局灶節段性腎小球硬化症 (Chinese Wikipedia)
Analysis of information sources in references of the Wikipedia article "局灶節段性腎小球硬化症" in Chinese language version.
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archive.org
- Kumar V, Fausto N, Abbas A (编). Robbins & Cotran Pathologic Basis of Disease 7th. Saunders. 2003: 982–3. ISBN 978-0-7216-0187-8.
- Thomas DB, Franceschini N, Hogan SL; et al. Clinical and pathologic characteristics of focal segmental glomerulosclerosis pathologic variants. Kidney Int. 2006, 69 (5): 920–6. PMID 16518352. doi:10.1038/sj.ki.5000160.
- Tsukaguchi H, Sudhakar A, Le TC; et al. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J. Clin. Invest. December 2002, 110 (11): 1659–66. PMC 151634
. PMID 12464671. doi:10.1172/JCI16242.
doi.org
dx.doi.org
- Thomas DB, Franceschini N, Hogan SL; et al. Clinical and pathologic characteristics of focal segmental glomerulosclerosis pathologic variants. Kidney Int. 2006, 69 (5): 920–6. PMID 16518352. doi:10.1038/sj.ki.5000160.
- Mukerji N, Damodaran TV, Winn MP. TRPC6 and FSGS: The latest TRP channelopathy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2007, 1772 (8): 859–68. PMID 17459670. doi:10.1016/j.bbadis.2007.03.005.
- Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, Kopp JB, Pays E, Pollak MR. Association of Trypanolytic ApoL1 Variants with Kidney Disease in African-Americans. Science. Jul 2010, 329 (5993): 841–5. PMC 2980843 . PMID 20647424. doi:10.1126/science.1193032.
- Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Mutations in the formin protein INF2 cause focal segmental glomerulosclerosis. Nature Genetics. Jan 2010, 42 (1): 72–6. PMC 2980844 . PMID 20023659. doi:10.1038/ng.505.
- Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Genet. Med. February 2006, 8 (2): 63–75 [2014-07-26]. PMID 16481888. doi:10.1097/01.gim.0000200947.09626.1c. （原始内容存档于2013-06-03）.
- Tsukaguchi H, Sudhakar A, Le TC; et al. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J. Clin. Invest. December 2002, 110 (11): 1659–66. PMC 151634 . PMID 12464671. doi:10.1172/JCI16242.
- Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler M-C, Niaudet P, Antignac C. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nature Genetics. May 2000, 24 (4): 349–354. PMID 10742096. doi:10.1038/74166.
mercksource.com
nih.gov
ncbi.nlm.nih.gov
- Thomas DB, Franceschini N, Hogan SL; et al. Clinical and pathologic characteristics of focal segmental glomerulosclerosis pathologic variants. Kidney Int. 2006, 69 (5): 920–6. PMID 16518352. doi:10.1038/sj.ki.5000160.
- Mukerji N, Damodaran TV, Winn MP. TRPC6 and FSGS: The latest TRP channelopathy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2007, 1772 (8): 859–68. PMID 17459670. doi:10.1016/j.bbadis.2007.03.005.
- Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, Kopp JB, Pays E, Pollak MR. Association of Trypanolytic ApoL1 Variants with Kidney Disease in African-Americans. Science. Jul 2010, 329 (5993): 841–5. PMC 2980843 . PMID 20647424. doi:10.1126/science.1193032.
- Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Mutations in the formin protein INF2 cause focal segmental glomerulosclerosis. Nature Genetics. Jan 2010, 42 (1): 72–6. PMC 2980844 . PMID 20023659. doi:10.1038/ng.505.
- Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Genet. Med. February 2006, 8 (2): 63–75 [2014-07-26]. PMID 16481888. doi:10.1097/01.gim.0000200947.09626.1c. （原始内容存档于2013-06-03）.
- Tsukaguchi H, Sudhakar A, Le TC; et al. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J. Clin. Invest. December 2002, 110 (11): 1659–66. PMC 151634 . PMID 12464671. doi:10.1172/JCI16242.
- Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler M-C, Niaudet P, Antignac C. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nature Genetics. May 2000, 24 (4): 349–354. PMID 10742096. doi:10.1038/74166.
sites.google.com
- Focal_segmental_glomerulosclerosis of the Kidney. [2009-11-20]. （原始内容存档于2012-11-14）.
uchc.edu
pathweb.uchc.edu
- Focal_segmental_glomerulosclerosis of the Kidney. [2008-11-25]. （原始内容存档于2009-01-07）.
web.archive.org
- Renal Pathology. [2008-11-25]. （原始内容存档于2018-10-17）.
- Focal_segmental_glomerulosclerosis of the Kidney. [2008-11-25]. （原始内容存档于2009-01-07）.
- Focal_segmental_glomerulosclerosis of the Kidney. [2009-11-20]. （原始内容存档于2012-11-14）.
- Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Genet. Med. February 2006, 8 (2): 63–75 [2014-07-26]. PMID 16481888. doi:10.1097/01.gim.0000200947.09626.1c. （原始内容存档于2013-06-03）.
- 存档副本. [2014-07-26]. （原始内容存档于2014-07-09）.
wkhealth.com
meta.wkhealth.com
- Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Genet. Med. February 2006, 8 (2): 63–75 [2014-07-26]. PMID 16481888. doi:10.1097/01.gim.0000200947.09626.1c. （原始内容存档于2013-06-03）.