Resultados de procura - Swarr, Daniel T.

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

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“PIK”ing Out New Epigenetic Markers in Lung Disease por 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 por Tolusso, Leandra K., Hazelton, Paige, Wong, Beatrix, Swarr, Daniel T.

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

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Unusual Cardiac “Masses” in a Newborn with Infantile Pompe Disease por 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 por 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 por 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 por 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 por 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... por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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