受强制性开放获取政策约束的文章 - Daniel T Swarr了解详情
无法在其他位置公开访问的文章：2 篇
Detection and impact of genetic disease in a level IV neonatal intensive care unit
L Hagen, D Khattar, K Whitehead, H He, DT Swarr, K Suhrie
Journal of Perinatology 42 (5), 580-588, 2022
强制性开放获取政策： US National Institutes of Health
Cell-and tissue-based therapies for lung disease
JA Whitsett, W Zacharias, D Swarr, VV Kalinichenko
Principles of Tissue Engineering, 1253-1272, 2020
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：22 篇
Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development
MJ Herriges, DT Swarr, MP Morley, KS Rathi, T Peng, KM Stewart, ...
Genes & development 28 (12), 1363-1379, 2014
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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
P Sen, Y Yang, C Navarro, I Silva, P Szafranski, KE Kolodziejska, ...
Human mutation 34 (6), 801-811, 2013
强制性开放获取政策： US National Institutes of Health
Lung endoderm morphogenesis: gasping for form and function
DT Swarr, EE Morrisey
Annual review of cell and developmental biology 31 (1), 553-573, 2015
强制性开放获取政策： US National Institutes of Health
Clinical features of three girls with mosaic genome‐wide paternal uniparental isodisomy
JM Kalish, LK Conlin, TR Bhatti, HA Dubbs, MC Harris, K Izumi, ...
American journal of medical genetics Part A 161 (8), 1929-1939, 2013
强制性开放获取政策： US National Institutes of Health
Congenital cystic lung lesions: redefining the natural distribution of subtypes and assessing the risk of malignancy
J Pogoriler, D Swarr, P Kreiger, NS Adzick, W Peranteau
The American journal of surgical pathology 43 (1), 47-55, 2019
强制性开放获取政策： US National Institutes of Health
Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit
TL Wenger, J Gerdes, K Taub, DT Swarr, MA Deardorff, NS Abend
Journal of Perinatology 34 (3), 234-240, 2014
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Novel molecular and phenotypic insights into congenital lung malformations
DT Swarr, WH Peranteau, J Pogoriler, DB Frank, NS Adzick, HL Hedrick, ...
American Journal of Respiratory and Critical Care Medicine 197 (10), 1328-1339, 2018
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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
P Kruszka, D Li, MH Harr, NR Wilson, D Swarr, EM McCormick, ...
Journal of medical genetics 52 (2), 104-110, 2015
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Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes
LK Tolusso, P Hazelton, B Wong, DT Swarr
Genetics in Medicine 23 (5), 909-917, 2021
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The long noncoding RNA Falcor regulates Foxa2 expression to maintain lung epithelial homeostasis and promote regeneration
DT Swarr, M Herriges, S Li, M Morley, S Fernandes, A Sridharan, S Zhou, ...
Genes & development 33 (11-12), 656-668, 2019
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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 …
J Nathanson, DT Swarr, A Singer, M Liu, A Chinn, W Jones, J Hurst, ...
American Journal of Medical Genetics Part A 161 (3), 473-478, 2013
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Perinatal outcomes of fetuses and infants diagnosed with trisomy 13 or trisomy 18
DME Cortezzo, LK Tolusso, DT Swarr
The Journal of Pediatrics 247, 116-123. e5, 2022
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Inflammatory blockade prevents injury to the developing pulmonary gas exchange surface in preterm primates
A Toth, S Steinmeyer, P Kannan, J Gray, CM Jackson, S Mukherjee, ...
Science Translational Medicine 14 (638), eabl8574, 2022
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Alveolar epithelial progenitor cells require Nkx2-1 to maintain progenitor-specific epigenomic state during lung homeostasis and regeneration
A Toth, P Kannan, J Snowball, M Kofron, JA Wayman, JP Bridges, ...
Nature Communications 14 (1), 8452, 2023
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PI3K signaling specifies proximal-distal fate by driving a developmental gene regulatory network in SOX9+ mouse lung progenitors
D Khattar, S Fernandes, J Snowball, M Guo, MC Gillen, SS Jain, D Sinner, ...
Elife 11, e67954, 2022
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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
LR Young, BC Trapnell, KD Mandl, DT Swarr, JA Wambach, CJ Blaisdell
Annals of the American Thoracic Society 13 (12), 385-393, 2016
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Expanding the differential diagnosis of fetal hydrops: an unusual prenatal presentation of megalencephaly-capillary malformation syndrome
DT Swarr, N Khalek, J Treat, MA Horton, GM Mirzaa, JB Riviere, ...
Prenatal diagnosis 33 (10), 1010, 2013
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Detection of mutually exclusive mosaicism in a girl with genotype‐phenotype discrepancies
M Luo, S Mulchandani, HA Dubbs, D Swarr, L Pyle, EH Zackai, ...
American Journal of Medical Genetics Part A 167 (12), 3091-3095, 2015
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