Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Ihor V. Yosypiv"'
Autor:
Euming Chong, Ihor V. Yosypiv
Publikováno v:
International Journal of Nephrology, Vol 2012 (2012)
A growing body of evidence supports the concept that changes in the intrauterine milieu during “sensitive” periods of embryonic development or in infant diet after birth affect the developing individual, resulting in general health alterations la
Externí odkaz:
https://doaj.org/article/3a6fc7b9db7c463bacfa3aded849ff0f
Autor:
Ihor V. Yosypiv
Publikováno v:
International Journal of Nephrology, Vol 2012 (2012)
Congenital anomalies of the kidney and urinary tract (CAKUTs) occur in 3–6 per 1000 live births, account for the most cases of pediatric end-stage kidney disease (ESKD), and predispose an individual to hypertension and cardiovascular disease throug
Externí odkaz:
https://doaj.org/article/70d73d92094c40ec89a189be9ea9295c
Autor:
Renfang Song, Ihor V. Yosypiv
Publikováno v:
International Journal of Nephrology, Vol 2011 (2011)
The renin-angiotensin system (RAS), a key regulator of the blood pressure and fluid/electrolyte homeostasis, also plays a critical role in kidney development. All the components of the RAS are expressed in the developing metanephros. Moreover, mutati
Externí odkaz:
https://doaj.org/article/b79a3687e94d4c8187d1e6e600dab5ff
Autor:
Ihor V. Yosypiv, Renfang Song
Publikováno v:
Pediatric Research. 90:205-211
BACKGROUND Multicystic dysplastic kidney (MCDK) is a common form of congenital cystic kidney disease in children. The etiology of MCDK remains unclear. Given an important role of the renin-angiotensin system in normal kidney development, we explored
Autor:
Mary Alice Rossi, Ihor V. Yosypiv
Publikováno v:
Diabetes and Kidney Disease ISBN: 9783030860196
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54395392df1f69a98adac8b84dbd63a8
https://doi.org/10.1007/978-3-030-86020-2_7
https://doi.org/10.1007/978-3-030-86020-2_7
Autor:
Ihor V. Yosypiv
Publikováno v:
Pediatric Nephrology. 36:479-489
Mutations in the genes of the renin-angiotensin system result in congenital anomalies of the kidney and urinary tract (CAKUT), the main cause of end-stage renal disease in children. The molecular mechanisms that cause CAKUT are unclear in most cases.
Autor:
Renfang Song, Yalan Liu, Ihor V. Yosypiv, Hua Peng, Jie Liu, Yafan Zhou, Yan Chen, Lei Li, Yali Liu, Yumei Feng
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
The (pro)renin receptor [(P)RR] binds to prorenin to activate the renin-angiotensin system and is essential for the development of many different organ systems. Whether the (P)RR also plays a role in lung development is unknown. Immunostaining was us
Publikováno v:
Clinical Pediatrics. 58:1557-1561
Publikováno v:
Pediatric research. 91(3)
Background Multicystic dysplastic kidney (MCDK) is a common form of congenital kidney anomaly. The cause of MCDK is unknown. We investigated whether MCDK in children is linked to cytogenomic aberrations. Methods We conducted array comparative genomic
Autor:
Renfang, Song, Ihor V, Yosypiv
Publikováno v:
Pediatric research. 90(1)
Multicystic dysplastic kidney (MCDK) is a common form of congenital cystic kidney disease in children. The etiology of MCDK remains unclear. Given an important role of the renin-angiotensin system in normal kidney development, we explored whether MCD