תוצאות חיפוש - Swarr, Daniel T.

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

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

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

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