Suchergebnisse - "GPI-Linked Proteins"

PubPharm (558)

1

Recombinant humanized Fab fragments targeting the CFC domain of human Cripto-1

enthalten in: Biochemical and biophysical research communications | 2024

von Sandomenico, A. | Selis, F. | Sivaccumar, J. | +8

2

ULBP2 is a biomarker related to prognosis and immunity in colon cancer

enthalten in: Molecular and cellular biochemistry | 2023

von Yang, X. | Su, X. | Wang, Z. | +3

3

Low MICA Gene Expression Confers an Increased Risk of Graves' Disease : A Mendelian Randomization Study

enthalten in: Thyroid : official journal of the American Thyroid Association | 2022

von Sutoh, Y. | Komaki, S. | Yamaji, T. | +11

4

CRIPTO-1 Is Immunolocalized in the Syncytiotrophoblast of Ampullary Pregnancies

enthalten in: BioMed research international | 2022

von Cabar, F. | Pereira, P. | Bandeira, C. | +3

5

Oncofetal Protein CRIPTO Is Involved in Wound Healing and Fibrogenesis in the Regenerating Liver and Is Associated with the Initial Stages of Cardiac Fibrosis

enthalten in: Cells | 2021

von Karkampouna, S. | van der Helm, D. | Scarpa, M. | +6

6

Cripto favors chondrocyte hypertrophy via TGF-β SMAD1/5 signaling during development of osteoarthritis

enthalten in: The Journal of pathology | 2021

von Garcia de Vinuesa, A. | Sanchez-Duffhues, G. | Blaney-Davidson, E. | +8

7

Altered NK-cell compartment and dysfunctional NKG2D/NKG2D-ligand axis in patients with ataxia-telangiectasia

enthalten in: Clinical immunology (Orlando, Fla.) | 2021

von Desimio, M. | Finocchi, A. | Di Matteo, G. | +10

8

Liver-specific over-expression of Cripto-1 in transgenic mice promotes hepatocyte proliferation and deregulated expression of hepatocarcinogenesis-related genes and signaling pathways

enthalten in: Aging | 2021

von Liu, Y. | Li, Y. | Huang, S. | +14

9

Cripto-1 as a Key Factor in Tumor Progression, Epithelial to Mesenchymal Transition and Cancer Stem Cells

enthalten in: International journal of molecular sciences | 2021

von Arnouk, H. | Yum, G. | Shah, D.

10

Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions

enthalten in: European journal of human genetics : EJHG | 2021

von Maya, I. | Basel-Salmon, L. | Sagi-Dain, L.

CommentIn: Eur J Hum Genet. 2022 Jan;30(1):5-6. - PMID 34819629

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