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Items: 1 to 50 of 356

1.

The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation.

Moriya K, Kadowaki S, Nakano T, Akarcan SE, Kutukculer N, Aksu G, Sasahara Y, Kure S, Ohnishi H, Casanova JL, Puel A, Fukao T.

J Clin Immunol. 2020 Mar 17. doi: 10.1007/s10875-020-00770-1. [Epub ahead of print] No abstract available.

PMID:
32185578
2.

Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation.

Moriya K, Suzuki T, Uchida N, Nakano T, Katayama S, Irie M, Rikiishi T, Niizuma H, Okada S, Imai K, Sasahara Y, Kure S.

Int J Hematol. 2020 Mar 16. doi: 10.1007/s12185-020-02860-7. [Epub ahead of print]

PMID:
32180118
3.

Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice.

Wada Y, Kikuchi A, Kaga A, Shimizu N, Ito J, Onuma R, Fujishima F, Totsune E, Sato R, Niihori T, Shirota M, Funayama R, Sato K, Nakazawa T, Nakayama K, Aoki Y, Aiba S, Nakagawa K, Kure S.

PLoS Genet. 2020 Feb 26;16(2):e1008628. doi: 10.1371/journal.pgen.1008628. eCollection 2020 Feb.

4.

Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.

Niitsuma S, Kudo H, Kikuchi A, Hayashi T, Kumakura S, Kobayashi S, Okuyama Y, Kumagai N, Niihori T, Aoki Y, So T, Funayama R, Nakayama K, Shirota M, Kondo S, Kagami S, Tsukaguchi H, Iijima K, Kure S, Ishii N.

Int Immunol. 2019 Dec 24. pii: dxz081. doi: 10.1093/intimm/dxz081. [Epub ahead of print]

PMID:
31954058
5.

Study profile of The Tohoku Medical Megabank Community-Based Cohort Study.

Hozawa A, Tanno K, Nakaya N, Nakamura T, Tsuchiya N, Hirata T, Narita A, Kogure M, Nochioka K, Sasaki R, Takanashi N, Otsuka K, Sakata K, Kuriyama S, Kikuya M, Tanabe O, Sugawara J, Suzuki K, Suzuki Y, Kodama EN, Fuse N, Kiyomoto H, Tomita H, Uruno A, Hamanaka Y, Metoki H, Ishikuro M, Obara T, Kobayashi T, Kitatani K, Takai-Igarashi T, Ogishima S, Satoh M, Ohmomo H, Tsuboi A, Egawa S, Ishii T, Ito K, Ito S, Taki Y, Minegishi N, Ishii N, Nagasaki M, Igarashi K, Koshiba S, Shimizu R, Tamiya G, Nakayama K, Motohashi H, Yasuda J, Shimizu A, Hachiya T, Shiwa Y, Tominaga T, Tanaka H, Oyama K, Tanaka R, Kawame H, Fukushima A, Ishigaki Y, Tokutomi T, Osumi N, Kobayashi T, Nagami F, Hashizume H, Arai T, Kawaguchi Y, Higuchi S, Sakaida M, Endo R, Nishizuka S, Tsuji I, Hitomi J, Nakamura M, Ogasawara K, Yaegashi N, Kinoshita K, Kure S, Sakai A, Kobayashi S, Sobue K, Sasaki M, Yamamoto M.

J Epidemiol. 2020 Jan 11. doi: 10.2188/jea.JE20190271. [Epub ahead of print]

6.

Multiple measurements of the urinary sodium-to-potassium ratio strongly related home hypertension: TMM Cohort Study.

Kogure M, Hirata T, Nakaya N, Tsuchiya N, Nakamura T, Narita A, Miyagawa K, Koshimizu H, Obara T, Metoki H, Uruno A, Kikuya M, Sugawara J, Kuriyama S, Tsuji I, Kure S, Hozawa A.

Hypertens Res. 2020 Jan;43(1):62-71. doi: 10.1038/s41440-019-0335-2. Epub 2019 Sep 27.

PMID:
31562419
7.

Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2.

Inui T, Iwama K, Miyabayashi T, Sato R, Okubo Y, Endo W, Togashi N, Kakisaka Y, Kikuchi A, Mizuguchi T, Kure S, Matsumoto N, Haginoya K.

Eur J Med Genet. 2020 Mar;63(3):103769. doi: 10.1016/j.ejmg.2019.103769. Epub 2019 Sep 16.

PMID:
31536832
8.

Reduced sleep efficiency, measured using an objective device, was related to an increased prevalence of home hypertension in Japanese adults.

Hirata T, Nakamura T, Kogure M, Tsuchiya N, Narita A, Miyagawa K, Nochioka K, Uruno A, Obara T, Nakaya N, Metoki H, Kikuya M, Sugawara J, Kuriyama S, Tsuji I, Kure S, Hozawa A.

Hypertens Res. 2020 Jan;43(1):23-29. doi: 10.1038/s41440-019-0329-0. Epub 2019 Sep 18.

PMID:
31534189
9.

Incidence of BRAF V600E mutation in patients with papillary thyroid carcinoma: a single-institution experience.

Kure S, Ishino K, Kudo M, Wada R, Saito M, Nagaoka R, Sugitani I, Naito Z.

J Int Med Res. 2019 Nov;47(11):5560-5572. doi: 10.1177/0300060519873481. Epub 2019 Sep 18. No abstract available.

10.

Cohort Profile: Tohoku Medical Megabank Project Birth and Three-Generation Cohort Study (TMM BirThree Cohort Study): Rationale, Progress and Perspective.

Kuriyama S, Metoki H, Kikuya M, Obara T, Ishikuro M, Yamanaka C, Nagai M, Matsubara H, Kobayashi T, Sugawara J, Tamiya G, Hozawa A, Nakaya N, Tsuchiya N, Nakamura T, Narita A, Kogure M, Hirata T, Tsuji I, Nagami F, Fuse N, Arai T, Kawaguchi Y, Higuchi S, Sakaida M, Suzuki Y, Osumi N, Nakayama K, Ito K, Egawa S, Chida K, Kodama E, Kiyomoto H, Ishii T, Tsuboi A, Tomita H, Taki Y, Kawame H, Suzuki K, Ishii N, Ogishima S, Mizuno S, Takai-Igarashi T, Minegishi N, Yasuda J, Igarashi K, Shimizu R, Nagasaki M, Tanabe O, Koshiba S, Hashizume H, Motohashi H, Tominaga T, Ito S, Tanno K, Sakata K, Shimizu A, Hitomi J, Sasaki M, Kinoshita K, Tanaka H, Kobayashi T, Kure S, Yaegashi N, Yamamoto M; Tohoku Medical Megabank Project Study Group .

Int J Epidemiol. 2019 Aug 25. pii: dyz169. doi: 10.1093/ije/dyz169. [Epub ahead of print] No abstract available.

PMID:
31504573
11.

Effectiveness of seasonal inactivated influenza vaccination in Japanese schoolchildren: an epidemiologic study at the community level.

Kuniyoshi Y, Obara T, Ishikuro M, Matsubara H, Nagai M, Murakami K, Noda A, Kikuya M, Kure S, Kuriyama S.

Hum Vaccin Immunother. 2020;16(2):295-300. doi: 10.1080/21645515.2019.1655833. Epub 2019 Sep 20.

PMID:
31424311
12.

The guanylate cyclase C agonist linaclotide ameliorates the gut-cardio-renal axis in an adenine-induced mouse model of chronic kidney disease.

Nanto-Hara F, Kanemitsu Y, Fukuda S, Kikuchi K, Asaji K, Saigusa D, Iwasaki T, Ho HJ, Mishima E, Suzuki T, Suzuki C, Tsukimi T, Matsuhashi T, Oikawa Y, Akiyama Y, Kure S, Owada Y, Tomioka Y, Soga T, Ito S, Abe T.

Nephrol Dial Transplant. 2020 Feb 1;35(2):250-264. doi: 10.1093/ndt/gfz126.

PMID:
31411705
13.

Long-term outcome of a group of Japanese children with myelin-oligodendrocyte glycoprotein encephalomyelitis without preventive immunosuppressive therapy.

Hino-Fukuyo N, Haginoya K, Takahashi T, Nakashima I, Fujihara K, Takai Y, Akasaka M, Kure S.

Brain Dev. 2019 Oct;41(9):790-795. doi: 10.1016/j.braindev.2019.06.004. Epub 2019 Jul 4.

PMID:
31281008
14.

Superficial Myofibroblastoma in the Vulva Mimicking Aggressive Angiomyxoma: A Case Report and Review of the Literature.

Peng WX, Wada R, Kure S, Fukunaga M, Naito Z.

Case Rep Pathol. 2019 May 26;2019:1582714. doi: 10.1155/2019/1582714. eCollection 2019.

15.

Construction of JRG (Japanese reference genome) with single-molecule real-time sequencing.

Nagasaki M, Kuroki Y, Shibata TF, Katsuoka F, Mimori T, Kawai Y, Minegishi N, Hozawa A, Kuriyama S, Suzuki Y, Kawame H, Nagami F, Takai-Igarashi T, Ogishima S, Kojima K, Misawa K, Tanabe O, Fuse N, Tanaka H, Yaegashi N, Kinoshita K, Kure S, Yasuda J, Yamamoto M.

Hum Genome Var. 2019 Jun 7;6:27. doi: 10.1038/s41439-019-0057-7. eCollection 2019.

16.

Prefabricated Temporary Housing and Eczema or Respiratory Symptoms in Schoolchildren after the Great East Japan Earthquake: The ToMMo Child Health Study.

Kuniyoshi Y, Kikuya M, Miyashita M, Yamanaka C, Ishikuro M, Obara T, Metoki H, Nakaya N, Nagami F, Tomita H, Hozawa A, Tsuji I, Kure S, Yaegashi N, Kuriyama S.

Disaster Med Public Health Prep. 2019 Dec;13(5-6):905-911. doi: 10.1017/dmp.2019.8.

PMID:
31156072
17.

Toll‑like receptor 4 plays a tumor‑suppressive role in cutaneous squamous cell carcinoma.

Mikami E, Kudo M, Ohashi R, Kawahara K, Kawamoto Y, Teduka K, Fujii T, Kitamura T, Kure S, Ishino K, Sakatani T, Wada R, Saeki H, Naito Z.

Int J Oncol. 2019 Jun;54(6):2179-2188. doi: 10.3892/ijo.2019.4790. Epub 2019 Apr 17.

PMID:
31081044
18.

Gut microbiome-derived phenyl sulfate contributes to albuminuria in diabetic kidney disease.

Kikuchi K, Saigusa D, Kanemitsu Y, Matsumoto Y, Thanai P, Suzuki N, Mise K, Yamaguchi H, Nakamura T, Asaji K, Mukawa C, Tsukamoto H, Sato T, Oikawa Y, Iwasaki T, Oe Y, Tsukimi T, Fukuda NN, Ho HJ, Nanto-Hara F, Ogura J, Saito R, Nagao S, Ohsaki Y, Shimada S, Suzuki T, Toyohara T, Mishima E, Shima H, Akiyama Y, Akiyama Y, Ichijo M, Matsuhashi T, Matsuo A, Ogata Y, Yang CC, Suzuki C, Breeggemann MC, Heymann J, Shimizu M, Ogawa S, Takahashi N, Suzuki T, Owada Y, Kure S, Mano N, Soga T, Wada T, Kopp JB, Fukuda S, Hozawa A, Yamamoto M, Ito S, Wada J, Tomioka Y, Abe T.

Nat Commun. 2019 Apr 23;10(1):1835. doi: 10.1038/s41467-019-09735-4.

19.

Association of Feeding Practice with Childhood Overweight and/or Obesity in Affected Areas Before and After the Great East Japan Earthquake.

Kuniyoshi Y, Kikuya M, Matsubara H, Ishikuro M, Obara T, Kure S, Kuriyama S.

Breastfeed Med. 2019 Jul/Aug;14(6):382-389. doi: 10.1089/bfm.2018.0254. Epub 2019 Apr 13.

PMID:
30985196
20.

Recurrent de novo MAPK8IP3 variants cause neurological phenotypes.

Iwasawa S, Yanagi K, Kikuchi A, Kobayashi Y, Haginoya K, Matsumoto H, Kurosawa K, Ochiai M, Sakai Y, Fujita A, Miyake N, Niihori T, Shirota M, Funayama R, Nonoyama S, Ohga S, Kawame H, Nakayama K, Aoki Y, Matsumoto N, Kaname T, Matsubara Y, Shoji W, Kure S.

Ann Neurol. 2019 Jun;85(6):927-933. doi: 10.1002/ana.25481. Epub 2019 Apr 25.

PMID:
30945334
21.

The prevalence of GALM mutations that cause galactosemia: A database of functionally evaluated variants.

Iwasawa S, Kikuchi A, Wada Y, Arai-Ichinoi N, Sakamoto O, Tamiya G, Kure S.

Mol Genet Metab. 2019 Apr;126(4):362-367. doi: 10.1016/j.ymgme.2019.01.018. Epub 2019 Mar 18.

PMID:
30910422
22.

Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals.

Yamaguchi-Kabata Y, Yasuda J, Uruno A, Shimokawa K, Koshiba S, Suzuki Y, Fuse N, Kawame H, Tadaka S, Nagasaki M, Kojima K, Katsuoka F, Kumada K, Tanabe O, Tamiya G, Yaegashi N, Kinoshita K, Yamamoto M, Kure S; Tohoku Medical Megabank Project Study Group.

Hum Genet. 2019 Apr;138(4):389-409. doi: 10.1007/s00439-019-01998-7. Epub 2019 Mar 18.

PMID:
30887117
23.

Successful use of an artificial placenta to support extremely preterm ovine fetuses at the border of viability.

Usuda H, Watanabe S, Saito M, Sato S, Musk GC, Fee ME, Carter S, Kumagai Y, Takahashi T, Kawamura MS, Hanita T, Kure S, Yaegashi N, Newnham JP, Kemp MW.

Am J Obstet Gynecol. 2019 Jul;221(1):69.e1-69.e17. doi: 10.1016/j.ajog.2019.03.001. Epub 2019 Mar 7.

PMID:
30853365
24.

Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndrome.

Suzuki-Muromoto S, Miyabayashi T, Nagai K, Yamamura-Suzuki S, Anzai M, Takezawa Y, Sato R, Okubo Y, Endo W, Inui T, Togashi N, Kikuchi A, Niihori T, Aoki Y, Kure S, Haginoya K.

J Hum Genet. 2019 May;64(5):499-504. doi: 10.1038/s10038-019-0579-3. Epub 2019 Mar 6.

PMID:
30842599
25.

Relationship between genetic alterations and clinicopathological characteristics of papillary thyroid carcinoma.

Kure S, Wada R, Naito Z.

Med Mol Morphol. 2019 Dec;52(4):181-186. doi: 10.1007/s00795-019-00217-6. Epub 2019 Feb 20. Review.

PMID:
30788603
26.

Maternity Log study: a longitudinal lifelog monitoring and multiomics analysis for the early prediction of complicated pregnancy.

Sugawara J, Ochi D, Yamashita R, Yamauchi T, Saigusa D, Wagata M, Obara T, Ishikuro M, Tsunemoto Y, Harada Y, Shibata T, Mimori T, Kawashima J, Katsuoka F, Igarashi-Takai T, Ogishima S, Metoki H, Hashizume H, Fuse N, Minegishi N, Koshiba S, Tanabe O, Kuriyama S, Kinoshita K, Kure S, Yaegashi N, Yamamoto M, Hiyama S, Nagasaki M.

BMJ Open. 2019 Feb 19;9(2):e025939. doi: 10.1136/bmjopen-2018-025939.

27.

Expression of protein disulfide isomerase A3 and its clinicopathological association in gastric cancer.

Shimoda T, Wada R, Kure S, Ishino K, Kudo M, Ohashi R, Fujita I, Uchida E, Yoshida H, Naito Z.

Oncol Rep. 2019 Apr;41(4):2265-2272. doi: 10.3892/or.2019.6999. Epub 2019 Feb 5.

PMID:
30720117
28.

Downregulation of protein disulfide‑isomerase A3 expression inhibits cell proliferation and induces apoptosis through STAT3 signaling in hepatocellular carcinoma.

Kondo R, Ishino K, Wada R, Takata H, Peng WX, Kudo M, Kure S, Kaneya Y, Taniai N, Yoshida H, Naito Z.

Int J Oncol. 2019 Apr;54(4):1409-1421. doi: 10.3892/ijo.2019.4710. Epub 2019 Feb 4.

PMID:
30720090
29.

Tetrahydrobipterin-responsive phenylalanine hydroxylase deficiency.

Kure S, Shintaku H.

J Hum Genet. 2019 Feb;64(2):67-71. doi: 10.1038/s10038-018-0529-5. Epub 2018 Nov 30. Review. No abstract available.

PMID:
30504912
30.

Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare.

Yasuda J, Kinoshita K, Katsuoka F, Danjoh I, Sakurai-Yageta M, Motoike IN, Kuroki Y, Saito S, Kojima K, Shirota M, Saigusa D, Otsuki A, Kawashima J, Yamaguchi-Kabata Y, Tadaka S, Aoki Y, Mimori T, Kumada K, Inoue J, Makino S, Kuriki M, Fuse N, Koshiba S, Tanabe O, Nagasaki M, Tamiya G, Shimizu R, Takai-Igarashi T, Ogishima S, Hozawa A, Kuriyama S, Sugawara J, Tsuboi A, Kiyomoto H, Ishii T, Tomita H, Minegishi N, Suzuki Y, Suzuki K, Kawame H, Tanaka H, Taki Y, Yaegashi N, Kure S, Nagami F; Tohoku Medical Megabank Project Study Group, Kosaki K, Sutoh Y, Hachiya T, Shimizu A, Sasaki M, Yamamoto M.

J Biochem. 2019 Feb 1;165(2):139-158. doi: 10.1093/jb/mvy096.

PMID:
30452759
31.

Biallelic GALM pathogenic variants cause a novel type of galactosemia.

Wada Y, Kikuchi A, Arai-Ichinoi N, Sakamoto O, Takezawa Y, Iwasawa S, Niihori T, Nyuzuki H, Nakajima Y, Ogawa E, Ishige M, Hirai H, Sasai H, Fujiki R, Shirota M, Funayama R, Yamamoto M, Ito T, Ohara O, Nakayama K, Aoki Y, Koshiba S, Fukao T, Kure S.

Genet Med. 2019 Jun;21(6):1286-1294. doi: 10.1038/s41436-018-0340-x. Epub 2018 Oct 19.

PMID:
30451973
32.

Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexes.

Umeki I, Niihori T, Abe T, Kanno SI, Okamoto N, Mizuno S, Kurosawa K, Nagasaki K, Yoshida M, Ohashi H, Inoue SI, Matsubara Y, Fujiwara I, Kure S, Aoki Y.

Hum Genet. 2019 Jan;138(1):21-35. doi: 10.1007/s00439-018-1951-7. Epub 2018 Oct 27.

PMID:
30368668
33.

Successful control of maternal phenylketonuria by tetrahydrobiopterin.

Sakamoto O, Arai-Ichinoi N, Murayama K, Kure S.

Pediatr Int. 2018 Oct;60(10):985-986. doi: 10.1111/ped.13678. No abstract available.

PMID:
30345699
34.

Potential identification of vitamin B6 responsiveness in autism spectrum disorder utilizing phenotype variables and machine learning methods.

Obara T, Ishikuro M, Tamiya G, Ueki M, Yamanaka C, Mizuno S, Kikuya M, Metoki H, Matsubara H, Nagai M, Kobayashi T, Kamiyama M, Watanabe M, Kakuta K, Ouchi M, Kurihara A, Fukuchi N, Yasuhara A, Inagaki M, Kaga M, Kure S, Kuriyama S.

Sci Rep. 2018 Oct 4;8(1):14840. doi: 10.1038/s41598-018-33110-w.

35.

Attachment Disorder and Early Media Exposure: Neurobehavioral symptoms mimicking autism spectrum disorder.

Numata-Uematsu Y, Yokoyama H, Sato H, Endo W, Uematsu M, Nara C, Kure S.

J Med Invest. 2018;65(3.4):280-282. doi: 10.2152/jmi.65.280.

36.

Reply to: Avoid valproate in patients with IARS2 mutations.

Takezawa Y, Fujie H, Kikuchi A, Kure S.

Brain Dev. 2019 Jan;41(1):122. doi: 10.1016/j.braindev.2018.09.004. Epub 2018 Sep 22. No abstract available.

PMID:
30253902
37.

[18F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome.

Haginoya K, Togashi N, Kaneta T, Hino-Fukuyo N, Ishitobi M, Kakisaka Y, Uematsu M, Inui T, Okubo Y, Sato R, Miyabayashi T, Arai A, Ogiwara I, Mazaki E, Yamakawa K, Iinuma K, Kure S.

Epilepsy Res. 2018 Nov;147:9-14. doi: 10.1016/j.eplepsyres.2018.08.008. Epub 2018 Aug 27.

PMID:
30176532
38.

Reply to: A genomic cause of cerebral palsy should not change the clinical classification.

Takezawa Y, Kikuchi A, Haginoya K, Kure S.

Ann Clin Transl Neurol. 2018 Jun 22;5(8):1012. doi: 10.1002/acn3.585. eCollection 2018 Aug. No abstract available.

39.

Menkes disease: Oral administration of glyoxal-bis(N(4)-methylthiosemicarbazonato)-copper(II) rescues the macular mouse.

Munakata M, Kodama H, Tani N, Kimura K, Takahashi H, Maruyama K, Sakamoto Y, Kure S.

Pediatr Res. 2018 Nov;84(5):770-777. doi: 10.1038/s41390-018-0116-7. Epub 2018 Jul 17.

PMID:
30127521
40.

Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome.

Takezawa Y, Fujie H, Kikuchi A, Niihori T, Funayama R, Shirota M, Nakayama K, Aoki Y, Sasaki M, Kure S.

Brain Dev. 2018 Nov;40(10):934-938. doi: 10.1016/j.braindev.2018.06.010. Epub 2018 Jul 2.

PMID:
30041933
41.

Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients.

Kawashima S, Nakamura A, Inoue T, Matsubara K, Horikawa R, Wakui K, Takano K, Fukushima Y, Tatematsu T, Mizuno S, Tsubaki J, Kure S, Matsubara Y, Ogata T, Fukami M, Kagami M.

J Clin Endocrinol Metab. 2018 Jun 1;103(6):2083-2088. doi: 10.1210/jc.2017-02780.

PMID:
29878129
42.

Early excessive growth with distinct seasonality in preschool obesity.

Isojima T, Kato N, Yokoya S, Ono A, Tanaka T, Yokomichi H, Yamagata Z, Tanaka S, Matsubara H, Ishikuro M, Kikuya M, Chida S, Hosoya M, Kuriyama S, Kure S.

Arch Dis Child. 2019 Jan;104(1):53-57. doi: 10.1136/archdischild-2018-314862. Epub 2018 Jun 5.

PMID:
29871900
43.

Asymptomatic left atrial appendage aneurysm (LAAA) with pericardial defect in a 1-year-old girl.

Ota C, Kimura M, Kitami M, Kure S.

BMJ Case Rep. 2018 Jun 4;2018. pii: bcr-2018-224573. doi: 10.1136/bcr-2018-224573. No abstract available.

44.
45.

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.

46.

Genomic analysis identifies masqueraders of full-term cerebral palsy.

Takezawa Y, Kikuchi A, Haginoya K, Niihori T, Numata-Uematsu Y, Inui T, Yamamura-Suzuki S, Miyabayashi T, Anzai M, Suzuki-Muromoto S, Okubo Y, Endo W, Togashi N, Kobayashi Y, Onuma A, Funayama R, Shirota M, Nakayama K, Aoki Y, Kure S.

Ann Clin Transl Neurol. 2018 Mar 26;5(5):538-551. doi: 10.1002/acn3.551. eCollection 2018 May.

47.

2-Deoxy-d-glucose increases GFAT1 phosphorylation resulting in endoplasmic reticulum-related apoptosis via disruption of protein N-glycosylation in pancreatic cancer cells.

Ishino K, Kudo M, Peng WX, Kure S, Kawahara K, Teduka K, Kawamoto Y, Kitamura T, Fujii T, Yamamoto T, Wada R, Naito Z.

Biochem Biophys Res Commun. 2018 Jun 27;501(3):668-673. doi: 10.1016/j.bbrc.2018.05.041.

48.

Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project.

Koshiba S, Motoike I, Saigusa D, Inoue J, Shirota M, Katoh Y, Katsuoka F, Danjoh I, Hozawa A, Kuriyama S, Minegishi N, Nagasaki M, Takai-Igarashi T, Ogishima S, Fuse N, Kure S, Tamiya G, Tanabe O, Yasuda J, Kinoshita K, Yamamoto M.

Genes Cells. 2018 Jun;23(6):406-417. doi: 10.1111/gtc.12588. Epub 2018 Apr 27. Review.

49.

Three case reports of radiation-induced glioblastoma after complete remission of acute lymphoblastic leukemia.

Kajitani T, Kanamori M, Saito R, Watanabe Y, Suzuki H, Watanabe M, Kure S, Tominaga T.

Brain Tumor Pathol. 2018 Apr;35(2):114-122. doi: 10.1007/s10014-018-0316-1. Epub 2018 Apr 17.

PMID:
29666969
50.

Mental Development and Surgical Prognosis of Pai Syndrome: A Case Report and Review of the Literature.

Imai Y, Kure S, Nara C, Takagi N, Tachi M.

Cleft Palate Craniofac J. 2019 Feb;56(2):273-279. doi: 10.1177/1055665618771419. Epub 2018 Apr 17. Review.

PMID:
29665340

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