Cytidine deaminase activity increases in the blood of breast cancer patients.
Scientific reports | 2022-08-18 | PMID 35982128
Buhagiar-Labarchède Géraldine, Onclercq-Delic Rosine, Vacher Sophie and 4 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 8978 of 10600
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Nature genetics | 2022-09-01 | PMID 35982159
Zhou Xueya, Feliciano Pamela, Shu Chang and 25 more
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Nature genetics | 2022-09-01 | PMID 35982160
Fu Jack M, Satterstrom F Kyle, Peng Minshi and 69 more
Genetic control of RNA splicing and its distinct role in complex trait variation.
Nature genetics | 2022-09-01 | PMID 35982161
Qi Ting, Wu Yang, Fang Hailing and 4 more
Differential ion mobility mass spectrometry in immunopeptidomics identifies neoantigens carrying colorectal cancer driver mutations.
Communications biology | 2022-08-18 | PMID 35982173
Minegishi Yuriko, Kiyotani Kazuma, Nemoto Kensaku and 6 more
Adaptive phenotypic plasticity is under stabilizing selection in Daphnia.
Nature ecology & evolution | 2022-10-01 | PMID 35982224
Becker Dörthe, Barnard-Kubow Karen, Porter Robert and 4 more
A thermodynamic investigation of amyloid precursor protein processing by human γ-secretase.
Communications biology | 2022-08-18 | PMID 35982231
Lu Xiaoli, Huang Jing
Associations between cardiometabolic phenotypes and levels of TNF-α, CRP, and interleukins in obstructive sleep apnea.
Sleep & breathing = Schlaf & Atmung | 2023-06-01 | PMID 35982289
Fei Quanming, Tan Yun, Yi Minhan and 2 more
Novel Hina alleles created by genome editing increase grain hardness and reduce grain width in barley.
Transgenic research | 2022-12-01 | PMID 35982368
Jiang Yanyan, Li Jianmin, Liu Baolong and 4 more
The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men.
Genes & genomics | 2023-04-01 | PMID 35982373
Jafari Leyla, Safinejad Kyumars, Nasiri Mahboobeh and 2 more
Development of markers using microsatellite loci of two rove beetle species, Paederus fuscipes Curtis and Aleochara (Aleochara) curtula Goeze (Coleoptera: Staphylinidae), followed by analyses of genetic diversity and population structure.
Genes & genomics | 2022-12-01 | PMID 35982374
Choi Yeon-Jae, Yi Jeesoo, Lee Chan-Jun and 4 more
Colorectal cancer risk in association with colorectal cancer as a second malignancy in relatives: a nationwide cohort study.
BMC cancer | 2022-08-18 | PMID 35982395
Zheng Guoqiao, Sundquist Jan, Sundquist Kristina and 1 more
Olverembatinib (HQP1351), a well-tolerated and effective tyrosine kinase inhibitor for patients with T315I-mutated chronic myeloid leukemia: results of an open-label, multicenter phase 1/2 trial.
Journal of hematology & oncology | 2022-08-18 | PMID 35982483
Jiang Qian, Li Zongru, Qin Yazhen and 20 more
Total mutational load and clinical features as predictors of the metastatic status in lung adenocarcinoma and squamous cell carcinoma patients.
Journal of translational medicine | 2022-08-18 | PMID 35982500
Oróstica Karen Y, Saez-Hidalgo Juan, de Santiago Pamela R and 6 more
Neurobiological sensitivity to unpredictable threat and familial risk for the internalizing and externalizing spectra in adolescents.
Psychological medicine | 2023-09-01 | PMID 35982518
Beatty Clare C, Ferry Rachel A, Eaton Nicholas R and 2 more
Difference in the nutritional, in vitro, and functional characteristics of protein and fat isolates of two Indian chia (Salvia hispanica L) seed genotypes with variation in seed coat color.
Journal of food science | 2022-09-01 | PMID 35982647
Malik Amanda Manoj, Riar Charanjit S
Aberrant splicing events caused by insertion of genes of interest into expression vectors.
International journal of biological sciences | 2022-01-01 | PMID 35982889
Cheng Yun, Kang Xiao-Zhuo, Chan Pearl and 3 more
CpG content in the Zika virus genome affects infection phenotypes in the adult brain and fetal lymph nodes.
Frontiers in immunology | 2022-01-01 | PMID 35983032
Udenze Daniel, Trus Ivan, Berube Nathalie and 1 more
The HMGB1 (C106A) mutation inhibits IL-10-producing CD19hiFcγRIIbhi B cell expansion by suppressing STAT3 activation in mice.
Frontiers in immunology | 2022-01-01 | PMID 35983056
Liu Mengru, Zhou Jingwen, Yin Rui and 4 more
Association of specific HLA alleles and haplotypes with pemphigus vulgaris in the Bulgarian population.
Frontiers in immunology | 2022-01-01 | PMID 35983062
Drenovska Kossara, Ivanova Milena, Vassileva Snejina and 2 more
The novel HLA-DQB1*03:493 allele, the first with glutamic acid at position-10 in the leader peptide.
HLA | 2022-12-01 | PMID 35983731
Niño Ramírez Jairo Eduardo, Gil Etayo Francisco Javier, Vicente Parra Ariadna and 2 more
Early Diagnosis of Wolfram Syndrome by Ophthalmologic Screening in a Patient with Type 1B Diabetes Mellitus: A Case Report
Journal of clinical research in pediatric endocrinology | 2024-03-11 | PMID 35983751
Kokumai Takahide, Suzuki Shigeru, Nishikawa Noriko and 4 more
Developmental genetic effects on externalizing behavior and alcohol use: Examination across two longitudinal samples.
Development and psychopathology | 2024-02-01 | PMID 35983793
Elam Kit K, Bountress Kaitlin E, Ha Thao and 5 more
Amivantamab: a monoclonal EGFR-MET bispecific antibody for EGFR exon 20 insertion in non-small cell lung cancer.
Drugs of today (Barcelona, Spain : 1998) | 2022-08-01 | PMID 35983925
Xie Yuhao, Lu Qisi, Wang Jing-Quan and 3 more
Compound-heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy.
Epilepsia | 2022-10-01 | PMID 35983985
Strehlow Vincent, Rieubland Claudine, Gallati Sabina and 7 more
Heterozygote advantage and pleiotropy contribute to intraspecific color trait variability.
Evolution; international journal of organic evolution | 2022-10-01 | PMID 35984008
De Pasqual Chiara, Suisto Kaisa, Kirvesoja Jimi and 3 more
Cytokine Mixtures Mimicking the Local Milieu in Patients with Inflammatory Bowel Disease Impact Phenotype and Function of Mesenchymal Stromal Cells.
Stem cells translational medicine | 2022-09-21 | PMID 35984079
Barnhoorn Marieke C, van der Meulen-de Jong Andrea E, Schrama Ellen C L M and 6 more
CNPY4 is a potential promising prognostic-related biomarker and correlated with immune infiltrates in gliomas.
Medicine | 2022-08-19 | PMID 35984129
Li Jian-Wen, Huang Qian-Rong, Mo Li-Gen
Effective treatment with icotinib in advanced lung adenocarcinoma harboring rare EGFR mutation G719A/L833V: A case report.
Medicine | 2022-08-19 | PMID 35984165
Zhou Bin, Wang Yanan, Liao Haijiang and 1 more
Efficacy and safety of pembrolizumab monotherapy in EGFR-mutant squamous cell lung cancer with PD-L1 over-expression: A case report.
Medicine | 2022-08-19 | PMID 35984168
Liu Qiu-Xia, Wei Jian-Guo, Chen Yi-Yi and 1 more
A new POLH mutation in a consanguineous Chinese family with xeroderma pigmentosum variant type.
Clinical and experimental dermatology | 2022-11-01 | PMID 35984432
OuYang Xiaoliang, Zhang Deng, Wang Xiuping and 3 more
Evaluating perinatal and neonatal outcomes among children with vascular Ehlers-Danlos syndrome.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-10-01 | PMID 35984436
Stephens Sara B, Russo Melissa, Shalhub Sherene and 4 more
Spectrum of qualitative and quantitative imaging of pilomyxoid, intermediate pilomyxoid and pilocytic astrocytomas in relation to their genetic alterations.
Neuroradiology | 2023-01-01 | PMID 35984480
Fadel Sandra Abi, von Reppert Marc, Kazarian Eve and 7 more
Multicenter clinical radiomics-integrated model based on [18F]FDG PET and multi-modal MRI predict ATRX mutation status in IDH-mutant lower-grade gliomas.
European radiology | 2023-02-01 | PMID 35984514
Zhang Liqiang, Pan Hongyu, Liu Zhi and 12 more
Identification of missense SNP-mediated mutations in the regulatory sites of aldose reductase (ALR2) responsible for treatment failure in diabetic complications.
Journal of molecular modeling | 2022-08-19 | PMID 35984530
Vyas Bhawna, Choudhary Shalki, Verma Himanshu and 2 more
Clinical and Therapeutic Aspects of Sideroblastic Anaemia with B-Cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) Syndrome: a Systematic Review.
Journal of clinical immunology | 2023-01-01 | PMID 35984545
Maccora Ilaria, Ramanan Athimalaipet V, Wiseman Daniel and 3 more
Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome.
Indian journal of pediatrics | 2022-11-01 | PMID 35984556
A Rekha, Chandran Shanu, Ghatak Arpita Roy and 2 more
Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease.
Familial cancer | 2023-04-01 | PMID 35984582
Bond Elysa, Yashar Beverly, Else Tobias and 2 more
Genetic variation and clonal diversity in floating aquatic plants: Comparative genomic analysis of water hyacinth species in their native range.
Molecular ecology | 2022-10-01 | PMID 35984729
da Cunha Nicolay Leme, Xue Haoran, Wright Stephen I and 1 more
Mutation of OsMYB60 reduces rice resilience to drought stress by attenuating cuticular wax biosynthesis.
The Plant journal : for cell and molecular biology | 2022-10-01 | PMID 35984735
Jian Lei, Kang Kiyoon, Choi Yumin and 2 more
Proteomic profiling platforms head to head: Leveraging genetics and clinical traits to compare aptamer- and antibody-based methods.
Science advances | 2022-08-19 | PMID 35984888
Katz Daniel H, Robbins Jeremy M, Deng Shuliang and 16 more
DNA repair in lung cancer: a large-scale quantitative analysis for polymorphisms in DNA repairing pathway genes and lung cancer susceptibility.
Expert review of respiratory medicine | 2022-09-01 | PMID 35984915
Liao Zexi, Yi Minhan, Li Jiaxin and 1 more
DHFR Mutants Modulate Their Synchronized Dynamics with the Substrate by Shifting Hydrogen Bond Occupancies.
Journal of chemical information and modeling | 2022-12-26 | PMID 35984987
Cetin Ebru, Atilgan Ali Rana, Atilgan Canan
Development of diagnostic SNP markers and a novel SNP genotyping assay for distinguishing opium poppies.
Forensic science international | 2022-10-01 | PMID 35985139
Chang Miwha, Kim Joo-Young, Lee Haeyong and 5 more
Oncohistones: Exposing the nuances and vulnerabilities of epigenetic regulation.
Molecular cell | 2022-08-18 | PMID 35985302
Mitchener Michelle M, Muir Tom W
Human tau mutations in cerebral organoids induce a progressive dyshomeostasis of cholesterol.
Stem cell reports | 2022-09-13 | PMID 35985329
Glasauer Stella M K, Goderie Susan K, Rauch Jennifer N and 13 more
De novo pyrimidine synthesis is a targetable vulnerability in IDH mutant glioma.
Cancer cell | 2022-09-12 | PMID 35985343
Shi Diana D, Savani Milan R, Levitt Michael M and 48 more
Genes: DHODH, IDH1
Mycobacterium Avium in Miniature Schnauzer From Argentina: A Series of Cases.
Topics in companion animal medicine | 2000-01-01 | PMID 35985408
Borrás Pablo, Marfil María Jimena, Tellado Matias and 5 more
Short variation of the sheep PDGFD gene is correlated with litter size.
Gene | 2022-11-30 | PMID 35985413
Su Peng, Luo Yunyun, Huang Yangming and 7 more
Cellular and molecular characterization of two novel asparagine synthetase gene mutations linked to asparagine synthetase deficiency.
The Journal of biological chemistry | 2022-09-01 | PMID 35985424
Staklinski Stephen J, Chang Mario C, Yu Fang and 7 more
Diverse mutational spectrum in the 13q14 chromosomal region in a Brazilian cohort of retinoblastoma.
Experimental eye research | 2022-11-01 | PMID 35985532
Mendonça Vanessa, Pereira Sena Priscila, Evangelista Dos Santos Anna Claudia and 10 more
Prediction and evaluation of combination pharmacotherapy using natural language processing, machine learning and patient electronic health records.
Journal of biomedical informatics | 2022-09-01 | PMID 35985621
Ding Pingjian, Pan Yiheng, Wang Quanqiu and 1 more
HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.
Molecular genetics & genomic medicine | 2022-10-01 | PMID 35985664
Wang Yanhong, Zheng Xuan, Feng Chao and 5 more
Mutational Signatures Associate With Survival in Gastrointestinal Carcinomas.
Cancer genomics & proteomics | 2000-01-01 | PMID 35985687
Karihtala Peeter, Porvari Katja, Kilpivaara Outi
Latrophilin-3 heterozygous versus homozygous mutations in Sprague Dawley rats: Effects on egocentric and allocentric memory and locomotor activity.
Genes, brain, and behavior | 2022-09-01 | PMID 35985692
Regan Samantha L, Sugimoto Chiho, Dawson Hannah E and 2 more
Obesity-related glomerulopathy in the presence of APOL1 risk alleles.
BMJ case reports | 2022-08-19 | PMID 35985743
Valdez Imbert Ronald, Hti Lar Seng Nang San, Stokes Michael B and 1 more
Assessing Cutaneous Mosaicism at the Molecular Level.
The Journal of investigative dermatology | 2022-09-01 | PMID 35985765
Park Jonathan J, Choate Keith
Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants.
Neurology | 2022-10-31 | PMID 35985819
Dalla Bella Eleonora, Bersano Enrica, Bruzzone Maria Grazia and 4 more
Genes: SOD1, FUS, OPTN, PFN1, SQSTM1, TARDBP, TUBA4A, UBQLN2
Thymocyte regulatory variant alters transcription factor binding and protects from type 1 diabetes in infants.
Scientific reports | 2022-08-19 | PMID 35986039
Sandholm Niina, Rubio García Arcadio, Pekalski Marcin L and 3 more
Prognostic significance of pathogenic variants in BRCA1, BRCA2, ATM and PALB2 genes in men undergoing hormonal therapy for advanced prostate cancer.
British journal of cancer | 2022-11-01 | PMID 35986085
Kimura Hiroko, Mizuno Kei, Shiota Masaki and 18 more
Precision oncology for intrahepatic cholangiocarcinoma in clinical practice.
British journal of cancer | 2022-11-01 | PMID 35986087
Tomczak Aurelie, Springfeld Christoph, Dill Michael T and 10 more
P21-activated kinase 2-mediated β-catenin signaling promotes cancer stemness and osimertinib resistance in EGFR-mutant non-small-cell lung cancer.
Oncogene | 2022-09-01 | PMID 35986102
Yi Yanmei, Li Pan, Huang Yuanfeng and 10 more
Understanding the comorbidity between posttraumatic stress severity and coronary artery disease using genome-wide information and electronic health records.
Molecular psychiatry | 2022-10-01 | PMID 35986173
Polimanti Renato, Wendt Frank R, Pathak Gita A and 10 more
Predictive value of common genetic variants in idiopathic pulmonary fibrosis survival.
Journal of molecular medicine (Berlin, Germany) | 2022-09-01 | PMID 35986225
Mota Patrícia Caetano, Soares Miguel Luz, Vasconcelos Carlos Daniel and 11 more
SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances.
BMC bioinformatics | 2022-08-19 | PMID 35986254
Hui Sandra, Nielsen Rasmus
Phenotypic, chemical component and molecular assessment of genetic diversity and population structure of Morinda officinalis germplasm.
BMC genomics | 2022-08-19 | PMID 35986256
Luo Zhenhua, Chen Zien, Liu Mengyun and 4 more
Mixed genotypes of Orientia tsutsugamushi in conserved genes and a single immune-dominant tsa56 genotype discovered from a patient with scrub typhus in Hainan Island, China: a case report.
BMC infectious diseases | 2022-08-19 | PMID 35986264
Tang Chuanning, Zhang Liyuan, Huang Yi and 13 more
Longitudinal single-cell transcriptomics reveals distinct patterns of recurrence in acute myeloid leukemia.
Molecular cancer | 2022-08-19 | PMID 35986270
Zhai Yanan, Singh Prashant, Dolnik Anna and 11 more
A novel CREBBP mutation and its phenotype in a case of Rubinstein-Taybi syndrome.
BMC medical genomics | 2022-08-19 | PMID 35986282
Wang Qian, Wang Cong, Wei Wen Bin and 2 more
Socioeconomic inequality in different phenotypes of childhood obesity and its determinants in Iran: a Blinder-Oaxaca decomposition method.
BMC public health | 2022-08-20 | PMID 35986309
Mahmoodi Zohreh, Gill Paramjit, Qorbani Mostafa and 5 more
Rabbit targeted genomic sequences after heterologous hybridization using human exome.
BMC research notes | 2022-08-19 | PMID 35986355
Iannuccelli Nathalie, Sarry Julien, Billon Yvon and 5 more
An epigenetically inherited UV hyper-resistance phenotype in Saccharomyces cerevisiae.
Epigenetics & chromatin | 2022-08-20 | PMID 35986361
Reardon Rachel M, Walsh Amanda K, Larsen Clairine I and 5 more
Extended genomic sequence of the HLA-DRB1*14:04:07 and -DRB1*15:53 alleles from Gujarati individuals.
HLA | 2022-12-01 | PMID 35986495
Thakker Nirali C, Dixit Hemangi, Buch Hiteshree and 2 more
HLA-A*24:244, a variant of HLA-A*24:02:01:01, detected in a Taiwanese individual.
HLA | 2022-12-01 | PMID 35986500
Yang Kuo-Liang, Lin Py-Yu
The EICA is dead? Long live the EICA!
Ecology letters | 2022-10-01 | PMID 35986512
Callaway Ragan M, Lucero Jacob E, Hierro José L and 1 more
TFG mutation induces haploinsufficiency and drives axonal Charcot-Marie-Tooth disease by causing neurite degeneration.
CNS neuroscience & therapeutics | 2022-12-01 | PMID 35986567
Chen Xihui, Liu Fangfang, Chen Kun and 9 more
Expanding the genotypic and phenotypic landscapes of rhizomelic chondrodysplasia punctata type 3 (RCDP3) with two novel families, and a review of the literature.
American journal of medical genetics. Part A | 2022-11-01 | PMID 35986576
İli Ezgi Gökpınar, Gezdirici Alper, Di Pietro Erminia and 2 more
Objective evaluation of facial features in Congolese newborns by facial measurements. The need for population-specific measurements.
American journal of medical genetics. Part A | 2022-10-01 | PMID 35986581
Mubungu Gerrye, Roelants Mathieu, Lumaka Aimé and 5 more
Presence of hepatitis E virus in testis of naturally infected wild boars.
Transboundary and emerging diseases | 2022-11-01 | PMID 35986711
Risalde María A, Frias Mario, Caballero-Gómez Javier and 10 more
Molecular characteristics of incidental lower-grade glioma for treatment decision-making.
Journal of neurosurgery | 2023-03-01 | PMID 35986732
Park Jeongman, Sim Jeongmin, Ahn Juwon and 8 more
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.
Genetics in medicine : official journal of the American College of Medical Genetics | 2022-10-01 | PMID 35986737
Park Joohyun, Tucci Arianna, Cipriani Valentina and 46 more
A Study of Combined Genotype Effects of SHCBP1 on Wool Quality Traits in Chinese Merino.
Biochemical genetics | 2023-04-01 | PMID 35986828
Ma Guang-Wei, Wang Shou-Zhi, Wang Ning and 2 more
Role of Germline Predisposition to Therapy-Related Myeloid Neoplasms.
Current hematologic malignancy reports | 2022-12-01 | PMID 35986863
Baranwal Anmol, Hahn Christopher N, Shah Mithun Vinod and 1 more
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese population.
European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry | 2022-12-01 | PMID 35986881
Elzein R, Abdel-Sater F, Mehawej C and 3 more
Clinical utility of serial serum dilutions for HLA antibody interpretation.
HLA | 2022-11-01 | PMID 35986896
Tambur Anat R, Schinstock Carrie
DDX58 Is Associated With Susceptibility to Severe Influenza Virus Infection in Children and Adolescents.
The Journal of infectious diseases | 2022-11-28 | PMID 35986912
Lee Sanghun, Zhang Yu, Newhams Margaret and 27 more
Circulating vitamin C and digestive system cancers: Mendelian randomization study.
Clinical nutrition (Edinburgh, Scotland) | 2022-09-01 | PMID 35986965
Larsson Susanna C, Mason Amy M, Vithayathil Mathew and 4 more
Common genetic driver mutation in NSCLC and their association with thromboembolic events: A retrospective study.
Lung cancer (Amsterdam, Netherlands) | 2022-10-01 | PMID 35986977
Lin Miaozhen, Lu Yujuan, Yu Qiwen and 3 more
Deficits in adolescent social functioning, dysfunctional family processes and genetic risk for schizophrenia spectrum disorders as risk factors for later psychiatric morbidity of adoptees.
Psychiatry research | 2022-10-01 | PMID 35987066
Tikkanen Ville, Siira Virva, Wahlberg Karl-Erik and 6 more
Comprehensive analysis of shared genetic loci between hippocampal volume and schizophrenia.
Psychiatry research | 2022-10-01 | PMID 35987069
Li Zongchang, Chen Xiaogang
Evaluation of Adenosine A2A receptor gene polymorphisms as risk factors of methamphetamine use disorder susceptibility and predictors of craving degree.
Psychiatry research | 2022-10-01 | PMID 35987070
Wang Huiying, Ma Yitian, Wang Xiaochen and 11 more
DIP2C polymorphisms are implicated in susceptibility and clinical phenotypes of autism spectrum disorder.
Psychiatry research | 2022-10-01 | PMID 35987071
Li Yan, Sun Chuanyong, Guo Yanbo and 7 more
Discovery of novel Quinazoline-based KRAS G12C inhibitors as potential anticancer agents.
Bioorganic & medicinal chemistry | 2022-10-01 | PMID 35987104
Li Ling, Zhao Huiting, Peng Xiaopeng and 8 more
Practical forensic use of kinship determination using high-density SNP profiling based on a microarray platform, focusing on low-quantity DNA.
Forensic science international. Genetics | 2022-11-01 | PMID 35987117
Yagasaki Kayoko, Mabuchi Akihiko, Higashino Toshihide and 4 more
Mutagenic effectiveness and efficiency of gamma rays and combinations with EMS in the induction of macro mutations in blackgram (Vigna mungo (L.) Hepper).
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine | 2022-10-01 | PMID 35987139
Tamilzharasi Murugesan, Dharmalingam Kumaresan, Venkatesan Thiruvengadam and 2 more
Point-of-care HIV viral load and targeted drug resistance mutation testing versus standard care for Kenyan children on antiretroviral therapy (Opt4Kids): an open-label, randomised controlled trial.
The Lancet. Child & adolescent health | 2022-10-01 | PMID 35987208
Patel Rena C, Oyaro Patrick, Thomas Katherine K and 14 more
A shared genetic architecture between adhesive capsulitis and Dupuytren disease.
Journal of shoulder and elbow surgery | 2023-01-01 | PMID 35987430
Kim Stuart K, Khan Condor, Ladd Amy L and 1 more
NPHP3 splice acceptor site variant is associated with infantile nephronophthisis and asphyxiating thoracic dystrophy; A rare combination.
European journal of medical genetics | 2022-10-01 | PMID 35987473
Ijaz Ambreen, Alfadhli Fatima, Alharbi Azizah and 5 more
Acute rapamycin rescues the hyperexcitable phenotype of accumbal medium spiny neurons in the valproic acid rat model of autism spectrum disorder.
Pharmacological research | 2022-09-01 | PMID 35987482
Iezzi D, Curti L, Ranieri G and 10 more
Novel homozygous CD46 variant with C-isoform expression affects C3b inactivation in atypical hemolytic uremic syndrome.
European journal of immunology | 2022-10-01 | PMID 35987516
Schack Vivien R, Herlin Morten K, Pedersen Henrik and 9 more