Cargando…

Comprehensive phenotyping of human peripheral blood B lymphocytes in pathological conditions

Several diseases are associated with alterations of the B‐cell compartment. Knowing how to correctly identify by flow cytometry the distribution of B‐cell populations in the peripheral blood is important to help in the early diagnosis. In the accompanying article we describe how to identify the diff...

Descripción completa

Detalles Bibliográficos
Autores principales:	Carsetti, Rita, Corrente, Francesco, Capponi, Claudia, Mirabella, Mattia, Cascioli, Simona, Palomba, Patrizia, Bertaina, Valentina, Pagliara, Daria, Colucci, Manuela, Piano Mortari, Eva
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2021
Materias:	Phenotype Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299869/ https://www.ncbi.nlm.nih.gov/pubmed/34851033 http://dx.doi.org/10.1002/cyto.a.24518

Ejemplares similares

Comprehensive phenotyping of human peripheral blood B lymphocytes in healthy conditions
por: Carsetti, Rita, et al.
Publicado: (2021)

CD21(–) CD27(–) Atypical B Cells in a Pediatric Cohort Study: An Extensive Single Center Flow Cytometric Analysis
por: Corrente, Francesco, et al.
Publicado: (2022)

Evaluation of Immune and Vaccine Competence in Steroid-Sensitive Nephrotic Syndrome Pediatric Patients
por: Colucci, Manuela, et al.
Publicado: (2021)

Immune Response of Neonates Born to Mothers Infected With SARS-CoV-2
por: Conti, Maria Giulia, et al.
Publicado: (2021)

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)

Different Innate and Adaptive Immune Responses to SARS-CoV-2 Infection of Asymptomatic, Mild, and Severe Cases
por: Carsetti, Rita, et al.
Publicado: (2020)

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study
por: Le Quesne Stabej, Polona, et al.
Publicado: (2011)

Temporal and Spatial Expression of CCN Genes in Zebrafish
por: Fernando, Carol A, et al.
Publicado: (2010)

Genetic targeting of the endoderm with claudin-6(CreER)
por: Anderson, William J, et al.
Publicado: (2008)

Differential Expression and Regulation by Activin of the Neurotrophins BDNF and NT4 During Human and Mouse Ovarian Development
por: Childs, Andrew J, et al.
Publicado: (2010)

Expression of Glycosaminoglycan Epitopes During Zebrafish Skeletogenesis
por: Hayes, Anthony J, et al.
Publicado: (2013)

A novel transgenic zebrafish line for red opsin expression in outer segments of photoreceptor cells
por: Crespo, Cátia, et al.
Publicado: (2018)

Expression analysis of limb element markers during mouse embryonic development
por: Rafipay, Alexandra, et al.
Publicado: (2018)

Limb specific Acvr1‐knockout during embryogenesis in mice exhibits great toe malformation as seen in Fibrodysplasia Ossificans Progressiva (FOP)
por: Hildebrand, Laura, et al.
Publicado: (2019)

LPA(1), LPA(2), LPA(4), and LPA(6) receptor expression during mouse brain development
por: Suckau, Olga, et al.
Publicado: (2019)

The platelet‐derived growth factor receptor alpha promoter‐directed expression of cre recombinase in mouse placenta
por: Wattez, Jean‐Sebastien, et al.
Publicado: (2019)

Differential localization of histone variant TH2B during the first round compared with subsequent rounds of spermatogenesis
por: Beedle, My‐Thanh, et al.
Publicado: (2019)

A novel conserved enhancer at zebrafish zic3 and zic6 loci drives neural expression
por: Minhas, Rashid, et al.
Publicado: (2019)

Comparison of sex determination mechanism of germ cells between birds and fish: Cloning and expression analyses of chicken forkhead box L3‐like gene
por: Ichikawa, Kennosuke, et al.
Publicado: (2019)

The requirement of SUMO2/3 for SENP2 mediated extraembryonic and embryonic development
por: Yu, H‐M Ivy, et al.
Publicado: (2019)

Depletion of Foxk transcription factors causes genome-wide transcriptional misregulation and developmental arrest in zebrafish embryos
por: Geng, Fan-Suo, et al.
Publicado: (2020)

Phylogenetic and developmental analyses indicate complex functions of calcium‐activated potassium channels in zebrafish embryonic development
por: Silic, Martin R., et al.
Publicado: (2021)

The real Nemo movie: Description of embryonic development in Amphiprion ocellaris from first division to hatching
por: Salis, Pauline, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_a37c73uefkl51em9bmdkc110nt