Suchergebnisse - "Castillejo-López, Casimiro"

PubPharm (42)

1

Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes and normal tissues

enthalten in: bioRxiv.org | 2024

von Diamanti, K. | Cavalli, M. | Pereira, M. | +10

2

A regulatory element associated to NAFLD in the promoter of DIO1 controls LDL-C, HDL-C and triglycerides in hepatic cells

enthalten in: Lipids in health and disease | 2024

von Castillejo-López, C. | Bárcenas-Walls, J. | Cavalli, M. | +2

3

A regulatory element associated to NAFLD in the promoter of DIO1 controls LDL-C, HDL-C and triglycerides in hepatic cells

enthalten in: Lipids in health and disease | 2024

von Castillejo-López, C. | Bárcenas-Walls, J. | Cavalli, M. | +2

4

Organ-specific metabolic pathways distinguish prediabetes, type 2 diabetes, and normal tissues

enthalten in: Cell reports. Medicine | 2022

von Diamanti, K. | Cavalli, M. | Pereira, M. | +10

5

CD44 Depletion in Glioblastoma Cells Suppresses Growth and Stemness and Induces Senescence

enthalten in: Cancers | 2022

von Kolliopoulos, C. | Ali, M. | Castillejo-Lopez, C. | +2

6

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

enthalten in: American journal of human genetics | 2022

von Fatima, A. | Hoeber, J. | Schuster, J. | +23

ErratumFor: Am J Hum Genet. 2021 Apr 1;108(4):739-748. - PMID 33711248

7

SIDT1 plays a key role in type I IFN responses to nucleic acids in plasmacytoid dendritic cells and mediates the pathogenesis of an imiquimod-induced psoriasis model

enthalten in: EBioMedicine | 2022

von Morell, M. | Varela, N. | Castillejo-López, C. | +10

8

Deubiquitinating enzymes USP4 and USP17 finetune the trafficking of PDGFRβ and affect PDGF-BB-induced STAT3 signalling

enthalten in: Cellular and molecular life sciences : CMLS | 2022

von Sarri, N. | Wang, K. | Tsioumpekou, M. | +4

9

Deubiquitinating enzymes USP4 and USP17 finetune the trafficking of PDGFRβ and affect PDGF-BB-induced STAT3 signalling

enthalten in: Cellular and molecular life sciences | 2022

von Sarri, N. | Wang, K. | Tsioumpekou, M. | +4

10

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

enthalten in: American journal of human genetics | 2021

von Fatima, A. | Hoeber, J. | Schuster, J. | +23

ErratumIn: Am J Hum Genet. 2022 Mar 3;109(3):542-546. - PMID 35245475

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