Effect of Ampicillin and Chloramphenicol Alone and in Combination on Ampicillin-Susceptible and -Resistant Haemophilus influenzae Type B

Por Cole, F. Sessions, Daum, Robert S., Teller, Lynn, Goldmann, Donald A., Smith, Arnold L.
Publicado em 1979

Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm, and Term Infants

Por Shen, Carol L., Zhang, Qunyuan, Meyer, Julia, Cole, F. Sessions, Wambach, Jennifer A.
Publicado no J Pediatr (2016)

Determination of Protein Turnover in Human Infants and Alveolar Type 2 Cells

Por Bereman, Michael, Heins, Hillary, Hamvas, Aaron, Guttentag, Susan, Cole, F. Sessions, MacCoss, Michael J.
Publicado em 2012

Respiratory Failure in a Term Infant with Cis and Trans Mutations in ABCA3

Por Jackson, Tara, Wegner, Daniel J., White, Frances V., Hamvas, Aaron, Cole, F. Sessions, Wambach, Jennifer A.
Publicado no J Perinatol (2015)

Congenital Lymphocytic Choriomeningitis Virus: When to consider the diagnosis

Por Anderson, Jacqueline L., Levy, Philip Thaler, Leonard, Kathryn B., Smyser, Christopher D., Tychsen, Lawrence, Cole, F. Sessions.
Publicado em 2013

An intronic ABCA3 mutation responsible for respiratory disease

Por Agrawal, Amit, Hamvas, Aaron, Cole, F. Sessions, Wambach, Jennifer, Wegner, Daniel, Coghill, Carl, Harrison, Keith, Nogee, Lawrence M.
Publicado em 2012

Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype

Por van Meel, Eline, Wegner, Daniel J, Cliften, Paul, Willing, Marcia C, White, Frances V, Kornfeld, Stuart, Cole, F Sessions
Publicado em 2013

Synonymous ABCA3 Variants Do Not Increase Risk for Neonatal Respiratory Distress Syndrome

Por Wambach, Jennifer A., Wegner, Daniel J., Heins, Hillary B., Druley, Todd E., Mitra, Robi D., Hamvas, Aaron, Cole, F. Sessions
Publicado em 2014

Genotype–Phenotype Correlations for Infants and Children with ABCA3 Deficiency

Por Wambach, Jennifer A., Casey, Alicia M., Fishman, Martha P., Wegner, Daniel J., Wert, Susan E., Cole, F. Sessions, Hamvas, Aaron, Nogee, Lawrence M.
Publicado no Am J Respir Crit Care Med (2014)

A Method to Determine the Kinetics of Multiple Proteins in Human Infants with Respiratory Distress Syndrome

Por Bereman, Michael S., Tomazela, Daniela M., Heins, Hillary S., Simonato, Manuela, Cogo, Paola E., Hamvas, Aaron, Patterson, Bruce W., Cole, F. Sessions, MacCoss, Michael J.
Publicado em 2012

Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations

Por Coghlan, Meghan A, Shifren, Adrian, Huang, Howard J, Russell, Tonya D, Mitra, Robi D, Zhang, Qunyuan, Wegner, Daniel J, Cole, F Sessions, Hamvas, Aaron
Publicado no BMJ Open Respir Res (2014)

Developmental and Genetic Regulation of Human Surfactant Protein B in vivo

Por Hamvas, Aaron, Heins, Hillary B., Guttentag, Susan H., Wegner, Daniel J., Trusgnich, Michelle A., Bennet, Kate W., Yang, Ping, Carlson, Christopher S., An, Ping, Cole, F. Sessions
Publicado em 2009

Comprehensive Genetic Variant Discovery in the Surfactant Protein B Gene

Por Hamvas, Aaron, Wegner, Daniel J., Carlson, Christopher S., Bergmann, Kelly R., Trusgnich, Michelle A., Fulton, Lucinda, Kasai, Yumi, An, Ping, Mardis, Elaine R., Wilson, Richard K., Cole, F. Sessions
Publicado em 2007

Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins

Por Szafranski, Przemyslaw, Dharmadhikari, Avinash V., Wambach, Jennifer A., Towe, Chris T., White, Frances V., Grady, R. Mark, Eghtesady, Pirooz, Cole, F. Sessions, Deutsch, Gail, Sen, Partha, Stankiewicz, Pawel
Publicado em 2014

Single ABCA3 Mutations Increase Risk for Neonatal Respiratory Distress Syndrome

Por Wambach, Jennifer A., Wegner, Daniel J., DePass, Kelcey, Heins, Hillary, Druley, Todd E., Mitra, Robi D., An, Ping, Zhang, Qunyuan, Nogee, Lawrence M., Cole, F. Sessions, Hamvas, Aaron
Publicado em 2012

Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome

Por Wambach, Jennifer A., Yang, Ping, Wegner, Daniel J., Heins, Hillary B., Kaliberova, Lyudmila N., Kaliberov, Sergey A., Curiel, David T., White, Frances V., Hamvas, Aaron, Hackett, Brian P., Cole, F. Sessions
Publicado no Am J Respir Cell Mol Biol (2016)

Measurement of human surfactant protein-B turnover in vivo from tracheal aspirates using targeted proteomics

Por Tomazela, Daniela, Patterson, Bruce W., Hanson, Elizabeth, Spence, Kimberly L., Kanion, Tiffany B., Salinger, David H., Vicini, Paolo, Barret, Hugh, Heins, Hillary B., Cole, F. Sessions, Hamvas, Aaron, MacCoss, Michael J.
Publicado em 2010

Population and Disease-based Prevalence of the Common Mutations Associated with Surfactant Deficiency

Por Garmany, Tami H., Wambach, Jennifer A., Heins, Hillary B., Watkins-Torry, Julie M., Wegner, Daniel J., Bennet, Kate, An, Ping, Land, Garland, Saugstad, O. D., Henderson, Howard, Nogee, Lawrence M., Cole, F. Sessions, Hamvas, Aaron
Publicado em 2008

Quantification of rare allelic variants from pooled genomic DNA

Por Druley, Todd E, Vallania, Francesco LM, Wegner, Daniel J, Varley, Katherine E, Knowles, Olivia L, Bonds, Jacqueline A, Robison, Sarah W, Doniger, Scott W, Hamvas, Aaron, Cole, F. Sessions, Fay, Justin C, Mitra, Robi D
Publicado em 2009

Recombination as a Mechanism for Sporadic Mutation in the Surfactant Protein-C Gene

Por McBee, Amy D., Wegner, Daniel J., Carlson, Christopher S., Wambach, Jennifer A., Yang, Ping, Heins, Hillary B., Saugstad, Ola D., Trusgnich, Michelle A., Watkins-Torry, Julie, Nogee, Lawrence M., Henderson, Howard, Cole, F. Sessions, Hamvas, Aaron
Publicado em 2008