Cargando…

Back to basics: Transcriptomics studies for deep phenotyping of osteoarthritis

Detalles Bibliográficos
Autor principal:	Rai, Muhammad Farooq
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Virtual Special Issue on: Omics Phenotyping; Edited by Mohit Kapoor, AliMobasheri, Shabana Amanda Ali and Annemarie Lang
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718213/ https://www.ncbi.nlm.nih.gov/pubmed/36474769 http://dx.doi.org/10.1016/j.ocarto.2021.100166

Ejemplares similares

The role of metabolomics in precision medicine of osteoarthritis: How far are we?
por: Zhai, Guangju
Publicado: (2021)

Mouse microRNA signatures in joint ageing and post-traumatic osteoarthritis
por: Castanheira, Catarina I.G.D., et al.
Publicado: (2021)

Targeted phospholipidomic analysis of synovial fluid as a tool for osteoarthritis deep phenotyping
por: Rocha, Beatriz, et al.
Publicado: (2021)

Proteomic clustering reveals the kinetics of disease biomarkers in bovine and human models of post-traumatic osteoarthritis
por: Black, Rebecca Mae, et al.
Publicado: (2021)

The lipid profile for the prediction of prednisolone treatment response in patients with inflammatory hand osteoarthritis: The HOPE study
por: Loef, Marieke, et al.
Publicado: (2021)

Osteoarthritis Data Integration Portal (OsteoDIP): A web-based gene and non-coding RNA expression database
por: Pastrello, Chiara, et al.
Publicado: (2022)

The future of deep phenotyping in osteoarthritis: How can high throughput omics technologies advance our understanding of the cellular and molecular taxonomy of the disease?
por: Mobasheri, Ali, et al.
Publicado: (2021)

DNA methylation and noncoding RNA in OA: Recent findings and methodological advances
por: Izda, Vladislav, et al.
Publicado: (2021)

In vivo mechanotransduction: Effect of acute exercise on the metabolomic profiles of mouse synovial fluid
por: Hahn, Alyssa K., et al.
Publicado: (2021)

Impact du confinement sur le suivi des immunothérapies orales alimentaires : étude multi-centrique dans 3 centres d’Île de France
por: Lethai, C., et al.
Publicado: (2021)

Epigenetic remodeling in heart failure with preserved ejection fraction
por: Ambrosini, Samuele, et al.
Publicado: (2022)

Structural genomic variants in thoracic aortic disease
por: Meester, Josephina A.N., et al.
Publicado: (2023)

Long noncoding RNAs in cardiovascular disease
por: Kohlmaier, Alexander, et al.
Publicado: (2023)

Viajes por Marruecos /
por: Ali Bey, 1766-1818
Publicado: (1997)

Alí Chumacero : retrato crítico /
Publicado: (1995)

OMIC-10. TRANSCRIPTOMIC ANALYSIS REVEALS SEX DIFFERENCES IN PEDIATRIC BRAIN MECHANISMS
por: Yang, Wei, et al.
Publicado: (2021)

Comparative transcriptomic analysis reveals the underlying molecular mechanism in high-fat diet-induced islet dysfunction
por: Wan, Shengrong, et al.
Publicado: (2023)

Editorial of Virtual Special Issue on Progress in Medicinal Chemistry
por: Guan, Xiangming
Publicado: (2016)

Online MR guided dose escalated radiotherapy for organ preservation in distal rectal cancer
por: Boeke, Simon, et al.
Publicado: (2022)

When faith moves mountains = cuando la fe mueve montañas /
por: Alÿs, Francis, 1959-
Publicado: (2005)

Mutaciones : elucubraciones mágicas de Rene Alis
Publicado: (1975)

Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6
por: Tezenas du Montcel, Sophie, et al.
Publicado: (2014)

Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein
por: Pescosolido, Matthew F, et al.
Publicado: (2014)

Fixed airflow obstruction in asthma: a descriptive study of patient profiles and effect on treatment responses
por: Tashkin, Donald P., et al.
Publicado: (2014)

A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia
por: Tsoi, Ho, et al.
Publicado: (2014)

Alternative splicing modifies the effect of mutations in COL11A1 and results in recessive type 2 Stickler syndrome with profound hearing loss
por: Richards, Allan J, et al.
Publicado: (2013)

Antiproteinuric therapy and Fabry nephropathy: factors associated with preserved kidney function during agalsidase-beta therapy
por: Warnock, David G, et al.
Publicado: (2015)

Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain
por: Zhang, Stella, et al.
Publicado: (2016)

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
por: Reijnders, Margot R F, et al.
Publicado: (2018)

Retrospective natural history of thymidine kinase 2 deficiency
por: Garone, Caterina, et al.
Publicado: (2018)

Variable expression of subclinical phenotypes instead of reduced penetrance in families with mild triphalangeal thumb phenotypes
por: Potuijt, Jacob W P, et al.
Publicado: (2020)

Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis
por: Gordon, Kristiana, et al.
Publicado: (2020)

Expanding the phenotype of COPA syndrome: a kindred with typical and atypical features
por: Taveira-DaSilva, Angelo M, et al.
Publicado: (2019)

Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
por: Chirita-Emandi, Adela, et al.
Publicado: (2021)

De novo TRPV4 Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathy
por: Ragamin, Aviel, et al.
Publicado: (2022)

Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transition
por: Peron, Angela, et al.
Publicado: (2022)

Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
por: Minatogawa, Mari, et al.
Publicado: (2022)

Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts
por: Mansour, Sahar, et al.
Publicado: (2023)

Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome
por: Otsuji, Shiomi, et al.
Publicado: (2023)

A Metabolomics Approach to Screening for Autism Risk in the Children's Autism Metabolome Project
por: Smith, Alan M., et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_i5ihc0osl66j1j788rb0klhg5t