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1
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
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Artigo
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Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

Haferlach, T ; Nagata, Y ; Grossmann, V ; Okuno, Y ; Bacher, U ; Nagae, G ; Schnittger, S ; Sanada, M ; Kon, A ; Alpermann, T ; Yoshida, K ; Roller, A ; Nadarajah, N ; Shiraishi, Y ; Shiozawa, Y ; Chiba, K ; Tanaka, H ; Koeffler, H P ; Klein, H-U ; Dugas, M ; Aburatani, H ; Kohlmann, A ; Miyano, S ; Haferlach, C ; Kern, W ; Ogawa, S

Leukemia, 2014-02, Vol.28 (2), p.241-247 [Periódico revisado por pares]

England: Nature Publishing Group

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2
PU.1 acts as tumor suppressor for myeloma cells through direct transcriptional repression of IRF4
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Artigo
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PU.1 acts as tumor suppressor for myeloma cells through direct transcriptional repression of IRF4

Ueno, N ; Nishimura, N ; Ueno, S ; Endo, S ; Tatetsu, H ; Hirata, S ; Hata, H ; Matsuoka, M ; Mitsuya, H ; Okuno, Y

Oncogene, 2017-08, Vol.36 (31), p.4481-4497 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia
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Artigo
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Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia

Kitamura, K. ; Okuno, Y. ; Yoshida, K. ; Sanada, M. ; Shiraishi, Y. ; Muramatsu, H. ; Kobayashi, R. ; Furukawa, K. ; Miyano, S. ; Kojima, S. ; Ogawa, S. ; Kunishima, S.

Journal of thrombosis and haemostasis, 2016-07, Vol.14 (7), p.1462-1469 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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4
Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation
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Artigo
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Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

Takeichi, T. ; Kobayashi, A. ; Ogawa, E. ; Okuno, Y. ; Kataoka, S. ; Kono, M. ; Sugiura, K. ; Okuyama, R. ; Akiyama, M.

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e133-e135 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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5
Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia
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Artigo
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Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia

Yoshida, N ; Sakaguchi, H ; Muramatsu, H ; Okuno, Y ; Song, C ; Dovat, S ; Shimada, A ; Ozeki, M ; Ohnishi, H ; Teramoto, T ; Fukao, T ; Kondo, N ; Takahashi, Y ; Matsumoto, K ; Kato, K ; Kojima, S

Leukemia, 2017-05, Vol.31 (5), p.1221-1223 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Restoring PU.1 induces apoptosis and modulates viral transactivation via interferon-stimulated genes in primary effusion lymphoma
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Artigo
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Restoring PU.1 induces apoptosis and modulates viral transactivation via interferon-stimulated genes in primary effusion lymphoma

Goto, H ; Kariya, R ; Kudo, E ; Okuno, Y ; Ueda, K ; Katano, H ; Okada, S

Oncogene, 2017-09, Vol.36 (37), p.5252-5262 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm
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Artigo
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Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm

Suzuki, K ; Suzuki, Y ; Hama, A ; Muramatsu, H ; Nakatochi, M ; Gunji, M ; Ichikawa, D ; Hamada, M ; Taniguchi, R ; Kataoka, S ; Murakami, N ; Kojima, D ; Sekiya, Y ; Nishikawa, E ; Kawashima, N ; Narita, A ; Nishio, N ; Nakazawa, Y ; Iwafuchi, H ; Watanabe, K-I ; Takahashi, Y ; Ito, M ; Kojima, S ; Kato, S ; Okuno, Y

Leukemia, 2017-07, Vol.31 (7), p.1629-1633 [Periódico revisado por pares]

England: Nature Publishing Group

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8
A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient
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Artigo
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A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient

Takeichi, T. ; Katayama, C. ; Tanaka, T. ; Okuno, Y. ; Murakami, N. ; Kono, M. ; Sugiura, K. ; Aoyama, Y. ; Akiyama, M.

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.e111-e113 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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9
Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations
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Artigo
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Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations

Takeuchi, S. ; Takeichi, T. ; Koike, Y. ; Takama, H. ; Tanahashi, K. ; Okuno, Y. ; Ishii, N. ; Muro, Y. ; Ogi, T. ; Suga, Y. ; Akiyama, M.

Journal of the European Academy of Dermatology and Venereology, 2022-03, Vol.36 (3), p.e215-e218 [Periódico revisado por pares]

England

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10
A cell-based assay to screen stimulators of the Hippo pathway reveals the inhibitory effect of dobutamine on the YAP-dependent gene transcription
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A cell-based assay to screen stimulators of the Hippo pathway reveals the inhibitory effect of dobutamine on the YAP-dependent gene transcription

Bao, Yijun ; Nakagawa, Kentaro ; Yang, Zeyu ; Ikeda, Mitsunobu ; Withanage, Kanchanamala ; Ishigami-Yuasa, Mari ; Okuno, Yukiko ; Hata, Shoji ; Nishina, Hiroshi ; Hata, Yutaka

Journal of biochemistry (Tokyo), 2011-08, Vol.150 (2), p.199-208 [Periódico revisado por pares]

England: Oxford University Press

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