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Items: 1 to 50 of 443

1.

Facile target validation in an animal model with intracellularly expressed monobodies.

Gupta A, Xu J, Lee S, Tsai ST, Zhou B, Kurosawa K, Werner MS, Koide A, Ruthenburg AJ, Dou Y, Koide S.

Nat Chem Biol. 2018 Jul 16. doi: 10.1038/s41589-018-0099-z. [Epub ahead of print]

PMID:
30013062
2.

Echocardiography-based pressure-volume loop assessment in the evaluation for the effects of indoxyl sulfate on cardiovascular function.

Obokata M, Kurosawa K, Ishida H, Ito K, Ogawa T, Ando Y, Kurabayashi M, Negishi K.

J Echocardiogr. 2018 Jul 7. doi: 10.1007/s12574-018-0385-5. [Epub ahead of print]

PMID:
29982976
3.

Biallelic mutations of EGFR in a compound heterozygous state cause ectodermal dysplasia with severe skin defects and gastrointestinal dysfunction.

Hayashi S, Yokoi T, Hatano C, Enomoto Y, Tsurusaki Y, Naruto T, Kobayashi M, Ida H, Kurosawa K.

Hum Genome Var. 2018 Jun 8;5:11. doi: 10.1038/s41439-018-0011-0. eCollection 2018.

4.

17q21.32-q22 Deletion in a girl with osteogenesis imperfecta, tricho-dento-osseous syndrome, and intellectual disability.

Yokoi T, Saito T, Nagai JI, Kurosawa K.

Congenit Anom (Kyoto). 2018 Jun 12. doi: 10.1111/cga.12292. [Epub ahead of print] No abstract available.

PMID:
29896840
5.

A Novel Laryngeal Preservation Technique following Total Glossectomy with Hyoid Bone Resection.

Kurosawa K, Imai T, Matsumoto K, Asada Y, Katoh K, Matsuura K, Goto T.

Plast Reconstr Surg Glob Open. 2018 Apr 9;6(4):e1756. doi: 10.1097/GOX.0000000000001756. eCollection 2018 Apr.

6.

The loss of BAP1 protein expression predicts poor prognosis in patients with nonmetastatic clear cell renal cell carcinoma with inferior vena cava tumor thrombosis.

Oka S, Inoshita N, Miura Y, Oki R, Miyama Y, Nagamoto S, Ogawa K, Sakaguchi K, Kondoh C, Kurosawa K, Urakami S, Takano T, Okaneya T.

Urol Oncol. 2018 May 28. pii: S1078-1439(18)30137-6. doi: 10.1016/j.urolonc.2018.04.015. [Epub ahead of print]

PMID:
29853346
7.

Targeting G-quadruplex DNA as cognitive function therapy for ATR-X syndrome.

Shioda N, Yabuki Y, Yamaguchi K, Onozato M, Li Y, Kurosawa K, Tanabe H, Okamoto N, Era T, Sugiyama H, Wada T, Fukunaga K.

Nat Med. 2018 Jun;24(6):802-813. doi: 10.1038/s41591-018-0018-6. Epub 2018 May 21.

PMID:
29785027
8.

Novel COL4A1 mutation in a fetus with early prenatal onset of schizencephaly.

Sato Y, Shibasaki J, Aida N, Hiiragi K, Kimura Y, Akahira-Azuma M, Enomoto Y, Tsurusaki Y, Kurosawa K.

Hum Genome Var. 2018 Apr 24;5:4. doi: 10.1038/s41439-018-0005-y. eCollection 2018.

9.

Loss of protein phosphatase 6 in mouse keratinocytes enhances K-rasG12D -driven tumor promotion.

Kurosawa K, Inoue Y, Kakugawa Y, Yamashita Y, Kanazawa K, Kishimoto K, Nomura M, Momoi Y, Sato I, Chiba N, Suzuki M, Ogoh H, Yamada H, Miura K, Watanabe T, Tanuma N, Tachi M, Shima H.

Cancer Sci. 2018 Jul;109(7):2178-2187. doi: 10.1111/cas.13638. Epub 2018 Jun 25.

10.

Acute lymphoblastic leukemia in a male with Simpson-Golabi-Behmel syndrome.

Minatogawa M, Iwasaki F, Yokoi T, Nagai J, Sakazume S, Goto H, Kurosawa K.

Am J Med Genet A. 2018 May 7. doi: 10.1002/ajmg.a.38664. [Epub ahead of print] No abstract available.

PMID:
29737011
11.

Complete Genome Sequence of Sphingobium sp. Strain YG1, a Lignin Model Dimer-Metabolizing Bacterium Isolated from Sediment in Kagoshima Bay, Japan.

Ohta Y, Shimane Y, Nishi S, Ichikawa J, Kurosawa K, Tsubouchi T, Ishii S.

Genome Announc. 2018 Apr 26;6(17). pii: e00267-18. doi: 10.1128/genomeA.00267-18.

12.

Refining the clinical phenotype of Okur-Chung neurodevelopmental syndrome.

Akahira-Azuma M, Tsurusaki Y, Enomoto Y, Mitsui J, Kurosawa K.

Hum Genome Var. 2018 Mar 29;5:18011. doi: 10.1038/hgv.2018.11. eCollection 2018.

13.

Complete Genome Sequence of Altererythrobacter sp. Strain B11, an Aromatic Monomer-Degrading Bacterium, Isolated from Deep-Sea Sediment under the Seabed off Kashima, Japan.

Maeda AH, Nishi S, Ishii S, Shimane Y, Kobayashi H, Ichikawa J, Kurosawa K, Arai W, Takami H, Ohta Y.

Genome Announc. 2018 Mar 22;6(12). pii: e00200-18. doi: 10.1128/genomeA.00200-18.

14.

PKM1 Confers Metabolic Advantages and Promotes Cell-Autonomous Tumor Cell Growth.

Morita M, Sato T, Nomura M, Sakamoto Y, Inoue Y, Tanaka R, Ito S, Kurosawa K, Yamaguchi K, Sugiura Y, Takizaki H, Yamashita Y, Katakura R, Sato I, Kawai M, Okada Y, Watanabe H, Kondoh G, Matsumoto S, Kishimoto A, Obata M, Matsumoto M, Fukuhara T, Motohashi H, Suematsu M, Komatsu M, Nakayama KI, Watanabe T, Soga T, Shima H, Maemondo M, Tanuma N.

Cancer Cell. 2018 Mar 12;33(3):355-367.e7. doi: 10.1016/j.ccell.2018.02.004.

PMID:
29533781
15.

Evaluation of a patient with classical Ehlers-Danlos syndrome due to a 9q34 duplication affecting COL5A1.

Kuroda Y, Ohashi I, Naruto T, Ida K, Enomoto Y, Saito T, Nagai JI, Kurosawa K.

Congenit Anom (Kyoto). 2018 Mar 9. doi: 10.1111/cga.12277. [Epub ahead of print]

PMID:
29520887
16.

Reduced variability of visual left ventricular ejection fraction assessment with reference images: The Japanese Association of Young Echocardiography Fellows multicenter study.

Kusunose K, Shibayama K, Iwano H, Izumo M, Kagiyama N, Kurosawa K, Mihara H, Oe H, Onishi T, Onishi T, Ota M, Sasaki S, Shiina Y, Tsuruta H, Tanaka H; JAYEF Investigators.

J Cardiol. 2018 Jul;72(1):74-80. doi: 10.1016/j.jjcc.2018.01.007. Epub 2018 Feb 19.

PMID:
29472129
17.

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 Feb 17. pii: jmedgenet-2017-104986. doi: 10.1136/jmedgenet-2017-104986. [Epub ahead of print]

PMID:
29455159
18.

Enhanced Recovery After Surgery program with dexamethasone administration for major head and neck surgery with free tissue transfer reconstruction: initial institutional experience.

Imai T, Kurosawa K, Yamaguchi K, Satake N, Asada Y, Matsumoto K, Morita S, Saijo S, Aoi J, Fujii K, Kishimoto K, Goto T, Matsuura K.

Acta Otolaryngol. 2018 Jul;138(7):664-669. doi: 10.1080/00016489.2018.1429651. Epub 2018 Jan 31.

PMID:
29385889
19.

Novel SYNGAP1 variant in a patient with intellectual disability and distinctive dysmorphisms.

Kimura Y, Akahira-Azuma M, Harada N, Enomoto Y, Tsurusaki Y, Kurosawa K.

Congenit Anom (Kyoto). 2018 Jan 30. doi: 10.1111/cga.12273. [Epub ahead of print]

PMID:
29381230
20.

Postprandial cardiogenic syncope caused by gastric polyp-induced pyloric obstruction in an elderly woman with a giant hiatal hernia: a case report.

Saito H, Miyazaki T, Sohda M, Sakai M, Honjyo H, Kumakura Y, Yoshida T, Yokobori T, Kurosawa K, Kuwano H.

Surg Case Rep. 2017 Dec 13;3(1):124. doi: 10.1186/s40792-017-0403-2.

21.

Redefining the phenotypic spectrum of de novo heterozygous CDK13 variants: Three patients without cardiac defects.

Uehara T, Takenouchi T, Kosaki R, Kurosawa K, Mizuno S, Kosaki K.

Eur J Med Genet. 2018 May;61(5):243-247. doi: 10.1016/j.ejmg.2017.12.004. Epub 2017 Dec 6.

PMID:
29222009
22.

CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations.

Okuno H, Renault Mihara F, Ohta S, Fukuda K, Kurosawa K, Akamatsu W, Sanosaka T, Kohyama J, Hayashi K, Nakajima K, Takahashi T, Wysocka J, Kosaki K, Okano H.

Elife. 2017 Nov 28;6. pii: e21114. doi: 10.7554/eLife.21114.

23.

Clinicopathological characteristics of patients with upper urinary tract urothelial cancer with loss of immunohistochemical expression of the DNA mismatch repair proteins in universal screening.

Urakami S, Inoshita N, Oka S, Miyama Y, Nomura S, Arai M, Sakaguchi K, Kurosawa K, Okaneya T.

Int J Urol. 2018 Feb;25(2):151-156. doi: 10.1111/iju.13481. Epub 2017 Nov 22.

PMID:
29164703
24.

A Novel Funnel-Shaped Flap for Reconstruction Surgery after Total Laryngopharyngectomy with Total Glossectomy.

Kurosawa K, Asada Y, Matsumoto K, Imai T, Matsuura K, Goto T.

Plast Reconstr Surg Glob Open. 2017 Sep 22;5(9):e1504. doi: 10.1097/GOX.0000000000001504. eCollection 2017 Sep.

25.

Novel AMER1 frameshift mutation in a girl with osteopathia striata with cranial sclerosis.

Enomoto Y, Tsurusaki Y, Harada N, Aida N, Kurosawa K.

Congenit Anom (Kyoto). 2018 Jul;58(4):145-146. doi: 10.1111/cga.12258. Epub 2017 Nov 16. No abstract available.

PMID:
28990699
26.

Fulminant myocardial bleeding: another clinical course of vascular Ehlers-Danlos Syndrome.

Tokue M, Hara H, Kurosawa K, Nakamura M.

BMJ Case Rep. 2017 Sep 23;2017. pii: bcr-2017-220786. doi: 10.1136/bcr-2017-220786.

27.

Differentiation of black writing ink on paper using luminescence lifetime by time-resolved luminescence spectroscopy.

Suzuki M, Akiba N, Kurosawa K, Akao Y, Higashikawa Y.

Forensic Sci Int. 2017 Oct;279:281-287. doi: 10.1016/j.forsciint.2017.09.003. Epub 2017 Sep 11.

PMID:
28938198
28.

Serum lithium levels and suicide attempts: a case-controlled comparison in lithium therapy-naive individuals.

Kanehisa M, Terao T, Shiotsuki I, Kurosawa K, Takenaka R, Sakamoto T, Shigemitsu O, Ishii N, Hatano K, Hirakawa H.

Psychopharmacology (Berl). 2017 Nov;234(22):3335-3342. doi: 10.1007/s00213-017-4729-z. Epub 2017 Aug 28.

PMID:
28849243
29.

CTCF deletion syndrome: clinical features and epigenetic delineation.

Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S.

J Med Genet. 2017 Dec;54(12):836-842. doi: 10.1136/jmedgenet-2017-104854. Epub 2017 Aug 28.

PMID:
28848059
30.

Haploinsufficiency of BCL11A associated with cerebellar abnormalities in 2p15p16.1 deletion syndrome.

Shimbo H, Yokoi T, Aida N, Mizuno S, Suzumura H, Nagai J, Ida K, Enomoto Y, Hatano C, Kurosawa K.

Mol Genet Genomic Med. 2017 May 22;5(4):429-437. doi: 10.1002/mgg3.289. eCollection 2017 Jul.

31.

Visualization of Aged Fingerprints with an Ultraviolet Laser.

Akiba N, Kuroki K, Kurosawa K, Tsuchiya K.

J Forensic Sci. 2018 Mar;63(2):556-562. doi: 10.1111/1556-4029.13588. Epub 2017 Jul 10.

PMID:
28691773
32.

Expansion of the phenotype of Kosaki overgrowth syndrome.

Minatogawa M, Takenouchi T, Tsuyusaki Y, Iwasaki F, Uehara T, Kurosawa K, Kosaki K, Curry CJ.

Am J Med Genet A. 2017 Sep;173(9):2422-2427. doi: 10.1002/ajmg.a.38310. Epub 2017 Jun 22.

PMID:
28639748
33.

Change in Calcaneal Bone Strength in Long-Term Care Residents Treated With Low-Intensity Pulsed Ultrasound.

Okuizumi H, Koyano K, Kurosawa K, Kamide N, Soyano A.

J Orthop Trauma. 2017 Jul;31(7):S4. doi: 10.1097/01.bot.0000520895.07718.ad.

PMID:
28632666
34.

A novel UBE2A mutation causes X-linked intellectual disability type Nascimento.

Tsurusaki Y, Ohashi I, Enomoto Y, Naruto T, Mitsui J, Aida N, Kurosawa K.

Hum Genome Var. 2017 Jun 8;4:17019. doi: 10.1038/hgv.2017.19. eCollection 2017.

35.

Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter.

Fukushi D, Kurosawa K, Suzuki Y, Suzuki K, Yamada K, Watanabe S, Yokochi K, Wakamatsu N.

Am J Med Genet A. 2017 Aug;173(8):2201-2209. doi: 10.1002/ajmg.a.38313. Epub 2017 Jun 9.

PMID:
28599099
36.

Two patients with 19p13.2 deletion (Malan syndrome) involving NFIX and CACNA1A with overgrowth, developmental delay, and epilepsy.

Kuroda Y, Mizuno Y, Mimaki M, Oka A, Sato Y, Ogawa S, Kurosawa K.

Clin Dysmorphol. 2017 Oct;26(4):224-227. doi: 10.1097/MCD.0000000000000185. No abstract available.

PMID:
28557812
37.

Effect of Lymphadenectomy During Radical Nephroureterectomy in Locally Advanced Upper Tract Urothelial Carcinoma.

Ikeda M, Matsumoto K, Sakaguchi K, Ishii D, Tabata KI, Kurosawa K, Urakami S, Okaneya T, Iwamura M.

Clin Genitourin Cancer. 2017 Oct;15(5):556-562. doi: 10.1016/j.clgc.2017.04.004. Epub 2017 Apr 10.

PMID:
28501481
38.

Neuroimaging findings in Joubert syndrome with C5orf42 gene mutations: A milder form of molar tooth sign and vermian hypoplasia.

Enokizono M, Aida N, Niwa T, Osaka H, Naruto T, Kurosawa K, Ohba C, Suzuki T, Saitsu H, Goto T, Matsumoto N.

J Neurol Sci. 2017 May 15;376:7-12. doi: 10.1016/j.jns.2017.02.065. Epub 2017 Mar 1.

PMID:
28431631
39.

Laryngeal function-preserving operation for T4a laryngeal cancer with vocal cord paralysis - A case report.

Asada Y, Kurosawa K, Matsumoto K, Goto T, Katoh K, Imai T, Saijo S, Matsuura K.

Auris Nasus Larynx. 2018 Feb;45(1):194-199. doi: 10.1016/j.anl.2017.03.012. Epub 2017 Apr 14.

PMID:
28416345
40.

Loss of BAP1 protein expression in the first metastatic site predicts prognosis in patients with clear cell renal cell carcinoma.

Miura Y, Inoshita N, Ikeda M, Miyama Y, Oki R, Oka S, Kondoh C, Ozaki Y, Tanabe Y, Kurosawa K, Urakami S, Kohno T, Okaneya T, Takano T.

Urol Oncol. 2017 Jun;35(6):386-391. doi: 10.1016/j.urolonc.2017.02.003. Epub 2017 Mar 9.

PMID:
28284891
41.

Incremental Prognostic Value of Ventricular-Arterial Coupling over Ejection Fraction in Patients with Maintenance Hemodialysis.

Obokata M, Kurosawa K, Ishida H, Ito K, Ogawa T, Ando Y, Kurabayashi M, Negishi K.

J Am Soc Echocardiogr. 2017 May;30(5):444-453.e2. doi: 10.1016/j.echo.2016.12.014. Epub 2017 Feb 27.

PMID:
28246005
42.

Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9.

Shimbo H, Oyoshi T, Kurosawa K.

Congenit Anom (Kyoto). 2018 Jan;58(1):33-35. doi: 10.1111/cga.12216. Epub 2017 May 2.

PMID:
28220539
43.

Genetic and prenatal findings in two Japanese patients with Schinzel-Giedion syndrome.

Hishimura N, Watari M, Ohata H, Fuseya N, Wakiguchi S, Tokutomi T, Okuhara K, Takahashi N, Iizuka S, Yamamoto H, Mishima T, Fujieda S, Kobayashi R, Cho K, Kuroda Y, Kurosawa K, Tonoki H.

Clin Case Rep. 2016 Nov 17;5(1):5-8. doi: 10.1002/ccr3.738. eCollection 2017 Jan.

44.

The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.

Hossain MA, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, Itagaki R, Eto K, Iwamoto T, Yokoi T, Kurosawa K, Numabe H, Eto Y.

Mol Genet Metab. 2017 Mar;120(3):173-179. doi: 10.1016/j.ymgme.2017.01.002. Epub 2017 Jan 7.

PMID:
28087245
45.

Hearing impairment in a female infant with interstitial deletion of 2q24.1q24.3.

Ono H, Kurosawa K, Wakamatsu N, Masuda S.

Congenit Anom (Kyoto). 2017 Jul;57(4):118-121. doi: 10.1111/cga.12207. Epub 2017 Mar 30.

PMID:
28039919
46.

[Significance of Urological Surgical Treatment for Viral Hemorrhagic Cystitis after Allogeneic Hematopoietic Stem Cell Transplantation].

Kurosawa K, Urakami S, Ishiwata K, Miyagawa J, Sakaguchi K, Fujioka M, Murata H, Inoshita N, Taniguchi S, Okaneya T.

Hinyokika Kiyo. 2016 Nov;62(11):563-567. doi: 10.14989/ActaUrolJap_62_11_563. Japanese.

47.

New radiological parameters for the assessment of atlantoaxial instability in children with Down syndrome: the normal values and the risk of spinal cord injury.

Nakamura N, Inaba Y, Aota Y, Oba M, Machida J, N Aida, Kurosawa K, Saito T.

Bone Joint J. 2016 Dec;98-B(12):1704-1710.

PMID:
27909135
48.

B Cell-Based Seamless Engineering of Antibody Fc Domains.

Hashimoto K, Kurosawa K, Murayama A, Seo H, Ohta K.

PLoS One. 2016 Dec 1;11(12):e0167232. doi: 10.1371/journal.pone.0167232. eCollection 2016.

49.

Enzymatic Specific Production and Chemical Functionalization of Phenylpropanone Platform Monomers from Lignin.

Ohta Y, Hasegawa R, Kurosawa K, Maeda AH, Koizumi T, Nishimura H, Okada H, Qu C, Saito K, Watanabe T, Hatada Y.

ChemSusChem. 2017 Jan 20;10(2):425-433. doi: 10.1002/cssc.201601235. Epub 2016 Dec 16.

50.

Arsenic and Heavy Metal Contamination in Soils under Different Land Use in an Estuary in Northern Vietnam.

Nguyen Van T, Ozaki A, Nguyen Tho H, Nguyen Duc A, Tran Thi Y, Kurosawa K.

Int J Environ Res Public Health. 2016 Nov 5;13(11). pii: E1091.

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