Scambler PJ - Search Results

1

Activation of podocyte Notch mediates early Wt1 glomerulopathy.

Asfahani RI, Tahoun MM, Miller-Hodges EV, Bellerby J, Virasami AK, Sampson RD, Moulding D, Sebire NJ, Hohenstein P, Scambler PJ, Waters AM. Asfahani RI, et al. Among authors: scambler pj. Kidney Int. 2018 Apr;93(4):903-920. doi: 10.1016/j.kint.2017.11.014. Epub 2018 Feb 2. Kidney Int. 2018. PMID: 29398135 Free PMC article.

2

Tissue Clearing and Deep Imaging of the Kidney Using Confocal and Two-Photon Microscopy.

Jafree DJ, Long DA, Scambler PJ, Moulding D. Jafree DJ, et al. Among authors: scambler pj. Methods Mol Biol. 2020;2067:103-126. doi: 10.1007/978-1-4939-9841-8_8. Methods Mol Biol. 2020. PMID: 31701448

3

Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease.

Jafree DJ, Moulding D, Kolatsi-Joannou M, Perretta Tejedor N, Price KL, Milmoe NJ, Walsh CL, Correra RM, Winyard PJ, Harris PC, Ruhrberg C, Walker-Samuel S, Riley PR, Woolf AS, Scambler PJ, Long DA. Jafree DJ, et al. Among authors: scambler pj. Elife. 2019 Dec 6;8:e48183. doi: 10.7554/eLife.48183. Elife. 2019. PMID: 31808745 Free PMC article.

4

Expression of Fraser syndrome genes in normal and polycystic murine kidneys.

Kerecuk L, Long DA, Ali Z, Anders C, Kolatsi-Joannou M, Scambler PJ, Woolf AS. Kerecuk L, et al. Among authors: scambler pj. Pediatr Nephrol. 2012 Jun;27(6):991-8. doi: 10.1007/s00467-012-2100-5. Epub 2011 Oct 13. Pediatr Nephrol. 2012. PMID: 21993971 Free PMC article.

5

Genetic inactivation of Semaphorin 3C protects mice from acute kidney injury.

Cai A, Ye G, Placier S, Frère P, Surin B, Vandermeersch S, Kormann R, Xu-Dubois YC, Genest M, Lannoy M, Chadjichristos CE, Dussaule JC, Scambler PJ, Chatziantoniou C, Calmont A. Cai A, et al. Among authors: scambler pj. Kidney Int. 2022 Apr;101(4):720-732. doi: 10.1016/j.kint.2021.12.028. Epub 2022 Jan 26. Kidney Int. 2022. PMID: 35090878

6

Generation of mice with a conditional null Fraser syndrome 1 (Fras1) allele.

Pitera JE, Turmaine M, Woolf AS, Scambler PJ. Pitera JE, et al. Among authors: scambler pj. Genesis. 2012 Dec;50(12):892-8. doi: 10.1002/dvg.22045. Epub 2012 Jul 23. Genesis. 2012. PMID: 22730198

7

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.

van Bueren KL, Papangeli I, Rochais F, Pearce K, Roberts C, Calmont A, Szumska D, Kelly RG, Bhattacharya S, Scambler PJ. van Bueren KL, et al. Among authors: scambler pj. Dev Biol. 2010 Apr 15;340(2):369-80. doi: 10.1016/j.ydbio.2010.01.020. Epub 2010 Feb 1. Dev Biol. 2010. PMID: 20122914 Free PMC article.

8

Novel exomphalos genetic mouse model: the importance of accurate phenotypic classification.

Carnaghan H, Roberts T, Savery D, Norris FC, McCann CJ, Copp AJ, Scambler PJ, Lythgoe MF, Greene ND, Decoppi P, Burns AJ, Pierro A, Eaton S. Carnaghan H, et al. Among authors: scambler pj. J Pediatr Surg. 2013 Oct;48(10):2036-42. doi: 10.1016/j.jpedsurg.2013.04.010. J Pediatr Surg. 2013. PMID: 24094954 Free PMC article.

9

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

Koziell A, Charmandari E, Hindmarsh PC, Rees L, Scambler P, Brook CG. Koziell A, et al. Clin Endocrinol (Oxf). 2000 Apr;52(4):519-24. doi: 10.1046/j.1365-2265.2000.00980.x. Clin Endocrinol (Oxf). 2000. PMID: 10762296 Review.

10

An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia.

Rix S, Calmont A, Scambler PJ, Beales PL. Rix S, et al. Among authors: scambler pj. Hum Mol Genet. 2011 Apr 1;20(7):1306-14. doi: 10.1093/hmg/ddr013. Epub 2011 Jan 12. Hum Mol Genet. 2011. PMID: 21227999 Free PMC article.

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