Resultats de la cerca - Swarr, Daniel T.

Lung Endoderm Morphogenesis: Gasping for Form and Function per Swarr, Daniel T., Morrisey, Edward E.

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“PIK”ing Out New Epigenetic Markers in Lung Disease per Swarr, Daniel, Putcha, Nirupama, Zacharias, William

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Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes per Tolusso, Leandra K., Hazelton, Paige, Wong, Beatrix, Swarr, Daniel T.

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Preterm infant with diprosopus and holoprosencephaly per Nair, Nitya M., Swarr, Daniel T., Barnes‐Davis, Maria E.

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Unusual Cardiac “Masses” in a Newborn with Infantile Pompe Disease per Swarr, Daniel T., Kaufman, Beth, Fogel, Mark A., Finkel, Richard, Ganesh, Jaya

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Congenital Cystic Lung Lesions: Redefining the natural distribution of subtypes and assessing the risk of malignancy per Pogoriler, Jennifer, Swarr, Daniel, Kreiger, Portia, Adzick, N Scott, Peranteau, William

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Telemedicine for genetic and neurologic evaluation in the Neonatal Intensive Care Unit per Wenger, Tara L., Gerdes, Jeffrey, Taub, Katherine, Swarr, Daniel T., Deardorff, Matthew A., Abend, Nicholas S.

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Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health–NHLBI Workshop, September 3 and 4, 2015 per Young, Lisa R., Trapnell, Bruce C., Mandl, Kenneth D., Swarr, Daniel T., Wambach, Jennifer A., Blaisdell, Carol J.

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Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development per Herriges, Michael J., Swarr, Daniel T., Morley, Michael P., Rathi, Komal S., Peng, Tien, Stewart, Kathleen M., Morrisey, Edward E.

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Novel FREM1 Mutations Expand the Phenotypic Spectrum Associated with Manitoba-Oculo-Tricho-Anal (MOTA) Syndrome and Bifid Nose Renal Agenesis Anorectal Malformations (BNAR) Syndrom... per Nathanson, Jared, Swarr, Daniel T., Singer, Amihood, Liu, Mochi, Chinn, Amy, Jones, Wendy, Hurst, Jane, Khalek, Nahla, Zackai, Elaine, Slavotinek, Anne

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Expanding the Differential Diagnosis of Fetal Hydrops: An Unusual Prenatal Presentation of Megalencephaly-Capillary Malformation Syndrome per Swarr, Daniel T., Khalek, Nahla, Treat, James, Horton, Margaret A., Mirzaa, Ghayda M., Riviere, Jean-Baptiste, Dobyns, William B, Zackai, Elaine H.

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The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration per Swarr, Daniel T., Herriges, Michael, Li, Shanru, Morley, Mike, Fernandes, Sharlene, Sridharan, Anusha, Zhou, Su, Garcia, Benjamin A., Stewart, Kathleen, Morrisey, Edward E.

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Novel Molecular and Phenotypic Insights into Congenital Lung Malformations per Swarr, Daniel T., Peranteau, William H., Pogoriler, Jennifer, Frank, David B., Adzick, N. Scott, Hedrick, Holly L., Morley, Mike, Zhou, Su, Morrisey, Edward E.

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Clinical Features of Three Girls With Mosaic Genome-Wide Paternal Uniparental Isodisomy per Kalish, Jennifer M., Conlin, Laura K., Bhatti, Tricia R., Dubbs, Holly A., Harris, Mary Catherine, Izumi, Kosuke, Mostoufi-Moab, Sogol, Mulchandani, Surabhi, Saitta, Sulagna, States, Lisa J., Swarr, Daniel T., Wilkens, Alisha B., Zackai, Elaine H., Zelley, Kristin, Bartolomei, Marisa S., Nichols, Kim E., Palladino, Andrew A., Spinner, Nancy B., Deardorff, Matthew A.

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Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome per Kruszka, Paul, Li, Dong, Harr, Margaret H, Wilson, Nathan R, Swarr, Daniel, McCormick, Elizabeth M, Chiavacci, Rosetta M, Li, Mindy, Martinez, Ariel F, Hart, Rachel A, McDonald-McGinn, Donna M, Deardorff, Matthew A, Falk, Marni J, Allanson, Judith E, Hudson, Cindy, Johnson, John P, Saadi, Irfan, Hakonarson, Hakon, Muenke, Maximilian, Zackai, Elaine H

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Inflammatory blockade prevents injury to the developing pulmonary gas exchange surface in preterm primates per Toth, Andrea, Steinmeyer, Shelby, Kannan, Paranthaman, Gray, Jerilyn, Jackson, Courtney M., Mukherjee, Shibabrata, Demmert, Martin, Sheak, Joshua R., Benson, Daniel, Kitzmiller, Joseph, Wayman, Joseph A., Presicce, Pietro, Cates, Christopher, Rubin, Rhea, Chetal, Kashish, Du, Yina, Miao, Yifei, Gu, Mingxia, Guo, Minzhe, Kalinichenko, Vladimir V., Kallapur, Suhas G., Miraldi, Emily R., Xu, Yan, Swarr, Daniel, Lewkowich, Ian, Salomonis, Nathan, Miller, Lisa, Sucre, Jennifer S., Whitsett, Jeffrey A., Chougnet, Claire A., Jobe, Alan H., Deshmukh, Hitesh, Zacharias, William J.

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Novel FOXF1 mutations in sporadic and familial cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins imply a role for its DNA binding domain per Sen, Partha, Yang, Yaping, Navarro, Colby, Silva, Iris, Szafranski, Przemyslaw, Kolodziejska, Katarzyna E., Dharmadhikari, Avinash V., Mostafa, Hasnaa, Kozakewich, Harry, Kearney, Debra, Cahill, John B., Whitt, Merrissa, Bilic, Masha, Margraf, Linda, Charles, Adrian, Goldblatt, Jack, Gibson, Kathleen, Lantz, Patrick, Garvin, Julian, Petty, John, Kiblawi, Zeina, Zuppan, Craig, McConkie-Rosell, Allyn, McDonald, Marie T., Peterson-Carmichael, Stacey L., Gaede, Jane T., Shivanna, Binoy, Schady, Deborah, Friedlich, Philippe S., Hays, Stephen R., Palafoll, Irene Valenzuela, Siebers-Renelt, Ulrike, Bohring, Axel, Finn, Laura S., Siebert, Joseph R., Galambos, Csaba, Nguyen, Lananh, Riley, Melissa, Chassaing, Nicolas, Vigouroux, Adeline, Rocha, Gustavo, Fernandes, Susana, Brumbaugh, Jane, Roberts, Kari, Ho-ming, Luk, Lo, Ivan, Lam, Stephen, Gerychova, Romana, Jezova, Marta, Valaskova, Iveta, Fellmann, Florence, Afshar, Katayoun, Giannoni, Eric, Muhlethaler, Vincent, Liang, Jinlong, Beckmann, Jacques S., Lioy, Janet, Deshmukh, Hitesh, Srinivasan, Lakshmi, Swarr, Daniel T., Sloman, Melissa, Shaw-Smith, Charles, van Loon, Rosa Laura, Hagman, Cecilia, Sznajer, Yves, Barrea, Catherine, Galant, Christine, Detaille, Thierry, Wambach, Jennifer A., Cole, F. Sessions, Hamvas, Aaron, Prince, Lawrence S., Diderich, Karin E.M., Brooks, Alice S., Verdijk, Rob M., Ravindranathan, Hari, Sugo, Ella, Mowat, David, Baker, Michael L., Langston, Claire, Welty, Stephen, Stankiewicz, Pawel

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