Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fadong Yu"'
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 438-443 (2023)
Neurofibromatosis-Noonan syndrome (NFNS), a rare autosomal-dominant hereditary disease, is characterized by clinical manifestations of both neurofibromatosis type 1 (NF1) and NS. We present a case of NFNS with short stature caused by a heterozygous n
Externí odkaz:
https://doaj.org/article/a8ead5fe0f814a2d882890474eaa8642
Publikováno v:
Clinical and Experimental Hypertension, Vol 45, Iss 1 (2023)
Background Endothelial dysfunction is a major pathophysiology observed in hypertension. Ghrelin, a key regulator of metabolism, has been shown to play protective roles in cardiovascular system. However, whether it has the effect of improving endothel
Externí odkaz:
https://doaj.org/article/fc2396fab05b45b5ae746d44560cf99d
Publikováno v:
Lipids in Health and Disease, Vol 22, Iss 1, Pp 1-16 (2023)
Abstract Background Curcumin (Cur) is a bioactive dietary polyphenol of turmeric with various biological activities against several cancers. Colorectal cancer (CRC) is one of the leading causes of cancer-related deaths. Intestinal cholesterol homeost
Externí odkaz:
https://doaj.org/article/38031df98b0b4733a1fa53201c881484
Background Curcumin (Cur) is a bioactive dietary polyphenol of turmeric with various biological activities against several cancers. Colorectal cancer (CRC) is one of the leading causes of cancer-related deaths. Intestinal cholesterol homeostasis is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c751638bd24eb180036ac01664b235c9
https://doi.org/10.21203/rs.3.rs-2032821/v1
https://doi.org/10.21203/rs.3.rs-2032821/v1
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Neurofibromatosis-Noonan syndrome (NFNS), a rare autosomal dominant hereditary disease, shows the manifestations of both neurofibromatosis type 1 (
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.