binds RNA G-quadruplex structures in genes associated with Parkinson's disease.
RNA biology | 2021-09-01 | PMID 33305682
Turcotte Marc-Antoine, Garant Jean-Michel, Cossette-Roberge Hélène and 1 more
Heterozygous deletion of Sox9 in mouse mimics the gonadal sex reversal phenotype associated with campomelic dysplasia in humans.
Human molecular genetics | 2021-02-04 | PMID 33305798
Bagheri-Fam Stefan, Combes Alexander N, Ling Cheuk K and 1 more
Characterization of TERT and BRAF copy number variation in papillary thyroid carcinoma: An analysis of the cancer genome atlas study.
Genes, chromosomes & cancer | 2021-06-01 | PMID 33305870
McKelvey Brittany A, Zeiger Martha A, Umbricht Christopher B
First patient with mosaic NOTCH3 gene pathogenic variant. Unrevealed mosaicisms and importance of their detection.
American journal of medical genetics. Part A | 2021-02-01 | PMID 33305890
Moreno-García Marta, Arteche-López Ana Rosa, Álvarez-Mora María Isabel and 8 more
Delineation of the clinical and radiological features of Stuve-Wiedemann syndrome childhood survivors, four new cases and review of the literature.
American journal of medical genetics. Part A | 2021-03-01 | PMID 33305909
Siccha Sofía M, Cueto Anna María, Parrón-Pajares Manuel and 11 more
Supervised learning methods for the recognition of melanoma cell lines through the analysis of their Raman spectra.
Journal of biophotonics | 2021-03-01 | PMID 33305912
Baria Enrico, Cicchi Riccardo, Malentacchi Francesca and 4 more
Hydride Transfer Catalyzed by Glycerol Phosphate Dehydrogenase: Recruitment of an Acidic Amino Acid Side Chain to Rescue a Damaged Enzyme.
Biochemistry | 2020-12-29 | PMID 33305938
He Rui, Cristobal Judith R, Gong Naiji Jabin and 1 more
Gene variants and haplotypes of Vitamin D biosynthesis, transport, and function in preeclampsia.
Hypertension in pregnancy | 2021-02-01 | PMID 33305962
Ghorbani Zahra, Shakiba Mohammad, Rezavand Negin and 4 more
Genotyping and Molecular Characterization of Fluoroquinolone's Resistance Among Multidrug-Resistant Mycobacterium tuberculosis in Southwest of China.
Microbial drug resistance (Larchmont, N.Y.) | 2021-07-01 | PMID 33305990
Hu Yan, Liu Jie, Shen Jing and 5 more
Characterization of the novel HLA-C*14:114 allele by next-generation sequencing.
HLA | 2021-04-01 | PMID 33306255
Genebrier Steve, Elsermans Vincent, Nivet Carl and 2 more
Multi-level convergence of complex traits and the evolution of bioluminescence.
Biological reviews of the Cambridge Philosophical Society | 2021-04-01 | PMID 33306257
Lau Emily S, Oakley Todd H
Two new HLA alleles, HLA-B*18:200 and HLA-C*04:435 detected in Russian donors.
HLA | 2021-05-01 | PMID 33306271
Loginova Maria, Smirnova Daria, Kutyavina Svetlana and 2 more
Identification of the novel HLA-C*15:210 allele by polymerase chain reaction sequence-based typing.
HLA | 2021-03-01 | PMID 33306272
He Yizhen, Wang Wei, Zhang Wei and 2 more
Identification of 11 novel HLA-A, -B, -C, -DRB1, and -DQB1 alleles in the 1000 Genomes Project panel.
HLA | 2021-03-01 | PMID 33306273
Di Cristofaro Julie, Gouret Philippe, Chiaroni Jacques and 2 more
Vitamin D receptor polymorphisms and bone health after kidney transplantation
Turkish journal of medical sciences | 2021-04-30 | PMID 33306336
Korucu Berfu, Tükün Ajlan, Helvacı Özant and 4 more
DNA Polymerase Variants with High Processivity and Accuracy for Encoding and Decoding Locked Nucleic Acid Sequences.
Journal of the American Chemical Society | 2020-12-23 | PMID 33306372
Hoshino Hidekazu, Kasahara Yuuya, Kuwahara Masayasu and 1 more
ATP induces contraction of cultured brain capillary pericytes via activation of P2Y-type purinergic receptors.
American journal of physiology. Heart and circulatory physiology | 2021-02-01 | PMID 33306443
Hørlyck Sofie, Cai Changsi, Helms Hans Christian Cederberg and 2 more
Exercise-induced mitral regurgitation and right ventricle to pulmonary circulation uncoupling across the heart failure phenotypes.
American journal of physiology. Heart and circulatory physiology | 2021-02-01 | PMID 33306448
Bandera Francesco, Barletta Marta, Fontana Marianna and 5 more
SARS-CoV-2 genomic characterization and clinical manifestation of the COVID-19 outbreak in Uruguay.
Emerging microbes & infections | 2021-12-01 | PMID 33306459
Elizondo Victoria, Harkins Gordon W, Mabvakure Batsirai and 22 more
Choice of biologics in asthma endotypes.
Current opinion in allergy and clinical immunology | 2021-02-01 | PMID 33306486
Wangberg Hannah, Woessner Katharine
Polycystic Ovarian Syndrome Genetics and Epigenetics.
Clinical obstetrics and gynecology | 2021-03-01 | PMID 33306497
Combs Joshua C, Hill Micah J, Decherney Alan H
Impact of the Association Between PNPLA3 Genetic Variation and Dietary Intake on the Risk of Significant Fibrosis in Patients With NAFLD.
The American journal of gastroenterology | 2021-05-01 | PMID 33306506
Vilar-Gomez Eduardo, Pirola Carlos Jose, Sookoian Silvia and 5 more
Effects of CYP2D6 Genotypes on Venlafaxine Metabolism in Japanese Psychiatric Patients With Depression.
Therapeutic drug monitoring | 2021-10-01 | PMID 33306568
Komahashi-Sasaki Hazuki, Yasui-Furukori Norio, Sasaki Taro and 8 more
The BDNF-Increasing Allele is Associated With Increased Proportion of Fast-Twitch Muscle Fibers, Handgrip Strength, and Power Athlete Status.
Journal of strength and conditioning research | 2022-07-01 | PMID 33306590
Guilherme João Paulo L F, Semenova Ekaterina A, Borisov Oleg V and 10 more
Immunohistochemical Examination is Highly Sensitive and Specific for Detection of the V600E BRAF Mutation in Colorectal Serrated Lesions.
Applied immunohistochemistry & molecular morphology : AIMM | 2021-07-01 | PMID 33306619
Yamada Noriyuki, Eizuka Makoto, Sugimoto Ryo and 6 more
Bud23 promotes the final disassembly of the small subunit Processome in Saccharomyces cerevisiae.
PLoS genetics | 2020-12-01 | PMID 33306676
Black Joshua J, Sardana Richa, Elmir Ezzeddine W and 1 more
Genes: BMS1, IMP4, NOP14
Genetic diversity, haplotype analysis, and risk factor assessment of hepatitis A virus isolates from the West Bank, Palestine during the period between 2014 and 2016.
PloS one | 2020-01-01 | PMID 33306686
Dumaidi Kamal, Qaraqe Hayah, Al-Jawabreh Amer and 3 more
Effects of the BDNF Val66Met polymorphism on functional status and disability in young stroke patients.
PloS one | 2020-01-01 | PMID 33306691
Braun Robynne G, Kittner Steven J, Ryan Kathleen A and 1 more
Genes: BDNF
Genetic variation in the TLL1 gene is not associated with fibrosis in patients with metabolic associated fatty liver disease.
PloS one | 2020-01-01 | PMID 33306709
Bayoumi Ali, Jalil Ismail, Metwally Mayada and 16 more
Genetic structure of coast redwood (Sequoia sempervirens [D. Don] Endl.) populations in and outside of the natural distribution range based on nuclear and chloroplast microsatellite markers.
PloS one | 2020-01-01 | PMID 33306715
Breidenbach Natalie, Gailing Oliver, Krutovsky Konstantin V
Genomic diversity of class I integrons from antimicrobial resistant strains of Salmonella Typhimurium isolated from livestock, poultry and humans.
PloS one | 2020-01-01 | PMID 33306723
Rao Sangeeta, Linke Lyndsey, Doster Enrique and 5 more
Phenotypical antimicrobial resistance data of clinical and non-clinical Escherichia coli from poultry in Germany between 2014 and 2017.
PloS one | 2020-01-01 | PMID 33306730
Mesa-Varona Octavio, Kaspar Heike, Grobbel Mirjam and 1 more
Quick and efficient approach to develop genomic resources in orphan species: Application in Lavandula angustifolia.
PloS one | 2020-01-01 | PMID 33306734
Fopa Fomeju Berline, Brunel Dominique, Bérard Aurélie and 4 more
[Study of the genotypic and hematological feature of hemoglobin H disease in West Guangxi area].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306814
Nong Xuejuan, Xu Guidan, Li Jia and 4 more
[Diagnosis and clinical phenotype analysis of a case with large fragment homozygous deletion of rare β gene cluster].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306815
Zhong Zeyan, Chen Jianhong, Chen Dina and 4 more
[Analysis of phenotype and CYP4V2 gene variants in two pedigrees affected with Bietti crystalline corneoretinal dystrophy].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306817
Xie Yanchuan, Bai Zhouxian, Sun Zongli and 3 more
[Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306818
Li Wenwen, Fang Rong, Shen Xueping and 3 more
[Molecular screening for Vel- blood type and analysis of SMIM1 gene variants].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306819
Liu Taixiang, Xu Ting, Liu Yanchun and 5 more
[Clinical features and gene variant of a pedigree affected with X-linked recessive mental retardation Claes-Jensen type].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306820
Ding Ning, Zhang Pingping, Mao Yingying and 4 more
[Clinical and genetic analysis of a case of dihydrolipoamide dehydrogenase deficiency caused by novel variant of DLD gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306821
Wu Shengnan, Chen Yongxing, Chen Qiong and 2 more
[Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with N-acetylglutamate synthase deficiency].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306822
Chen Jia, Yuan Huizhen, Xie Kang and 5 more
[Detection and analysis of dynamic variant in a pedigree affected with spinocerebellar ataxia type 3].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306823
Chen Chen, Zhao Xuechao, Kong Xiangdong
[Identification of pathological variants of SLC12A3 gene in a pedigree affected with Gitelman syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306824
Ma Qian, Wu Jinlin, Che Lingyi and 1 more
[Analysis of a sib-pair with Finnish type congenital nephrotic syndrome due to variant of NPHS1 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306827
Liu Zhufeng, Wang Wenhong, Zhang Xuan and 3 more
[Analysis of a case of Warburg micro syndrome type 1 due to variant of RAB3GAP1 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306828
Yang Dongmei, Wang Xizhen, Yang Jian and 2 more
[Prenatal diagnosis of a fetus with Phelan-McDermid syndrome and 21q21 microdeletion by multiple genetic techniques].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306829
Shen Huaxiang, Li Suping, Jin Yuxia
[A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306830
Wang Xiaoou, Yang Xiao, Wang Jinle and 6 more
[Evolvement of a five-way translocation t(5;9;22;6;17) from a four-way Philadelphia translocation t(5;9;22;6) in a rare case of chronic myeloid leukemia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306831
Kong Shu, Gu Yuqing, Qin Yazhen and 4 more
[Characterization of a pair of twins as blood group chimeras].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306832
Zhu Yuli, Ma Wenhui, Wang Haiyan and 2 more
[Exploration of the pathogenesis for a SRY-negative male with 46,XX disorder of sex development].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020-12-10 | PMID 33306833
Liu Ailing, Zhang Lanxue, Xu Hongyan and 3 more
A Multi-Omics Analysis of PON1 Lactonase Activity in Relation to Human Health and Disease.
Omics : a journal of integrative biology | 2021-01-01 | PMID 33306925
Petrič Boštjan, Kunej Tanja, Bavec Aljoša
Seroprevalence, Risk Factors, and Genotypes of Toxoplasma gondii in Free-Range Chickens Intended for Human Consumption in China.
Foodborne pathogens and disease | 2021-04-01 | PMID 33306935
Lv Qiu-Yan, Quan Min-Xiu, Tang Hua-Li and 4 more
Cas9 in Human Embryos: On Target but No Repair.
Cell | 2020-12-10 | PMID 33306952
Hoffmann Eva R, Roig Ignasi
D614G Spike Mutation Increases SARS CoV-2 Susceptibility to Neutralization.
Cell host & microbe | 2021-01-13 | PMID 33306985
Weissman Drew, Alameh Mohamad-Gabriel, de Silva Thushan and 22 more
Chitotriosidase gene polymorphisms and mutations limit the determination of chitotriosidase expression in sarcoidosis.
Clinica chimica acta; international journal of clinical chemistry | 2021-02-01 | PMID 33307063
Csongrádi Alexandra, Altorjay István T, Fülöp Gábor Á and 7 more
Architecture of the Tuberous Sclerosis Protein Complex.
Journal of molecular biology | 2021-01-22 | PMID 33307091
Ramlaul Kailash, Fu Wencheng, Li Hua and 6 more
Inflammatory phenotype of depression symptom structure: A network perspective.
Brain, behavior, and immunity | 2021-03-01 | PMID 33307169
Moriarity Daniel P, van Borkulo Claudia, Alloy Lauren B
Polymorphism rs3737787 of Upstream Stimulatory Factor 1 gene is associated with serum lipid phenotype in Nigerian population.
Molecular and cellular probes | 2021-02-01 | PMID 33307180
Onadeko Oluwadamilola T, Okunowo Wahab O, Imaga Ngozi O A and 4 more
A population scale analysis of rare SNCA variation in the UK Biobank.
Neurobiology of disease | 2021-01-01 | PMID 33307186
Blauwendraat Cornelis, Makarious Mary B, Leonard Hampton L and 5 more
Clinical Implications of KEAP1-NFE2L2 Mutations in NSCLC.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2021-03-01 | PMID 33307193
Hellyer Jessica A, Padda Sukhmani K, Diehn Maximilian and 1 more
A Gene Mutation Signature Predicting Immunotherapy Benefits in Patients With NSCLC.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer | 2021-03-01 | PMID 33307194
Pan Dong, Hu Angela Y, Antonia Scott J and 1 more
The effect of age on the acquisition and selection of cancer driver mutations in sun-exposed normal skin.
Annals of oncology : official journal of the European Society for Medical Oncology | 2021-03-01 | PMID 33307203
Hernando B, Dietzen M, Parra G and 6 more
Successful expansion of Mycobacterium tuberculosis Latin American and Mediterranean sublineage (L4.3/LAM) in Tunisia mainly driven by a single, long-established clonal complex.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases | 2021-02-01 | PMID 33307222
Skhairia Mohamed Amine, Dekhil Naira, Mhenni Besma and 2 more
Milder presentation of TELO2-related syndrome in two sisters homozygous for the p.Arg609His pathogenic variant.
European journal of medical genetics | 2021-01-01 | PMID 33307281
Ciaccio Claudia, Duga Valentina, Pantaleoni Chiara and 7 more
The complexities of PKCα signaling in cancer.
Advances in biological regulation | 2021-05-01 | PMID 33307285
Black Adrian R, Black Jennifer D
Cancer-related SRCAP and TPR mutations in colon cancers.
Pathology, research and practice | 2021-01-01 | PMID 33307343
Moon Seong Won, Mo Ha Yoon, Choi Eun Ji and 2 more
Hepatocellular carcinoma: Clinicopathologic associations amidst marked phenotypic heterogeneity.
Pathology, research and practice | 2021-01-01 | PMID 33307344
Rastogi Archana, Maiwall Rakhi, Ramakrishna Gayatri and 10 more
Diagnostic performance between MR amide proton transfer (APT) and diffusion kurtosis imaging (DKI) in glioma grading and IDH mutation status prediction at 3 T.
European journal of radiology | 2021-01-01 | PMID 33307459
Xu Zongwei, Ke Chao, Liu Jie and 8 more
The impact of chimerism on DNA-based human identification from skin surface cells of post-allogenic hematopoietic stem cell transplantation (HCST) patients.
Forensic science international | 2021-01-01 | PMID 33307474
Alsaleh Abrar B, Alokail Majed S, Kassab Ahmed Ch and 5 more
Association of IL-35 expression and gene polymorphisms in rheumatoid arthritis.
International immunopharmacology | 2021-01-01 | PMID 33307515
Xie Qiang, Xu Wang-Dong, Pan Min and 4 more
[Molecular and functional testing in case of hereditary hearing loss associated with the SLC26A4 gene].
Laryngo- rhino- otologie | 2020-12-01 | PMID 33307573
Roesch Sebastian, Bernardinelli Emanuele, Wortmann Saskia and 5 more
A low-cost platform suitable for sequencing-based recovery of natural variation in understudied plants.
BioTechniques | 2021-02-01 | PMID 33307792
Howard-Till Rachel, E Osorio Claudia, J Till Bradley
Hsa_circ_0037897 may be a risk factor for essential hypertension via hsa-miR-145-5p.
Clinical and experimental hypertension (New York, N.Y. : 1993) | 2021-04-03 | PMID 33307836
Tao Zhenbo, Zheng Shuying, He Xin and 3 more
Frequency and characteristics of the JAK2 V617F mutation in 23 cerebral venous sinus thrombosis patients with thrombocytosis.
The Journal of international medical research | 2020-12-01 | PMID 33307939
Ma Qiang
Differentiation of the 50B11 dorsal ganglion cells into NGF and GDNF responsive nociceptor subtypes.
Molecular pain | 2000-01-01 | PMID 33307981
Dusan Matusica, Jastrow Canlas, Alyce Martin M and 10 more
Association analysis of KISS1 polymorphisms and haplotypes with polycystic ovary syndrome.
British journal of biomedical science | 2021-10-01 | PMID 33308008
Farsimadan M, Moammadzadeh Ghosi F, Takamoli S and 1 more
Pro64His (rs4644) Polymorphism Within Galectin-3 Is a Risk Factor of Differentiated Thyroid Carcinoma and Affects the Transcriptome of Thyrocytes Engineered via CRISPR/Cas9 System.
Thyroid : official journal of the American Thyroid Association | 2021-07-01 | PMID 33308024
Corrado Alda, Aceto Romina, Silvestri Roberto and 15 more
Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1.
Modern rheumatology case reports | 2021-07-01 | PMID 33308032
Ishizuka Tatsuo, Fujioka Kei, Mori Ichiro and 7 more
A Fusion Method Based on Alignment Software with SNP and Indel Detection Methods.
Combinatorial chemistry & high throughput screening | 2022-01-01 | PMID 33308124
Chen Guobing, Tang Chao, Qi Jun and 2 more
Autosomal dominant polycystic kidney disease and pioglitazone for its therapy: a comprehensive review with an emphasis on the molecular pathogenesis and pharmacological aspects.
Molecular medicine (Cambridge, Mass.) | 2020-12-11 | PMID 33308138
Saini Aryendu Kumar, Saini Rakesh, Singh Shubham
Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis.
BMC medical genetics | 2020-12-12 | PMID 33308164
Ouhenach Mouna, Zrhidri Abdelali, Jaouad Imane Cherkaoui and 2 more
Macrolide and fluoroquinolone associated mutations in Mycoplasma genitalium in a retrospective study of male and female patients seeking care at a STI Clinic in Guangzhou, China, 2016-2018.
BMC infectious diseases | 2020-12-11 | PMID 33308173
Ke Wujian, Li Dongling, Tso Lai Sze and 11 more
Genetic association study of interferon lambda 3, CD27, and human leukocyte antigen-DPB1 with dengue severity in Thailand.
BMC infectious diseases | 2020-12-11 | PMID 33308178
Arayasongsak Unchana, Naka Izumi, Ohashi Jun and 6 more
Mutation screening of the UBE3A gene in Chinese Han population with autism.
BMC psychiatry | 2020-12-11 | PMID 33308194
Zhao Xue, Zhang Ran, Yu Shunying
Total knee arthroplasty according to the original knee phenotypes with kinematic alignment surgical technique-early clinical and functional outcomes.
BMC musculoskeletal disorders | 2020-12-11 | PMID 33308196
Hsu Cheng-En, Huang Jen-Ting, Tong Kwok-Man and 1 more
Genetic and clinical phenotypic analysis of familial stapes sclerosis caused by an NOG mutation.
BMC medical genomics | 2020-12-11 | PMID 33308208
Yu Rong, Jiang Hongqun, Liao Huihuang and 1 more
Identification of biological correlates associated with respiratory failure in COVID-19.
BMC medical genomics | 2020-12-11 | PMID 33308225
Oh Jung Hun, Tannenbaum Allen, Deasy Joseph O
Novel gene variants in Polish patients with Leber congenital amaurosis (LCA).
Orphanet journal of rare diseases | 2020-12-11 | PMID 33308271
Skorczyk-Werner Anna, Niedziela Zuzanna, Stopa Marcin and 1 more
Gene functional networks and autism spectrum characteristics in young people with intellectual disability: a dimensional phenotyping study.
Molecular autism | 2020-12-11 | PMID 33308299
Brkić Diandra, Ng-Cordell Elise, O'Brien Sinéad and 3 more
The Number of Larval Molts Is Controlled by Hox in Caterpillars.
Current biology : CB | 2021-02-22 | PMID 33308417
Daimon Takaaki, Koyama Takashi, Yamamoto Gaku and 3 more
Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stability.
American journal of human genetics | 2021-01-07 | PMID 33308442
Meili Fabian, Wei William J, Sin Wun-Chey and 6 more
Probabilistic colocalization of genetic variants from complex and molecular traits: promise and limitations.
American journal of human genetics | 2021-01-07 | PMID 33308443
Hukku Abhay, Pividori Milton, Luca Francesca and 3 more
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.
American journal of human genetics | 2021-01-07 | PMID 33308445
Ortiz-Fernández Lourdes, Saruhan-Direskeneli Güher, Alibaz-Oner Fatma and 68 more
Prophylactic risk-reducing salpingo-oophorectomy in BRCA mutation carriers: what is going on in a region of northern Italy?
Maturitas | 2021-01-01 | PMID 33308637
Grandi Giovanni, Perrone Anna Myriam, Perrone Antonino and 9 more
Astragaloside IV antagonizes M2 phenotype macrophage polarization-evoked ovarian cancer cell malignant progression by suppressing the HMGB1-TLR4 axis.
Molecular immunology | 2021-02-01 | PMID 33308900
Wang Xue, Gao ShouYang, Song LiYou and 3 more
Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia.
Molecular genetics and metabolism | 2021-01-01 | PMID 33309011
Becker Pierre-Hadrien, Demir Zeynep, Mozer Glassberg Yael and 12 more
The PEAPOD Pathway and Its Potential To Improve Crop Yield.
Trends in plant science | 2021-03-01 | PMID 33309102
Schneider Michele, Gonzalez Nathalie, Pauwels Laurens and 2 more