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Items: 1 to 50 of 63

1.

Factors Related to Osteosarcopenia in Kidney Transplant Recipients.

Yanishi M, Kinoshita H, Tsukaguchi H, Kimura Y, Koito Y, Sugi M, Matsuda T.

Transplant Proc. 2018 Dec;50(10):3371-3375. doi: 10.1016/j.transproceed.2018.04.032. Epub 2018 Apr 18.

PMID:
30586836
2.

Homozygous splicing mutation in NUP133 causes Galloway-Mowat syndrome.

Fujita A, Tsukaguchi H, Koshimizu E, Nakazato H, Itoh K, Kuraoka S, Komohara Y, Shiina M, Nakamura S, Kitajima M, Tsurusaki Y, Miyatake S, Ogata K, Iijima K, Matsumoto N, Miyake N.

Ann Neurol. 2018 Dec;84(6):814-828. doi: 10.1002/ana.25370. Erratum in: Ann Neurol. 2019 Mar;85(3):462-463.

PMID:
30427554
3.

A Nationwide Survey on Danon Disease in Japan.

Sugie K, Komaki H, Eura N, Shiota T, Onoue K, Tsukaguchi H, Minami N, Ogawa M, Kiriyama T, Kataoka H, Saito Y, Nonaka I, Nishino I.

Int J Mol Sci. 2018 Nov 8;19(11). pii: E3507. doi: 10.3390/ijms19113507.

4.

The creatinine/cystatin C ratio provides effective evaluation of muscle mass in kidney transplant recipients.

Yanishi M, Kinoshita H, Tsukaguchi H, Kimura Y, Koito Y, Sugi M, Matsuda T.

Int Urol Nephrol. 2019 Jan;51(1):79-83. doi: 10.1007/s11255-018-2015-6. Epub 2018 Oct 25.

PMID:
30361963
5.

A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report.

Hyun HS, Kim SH, Park E, Cho MH, Kang HG, Lee HS, Miyake N, Matsumoto N, Tsukaguchi H, Cheong HI.

BMC Med Genet. 2018 Jul 27;19(1):131. doi: 10.1186/s12881-018-0649-y.

6.

A mutation in transcription factor MAFB causes Focal Segmental Glomerulosclerosis with Duane Retraction Syndrome.

Sato Y, Tsukaguchi H, Morita H, Higasa K, Tran MTN, Hamada M, Usui T, Morito N, Horita S, Hayashi T, Takagi J, Yamaguchi I, Nguyen HT, Harada M, Inui K, Maruta Y, Inoue Y, Koiwa F, Sato H, Matsuda F, Ayabe S, Mizuno S, Sugiyama F, Takahashi S, Yoshimura A.

Kidney Int. 2018 Aug;94(2):396-407. doi: 10.1016/j.kint.2018.02.025. Epub 2018 May 18.

PMID:
29779709
7.

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.

Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A, Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F.

Nat Commun. 2018 May 17;9(1):1960. doi: 10.1038/s41467-018-04193-w.

8.

Long-term clinicopathologic observation in a case of steroid-resistant nephrotic syndrome caused by a novel Crumbs homolog 2 mutation.

Watanabe S, Aizawa T, Tsukaguchi H, Tsugawa K, Tsuruga K, Shono A, Nozu K, Iijima K, Joh K, Tanaka H.

Nephrology (Carlton). 2018 Jul;23(7):697-702. doi: 10.1111/nep.13244.

PMID:
29473663
9.

Small-Vessel Vasculopathy Due to Aberrant Autophagy in LAMP-2 Deficiency.

Nguyen HT, Noguchi S, Sugie K, Matsuo Y, Nguyen CTH, Koito H, Shiojima I, Nishino I, Tsukaguchi H.

Sci Rep. 2018 Feb 20;8(1):3326. doi: 10.1038/s41598-018-21602-8.

10.

Dual Energy X-ray Absorptiometry and Bioimpedance Analysis are Clinically Useful for Measuring Muscle Mass in Kidney Transplant Recipients With Sarcopenia.

Yanishi M, Kinoshita H, Tsukaguchi H, Kimura Y, Koito Y, Jino E, Watanabe M, Sugi M, Matsuda T.

Transplant Proc. 2018 Jan - Feb;50(1):150-154. doi: 10.1016/j.transproceed.2017.12.023.

PMID:
29407300
11.

Determinants of the Change in Arterial Stiffness in Peritoneal Dialysis Patients.

Nakahigashi M, Tsukaguchi H, Morimoto S, Nakano C, Ueda H, Someya K, Kusabe M, Kikuchi S, Imada T, Shiojima I.

Int Heart J. 2017 Dec 12;58(6):915-925. doi: 10.1536/ihj.16-624. Epub 2017 Nov 17.

12.

Erratum to: Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations.

Kin J, Tsukaguchi H, Kimata T, Nguyen HT, Nakano Y, Miyake N, Matsumoto N, Kaneko K.

BMC Nephrol. 2017 Aug 17;18(1):271. doi: 10.1186/s12882-017-0682-7. No abstract available.

13.

Evaluation of physical activity in sarcopenic conditions of kidney transplantation recipients.

Yanishi M, Tsukaguchi H, Kimura Y, Koito Y, Yoshida K, Seo M, Jino E, Sugi M, Kinoshita H, Matsuda T.

Int Urol Nephrol. 2017 Oct;49(10):1779-1784. doi: 10.1007/s11255-017-1661-4. Epub 2017 Jul 19.

PMID:
28726035
14.

Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations.

Kino J, Tsukaguchi H, Kimata T, Nguyen HT, Nakano Y, Miyake N, Matsumoto N, Kaneko K.

BMC Nephrol. 2017 Jul 6;18(1):220. doi: 10.1186/s12882-017-0632-4. Erratum in: BMC Nephrol. 2017 Aug 17;18(1):271.

15.

Monoclonal immunoglobulin-associated proliferative glomerulonephritis characterized by organized deposits of striated ultra-substructures: A case report.

Hara S, Tsukaguchi H, Oka T, Kusabe M, Mizui M, Joh K.

Ultrastruct Pathol. 2017 Jul-Aug;41(4):301-307. doi: 10.1080/01913123.2017.1336189. Epub 2017 Jun 19.

PMID:
28628381
16.

Short-term outcome and quality of life in kidney transplant recipient with monoclonal gammopathy.

Yanishi M, Tsukaguchi H, Yoshida T, Taniguchi H, Yoshida K, Mishima T, Komai Y, Yasuda K, Watanabe M, Sugi M, Kinoshita H, Matsuda T.

CEN Case Rep. 2016 Nov;5(2):168-172. doi: 10.1007/s13730-016-0218-1. Epub 2016 Apr 5.

17.

Factors Associated With the Development of Sarcopenia in Kidney Transplant Recipients.

Yanishi M, Kimura Y, Tsukaguchi H, Koito Y, Taniguchi H, Mishima T, Fukushima Y, Sugi M, Kinoshita H, Matsuda T.

Transplant Proc. 2017 Mar;49(2):288-292. doi: 10.1016/j.transproceed.2016.12.015.

PMID:
28219586
18.

Decreased urinary excretion of the ectodomain form of megalin (A-megalin) in children with OCRL gene mutations.

Suruda C, Tsuji S, Yamanouchi S, Kimata T, Huan NT, Kurosawa H, Hirayama Y, Tsukaguchi H, Saito A, Kaneko K.

Pediatr Nephrol. 2017 Apr;32(4):621-625. doi: 10.1007/s00467-016-3535-x. Epub 2016 Oct 20.

PMID:
27766457
19.

Correlation of whole kidney hypertrophy with glomerular over-filtration in live, gender-mismatched renal transplant allografts.

Yanishi M, Tsukaguchi H, Huan NT, Koito Y, Taniguchi H, Yoshida K, Mishima T, Sugi M, Kinoshita H, Matsuda T.

Nephrology (Carlton). 2017 Dec;22(12):1002-1007. doi: 10.1111/nep.12915.

PMID:
27576505
20.

Comparison of Nephroscope-assisted "Pulling Thread" Technique and Conventional Open Placement of Peritoneal Dialysis Catheters in Patients With End-stage Renal Disease.

Yoshida T, Nakamoto T, Yoshida K, Yanishi M, Inoue T, Murota T, Kinoshita H, Tsukaguchi H, Matsuda T.

Urology. 2016 Nov;97:261-265. doi: 10.1016/j.urology.2016.06.019. Epub 2016 Jul 7.

PMID:
27397096
21.

NUP107 mutations in children with steroid-resistant nephrotic syndrome.

Park E, Ahn YH, Kang HG, Miyake N, Tsukaguchi H, Cheong HI.

Nephrol Dial Transplant. 2017 Jun 1;32(6):1013-1017. doi: 10.1093/ndt/gfw103.

PMID:
27190346
22.

Comparison of live donor pre-transplant and recipient post-transplant renal volumes.

Yanishi M, Kinoshita H, Yoshida T, Takayasu K, Yoshida K, Mishima T, Sugi M, Tsukaguchi H, Kawa G, Matsuda T.

Clin Transplant. 2016 May;30(5):613-8. doi: 10.1111/ctr.12727. Epub 2016 Mar 29.

PMID:
26928366
23.

Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome.

Miyake N, Tsukaguchi H, Koshimizu E, Shono A, Matsunaga S, Shiina M, Mimura Y, Imamura S, Hirose T, Okudela K, Nozu K, Akioka Y, Hattori M, Yoshikawa N, Kitamura A, Cheong HI, Kagami S, Yamashita M, Fujita A, Miyatake S, Tsurusaki Y, Nakashima M, Saitsu H, Ohashi K, Imamoto N, Ryo A, Ogata K, Iijima K, Matsumoto N.

Am J Hum Genet. 2015 Oct 1;97(4):555-66. doi: 10.1016/j.ajhg.2015.08.013. Epub 2015 Sep 24.

24.

[The genetic basis of nephrotic syndrome].

Tsukaguchi H.

Nihon Jinzo Gakkai Shi. 2015;57(4):726-35. Japanese. No abstract available.

PMID:
26126329
25.

[Case report; A case of familial focal segmental glomerulosclerosis with a mutation in the formin INF2].

Yamamoto J, Nakazawa D, Tsukaguchi H, Toyoyama T, Sato A, Nakagaki T, Ishikawa Y, Shibazaki S, Nishio S, Atsumi T.

Nihon Naika Gakkai Zasshi. 2013 May 10;102(5):1220-2. Japanese. No abstract available.

PMID:
23847988
26.

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.

Toyota K, Ogino D, Hayashi M, Taki M, Saito K, Abe A, Hashimoto T, Umetsu K, Tsukaguchi H, Hayasaka K.

J Peripher Nerv Syst. 2013 Mar;18(1):97-8. doi: 10.1111/jns5.12014. No abstract available.

PMID:
23521651
27.

Methicillin-resistant Staphylococcus aureus-related glomerulonephritis in a child.

Kimata T, Tsuji S, Yoshimura K, Tsukaguchi H, Kaneko K.

Pediatr Nephrol. 2012 Nov;27(11):2149-2152. doi: 10.1007/s00467-012-2229-2. Epub 2012 Jun 20.

PMID:
22714673
28.

[Molecular basis of hereditary nephrotic syndromes].

Iijima K, Tsukaguchi H.

Nihon Jinzo Gakkai Shi. 2010;52(7):914-23. Review. Japanese. No abstract available.

PMID:
21077341
29.

More on clinical renal genetics.

Grünfeld JP, Hwu W, Chien Y, Lee N, Chiang S, Dobrovolny R, Huang A, Yeh H, Chao M, Lin S, Kitagawa T, Desnick R, Hsu L, Van Keimpema L, Nevens F, Vanslembrouck R, Van Oijen G, Hoffmann A, Dekker H, De Man R, Drenth J, Alamovitch S, Plaisier E, Favrole P, Prost C, Chen Z, Van Agrmael T, Marro B, Ronco P, Zivna M, Hulkova H, Matignon M, Hodanova K, Vylet'al P, Kalbacova M, Baresova V, Sikora J, Blazkova H, Zivny J, Ivanek R, Stranecky V, Sovova J, Claes K, Lerut E, Fryns J, Hart P, Hart T, Adams J, Pawtowski A, Clemessy M, Gasc J, Gubler M, Antignac C, Elleder M, Kapp K, Grimbert P, Bleyer A, Kmoch S, Brown E, Schlöndorff J, Becker Dj, Tsukaguchi H, Uschinski A, Higgs H, Henderson J, Pollak M.

Clin J Am Soc Nephrol. 2010 Apr;5(4):563-7. doi: 10.2215/CJN.01720210. Epub 2010 Mar 25. No abstract available.

30.

Glomerular proteins related to slit diaphragm and matrix adhesion in the foot processes are highly tyrosine phosphorylated in the normal rat kidney.

Zhang Y, Yoshida Y, Nameta M, Xu B, Taguchi I, Ikeda T, Fujinaka H, Magdeldin S, Tsukaguchi H, Harita Y, Yaoita E, Yamamoto T.

Nephrol Dial Transplant. 2010 Jun;25(6):1785-95. doi: 10.1093/ndt/gfp697. Epub 2010 Jan 12. Erratum in: Nephrol Dial Transplant. 2012 Jun;27(6):2606. Mohamed, Sameh Magdeldin [corrected to Magdeldin, Sameh].

PMID:
20067908
31.

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.

Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR.

Nat Genet. 2010 Jan;42(1):72-6. doi: 10.1038/ng.505. Epub 2009 Dec 20. Erratum in: Nat Genet. 2010 Apr;42(4):361. Tonna, Stephen J [added].

32.

Phosphorylation of nephrin triggers its internalization by raft-mediated endocytosis.

Qin XS, Tsukaguchi H, Shono A, Yamamoto A, Kurihara H, Doi T.

J Am Soc Nephrol. 2009 Dec;20(12):2534-45. doi: 10.1681/ASN.2009010011. Epub 2009 Oct 22.

33.

Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains.

Shono A, Tsukaguchi H, Kitamura A, Hiramoto R, Qin XS, Doi T, Iijima K.

Hum Mol Genet. 2009 Aug 15;18(16):2943-56. doi: 10.1093/hmg/ddp232. Epub 2009 May 14.

PMID:
19443487
34.

Toll-like receptor 9 affects severity of IgA nephropathy.

Suzuki H, Suzuki Y, Narita I, Aizawa M, Kihara M, Yamanaka T, Kanou T, Tsukaguchi H, Novak J, Horikoshi S, Tomino Y.

J Am Soc Nephrol. 2008 Dec;19(12):2384-95. doi: 10.1681/ASN.2007121311. Epub 2008 Sep 5.

35.

Steroid-resistant nephrotic syndrome.

Kitamura A, Tsukaguchi H, Maruyama K, Shono A, Iijima K, Kagami S, Doi T.

Kidney Int. 2008 Nov;74(9):1209-15. doi: 10.1038/ki.2008.297. Epub 2008 Jul 2. No abstract available.

36.

Increase of integrin-linked kinase activity in cultured podocytes upon stimulation with plasma from patients with recurrent FSGS.

Hattori M, Akioka Y, Chikamoto H, Kobayashi N, Tsuchiya K, Shimizu M, Kagami S, Tsukaguchi H.

Am J Transplant. 2008 Jul;8(7):1550-6. doi: 10.1111/j.1600-6143.2008.02287.x.

37.

Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.

Furue T, Hattori M, Tsukaguchi H, Kitamura A, Oomori T, Ogino D, Nakakura H, Ashida A, Miura K, Hisano M, Takahashi K, Chikamoto H, Akioka Y, Sakano T.

Pediatr Transplant. 2008 May;12(3):341-6. doi: 10.1111/j.1399-3046.2007.00752.x. Epub 2008 Jan 16.

PMID:
18208440
38.

Podocin participates in the assembly of tight junctions between foot processes in nephrotic podocytes.

Shono A, Tsukaguchi H, Yaoita E, Nameta M, Kurihara H, Qin XS, Yamamoto T, Doi T.

J Am Soc Nephrol. 2007 Sep;18(9):2525-33. Epub 2007 Aug 5.

39.

[The genetic basis of familial focal segmental glomerulosclerosis and related nephrotic syndrome].

Tsukaguchi H, Kitamura A.

Nihon Jinzo Gakkai Shi. 2007;49(2):88-97. Japanese. No abstract available.

PMID:
17375615
40.

A familial childhood-onset relapsing nephrotic syndrome.

Kitamura A, Tsukaguchi H, Hiramoto R, Shono A, Doi T, Kagami S, Iijima K.

Kidney Int. 2007 May;71(9):946-51. Epub 2007 Feb 7. No abstract available.

41.

Genetics and clinical features of 15 Asian families with steroid-resistant nephrotic syndrome.

Kitamura A, Tsukaguchi H, Iijima K, Araki J, Hattori M, Ikeda M, Honda M, Nozu K, Nakazato H, Yoshikawa N, Kagami S, Muramatsu M, Choi Y, Cheong HI, Doi T.

Nephrol Dial Transplant. 2006 Nov;21(11):3133-8. Epub 2006 Sep 12. No abstract available.

PMID:
16968734
42.

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.

Maruyama K, Iijima K, Ikeda M, Kitamura A, Tsukaguchi H, Yoshiya K, Hoshii S, Wada N, Uemura O, Satomura K, Honda M, Yoshikawa N.

Pediatr Nephrol. 2003 May;18(5):412-6. Epub 2003 Apr 5.

PMID:
12687458
43.

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.

Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR.

J Clin Invest. 2002 Dec;110(11):1659-66.

44.

Molecular characterization of a novel urea transporter from kidney inner medullary collecting ducts.

Shayakul C, Tsukaguchi H, Berger UV, Hediger MA.

Am J Physiol Renal Physiol. 2001 Mar;280(3):F487-94.

45.

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31.

Tsukaguchi H, Yager H, Dawborn J, Jost L, Cohlmia J, Abreu PF, Pereira AB, Pollak MR.

J Am Soc Nephrol. 2000 Sep;11(9):1674-80.

46.

Human vitamin C (L-ascorbic acid) transporter SVCT1.

Wang Y, Mackenzie B, Tsukaguchi H, Weremowicz S, Morton CC, Hediger MA.

Biochem Biophys Res Commun. 2000 Jan 19;267(2):488-94.

PMID:
10631088
47.

Functional and molecular characterization of the human neutral solute channel aquaporin-9.

Tsukaguchi H, Weremowicz S, Morton CC, Hediger MA.

Am J Physiol. 1999 Nov;277(5):F685-96. doi: 10.1152/ajprenal.1999.277.5.F685.

PMID:
10564231
48.

Molecular cloning and characterization of a channel-like transporter mediating intestinal calcium absorption.

Peng JB, Chen XZ, Berger UV, Vassilev PM, Tsukaguchi H, Brown EM, Hediger MA.

J Biol Chem. 1999 Aug 6;274(32):22739-46.

49.

A family of mammalian Na+-dependent L-ascorbic acid transporters.

Tsukaguchi H, Tokui T, Mackenzie B, Berger UV, Chen XZ, Wang Y, Brubaker RF, Hediger MA.

Nature. 1999 May 6;399(6731):70-5.

PMID:
10331392
50.

Molecular and functional analysis of SDCT2, a novel rat sodium-dependent dicarboxylate transporter.

Chen X, Tsukaguchi H, Chen XZ, Berger UV, Hediger MA.

J Clin Invest. 1999 Apr;103(8):1159-68.

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