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Expression of type IV collagen in the developing human kidney.
Kuroda N, Yoshikawa N, Nakanishi K, Iijima K, Hanioka K, Hayashi Y, Imai Y, Sado Y, Nakayama M, Itoh H. Kuroda N, et al. Among authors: nakayama m. Pediatr Nephrol. 1998 Sep;12(7):554-8. doi: 10.1007/s004670050503. Pediatr Nephrol. 1998. PMID: 9761353
Chronic glomerulonephritis associated with IgG subclass deficiency.
Kamei K, Nakagawa A, Otsuka Y, Nakayama M, Kobayashi S, Matsuoka K, Iijima K. Kamei K, et al. Among authors: nakayama m. Pediatr Nephrol. 2007 Aug;22(8):1229-34. doi: 10.1007/s00467-007-0474-6. Epub 2007 Apr 17. Pediatr Nephrol. 2007. PMID: 17437134
Rituximab for refractory focal segmental glomerulosclerosis.
Nakayama M, Kamei K, Nozu K, Matsuoka K, Nakagawa A, Sako M, Iijima K. Nakayama M, et al. Pediatr Nephrol. 2008 Mar;23(3):481-5. doi: 10.1007/s00467-007-0640-x. Epub 2007 Nov 1. Pediatr Nephrol. 2008. PMID: 17973121
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F. van der Ven AT, et al. Among authors: nakayama m. J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24. J Am Soc Nephrol. 2018. PMID: 30143558 Free PMC article.
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT).
Wu CW, Mann N, Nakayama M, Connaughton DM, Dai R, Kolvenbach CM, Kause F, Ottlewski I, Wang C, Klämbt V, Seltzsam S, Lai EW, Selvin A, Senguttuva P, Bodamer O, Stein DR, El Desoky S, Kari JA, Tasic V, Bauer SB, Shril S, Hildebrandt F. Wu CW, et al. Among authors: nakayama m. Genet Med. 2020 Oct;22(10):1673-1681. doi: 10.1038/s41436-020-0844-z. Epub 2020 Jun 1. Genet Med. 2020. PMID: 32475988 Free PMC article.
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
Zheng B, Seltzsam S, Wang C, Schierbaum L, Schneider S, Wu CW, Dai R, Connaughton DM, Nakayama M, Mann N, Stajic N, Mane S, Bauer SB, Tasic V, Nam HJ, Shril S, Hildebrandt F. Zheng B, et al. Among authors: nakayama m. Nephrol Dial Transplant. 2022 Sep 22;37(10):1833-1843. doi: 10.1093/ndt/gfab253. Nephrol Dial Transplant. 2022. PMID: 34473308 Free PMC article.
3,255 results