Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Lorine Wilkinson"'
Publikováno v:
The Journal of Pathology. 238:665-676
Congenital medullary dysplasia with obstructive nephropathy is a common congenital disorder observed in paediatric patients and represents the foremost cause of renal failure. However, the molecular processes regulating normal papillary outgrowth dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfd35b225481563943eb55a92c8673dd
https://doi.org/10.1002/path.4690
https://doi.org/10.1002/path.4690
Autor:
Oliver H. Tam, David J. Pennisi, Lorine Wilkinson, Victor L. Wan, Melissa H. Little, Fatima Wazin, Frank J. Lovicu
Publikováno v:
Experimental eye research. 170
The development and growth of the vertebrate ocular lens is dependent on the regulated proliferation of an anterior monolayer of epithelial cells, and their subsequent differentiation into elongate fiber cells. The growth factor rich ocular media tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c6c4ab1fc3dd1dd2d38d171bc78c6e
https://pubmed.ncbi.nlm.nih.gov/29458060
https://pubmed.ncbi.nlm.nih.gov/29458060
Autor:
Sarah L. Walton, Helle Bielefeldt-Ohmann, Jereme G. Spiers, Lorine Wilkinson, Reetu R. Singh, Karen M. Moritz, Melissa H. Little, James S. M. Cuffe
Publikováno v:
The Journal of Physiology. 592:3127-3141
Maternal hypoxia is a common perturbation that can disrupt placental and thus fetal development, contributing to neonatal impairments. Recently, evidence has suggested that physiological outcomes are dependent upon the sex of the fetus, with males mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f46d8e528fde2a18ebd6eaa48cdeddc
https://doi.org/10.1113/jphysiol.2014.272856
https://doi.org/10.1113/jphysiol.2014.272856
Publikováno v:
The Journal of Pathology. 229:685-696
Crim1 is a transmembrane protein that regulates the bioavailability of growth factors such as VEGFA. Crim1(KST264)(/)(KST264) hypomorphic mice develop renal disease characterized by glomerular cysts and loss of endothelial integrity, progressing to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a3fbb3f17f024d24f60e5051ea58deb
https://doi.org/10.1002/path.4155
https://doi.org/10.1002/path.4155
Publikováno v:
The Journal of pathology. 238(5)
Congenital medullary dysplasia with obstructive nephropathy is a common congenital disorder observed in paediatric patients and represents the foremost cause of renal failure. However, the molecular processes regulating normal papillary outgrowth dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26cb50acb51e2e2d1be8dbd48a303d45
https://pubmed.ncbi.nlm.nih.gov/26800422
https://pubmed.ncbi.nlm.nih.gov/26800422
Publikováno v:
The Journal of pathology. 229(5)
Crim1 is a transmembrane protein that regulates the bioavailability of growth factors such as VEGFA. Crim1(KST264)(/)(KST264) hypomorphic mice develop renal disease characterized by glomerular cysts and loss of endothelial integrity, progressing to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f71ae6ed7a906c63e821cc58067a2882
https://pubmed.ncbi.nlm.nih.gov/23224993
https://pubmed.ncbi.nlm.nih.gov/23224993
Autor:
David J. Pennisi, J. Philippe York, Melissa H. Little, Pumin Zhang, Han Sheng Chiu, Lorine Wilkinson
Publikováno v:
Genesis (New York, N.Y. : 2000). 50(9)
Crim1 is a developmentally expressed, transmembrane protein essential for normal embryonic development. We generated mice engineered to contain a Crim1 conditional null allele by flanking exons three and four of Crim1 with unidirectional LoxP sites.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0b781900b4fa9d5be2ffce43961b7fe
https://pubmed.ncbi.nlm.nih.gov/22511315
https://pubmed.ncbi.nlm.nih.gov/22511315
Autor:
Graham J. Galloway, Richard J Lang, Yu Leng Phua, Joan Li, Melissa H. Little, Lorine Wilkinson, Michael J Nguyen, Hikaru Hashitani, Nyoman D. Kurniawan
Publikováno v:
The Journal of pathology. 227(4)
Crim1 hypomorphic (Crim1(KST264/KST264)) mice display progressive renal disease characterized by glomerular defects, leaky peritubular vasculature, and progressive interstitial fibrosis. Here we show that 27% of these mice also present with hydroneph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85bbe47b112b970f874f7a91a456198
https://pubmed.ncbi.nlm.nih.gov/22488641
https://pubmed.ncbi.nlm.nih.gov/22488641
Autor:
David J. Pennisi, Genevieve Kinna, Melissa H. Little, Han Sheng Chiu, David G. Simmons, Lorine Wilkinson
Publikováno v:
Placenta. 33(3)
Normal placental development and function is essential for fetal growth of eutherian mammals. Mutational studies have shown that numerous growth factors are required for placental development and differentiation of placental lineages. Here, using a g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f74196a518c1fff3dbb0f60a255f5165
https://pubmed.ncbi.nlm.nih.gov/22225908
https://pubmed.ncbi.nlm.nih.gov/22225908
Publikováno v:
Current topics in developmental biology. 90
The mammalian kidney may well be one of the most complex organs of postnatal life. Each adult human kidney contains on average more than one million functional filtration units, the nephrons, residing within a specialized cellular interstitium. Each
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9f5f499fecd4b21ba01ef6cc9c138d0b
https://pubmed.ncbi.nlm.nih.gov/20691850
https://pubmed.ncbi.nlm.nih.gov/20691850