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Material Type: Artigo
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Haplotype Insufficiency for Suppressor of Cytokine Signaling-2 Enhances Intestinal Growth and Promotes Polyp Formation in Growth Hormone-Transgenic MiceMichaylira, Carmen Z ; Ramocki, Nicole M ; Simmons, James G ; Tanner, C. Kirby ; McNaughton, Kirk K ; Woosley, John T ; Greenhalgh, Christopher J ; Lund, P. KayEndocrinology (Philadelphia), 2006-04, Vol.147 (4), p.1632-1641 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Insulin Receptor Substrate-1 Deficiency Promotes Apoptosis in the Putative Intestinal Crypt Stem Cell Region, Limits Apcmin/+ Tumors, and Regulates Sox9Ramocki, Nicole M ; Wilkins, Heather R ; Magness, Scott T ; Simmons, James G ; Scull, Brooks P ; Lee, Ginny H ; McNaughton, Kirk K ; Lund, P. KayEndocrinology (Philadelphia), 2008-01, Vol.149 (1), p.261-267 [Periódico revisado por pares]United States: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 geneCARDOSO, Carlos ; LEVENTER, Richard J ; PILZ, Daniela T ; DOBYNS, William B ; LEDBETTER, David H ; MATSUMOTO, Naomichi ; KUC, Julie A ; RAMOCKI, Melissa B ; MEWBORN, Stephanie K ; DUDLICEK, Laura L ; MAY, Lorraine F ; MILLS, Patti L ; DAS, SomaHuman molecular genetics, 2000-12, Vol.9 (20), p.3019-3028 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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4 |
Material Type: Artigo
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Insulin Receptor Substrate-1 Deficiency Promotes Apoptosis in the Putative Intestinal Crypt Stem Cell Region, Limits Apc super(min/+) Tumors, and Regulates Sox9Ramocki, Nicole M ; Wilkins, Heather R ; Magness, Scott T ; Simmons, James G ; Scull, Brooks P ; Lee, Ginny H ; McNaughton, Kirk K ; Lund, PKayEndocrinology (Philadelphia), 2008-01, Vol.149 (1), p.261-267 [Periódico revisado por pares]Texto completo disponível |
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5 |
Material Type: Artigo
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The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 geneCardoso, C ; Leventer, R J ; Matsumoto, N ; Kuc, JA ; Ramocki, M B ; Mewborn, S K ; Dudlicek, L L ; May, L F ; Mills, P L ; Das, S ; Pilz, D T ; Dobyns, W B ; Ledbetter, D HHuman molecular genetics, 2000-12, Vol.19 (20), p.3019-3028 [Periódico revisado por pares]Texto completo disponível |
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6 |
Material Type: Artigo
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Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingCarvalho, Claudia M.B. ; Zhang, Feng ; Liu, Pengfei ; Patel, Ankita ; Sahoo, Trilochan ; Bacino, Carlos A. ; Shaw, Chad ; Peacock, Sandra ; Pursley, Amber ; Tavyev, Y. Jane ; Ramocki, Melissa B. ; Nawara, Magdalena ; Obersztyn, Ewa ; Vianna-Morgante, Angela M. ; Stankiewicz, Pawel ; Zoghbi, Huda Y. ; Cheung, Sau Wai ; Lupski, James R.Human molecular genetics, 2009-06, Vol.18 (12), p.2188-2203 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |