Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Julia A Brickey"'
Publikováno v:
Journal of Cardiac Surgery. 37:574-578
Background: Manouguian aortic root enlargement (ARE) has been a standard root enlargement procedure to assist in patients with a small annular size. We describe a modification to the Manouguian ARE similar to Yang et al. This approach could serve as
Autor:
Janet L. Funk, Claus Schneider, Julia A. Brickey, Andrew G. Kunihiro, Paula B. Luis, Jennifer B. Frye
Publikováno v:
The Journal of Nutritional Biochemistry. 63:150-156
Breast cancer (BCa) bone metastases (BMETs) drive osteolysis via a feed-forward loop involving tumoral secretion of osteolytic factors (e.g., PTHrP) induced by bone-matrix-derived growth factors (e.g., TGFβ). In prior experiments, turmeric-derived c
Autor:
Susan A. Whitman, Julia N. Cheng, Andrew G. Kunihiro, Jennifer B. Frye, Julia A. Brickey, Janet L. Funk
Publikováno v:
Journal of cancer metastasis and treatment
Aim Estrogen receptor α-positive (ER+) subtypes of breast cancer have the greatest predilection for forming osteolytic bone metastases (BMETs). Because tumor-derived factors mediate osteolysis, a possible role for tumoral ERα signaling in driving E
Autor:
Jeanne Cho, Julia A Brickey, Mara Flannery, Corita R. Grudzen, EMPallA Investigators, Allison M. Cuthel
Background: Emergency department (ED) visits among older adults are common near the end of life. Palliative care has been shown to reduce ED visits and to increase quality of life among patients, but recruitment into these programs is often challengi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6752c699aa1eec6a806077e2fc7cfec
https://doi.org/10.21203/rs.3.rs-21202/v2
https://doi.org/10.21203/rs.3.rs-21202/v2
Background Emergency department (ED) visits among older adults are common near the end of life. Palliative care has been shown to reduce ED visits and to increase quality of life among patients, but recruitment into these programs is often challengin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b43bcf54eaca6411277313eff10eef1
https://doi.org/10.21203/rs.3.rs-21202/v1
https://doi.org/10.21203/rs.3.rs-21202/v1
Autor:
Andrew G. Kunihiro, Julia N. Cheng, Janet L. Funk, Julia A. Brickey, Paula B. Luis, Jennifer B. Frye, Claus Schneider
Publikováno v:
J Nutr Biochem
TGFβ signaling promotes progression of bone-metastatic (BMET) breast cancer (BCa) cells by driving tumor-associated osteolysis, a hallmark of BCa BMETs, thus allowing for tumor expansion within bone. Turmeric-derived bioactive curcumin, enriched in
Autor:
Paula B. Luis, Julia A. Brickey, Jennifer B. Frye, Janet L. Funk, Andrew G. Kunihiro, Claus Schneider
Publikováno v:
Cancer Research. 77:P6-18
The majority of women with advanced breast cancer (BCa) develop incurable osteolytic bone metastases. Our laboratory has previously demonstrated that curcuminoids, bioactive compounds isolated from turmeric rhizomes, prevent the development of lytic
Autor:
Andrew Kunihiro, Julia A. Brickey, jennifer B. Frye, Paula B. Luis, Claus Schneider, Janet L. Funk
Publikováno v:
Cancer Research. 79:3002-3002
Curcumin (CURC), a turmeric-derived dietary polyphenol, prevents osteoclast formation and bone resorption in murine models of arthritis, post-menopausal osteoporosis, and bone metastatic breast cancer despite being rapidly conjugated upon ingestion i
Autor:
Julia N. Cheng, Madison M. Egan, Andrew G. Kunihiro, Susan A. Whitman, Julia A. Brickey, Janet L. Funk, Jennifer B. Frye
Publikováno v:
Cancer Research. 78:2116-2116
Estrogen receptor α-positive (ER+) breast cancers (BrCAs) have the greatest predilection for forming bone metastases (BMETs). To begin to query ERα's role in osteolytic BrCA BMET progression, tumoral vs bone microenvironment effects of 17β-estradi
Publikováno v:
Cancer Research. 78:2685-2685
Tumor-cell TGFβ signaling has been demonstrated to drive osteolytic breast cancer bone metastases (BrCa BMET) in mouse models. This established an important link between the microenvironment and tumor cells in bone, wherein osteoclast-mediated bone