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Items: 1 to 50 of 253

1.

Functional evaluation of the pathological significance of MEFV variants using induced pluripotent stem cell-derived macrophages.

Shiba T, Tanaka T, Ida H, Watanabe M, Nakaseko H, Osawa M, Shibata H, Izawa K, Yasumi T, Kawasaki Y, Saito MK, Takita J, Heike T, Nishikomori R.

J Allergy Clin Immunol. 2019 Nov;144(5):1438-1441.e12. doi: 10.1016/j.jaci.2019.07.039. Epub 2019 Sep 18. No abstract available.

PMID:
31542286
2.

Phenotype-Based High-Throughput Classification of Long QT Syndrome Subtypes Using Human Induced Pluripotent Stem Cells.

Yoshinaga D, Baba S, Makiyama T, Shibata H, Hirata T, Akagi K, Matsuda K, Kohjitani H, Wuriyanghai Y, Umeda K, Yamamoto Y, Conklin BR, Horie M, Takita J, Heike T.

Stem Cell Reports. 2019 Aug 13;13(2):394-404. doi: 10.1016/j.stemcr.2019.06.007. Epub 2019 Aug 1.

3.

Cerebral Sinovenous Thrombosis and Subdural Hematoma as Treatment-Related Complications in Suprasellar Germ Cell Tumor Associated with Adipsic Diabetes Insipidus.

Kobayashi K, Suehiro M, Maihara T, Usami I, Kageyama Y, Okazaki S, Heike T.

Pediatr Neurosurg. 2019;54(4):288-292. doi: 10.1159/000501044. Epub 2019 Jul 10.

PMID:
31291634
4.

The intracellular Ca2+ concentration is elevated in cardiomyocytes differentiated from hiPSCs derived from a Duchenne muscular dystrophy patient.

Tsurumi F, Baba S, Yoshinaga D, Umeda K, Hirata T, Takita J, Heike T.

PLoS One. 2019 Mar 15;14(3):e0213768. doi: 10.1371/journal.pone.0213768. eCollection 2019.

5.

Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency.

Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova JL, Hagiwara M, Yasumi T.

J Clin Invest. 2019 Feb 1;129(2):583-597. doi: 10.1172/JCI124011. Epub 2018 Dec 18.

6.

Integrative network analysis reveals biological pathways associated with Williams syndrome.

Kimura R, Swarup V, Tomiwa K, Gandal MJ, Parikshak NN, Funabiki Y, Nakata M, Awaya T, Kato T, Iida K, Okazaki S, Matsushima K, Kato T, Murai T, Heike T, Geschwind DH, Hagiwara M.

J Child Psychol Psychiatry. 2019 May;60(5):585-598. doi: 10.1111/jcpp.12999. Epub 2018 Oct 25.

7.

Williams-Beuren Syndrome as a Potential Risk Factor for Burkitt Lymphoma.

Kimura R, Ishii Y, Tomiwa K, Awaya T, Nakata M, Kato T, Okazaki S, Heike T, Hagiwara M.

Front Genet. 2018 Sep 4;9:368. doi: 10.3389/fgene.2018.00368. eCollection 2018.

8.

Paraneoplastic hypereosinophilic syndrome associated with IL3-IgH positive acute lymphoblastic leukemia.

Kobayashi K, Mizuta S, Yamane N, Ueno H, Yoshida K, Kato I, Umeda K, Hiramatsu H, Suehiro M, Maihara T, Usami I, Shiraishi Y, Chiba K, Miyano S, Adachi S, Ogawa S, Kiyokawa N, Heike T.

Pediatr Blood Cancer. 2019 Jan;66(1):e27449. doi: 10.1002/pbc.27449. Epub 2018 Sep 11. No abstract available.

PMID:
30207070
9.

Living-donor lung transplantation after surgical repair of transposition of the great arteries.

Yoshinaga D, Baba S, Hirata T, Fukushima H, Hamaji M, Aoyama A, Chen-Yoshikawa TF, Yamagishi H, Date H, Heike T.

Gen Thorac Cardiovasc Surg. 2019 Jul;67(7):640-643. doi: 10.1007/s11748-018-1006-y. Epub 2018 Sep 6.

PMID:
30191531
10.

Current state of therapeutic development for rare cancers in Japan, and proposals for improvement.

Kawai A, Goto T, Shibata T, Tani K, Mizutani S, Nishikawa A, Shibata T, Matsumoto S, Nagata K, Narukawa M, Matsui S, Ando M, Toguchida J, Monden M, Heike T, Kimura S, Ueda R.

Cancer Sci. 2018 May;109(5):1731-1737. doi: 10.1111/cas.13568.

11.

Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3.

Hiejima E, Shibata H, Yasumi T, Shimodera S, Hori M, Izawa K, Kawai T, Matsuoka M, Kojima Y, Ohara A, Nishikomori R, Ohara O, Heike T.

Clin Immunol. 2018 Jun;191:63-66. doi: 10.1016/j.clim.2018.03.012. Epub 2018 Mar 26.

PMID:
29596912
12.

Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation.

Kawaguchi K, Umeda K, Hiejima E, Iwai A, Mikami M, Nodomi S, Saida S, Kato I, Hiramatsu H, Yasumi T, Nishikomori R, Kondo T, Takaori-Kondo A, Heike T, Adachi S.

Int J Hematol. 2018 Jul;108(1):66-75. doi: 10.1007/s12185-018-2442-2. Epub 2018 Mar 26.

PMID:
29582333
13.

Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis.

Shibata H, Yasumi T, Shimodera S, Hiejima E, Izawa K, Kawai T, Shirakawa R, Wada T, Nishikomori R, Horiuchi H, Ohara O, Ishii E, Heike T.

Blood. 2018 May 3;131(18):2016-2025. doi: 10.1182/blood-2017-10-812503. Epub 2018 Mar 16.

PMID:
29549174
14.

[Pediatric acute lymphoblastic leukemia presenting with bone and joint pain].

Kubota H, Saida S, Kouzuki K, Hamabata T, Daifu T, Kato I, Umeda K, Hiramatsu H, Nishikomori R, Heike T, Okamoto T, Adachi S.

Rinsho Ketsueki. 2018;59(2):167-173. doi: 10.11406/rinketsu.59.167. Japanese.

PMID:
29515068
15.

National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics.

Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T.

Mod Rheumatol. 2019 Jan;29(1):181-187. doi: 10.1080/14397595.2018.1442639. Epub 2018 Mar 2.

PMID:
29451047
16.

Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders.

Kadowaki T, Ohnishi H, Kawamoto N, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Kawai T, Hiejima E, Takagi M, Imai K, Nishikomori R, Ito S, Heike T, Ohara O, Morio T, Fukao T, Kanegane H.

J Allergy Clin Immunol. 2018 Apr;141(4):1485-1488.e11. doi: 10.1016/j.jaci.2017.10.039. Epub 2017 Dec 11. No abstract available.

PMID:
29241730
17.

Live-attenuated vaccines in a cryopyrin-associated periodic syndrome patient receiving canakinumab treatment during infancy.

Watanabe M, Nishikomori R, Fujimaki Y, Heike T, Ohara A, Saji T.

Clin Case Rep. 2017 Sep 12;5(11):1750-1755. doi: 10.1002/ccr3.1149. eCollection 2017 Nov.

18.

Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report.

Hiejima E, Yasumi T, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Okafuji I, Yorifuji T, Tanaka T, Izawa K, Kawai T, Nishikomori R, Heike T.

Medicine (Baltimore). 2017 Nov;96(46):e8601. doi: 10.1097/MD.0000000000008601.

19.

A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells.

Yoshida T, Awaya T, Jonouchi T, Kimura R, Kimura S, Era T, Heike T, Sakurai H.

Sci Rep. 2017 Oct 18;7(1):13473. doi: 10.1038/s41598-017-14063-y.

20.

Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren.

Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Higashi A, Heike T.

Pediatr Allergy Immunol. 2017 Dec;28(8):793-800. doi: 10.1111/pai.12817. Epub 2017 Nov 2.

PMID:
29024078
21.

Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq.

Nakayama M, Oda H, Nakagawa K, Yasumi T, Kawai T, Izawa K, Nishikomori R, Heike T, Ohara O.

Biochem Biophys Rep. 2016 Dec 23;9:146-152. doi: 10.1016/j.bbrep.2016.12.002. eCollection 2017 Mar.

22.

Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency.

Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, Nambu M, Miyagawa-Hayashino A, Nomura T, Kabashima K, Ito M, Iwaki-Egawa S, Sasahara Y, Nakayama M, Heike T.

Scand J Rheumatol. 2018 Mar;47(2):170-172. doi: 10.1080/03009742.2017.1324912. Epub 2017 Jun 30. No abstract available.

PMID:
28665179
23.

A 6-year-old girl diagnosed with mevalonate kinase deficiency who had hydrops fetalis and neonatal-onset cholestasis.

Yamashita Y, Matsumoto S, Hiramoto R, Komori I, Tanaka T, Nishikomori R, Heike T, Umetsu S, Inui A.

Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(2):131-137. doi: 10.2177/jsci.40.131. Japanese.

24.

Pluripotent stem cell models of Blau syndrome reveal an IFN-γ-dependent inflammatory response in macrophages.

Takada S, Kambe N, Kawasaki Y, Niwa A, Honda-Ozaki F, Kobayashi K, Osawa M, Nagahashi A, Semi K, Hotta A, Asaka I, Yamada Y, Nishikomori R, Heike T, Matsue H, Nakahata T, Saito MK.

J Allergy Clin Immunol. 2018 Jan;141(1):339-349.e11. doi: 10.1016/j.jaci.2017.04.013. Epub 2017 Jun 3.

PMID:
28587749
25.

Gonadotropin levels in urine during early postnatal period in small for gestational age preterm male infants with fetal growth restriction.

Nagai S, Kawai M, Myowa-Yamakoshi M, Morimoto T, Matsukura T, Heike T.

J Perinatol. 2017 Jul;37(7):843-847. doi: 10.1038/jp.2017.55. Epub 2017 Apr 27.

PMID:
28448063
26.

Hypoxic adaptation of leukemic cells infiltrating the CNS affords a therapeutic strategy targeting VEGFA.

Kato I, Nishinaka Y, Nakamura M, Akarca AU, Niwa A, Ozawa H, Yoshida K, Mori M, Wang D, Morita M, Ueno H, Shiozawa Y, Shiraishi Y, Miyano S, Gupta R, Umeda K, Watanabe K, Koh K, Adachi S, Heike T, Saito MK, Sanada M, Ogawa S, Marafioti T, Watanabe A, Nakahata T, Enver T.

Blood. 2017 Jun 8;129(23):3126-3129. doi: 10.1182/blood-2016-06-721712. Epub 2017 Apr 19. No abstract available.

27.

Impact of post-transplant minimal residual disease on the clinical outcome of pediatric acute leukemia.

Umeda K, Iwai A, Kawaguchi K, Mikami M, Nodomi S, Saida S, Hiramatsu H, Heike T, Ohmori K, Adachi S.

Pediatr Transplant. 2017 Jun;21(4). doi: 10.1111/petr.12926. Epub 2017 Mar 31.

PMID:
28370903
28.

Reply to Walsh et al.

Kawai T, Hiejima E, Oda H, Izawa K, Yasumi T, Nishikomori R, Okamoto S, Heike T.

Eur J Hum Genet. 2017 Aug;25(8):907. doi: 10.1038/ejhg.2016.192. Epub 2017 Jan 4. No abstract available.

29.

Whole brain radiotherapy with volumetric-modulated arc therapy for pediatric intracranial embryonic carcinoma prevents permanent alopecia.

Iwai A, Umeda K, Uto M, Nihira H, Kawaguchi K, Mikami M, Nodomi S, Saida S, Hiramatsu H, Ogura K, Tanji M, Arakawa Y, Sakamoto T, Adachi S, Mizowaki T, Heike T.

Pediatr Blood Cancer. 2017 Aug;64(8). doi: 10.1002/pbc.26434. Epub 2017 Jan 2. No abstract available.

PMID:
28042910
30.

A clinical course of patient with Aicardi-Goutieres syndrome due to SAMHD1 gene abnormality.

Watanabe E, Onozawa K, Fujita T, Tomonoh Y, Ihara Y, Yasumoto S, Nishikomori R, Heike T, Hirose S.

No To Hattatsu. 2017 Jan;49(1):51-2. Japanese. No abstract available.

PMID:
30011156
31.

Long-term safety and efficacy of canakinumab in cryopyrin-associated periodic syndrome: results from an open-label, phase III pivotal study in Japanese patients.

Yokota S, Imagawa T, Nishikomori R, Takada H, Abrams K, Lheritier K, Heike T, Hara T.

Clin Exp Rheumatol. 2017 Nov-Dec;35 Suppl 108(6):19-26. Epub 2016 Dec 14.

32.

A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.

Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Oda H, Izawa K, Kawai T, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Morita S, Horiuchi H, Ohara O, Ishii E, Heike T.

J Clin Immunol. 2017 Jan;37(1):92-99. doi: 10.1007/s10875-016-0357-3. Epub 2016 Nov 28.

PMID:
27896523
33.

Efficacy of Ifosfamide-Cisplatin-Etoposide (ICE) Chemotherapy for a CNS Germinoma in a Child With Down Syndrome.

Nodomi S, Umeda K, Ueno H, Saida S, Hiramatsu H, Funaki T, Arakawa Y, Mizowaki T, Adachi S, Heike T.

J Pediatr Hematol Oncol. 2017 Jan;39(1):e39-e42.

PMID:
27879538
34.

Dasatinib induces autophagy in mice with Bcr-Abl-positive leukemia.

Morita M, Nishinaka Y, Kato I, Saida S, Hiramatsu H, Kamikubo Y, Heike T, Nakahata T, Adachi S.

Int J Hematol. 2017 Mar;105(3):335-340. doi: 10.1007/s12185-016-2137-5. Epub 2016 Nov 15.

PMID:
27848186
35.

Screening for secondary hyperparathyroidism in preterm infants.

Dowa Y, Kawai M, Kanazawa H, Iwanaga K, Matsukura T, Heike T.

Pediatr Int. 2016 Oct;58(10):988-992. doi: 10.1111/ped.12961. Epub 2016 Jun 8.

PMID:
26916393
36.

Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children.

Eroglu FK, Kasapcopur O, Beşbaş N, Ozaltin F, Bilginer Y, Barut K, Mensa-Vilaro A, Nakagawa K, Heike T, Nishikomori R, Arostegui J, Ozen S.

Clin Exp Rheumatol. 2016 Sep-Oct;34(6 Suppl 102):S115-S120. Epub 2016 May 10.

PMID:
27191192
37.

Identification of a High-Frequency Somatic NLRC4 Mutation as a Cause of Autoinflammation by Pluripotent Cell-Based Phenotype Dissection.

Kawasaki Y, Oda H, Ito J, Niwa A, Tanaka T, Hijikata A, Seki R, Nagahashi A, Osawa M, Asaka I, Watanabe A, Nishimata S, Shirai T, Kawashima H, Ohara O, Nakahata T, Nishikomori R, Heike T, Saito MK.

Arthritis Rheumatol. 2017 Feb;69(2):447-459. doi: 10.1002/art.39960.

38.

Secondary bladder amyloidosis with familial Mediterranean fever in a living donor kidney transplant recipient: a case report.

Imamura S, Narita S, Nishikomori R, Tsuruta H, Numakura K, Maeno A, Saito M, Inoue T, Tsuchiya N, Nanjo H, Heike T, Satoh S, Habuchi T.

BMC Res Notes. 2016 Oct 19;9(1):473.

39.

A portable platform for stepwise hematopoiesis from human pluripotent stem cells within PET-reinforced collagen sponges.

Sugimine Y, Niwa A, Matsubara H, Kobayashi K, Tabata Y, Heike T, Nakahata T, Saito MK.

Int J Hematol. 2016 Dec;104(6):647-660. Epub 2016 Sep 6.

PMID:
27599982
40.

A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases.

Nanishi E, Hoshina T, Takada H, Ishimura M, Nishio H, Uehara T, Mizuno Y, Hasegawa S, Ohga S, Nagao M, Igarashi M, Yajima S, Kusumoto Y, Onishi N, Sasahara Y, Yasumi T, Heike T, Hara T; PID-Infection Study Group.

J Infect. 2016 Oct;73(4):358-68. doi: 10.1016/j.jinf.2016.07.018. Epub 2016 Aug 4.

PMID:
27498293
41.

Nod2-Nodosome in a Cell-Free System: Implications in Pathogenesis and Drug Discovery for Blau Syndrome and Early-Onset Sarcoidosis.

Iwasaki T, Kaneko N, Ito Y, Takeda H, Sawasaki T, Heike T, Migita K, Agematsu K, Kawakami A, Morikawa S, Mokuda S, Kurata M, Masumoto J.

ScientificWorldJournal. 2016;2016:2597376. doi: 10.1155/2016/2597376. Epub 2016 Jun 15.

42.

Febrile attacks triggered by milk allergy in an infant with mevalonate kinase deficiency.

Nakashimai H, Miyake F, Ohki S, Hattori S, Matsubayashi T, Izawa K, Nishikomori R, Heike T, Honda Y, Shigematsu Y.

Rheumatol Int. 2016 Oct;36(10):1477-8. doi: 10.1007/s00296-016-3522-3. Epub 2016 Jul 7. No abstract available.

43.

Brief Report: Late-Onset Cryopyrin-Associated Periodic Syndrome Due to Myeloid-Restricted Somatic NLRP3 Mosaicism.

Mensa-Vilaro A, Teresa Bosque M, Magri G, Honda Y, Martínez-Banaclocha H, Casorran-Berges M, Sintes J, González-Roca E, Ruiz-Ortiz E, Heike T, Martínez-Garcia JJ, Baroja-Mazo A, Cerutti A, Nishikomori R, Yagüe J, Pelegrín P, Delgado-Beltran C, Aróstegui JI.

Arthritis Rheumatol. 2016 Dec;68(12):3035-3041. doi: 10.1002/art.39770.

44.

Impact of pretransplant minimal residual disease on the post-transplant outcome of pediatric acute lymphoblastic leukemia.

Umeda K, Hiramatsu H, Kawaguchi K, Iwai A, Mikami M, Nodomi S, Saida S, Heike T, Ohomori K, Adachi S.

Pediatr Transplant. 2016 Aug;20(5):692-6. doi: 10.1111/petr.12732. Epub 2016 Jun 3.

PMID:
27256540
45.

A Pediatric Case of Metastatic Conventional Parosteal Osteosarcoma Treated With Multidrug Chemotherapy.

Nodomi S, Umeda K, Okamoto T, Saida S, Hiramatsu H, Watanabe K, Adachi S, Heike T.

Pediatr Blood Cancer. 2016 Aug;63(8):1471-3. doi: 10.1002/pbc.26052. Epub 2016 May 3.

PMID:
27149276
46.

CD146 is a novel marker for highly tumorigenic cells and a potential therapeutic target in malignant rhabdoid tumor.

Nodomi S, Umeda K, Saida S, Kinehara T, Hamabata T, Daifu T, Kato I, Hiramatsu H, Watanabe KI, Kuwahara Y, Iehara T, Adachi S, Konishi E, Nakahata T, Hosoi H, Heike T.

Oncogene. 2016 Oct 6;35(40):5317-5327. doi: 10.1038/onc.2016.72. Epub 2016 Apr 4.

47.

Central nervous system recurrence of desmoplastic small round cell tumor following aggressive multimodal therapy: A case report.

Umeda K, Saida S, Yamaguchi H, Okamoto S, Okamoto T, Kato I, Hiramatsu H, Imai T, Kodaira T, Heike T, Adachi S, Watanabe KI.

Oncol Lett. 2016 Jan;11(1):856-860. Epub 2015 Nov 17.

48.

Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease.

Hiejima E, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Saida S, Umeda K, Hiramatsu H, Adachi S, Izawa K, Kawai T, Yasumi T, Nishikomori R, Heike T.

Dig Endosc. 2016 Jul;28(5):548-55. doi: 10.1111/den.12604. Epub 2016 Feb 18.

PMID:
26773564
49.

Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.

Saida S, Umeda K, Yasumi T, Matsumoto A, Kato I, Hiramatsu H, Ohara O, Heike T, Adachi S.

Pediatr Transplant. 2016 Mar;20(2):333-6. doi: 10.1111/petr.12667. Epub 2016 Jan 8.

PMID:
26748574
50.

[A girl with dyslexia suspected to have Irlen syndrome, completely relieved by wearing tinted lenses].

Kusano Y, Awaya T, Saito K, Yoshida T, Ide M, Kato T, Heike T, Kato T.

No To Hattatsu. 2015 Nov;47(6):445-8. Japanese.

PMID:
26717646

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