Results 41 to 50 of about 80,394 (263)
Repurposing a Small Molecule Plant Hormone as a Tunable ON‐Switch for CAR‐T Cell Immunotherapy
By engineering a receptor system integrating the plant auxin receptor AFB1 with its co‐receptor IAA7, we enable ligand‐dependent interactions triggered by the plant hormone auxins. This design allows rapid, reversible, and dose‐dependent T cell activation, resulting in potent cytotoxicity against B‐cell lymphoma in vitro and in vivo.
Hongxiang Zeng +16 more
wiley +1 more source
The Scarlet - October 25, 2021 [PDF]
The October 25, 2021 edition of The Scarlet (est. 1939), Clark University\u27s student-run newspaper. The Scarlet is intellectually and editorially independent of the University.https://commons.clarku.edu/scarlet/1096/thumbnail ...
Scarlet Staff
core +1 more source
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto +5 more
wiley +1 more source
Determination of antioxidant activities of some apple cultivars
This study was conducted in order to determine the antioxidant activities of certain apple varieties. 'Galaxy Gala', 'Scarlet Spur', 'Fuji', 'Pink Lady' and 'Granny Smith' were characterized in this study.
Lütfi Pirlak +2 more
doaj +1 more source
BackgroundInternet-derived data and the autoregressive integrated moving average (ARIMA) and ARIMA with explanatory variable (ARIMAX) models are extensively used for infectious disease surveillance.
Tingyan Luo +11 more
doaj +1 more source
The Scarlet - November 2, 2018 [PDF]
The November 2, 2018 edition of The Scarlet (est. 1939), Clark University\u27s student-run newspaper. The Scarlet is intellectually and editorially independent of the University.https://commons.clarku.edu/scarlet/1069/thumbnail ...
Scarlet Staff
core
Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley +1 more source
The Scarlet - September 13, 2019 [PDF]
The September 13, 2019 edition of The Scarlet (est. 1939), Clark University\u27s student-run newspaper. The Scarlet is intellectually and editorially independent of the University.https://commons.clarku.edu/scarlet/1080/thumbnail ...
Scarlet Staff
core +1 more source
Posthumously Diagnosed Myhre Syndrome Presenting With Pleural Remodeling and Endometrial Cancer
ABSTRACT Myhre syndrome (OMIM 139210) is a genetic condition defined by neurodevelopmental disability, characteristic facial features, and multisystem proliferative fibrosis. While various types of lung disease have been reported, pleural remodeling leading to restrictive lung disease has not yet been described.
Jeanette Saffir +6 more
wiley +1 more source

