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Items: 1 to 50 of 186

1.

IGF2 Mutations: Report of Five Cases, Review of the Literature, and Comparison with H19/IGF2:IG-DMR Epimutations.

Masunaga Y, Inoue T, Yamoto K, Fujisawa Y, Sato Y, Kawashima-Sonoyama Y, Morisada N, Iijima K, Ohata Y, Namba N, Suzumura H, Kuribayashi R, Yamaguchi Y, Yoshihashi H, Fukami M, Saitsu H, Kagami M, Ogata T.

J Clin Endocrinol Metab. 2019 Sep 23. pii: dgz034. doi: 10.1210/clinem/dgz034. [Epub ahead of print]

PMID:
31544945
2.

The potential of zooplankton in constraining chytrid epidemics in phytoplankton hosts.

Frenken T, Miki T, Kagami M, Van de Waal DB, Van Donk E, Rohrlack T, Gsell AS.

Ecology. 2019 Sep 23:e02900. doi: 10.1002/ecy.2900. [Epub ahead of print]

PMID:
31544240
3.

Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool.

Yoshida T, Miyado M, Mikami M, Suzuki E, Kinjo K, Matsubara K, Ogata T, Akutsu H, Kagami M, Fukami M.

Hum Reprod. 2019 Sep 29;34(9):1762-1769. doi: 10.1093/humrep/dez117.

PMID:
31398259
4.

DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations.

Ogushi K, Hattori A, Suzuki E, Shima H, Izawa M, Yagasaki H, Horikawa R, Uetake K, Umezawa A, Ishii T, Muroya K, Namba N, Tanaka T, Hirano Y, Yamamoto H, Soneda S, Matsubara K, Kagami M, Miyado M, Fukami M.

Cytogenet Genome Res. 2019;158(2):56-62. doi: 10.1159/000500468. Epub 2019 Jun 4.

5.

Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.

Hattori A, Okamura K, Terada Y, Tanaka R, Katoh-Fukui Y, Matsubara Y, Matsubara K, Kagami M, Horikawa R, Fukami M.

BMC Med Genomics. 2019 May 28;12(1):77. doi: 10.1186/s12920-019-0526-3.

6.

Photonic technologies for autonomous cars: feature introduction.

Shi JW, Guo JI, Kagami M, Suni P, Ziemann O.

Opt Express. 2019 Mar 4;27(5):7627-7628. doi: 10.1364/OE.27.007627.

PMID:
30876324
7.

Fungi in aquatic ecosystems.

Grossart HP, Van den Wyngaert S, Kagami M, Wurzbacher C, Cunliffe M, Rojas-Jimenez K.

Nat Rev Microbiol. 2019 Jun;17(6):339-354. doi: 10.1038/s41579-019-0175-8. Review.

PMID:
30872817
8.

Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR.

Kagami M, Yanagisawa A, Ota M, Matsuoka K, Nakamura A, Matsubara K, Nakabayashi K, Takada S, Fukami M, Ogata T.

Clin Epigenetics. 2019 Mar 7;11(1):42. doi: 10.1186/s13148-019-0640-2.

9.

Fungi in the Marine Environment: Open Questions and Unsolved Problems.

Amend A, Burgaud G, Cunliffe M, Edgcomb VP, Ettinger CL, Gutiérrez MH, Heitman J, Hom EFY, Ianiri G, Jones AC, Kagami M, Picard KT, Quandt CA, Raghukumar S, Riquelme M, Stajich J, Vargas-Muñiz J, Walker AK, Yarden O, Gladfelter AS.

MBio. 2019 Mar 5;10(2). pii: e01189-18. doi: 10.1128/mBio.01189-18. Review.

10.

Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.

Matsubara K, Itoh M, Shimizu K, Saito S, Enomoto K, Nakabayashi K, Hata K, Kurosawa K, Ogata T, Fukami M, Kagami M.

Clin Epigenetics. 2019 Feb 28;11(1):36. doi: 10.1186/s13148-019-0633-1.

11.

Taming chlorophylls by early eukaryotes underpinned algal interactions and the diversification of the eukaryotes on the oxygenated Earth.

Kashiyama Y, Yokoyama A, Shiratori T, Hess S, Not F, Bachy C, Gutierrez-Rodriguez A, Kawahara J, Suzaki T, Nakazawa M, Ishikawa T, Maruyama M, Wang M, Chen M, Gong Y, Seto K, Kagami M, Hamamoto Y, Honda D, Umetani T, Shihongi A, Kayama M, Matsuda T, Taira J, Yabuki A, Tsuchiya M, Hirakawa Y, Kawaguchi A, Nomura M, Nakamura A, Namba N, Matsumoto M, Tanaka T, Yoshino T, Higuchi R, Yamamoto A, Maruyama T, Yamaguchi A, Uzuka A, Miyagishima S, Tanifuji G, Kawachi M, Kinoshita Y, Tamiaki H.

ISME J. 2019 Aug;13(8):1899-1910. doi: 10.1038/s41396-019-0377-0. Epub 2019 Feb 26.

12.

Association of four imprinting disorders and ART.

Hattori H, Hiura H, Kitamura A, Miyauchi N, Kobayashi N, Takahashi S, Okae H, Kyono K, Kagami M, Ogata T, Arima T.

Clin Epigenetics. 2019 Feb 7;11(1):21. doi: 10.1186/s13148-019-0623-3.

13.

Severe in utero under-virilization in a 46,XY patient with Silver-Russell syndrome with 11p15 loss of methylation.

Adachi M, Fukami M, Kagami M, Sho N, Yamazaki Y, Tanaka Y, Asakura Y, Hanakawa J, Muroya K.

J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):191-196. doi: 10.1515/jpem-2018-0464.

PMID:
30676999
14.

(Epi)genetic defects of MKRN3 are rare in Asian patients with central precocious puberty.

Suzuki E, Shima H, Kagami M, Soneda S, Tanaka T, Yatsuga S, Nishioka J, Oto Y, Kamiya T, Naiki Y, Ogata T, Fujisawa Y, Nakamura A, Kawashima S, Morikawa S, Horikawa R, Sano S, Fukami M.

Hum Genome Var. 2019 Jan 21;6:7. doi: 10.1038/s41439-019-0039-9. eCollection 2019.

15.

Temple syndrome diagnosed in an adult patient with clinical autism spectrum disorder.

Kimura T, Kagami M, Matsubara K, Yatsuga S, Mukasa R, Yatsuga C, Matsumoto T, Koga Y.

Clin Case Rep. 2018 Nov 8;7(1):15-18. doi: 10.1002/ccr3.1895. eCollection 2019 Jan.

16.

Molecular and clinical analyses of two patients with UPD(16)mat detected by screening 94 patients with Silver-Russell syndrome phenotype of unknown aetiology.

Inoue T, Yagasaki H, Nishioka J, Nakamura A, Matsubara K, Narumi S, Nakabayashi K, Yamazawa K, Fuke T, Oka A, Ogata T, Fukami M, Kagami M.

J Med Genet. 2019 Jun;56(6):413-418. doi: 10.1136/jmedgenet-2018-105463. Epub 2018 Sep 21.

17.

Introducing ribosomal tandem repeat barcoding for fungi.

Wurzbacher C, Larsson E, Bengtsson-Palme J, Van den Wyngaert S, Svantesson S, Kristiansson E, Kagami M, Nilsson RH.

Mol Ecol Resour. 2019 Jan;19(1):118-127. doi: 10.1111/1755-0998.12944. Epub 2018 Oct 24.

PMID:
30240145
18.

Anaphylaxis to xylitol diagnosed by skin prick test and basophil activation test.

Okamoto K, Kagami M, Kawai M, Mori Y, Yamawaki K, Nakajima Y, Kondo Y, Tsuge I.

Allergol Int. 2019 Jan;68(1):130-131. doi: 10.1016/j.alit.2018.08.001. Epub 2018 Sep 3. No abstract available.

19.

Influence of parasitic chytrids on the quantity and quality of algal dissolved organic matter (AOM).

Senga Y, Yabe S, Nakamura T, Kagami M.

Water Res. 2018 Nov 15;145:346-353. doi: 10.1016/j.watres.2018.08.037. Epub 2018 Aug 22.

PMID:
30170302
20.

Uniparental disomy as a cause of pediatric endocrine disorders.

Matsubara K, Kagami M, Fukami M.

Clin Pediatr Endocrinol. 2018;27(3):113-121. doi: 10.1297/cpe.27.113. Epub 2018 Jul 31.

21.

Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform.

Hernandez Mora JR, Tayama C, Sánchez-Delgado M, Monteagudo-Sánchez A, Hata K, Ogata T, Medrano J, Poo-Llanillo ME, Simón C, Moran S, Esteller M, Tenorio J, Lapunzina P, Kagami M, Monk D, Nakabayashi K.

Epigenomics. 2018 Jul;10(7):941-954. doi: 10.2217/epi-2017-0172. Epub 2018 Jul 2.

PMID:
29962238
22.

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
23.

Diversity and Hidden Host Specificity of Chytrids Infecting Colonial Volvocacean Algae.

Van den Wyngaert S, Rojas-Jimenez K, Seto K, Kagami M, Grossart HP.

J Eukaryot Microbiol. 2018 Nov;65(6):870-881. doi: 10.1111/jeu.12632. Epub 2018 Jun 5.

PMID:
29752884
24.

A case of paternal uniparental isodisomy for chromosome 7 associated with overgrowth.

Nakamura A, Muroya K, Ogata-Kawata H, Nakabayashi K, Matsubara K, Ogata T, Kurosawa K, Fukami M, Kagami M.

J Med Genet. 2018 Aug;55(8):567-570. doi: 10.1136/jmedgenet-2017-104986. Epub 2018 Feb 17.

PMID:
29455159
25.

(Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I.

Sano S, Nakamura A, Matsubara K, Nagasaki K, Fukami M, Kagami M, Ogata T.

J Endocr Soc. 2017 Nov 21;2(1):9-23. doi: 10.1210/js.2017-00293. eCollection 2018 Jan 1.

26.

Mosaic upd(14)pat in a patient with mild features of Kagami-Ogata syndrome.

Haug MG, Brendehaug A, Houge G, Kagami M, Ogata T.

Clin Case Rep. 2017 Nov 28;6(1):91-95. doi: 10.1002/ccr3.1300. eCollection 2018 Jan.

27.

Effectiveness of Sodium-Glucose Cotransporter-2 Inhibitor as an Add-on Drug to GLP-1 Receptor Agonists for Glycemic Control of a Patient with Prader-Willi Syndrome: A Case Report.

Horikawa Y, Enya M, Komagata M, Hashimoto KI, Kagami M, Fukami M, Takeda J.

Diabetes Ther. 2018 Feb;9(1):421-426. doi: 10.1007/s13300-018-0369-5. Epub 2018 Jan 15.

28.

A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1a.

Suzuki E, Bo R, Sue K, Awano H, Ogata T, Narumi S, Kagami M, Sano S, Fukami M.

Cytogenet Genome Res. 2017;153(3):125-130. doi: 10.1159/000485644. Epub 2018 Jan 11.

PMID:
29320763
29.

A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism.

Ushijima K, Yatsuga S, Matsumoto T, Nakamura A, Fukami M, Kagami M.

J Hum Genet. 2018 Mar;63(3):377-381. doi: 10.1038/s10038-017-0381-z. Epub 2018 Jan 9. Review.

PMID:
29311684
30.

Sustained endocrine profiles of a girl with WAGR syndrome.

Takada Y, Sakai Y, Matsushita Y, Ohkubo K, Koga Y, Akamine S, Torio M, Ishizaki Y, Sanefuji M, Torisu H, Shaw CA, Kagami M, Hara T, Ohga S.

BMC Med Genet. 2017 Oct 23;18(1):117. doi: 10.1186/s12881-017-0477-5.

31.

Continuous hypomethylation of the KCNQ1OT1:TSS-DMR in monochorionic twins discordant for Beckwith-Wiedemann syndrome.

Inoue T, Nakamura A, Matsubara K, Nyuzuki H, Nagasaki K, Oka A, Fukami M, Kagami M.

Am J Med Genet A. 2017 Oct;173(10):2847-2850. doi: 10.1002/ajmg.a.38419. Epub 2017 Aug 16. No abstract available.

PMID:
28816024
32.

A New Parasitic Chytrid, Staurastromyces oculus (Rhizophydiales, Staurastromycetaceae fam. nov.), Infecting the Freshwater Desmid Staurastrum sp.

Van den Wyngaert S, Seto K, Rojas-Jimenez K, Kagami M, Grossart HP.

Protist. 2017 Aug;168(4):392-407. doi: 10.1016/j.protis.2017.05.001. Epub 2017 May 13.

PMID:
28704705
33.

Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients.

Kagami M, Nagasaki K, Kosaki R, Horikawa R, Naiki Y, Saitoh S, Tajima T, Yorifuji T, Numakura C, Mizuno S, Nakamura A, Matsubara K, Fukami M, Ogata T.

Genet Med. 2017 Dec;19(12):1356-1366. doi: 10.1038/gim.2017.53. Epub 2017 May 31.

34.

Impact of borderline-subclinical hypothyroidism on subsequent pregnancy outcome in women with unexplained recurrent pregnancy loss.

Uchida S, Maruyama T, Kagami M, Miki F, Hihara H, Katakura S, Yoshimasa Y, Masuda H, Uchida H, Tanaka M.

J Obstet Gynaecol Res. 2017 Jun;43(6):1014-1020. doi: 10.1111/jog.13319.

PMID:
28621046
35.

Integrating chytrid fungal parasites into plankton ecology: research gaps and needs.

Frenken T, Alacid E, Berger SA, Bourne EC, Gerphagnon M, Grossart HP, Gsell AS, Ibelings BW, Kagami M, Küpper FC, Letcher PM, Loyau A, Miki T, Nejstgaard JC, Rasconi S, Reñé A, Rohrlack T, Rojas-Jimenez K, Schmeller DS, Scholz B, Seto K, Sime-Ngando T, Sukenik A, Van de Waal DB, Van den Wyngaert S, Van Donk E, Wolinska J, Wurzbacher C, Agha R.

Environ Microbiol. 2017 Oct;19(10):3802-3822. doi: 10.1111/1462-2920.13827. Epub 2017 Jul 13. Review.

PMID:
28618196
36.

Maternally derived 15q11.2-q13.1 duplication and H19-DMR hypomethylation in a patient with Silver-Russell syndrome.

Dateki S, Kagami M, Matsubara K, Izumi K, Watanabe S, Nakatomi A, Kondoh T, Fukami M, Moriuchi H.

J Hum Genet. 2017 Oct;62(10):919-922. doi: 10.1038/jhg.2017.62. Epub 2017 Jun 8.

PMID:
28592837
37.

Light-induced self-written waveguide fabrication using 1550  nm laser light.

Terasawa H, Tan F, Sugihara O, Kawasaki A, Inoue D, Yamashita T, Kagami M, Maury O, Bretonnière Y, Andraud C.

Opt Lett. 2017 Jun 1;42(11):2236-2238. doi: 10.1364/OL.42.002236.

PMID:
28569890
38.

Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defects.

Inoue T, Nakamura A, Fuke T, Yamazawa K, Sano S, Matsubara K, Mizuno S, Matsukura Y, Harashima C, Hasegawa T, Nakajima H, Tsumura K, Kizaki Z, Oka A, Ogata T, Fukami M, Kagami M.

Clin Epigenetics. 2017 May 15;9:52. doi: 10.1186/s13148-017-0350-6. eCollection 2017.

39.

De novo IGF2 mutation on the paternal allele in a patient with Silver-Russell syndrome and ectrodactyly.

Yamoto K, Saitsu H, Nakagawa N, Nakajima H, Hasegawa T, Fujisawa Y, Kagami M, Fukami M, Ogata T.

Hum Mutat. 2017 Aug;38(8):953-958. doi: 10.1002/humu.23253. Epub 2017 May 29.

PMID:
28489339
40.

Temperature during pregnancy influences the fetal growth and birth size.

Rashid H, Kagami M, Ferdous F, Ma E, Terao T, Hayashi T, Wagatsuma Y.

Trop Med Health. 2016 Dec 14;45:1. doi: 10.1186/s41182-016-0041-6. eCollection 2017.

41.

Sporadic pseudohypoparathyroidism type-1b with asymptomatic hypocalcemia.

Goto M, Yamamoto Y, Ishii M, Nakamura A, Sano S, Kagami M, Fukami M, Saito R, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K.

Pediatr Int. 2016 Nov;58(11):1229-1231. doi: 10.1111/ped.13096.

PMID:
27882740
42.

Diagnosis and management of Silver-Russell syndrome: first international consensus statement.

Wakeling EL, Brioude F, Lokulo-Sodipe O, O'Connell SM, Salem J, Bliek J, Canton AP, Chrzanowska KH, Davies JH, Dias RP, Dubern B, Elbracht M, Giabicani E, Grimberg A, Grønskov K, Hokken-Koelega AC, Jorge AA, Kagami M, Linglart A, Maghnie M, Mohnike K, Monk D, Moore GE, Murray PG, Ogata T, Petit IO, Russo S, Said E, Toumba M, Tümer Z, Binder G, Eggermann T, Harbison MD, Temple IK, Mackay DJ, Netchine I.

Nat Rev Endocrinol. 2017 Feb;13(2):105-124. doi: 10.1038/nrendo.2016.138. Epub 2016 Sep 2.

PMID:
27585961
43.

Phylogenetic Position of Parasitic Chytrids on Diatoms: Characterization of a Novel Clade in Chytridiomycota.

Seto K, Kagami M, Degawa Y.

J Eukaryot Microbiol. 2017 May;64(3):383-393. doi: 10.1111/jeu.12373. Epub 2016 Nov 14.

PMID:
27714973
44.

Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome.

Kagami M, Matsubara K, Nakabayashi K, Nakamura A, Sano S, Okamura K, Hata K, Fukami M, Ogata T.

Genet Med. 2017 Apr;19(4):476-482. doi: 10.1038/gim.2016.123. Epub 2016 Sep 15.

45.

Chromosome 6q24 methylation defects are uncommon in childhood-onset non-autoimmune diabetes mellitus patients born appropriate- or large-for-gestational age.

Okuno M, Yorifuji T, Kagami M, Ayabe T, Urakami T, Kawamura T, Kikuchi N, Yokota I, Kikuchi T, Amemiya S, Suzuki J, Ogata T, Sugihara S, Fukami M; Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT).

Clin Pediatr Endocrinol. 2016 Jul;25(3):99-102. doi: 10.1297/cpe.25.99. Epub 2016 Jul 20. No abstract available.

46.

A patient with Temple syndrome satisfying the clinical diagnostic criteria of Silver-Russell syndrome.

Goto M, Kagami M, Nishimura G, Yamagata T.

Am J Med Genet A. 2016 Sep;170(9):2483-5. doi: 10.1002/ajmg.a.37827. Epub 2016 Jun 30. No abstract available.

47.

Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1b.

Nakamura A, Hamaguchi E, Horikawa R, Nishimura Y, Matsubara K, Sano S, Nagasaki K, Matsubara Y, Umezawa A, Tajima T, Ogata T, Kagami M, Okamura K, Fukami M.

J Clin Endocrinol Metab. 2016 Jul;101(7):2623-7. doi: 10.1210/jc.2016-1725. Epub 2016 Jun 2.

PMID:
27253667
48.

Silver-Russell syndrome in a patient with somatic mosaicism for upd(11)mat identified by buccal cell analysis.

Luk HM, Ivan Lo FM, Sano S, Matsubara K, Nakamura A, Ogata T, Kagami M.

Am J Med Genet A. 2016 Jul;170(7):1938-41. doi: 10.1002/ajmg.a.37679. Epub 2016 May 6. No abstract available.

49.

Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type Ib in a patient with multilocus imprinting disturbance: a female-dominant phenomenon?

Sano S, Matsubara K, Nagasaki K, Kikuchi T, Nakabayashi K, Hata K, Fukami M, Kagami M, Ogata T.

J Hum Genet. 2016 Aug;61(8):765-9. doi: 10.1038/jhg.2016.45. Epub 2016 Apr 28.

PMID:
27121328
50.

Evaluation of Daphnid Grazing on Microscopic Zoosporic Fungi by Using Comparative Threshold Cycle Quantitative PCR.

Maier MA, Uchii K, Peterson TD, Kagami M.

Appl Environ Microbiol. 2016 Jun 13;82(13):3868-3874. doi: 10.1128/AEM.00087-16. Print 2016 Jul 1.

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