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Material Type: Artigo
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Growth hormone deficiency with advanced bone age phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencingFernanda A. Correa Marcela M França; Qing Fang; Qianyi Ma; Tânia Aparecida Sartori Sanchez Bachega; Andresa Rodrigues; Bilge A Ozel; Jun Z Li; Berenice Bilharinho de Mendonça; Alexander Augusto de Lima Jorge; Luciani R Carvalho; Sally A Camper; Ivo J ArnholdArchives of endocrinology metabolism v. 61, n. 6, p. 633-636, 2017Rio De Janeiro, Rj 2017Localização: FM - Fac. Medicina (BCSEP 250 2017 )(Acessar) |
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Material Type: Artigo
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Single-Cell RNA Sequencing Reveals Novel Markers of Male Pituitary Stem Cells and Hormone-Producing Cell TypesCheung, Leonard Y M ; George, Akima S ; McGee, Stacey R ; Daly, Alexandre Z ; Brinkmeier, Michelle L ; Ellsworth, Buffy S ; Camper, Sally AEndocrinology (Philadelphia), 2018-12, Vol.159 (12), p.3910-3924 [Periódico revisado por pares]Washington, DC: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Gata2 is required for HSC generation and survivalde Pater, Emma ; Kaimakis, Polynikis ; Vink, Chris S ; Yokomizo, Tomomasa ; Yamada-Inagawa, Tomoko ; van der Linden, Reinier ; Kartalaei, Parham Solaimani ; Camper, Sally A ; Speck, Nancy ; Dzierzak, ElaineThe Journal of experimental medicine, 2013-12, Vol.210 (13), p.2843-2850 [Periódico revisado por pares]United States: The Rockefeller University PressTexto completo disponível |
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Material Type: Artigo
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Advances in Skeletal Dysplasia GeneticsGeister, Krista A ; Camper, Sally AAnnual review of genomics and human genetics, 2015-01, Vol.16 (1), p.199-227 [Periódico revisado por pares]United States: Annual ReviewsTexto completo disponível |
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Material Type: Artigo
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Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and manBando, Hironori ; Brinkmeier, Michelle L ; Castinetti, Frederic ; Fang, Qing ; Lee, Mi-Sun ; Saveanu, Alexandru ; Albarel, Frédérique ; Dupuis, Clémentine ; Brue, Thierry ; Camper, Sally AHuman molecular genetics, 2023-01, Vol.32 (3), p.367-385 [Periódico revisado por pares]England: Oxford University Press (OUP)Texto completo disponível |
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Material Type: Artigo
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Conditional Gata2 inactivation results in HSC loss and lymphatic mispatterningLim, Kim-Chew ; Hosoya, Tomonori ; Brandt, William ; Ku, Chia-Jui ; Hosoya-Ohmura, Sakie ; Camper, Sally A ; Yamamoto, Masayuki ; Engel, James DouglasThe Journal of clinical investigation, 2012-10, Vol.122 (10), p.3705-3717 [Periódico revisado por pares]United States: American Society for Clinical InvestigationTexto completo disponível |
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Material Type: Artigo
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Deletion of OTX2 in neural ectoderm delays anterior pituitary developmentMortensen, Amanda H ; Schade, Vanessa ; Lamonerie, Thomas ; Camper, Sally AHuman molecular genetics, 2015-02, Vol.24 (4), p.939-953 [Periódico revisado por pares]England: Oxford University Press (OUP)Texto completo disponível |
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Material Type: Artigo
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A Gata2-Dependent Transcription Network Regulates Uterine Progesterone Responsiveness and Endometrial FunctionRubel, Cory A. ; Wu, San-Pin ; Lin, Lin ; Wang, Tianyuan ; Lanz, Rainer B. ; Li, Xilong ; Kommagani, Ramakrishna ; Franco, Heather L. ; Camper, Sally A. ; Tong, Qiang ; Jeong, Jae-Wook ; Lydon, John P. ; DeMayo, Francesco J.Cell reports (Cambridge), 2016-10, Vol.17 (5), p.1414-1425 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in miceDing, Feng ; Li, Hong Hua ; Zhang, Shengwen ; Solomon, Nicola M ; Camper, Sally A ; Cohen, Pinchas ; Francke, Uta Akbarian, SchahramPloS one, 2008-03, Vol.3 (3), p.e1709 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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Material Type: Artigo
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Pituitary Stem Cell Update and Potential Implications for Treating HypopituitarismCastinetti, Frederic ; Davis, Shannon W ; Brue, Thierry ; Camper, Sally AEndocrine reviews, 2011-08, Vol.32 (4), p.453-471 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |