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Items: 1 to 50 of 343

1.

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 Jul 4. pii: S0387-7604(18)30626-0. doi: 10.1016/j.braindev.2019.06.004. [Epub ahead of print]

PMID:
31281008
2.

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.

3.

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.

4.

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 Jun 3:1-7. doi: 10.1017/dmp.2019.8. [Epub ahead of print]

PMID:
31156072
5.

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
6.

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.

7.

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
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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

Kure S, Wada R, Naito Z.

Med Mol Morphol. 2019 Feb 20. doi: 10.1007/s00795-019-00217-6. [Epub ahead of print] Review.

PMID:
30788603
14.

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.

15.

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
16.

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
17.

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
18.

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
19.

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
20.

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
21.

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
22.

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.

23.

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.

24.

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
25.

[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
26.

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.

27.

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
28.

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
29.

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
30.

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
31.

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.

32.
33.

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.

34.

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.

35.

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.

36.

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.

37.

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
38.

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.

PMID:
29665340
39.

Severity of eczema and mental health problems in Japanese schoolchildren: 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, Yamamoto M, Kuriyama S.

Allergol Int. 2018 Oct;67(4):481-486. doi: 10.1016/j.alit.2018.02.009. Epub 2018 Apr 13.

40.

Effect of the Fukushima earthquake on weight in early childhood: a retrospective analysis.

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

BMJ Paediatr Open. 2018 Feb 7;2(1):e000229. doi: 10.1136/bmjpo-2017-000229. eCollection 2018.

41.

A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in INSR.

Saito-Hakoda A, Nishii A, Uchida T, Kikuchi A, Kanno J, Fujiwara I, Kure S.

Clin Pediatr Endocrinol. 2018;27(1):53-57. doi: 10.1297/cpe.27.53. Epub 2018 Jan 30. No abstract available.

42.

Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation.

Nakamura H, Uematsu M, Numata-Uematsu Y, Abe Y, Endo W, Kikuchi A, Takezawa Y, Funayama R, Shirota M, Nakayama K, Niihori T, Aoki Y, Haginoya K, Kure S.

Brain Dev. 2018 May;40(5):410-414. doi: 10.1016/j.braindev.2017.12.015. Epub 2018 Feb 1.

PMID:
29395664
43.

Somatic mosaic deletions involving SCN1A cause Dravet syndrome.

Nakayama T, Ishii A, Yoshida T, Nasu H, Shimojima K, Yamamoto T, Kure S, Hirose S.

Am J Med Genet A. 2018 Mar;176(3):657-662. doi: 10.1002/ajmg.a.38596. Epub 2018 Jan 17.

PMID:
29341473
44.

Impact of the Great East Japan Earthquake on Body Mass Index, Weight, and Height of Infants and Toddlers: An Infant Survey.

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

J Epidemiol. 2018 May 5;28(5):237-244. doi: 10.2188/jea.JE20170006. Epub 2018 Jan 13.

45.

Evolution into moyamoya disease in an infant with internal carotid artery aneurysms.

Tanaka R, Takahashi S, Okano S, Okayama A, Suzuki N, Kure S, Azuma H.

eNeurologicalSci. 2017 Jan 31;6:80-82. doi: 10.1016/j.ensci.2017.01.002. eCollection 2017 Mar.

46.

A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation.

Okubo Y, Endo W, Inui T, Suzuki-Muromoto S, Miyabayashi T, Togashi N, Sato R, Arai-Ichinoi N, Kikuchi A, Kure S, Haginoya K.

Brain Dev. 2018 Apr;40(4):334-338. doi: 10.1016/j.braindev.2017.11.011. Epub 2017 Dec 16.

PMID:
29254829
47.

Parapharyngeal neuroglial heterotopia appearing as high uptake on 18F-FDG PET: case report and literature review of radiographical findings.

Kameyama M, Kawaguchi T, Niizuma H, Ogawa T, Watanabe K, Hayashi T, Sato K, Kanamori M, Watanabe M, Katori Y, Kure S, Tominaga T.

Acta Neurochir (Wien). 2018 Apr;160(4):801-809. doi: 10.1007/s00701-017-3403-x. Epub 2017 Dec 2. Review.

PMID:
29197937
48.

Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.

Yamaguchi-Kabata Y, Yasuda J, Tanabe O, Suzuki Y, Kawame H, Fuse N, Nagasaki M, Kawai Y, Kojima K, Katsuoka F, Saito S, Danjoh I, Motoike IN, Yamashita R, Koshiba S, Saigusa D, Tamiya G, Kure S, Yaegashi N, Kawaguchi Y, Nagami F, Kuriyama S, Sugawara J, Minegishi N, Hozawa A, Ogishima S, Kiyomoto H, Takai-Igarashi T; ToMMo Study Group, Kinoshita K, Yamamoto M.

J Hum Genet. 2018 Feb;63(2):213-230. doi: 10.1038/s10038-017-0347-1. Epub 2017 Dec 1.

PMID:
29192238
49.

Earlier BMI rebound and lower pre-rebound BMI as risk of obesity among Japanese preschool children.

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

Int J Obes (Lond). 2018 Jan;42(1):52-58. doi: 10.1038/ijo.2017.242. Epub 2017 Oct 3.

PMID:
29064477
50.

Suppressive effects of RXR agonist PA024 on adrenal CYP11B2 expression, aldosterone secretion and blood pressure.

Suzuki D, Saito-Hakoda A, Ito R, Shimizu K, Parvin R, Shimada H, Noro E, Suzuki S, Fujiwara I, Kagechika H, Rainey WE, Kure S, Ito S, Yokoyama A, Sugawara A.

PLoS One. 2017 Aug 11;12(8):e0181055. doi: 10.1371/journal.pone.0181055. eCollection 2017.

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