Suchergebnisse - "Endoglin"

PubPharm (2.868)

1

Endothelial progenitor cells control remodeling of uterine spiral arteries for the establishment of utero-placental circulation

enthalten in: Developmental cell | 2024

von Tan, B. | Lin, L. | Yuan, Y. | +7

2

Antisense oligonucleotide-mediated terminal intron retention of endoglin : A potential strategy to inhibit renal interstitial fibrosis

enthalten in: Biochimica et biophysica acta. Molecular basis of disease | 2024

von Gerrits, T. | Dijkstra, K. | Bruijn, J. | +3

3

A chemical proteomics approach for global mapping of functional lysines on cell surface of living cell

enthalten in: Nature communications | 2024

von Wang, T. | Ma, S. | Ji, G. | +5

4

Dapagliflozin prevents ERK activation and SGLT2-dependent endoglin upregulation in a mechanically provoked cardiac injury model

enthalten in: Physiological reports | 2024

von Yeh, T. | Wu, Y. | Wong, T. | +3

5

Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia

enthalten in: Clinical genetics | 2024

von Morita, S. | Nomura, S. | Azuma, K. | +11

6

Angiogenic and vasoactive proteins in the maternal-fetal interface in healthy pregnancies and preeclampsia

enthalten in: American journal of obstetrics and gynecology | 2024

von Westerberg, A. | Degnes, M. | Andresen, I. | +2

7

Impact of physical activity on preeclampsia and angiogenic markers in the Finnish Genetics of Pre-eclampsia Consortium (FINNPEC) cohort

enthalten in: Annals of medicine | 2024

von Jaatinen, N. | Ekholm, E. | Laivuori, F. | +1

8

HDAC6 Enhances Endoglin Expression through Deacetylation of Transcription Factor SP1, Potentiating BMP9-Induced Angiogenesis

enthalten in: Cells | 2024

von Sun, C. | Xie, K. | Yang, L. | +5

9

Iron deficiency responses and integrated compensations in patients according to hereditary hemorrhagic telangiectasia ACVRL1, ENG and SMAD4 genotypes

enthalten in: Haematologica | 2024

von Sharma, L. | Almaghlouth, F. | Mckernan, H. | +3

10

Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families

enthalten in: European journal of medical genetics | 2024

von Tusseau, M. | Eyries, M. | Chatron, N. | +14

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