Results 1 to 10 of about 569,127 (341)

Triple-hit explanation for the worse prognosis of pediatric acute lymphoblastic leukemia among Mexican and Hispanic children

open access: yesFrontiers in Oncology, 2022
Acute lymphoblastic leukemia (ALL) is the most common malignancy among Mexican and Hispanic children and the first cause of death by disease in Mexico. We propose a “triple-hit” explanation for the survival gap affecting this population.
Roberto Rivera-Luna   +8 more
doaj   +1 more source

Bronchiolar Progenitor Cells [PDF]

open access: yesProceedings of the American Thoracic Society, 2009
A comprehensive appreciation of mechanisms regulating epithelial maintenance and repair in pulmonary airways is fundamental to our understanding of tissue remodeling and dysfunction in chronic lung disease. This review provides an update on current concepts that have emerged from recent work in the field of airway epithelial repair and progenitor cell ...
Huaiyong Chen   +2 more
openaire   +3 more sources

Categorisation of patients based on immune profiles: a new approach to identifying candidates for response to checkpoint inhibitors

open access: yesClinical & Translational Immunology, 2021
Objectives Inhibitors to the checkpoint proteins cytotoxic T‐lymphocyte‐associated protein 4 (CTLA‐4) and programmed cell death protein 1 (PD‐1) are becoming widely used in cancer treatment.
Svetlana Bornschlegl   +11 more
doaj   +1 more source

Characterization of The Retinal Progenitor Cells Generated Using Co-Culture Systems [PDF]

open access: yesCell Journal, 2022
Objective: Degeneration of the photoreceptors due to retinal disorders can affect vision, and even lead to blindness. Recently therapeutic progress in retinal degeneration, using human embryonic stem cells (hESCs), has been facing technical challenges,
Sara Momenzadeh   +3 more
doaj   +1 more source

HSPCs display within-family homogeneity in differentiation and proliferation despite population heterogeneity

open access: yeseLife, 2021
High-throughput single-cell methods have uncovered substantial heterogeneity in the pool of hematopoietic stem and progenitor cells (HSPCs), but how much instruction is inherited by offspring from their heterogeneous ancestors remains unanswered. Using a
Tamar Tak   +8 more
doaj   +1 more source

Brain isoform glycogen phosphorylase as a novel hepatic progenitor cell marker. [PDF]

open access: yesPLoS ONE, 2015
An appropriate liver-specific progenitor cell marker is a stepping stone in liver regenerative medicine. Here, we report brain isoform glycogen phosphorylase (GPBB) as a novel liver progenitor cell marker.
Yu-Wen Huang   +6 more
doaj   +1 more source

Single-nuclei analysis reveals depot-specific transcriptional heterogeneity and depot-specific cell types in adipose tissue of dairy cows

open access: yesFrontiers in Cell and Developmental Biology, 2022
Adipose tissue (AT) is an endocrine organ with a central role on whole-body energy metabolism and development of metabolic diseases. Single-cell and single-nuclei RNA sequencing (scRNA-seq and snRNA-seq, respectively) analyses in mice and human AT have ...
Tainara C. Michelotti   +11 more
doaj   +1 more source

Hindlimb Immobilization Increases IL-1β and Cdkn2a Expression in Skeletal Muscle Fibro-Adipogenic Progenitor Cells: A Link Between Senescence and Muscle Disuse Atrophy

open access: yesFrontiers in Cell and Developmental Biology, 2022
Loss of muscle mass and strength contributes to decreased independence and an increased risk for morbidity and mortality. A better understanding of the cellular and molecular mechanisms underlying muscle atrophy therefore has significant clinical and ...
Emily Parker   +12 more
doaj   +1 more source

Nuclear GSK-3β and Oncogenic KRas Lead to the Retention of Pancreatic Ductal Progenitor Cells Phenotypically Similar to Those Seen in IPMN

open access: yesFrontiers in Cell and Developmental Biology, 2022
Glycogen synthase kinase-3β (GSK-3β) is a downstream target of oncogenic KRas and can accumulate in the nucleus in pancreatic ductal adenocarcinoma (PDA).
Li Ding   +13 more
doaj   +1 more source

Therapeutic Strategies for Dystrophin Replacement in Duchenne Muscular Dystrophy

open access: yesFrontiers in Medicine, 2022
Duchenne muscular dystrophy (DMD) is an X-linked hereditary disease characterized by progressive muscle wasting due to modifications in the DMD gene (exon deletions, nonsense mutations, intra-exonic insertions or deletions, exon duplications, splice site
Cedric Happi Mbakam   +5 more
doaj   +1 more source

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