Resultados da pesquisa - Sanchez-Lara, Pedro A
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X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female Por Vidmar, Alaina P., Miyazaki, Brian, Sanchez-Lara, Pedro A., Pitukcheewanont, Pisit
Publicado em 2017Text -
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Transforming Growth Factor-β Regulates Basal Transcriptional Regulatory Machinery to Control Cell Proliferation and Differentiation in Cranial Neural Crest-derived Osteoprogenitor... Por Iwata, Jun-ichi, Hosokawa, Ryoichi, Sanchez-Lara, Pedro A., Urata, Mark, Slavkin, Harold, Chai, Yang
Publicado em 2010Text -
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Generation and Characterization of Tamoxifen-Inducible Pax9-CreER Knock-In Mice using CrispR/Cas9 Por Feng, Jifan, Jing, Junjun, Sanchez-Lara, Pedro A, Bootwalla, Moiz S, Buckley, Jonathan, Wu, Nancy, Yan, Youzhen, Chai, Yang
Publicado em 2016Text -
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Whole genome sequencing identifies a cryptic SOX9 regulatory element duplication underlying a case of 46,XX ovotesticular difference of sexual development Por Qian, Zhiyu, Grand, Katheryn, Freedman, Andrew, Nieto, Maria C., Behlmann, Andrea, Schweiger, Bahareh M., Sanchez‐Lara, Pedro A.
Publicado em 2021Text -
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Integration of comprehensive 3D microCT and signaling analysis reveals differential regulatory mechanisms of craniofacial bone development Por Ho, Thach-Vu, Iwata, Junichi, Ho, Hoang Anh, Grimes, Weston C., Park, Shery, Sanchez-Lara, Pedro A., Chai, Yang
Publicado em 2015Text -
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TGFβ regulates epithelial-mesenchymal interactions through WNT signaling activity to control muscle development in the soft palate Por Iwata, Jun-ichi, Suzuki, Akiko, Yokota, Toshiaki, Ho, Thach-Vu, Pelikan, Richard, Urata, Mark, Sanchez-Lara, Pedro A., Chai, Yang
Publicado em 2014Text -
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Smad4-Irf6 genetic interaction and TGFβ-mediated IRF6 signaling cascade are crucial for palatal fusion in mice Por Iwata, Jun-ichi, Suzuki, Akiko, Pelikan, Richard C., Ho, Thach-Vu, Sanchez-Lara, Pedro A., Urata, Mark, Dixon, Michael J., Chai, Yang
Publicado em 2013Text -
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Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibroma... Por Davidson, Tom B, Sanchez-Lara, Pedro A, Randolph, Linda M, Krieger, Mark D, Wu, Shi-Qi, Panigrahy, Ashok, Shimada, Hiroyuki, Erdreich-Epstein, Anat
Publicado em 2012Text -
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Hypertrophic scarring in cleft lip repair: a comparison of incidence among ethnic groups Por Soltani, Ali M, Francis, Cameron S, Motamed, Arash, Karatsonyi, Ashley L, Hammoudeh, Jeffrey A, Sanchez-Lara, Pedro A, Reinisch, John F, Urata, Mark M
Publicado em 2012Text