S. Wert

M. Dishop, C. Langston, E. Cutz, 2006, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A mutation in the surfactant protein C gene associated with familial interstitial lung disease.

F. Askin, A. Hamvas, J. Whitsett, 2001, The New England journal of medicine.

ABCA3 mutations associated with pediatric interstitial lung disease.

J. Whitsett, M. Dean, S. Wert, 2005, American journal of respiratory and critical care medicine.

STAT3 regulates ABCA3 expression and influences lamellar body formation in alveolar type II cells.

J. Whitsett, Yan Xu, V. Besnard, 2008, American journal of respiratory cell and molecular biology.

Hepatocyte nuclear factor 3 activates transcription of thyroid transcription factor 1 in respiratory epithelial cells

J. Whitsett, K. Ikeda, S. Wert, 1996, Molecular and cellular biology.

Adenoviral-mediated gene transfer of human surfactant protein B to respiratory epithelial cells.

J. Whitsett, B. Trapnell, J. Whitsett, 1994, American journal of respiratory cell and molecular biology.

Transcriptional elements from the human SP-C gene direct expression in the primordial respiratory epithelium of transgenic mice.

J. Whitsett, T. Korfhagen, S. Wert, 1993, Developmental biology.

Glucocorticoids regulate surfactant protein synthesis in a pulmonary adenocarcinoma cell line.

A. Gazdar, T. Pilot‐Matias, J. Whitsett, 1989, The American journal of physiology.

Cis-acting sequences from a human surfactant protein gene confer pulmonary-specific gene expression in transgenic mice.

S. Potter, J. Whitsett, J. Stock, 1990, Proceedings of the National Academy of Sciences of the United States of America.

VEGF enhances pulmonary vasculogenesis and disrupts lung morphogenesis in vivo

J. Whitsett, K. Peters, S. Wert, 1998, Developmental dynamics : an official publication of the American Association of Anatomists.

Interleukin-1beta causes pulmonary inflammation, emphysema, and airway remodeling in the adult murine lung.

J. Tichelaar, J. Whitsett, S. Wert, 2005, American journal of respiratory cell and molecular biology.

36 – Trachea, Bronchi, and Lungs

J. Whitsett, R. Elluru, S. Wert, 2004 .

Activation of Sterol-response Element-binding Proteins (SREBP) in Alveolar Type II Cells Enhances Lipogenesis Causing Pulmonary Lipotoxicity*

J. Whitsett, Yan Xu, L. Plantier, 2012, The Journal of Biological Chemistry.

Arrested lung morphogenesis in transgenic mice bearing an SP-C-TGF-beta 1 chimeric gene.

J. Whitsett, L. Zhou, S. Wert, 1996, Developmental biology.

Surfactant protein-B-deficient mice are susceptible to hyperoxic lung injury.

J. Whitsett, H. Iwamoto, C. Bachurski, 1999, American journal of respiratory cell and molecular biology.

Temporal/spatial expression of nuclear receptor coactivators in the mouse lung.

J. Whitsett, S. Wert, C. Yan, 2000, American journal of physiology. Lung cellular and molecular physiology.

Respiratory epithelial cell expression of human transforming growth factor-alpha induces lung fibrosis in transgenic mice.

J. Whitsett, T. Korfhagen, J. McCarty, 1994, The Journal of clinical investigation.

61 – Normal and Abnormal Structural Development of the Lung

S. Wert, 2017 .

Conditional recombination reveals distinct subsets of epithelial cells in trachea, bronchi, and alveoli.

J. Whitsett, A. Perl, S. Wert, 2005, American journal of respiratory cell and molecular biology.

Immunolocalization of Sonic Hedgehog (Shh) in Developing Mouse Lung

J. Whitsett, S. Wert, L. Miller, 2001, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

GM-CSF autoantibodies and neutrophil dysfunction in pulmonary alveolar proteinosis.

B. Trapnell, L. Denson, M. Filippi, 2007, The New England journal of medicine.

Chapter 1 – Molecular Determinants of Lung Morphogenesis

J. Whitsett, S. Wert, 2006 .

Genetic Disorders of Surfactant Dysfunction

J. Whitsett, S. Wert, L. Nogee, 2009, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.

S. Wert, L. Nogee, J. Bullard, 2006, Seminars in perinatology.

Altered surfactant function and structure in SP-A gene targeted mice.

B. Stripp, A. Jobe, J. Whitsett, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Muc5ac expression in mouse lung Monocyte inflammation augments acrolein-induced

S. Shapiro, M. Borchers, S. Wesselkamper, 2016 .

Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C gene.

A. Hamvas, F. Hsu, P. Ballard, 2004, American journal of respiratory cell and molecular biology.

Surfactant protein deficiency in familial interstitial lung disease.

J. Whitsett, J. Tomashefski, R. Baughman, 2001, The Journal of pediatrics.

HNF-3/Forkhead Homologue-4 (HFH-4) Is Expressed in Ciliated Epithelial Cells in the Developing Mouse Lung

J. Tichelaar, J. Whitsett, R. Costa, 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Characteristics of surfactant from SP-A-deficient mice.

A. Jobe, J. Whitsett, M. Bruno, 1998, American journal of physiology. Lung cellular and molecular physiology.

Hyaluronic acid synthesis and gap junction endocytosis are necessary for normal expansion of the cumulus mass

S. Wert, W. J. Larsen, Lin Chen, 1990, Molecular reproduction and development.

Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapy.

B. Rubin, J. Whitsett, B. Trapnell, 2010, American journal of respiratory and critical care medicine.

Genome-wide transcriptional profiling reveals connective tissue mast cell accumulation in bronchopulmonary dysplasia.

S. Bhattacharya, T. Mariani, G. Pryhuber, 2012, American journal of respiratory and critical care medicine.

Genetic Abnormalities of Surfactant Metabolism

S. Wert, L. Nogee, 2010, Molecular Pathology of Lung Diseases.

Patient-derived granulocyte/macrophage colony-stimulating factor autoantibodies reproduce pulmonary alveolar proteinosis in nonhuman primates.

J. Krischer, J. Whitsett, B. Trapnell, 2010, American journal of respiratory and critical care medicine.

A common mutation in the surfactant protein C gene associated with lung disease.

A. Hamvas, J. Whitsett, G. Deutsch, 2005, The Journal of pediatrics.

Forkhead Box m1 transcription factor is required for perinatal lung function

J. Whitsett, T. Kalin, V. Kalinichenko, 2008, Proceedings of the National Academy of Sciences.

Pulmonary malformation in transgenic mice expressing human keratinocyte growth factor in the lung.

J. Whitsett, T. Ulich, L. Zhou, 1995, Proceedings of the National Academy of Sciences of the United States of America.

cis-acting elements that confer lung epithelial cell expression of the CC10 gene.

B. Stripp, J. Whitsett, D. Luse, 1992, The Journal of biological chemistry.

Role of Sonic hedgehog in patterning of tracheal–bronchial cartilage and the peripheral lung

J. Whitsett, Yan Xu, A. Perl, 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

R-spondin 2 is required for normal laryngeal-tracheal, lung and limb morphogenesis

J. Whitsett, W. Scott, M. Mucenski, 2008, Development.

Congenital cystic adenomatoid malformation of the lung (CCAM): evaluation of the cellular components.

F. Askin, J. Whitsett, J. Jagirdar, 1999, Human pathology.

Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease

F. Reinholt, A. Hamvas, J. Whitsett, 2007, Acta paediatrica.

Genetic Disorders of Surfactant Homeostasis

J. Whitsett, Yan Xu, S. Wert, 2005, Neonatology.

Mutations in the surfactant protein C gene associated with interstitial lung disease.

F. Askin, A. Hamvas, J. Whitsett, 2002, Chest.

Absence of Lamellar Bodies with Accumulation of Dense Bodies Characterizes a Novel Form of Congenital Surfactant Defect

J. Mazursky, S. Wert, L. Nogee, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

SP-D and GM-CSF regulate surfactant homeostasis via distinct mechanisms.

J. Whitsett, M. Ikegami, S. Wert, 2001, American journal of physiology. Lung cellular and molecular physiology.

GM-CSF enhances lung growth and causes alveolar type II epithelial cell hyperplasia in transgenic mice.

G. Dranoff, J. Whitsett, S. Wert, 1997, American journal of physiology. Lung cellular and molecular physiology.

GM-CSF enhances lung growth and causes alveolar type II epithelial cell hyperplasia in transgenic mice.

G. Dranoff, J. Whitsett, S. Wert, 1997, American journal of physiology. Lung cellular and molecular physiology.

Genetic disorders of surfactant homeostasis.

J. Whitsett, Yan Xu, S. Wert, 2005, Biology of the neonate.

Increased metalloproteinase activity, oxidant production, and emphysema in surfactant protein D gene-inactivated mice.

M Ikegami, J. Whitsett, G. Ross, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Inherited Surfactant Disorders

S. Wert, L. Nogee, W. Gower, 2008 .

Persistent tachypnea and hypoxia in a 3-month-old term infant.

J. Whitsett, L. Young, G. Deutsch, 2006, The Journal of pediatrics.

InfectionRespiratory Epithelium during Adenoviral Stat3 Is Required for Cytoprotection of the

Kwon-Sik Park, J. Whitsett, Yan Xu, 2006 .

Preendocytotic alterations in cumulus cell gap junctions precede meiotic resumption in the rat cumulus-oocyte complex.

S. Wert, W. J. Larsen, 1990, Tissue & cell.

Meiotic resumption and gap junction modulation in the cultured rat cumulus-oocyte complex.

S. Wert, W. J. Larsen, 1989, Gamete research.

Differential modulation of rat follicle cell gap junction populations at ovulation.

S. Wert, W. J. Larsen, G. D. Brunner, 1987, Developmental biology.

A dramatic loss of cumulus cell gap junctions is correlated with germinal vesicle breakdown in rat oocytes.

S. Wert, W. J. Larsen, G. D. Brunner, 1986, Developmental biology.

Recombinant adenoviral vector disrupts surfactant homeostasis in mouse lung.

B. Trapnell, J. Whitsett, C. Bachurski, 1997, Human gene therapy.

Adenovirus-mediated gene transfer to the respiratory tract of fetal sheep in utero.

B. Trapnell, R. Baughman, J. Whitsett, 1995, Human gene therapy.

Cell‐ and developmental stage‐specific Dicer1 ablation in the lung epithelium models cystic pleuropulmonary blastoma

K. Wikenheiser-Brokamp, J. Shannon, S. Wert, 2015, The Journal of pathology.

Distinct effects of oxygen on surfactant protein B expression in bronchiolar and alveolar epithelium.

J. Whitsett, J. Wispé, M. Stahlman, 1992, The American journal of physiology.

Chapter 76 – Normal and Abnormal Structural Development of the Lung

S. Wert, 2004 .

surfactant treatment effects in preterm lambs Surfactant inhibition by plasma: gestational age and

A. Jobe, B. Yoder, J. Whitsett, 2015 .

Pathogenesis, Presentation, Diagnosis, and Therapy

B. Rubin, J. Whitsett, B. Trapnell, 2010 .

Tissue-specific regulation of the alpha-myosin heavy chain gene promoter in transgenic mice.

J. Robbins, J. Gulick, A. Subramaniam, 1991, The Journal of biological chemistry.

Reduced Surfactant Protein C Expression in Full-Term Infants with Respiratory Distress Syndrome • 1776

J. Whitsett, S. Wert, L. Nogee, 1998, Pediatric Research.

Pulmonary pathology in thyroid transcription factor-1 deficiency syndrome.

J. Whitsett, R. Lindeman, A. Perez-Atayde, 2010, American journal of respiratory and critical care medicine.

Human GM-CSF autoantibodies and reproduction of pulmonary alveolar proteinosis.

J. Whitsett, B. Trapnell, R. Wood, 2009, The New England journal of medicine.

Pulmonary Surfactant Protein A, B, and C mRNA and Protein Expression in the Nitrofen-Induced Congenital Diaphragmatic Hernia Rat Model

J. Ruijter, D. Tibboel, W. Lamers, 2003, Pediatric Research.

Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice.

B. Stripp, J. Whitsett, J. C. Clark, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Roles of cell junctions in gametogenesis and in early embryonic development.

S. Wert, W. J. Larsen, 1988, Tissue & cell.

MEK-ERK pathway modulation ameliorates pulmonary fibrosis associated with epidermal growth factor receptor activation.

Cynthia Davidson, S. Madala, W. Hardie, 2012, American journal of respiratory cell and molecular biology.

Molecular Determinants of Lung Morphogenesis

J. Whitsett, S. Wert, D. Swarr, 2019, Kendig's Disorders of the Respiratory Tract in Children.

Stage-specific regulation of respiratory epithelial cell differentiation by Foxa1.

K. Kaestner, J. Whitsett, V. Besnard, 2005, American journal of physiology. Lung cellular and molecular physiology.

SPDEF is required for mouse pulmonary goblet cell differentiation and regulates a network of genes associated with mucus production.

Susan E Wert, Hans Clevers, Jeffrey A Whitsett, 2009, The Journal of clinical investigation.

Sox17 influences the differentiation of respiratory epithelial cells.

Kwon-Sik Park, J. Whitsett, A. Zorn, 2006, Developmental biology.

Lung Kruppel-like Factor, a Zinc Finger Transcription Factor, Is Essential for Normal Lung Development*

J. Lingrel, S. Wert, M. Wani, 1999, The Journal of Biological Chemistry.

Gsh‐4 encodes a LIM‐type homeodomain, is expressed in the developing central nervous system and is required for early postnatal survival.

J. Whitsett, Gurparkash Singh, M. Weinstein, 1994, The EMBO journal.

Compensatory Roles of Foxa1 and Foxa2 during Lung Morphogenesis*

Jeffrey A Whitsett, K. Kaestner, J. Whitsett, 2005, Journal of Biological Chemistry.

Sox2 Is Required for Maintenance and Differentiation of Bronchiolar Clara, Ciliated, and Goblet Cells

J. Whitsett, R. Lang, V. Besnard, 2009, PloS one.

Beta-catenin regulates differentiation of respiratory epithelial cells in vivo.

A. R. Thitoff, J. Whitsett, Yan Xu, 2005, American journal of physiology. Lung cellular and molecular physiology.

Early restriction of peripheral and proximal cell lineages during formation of the lung

Susan E. Wert, Andras Nagy, Jeffrey A. Whitsett, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Hepatocyte nuclear factor‐3β limits cellular diversity in the developing respiratory epithelium and alters lung morphogenesis in vivo

J. Whitsett, R. Costa, S. Wert, 1997, Developmental dynamics : an official publication of the American Association of Anatomists.

Targeted expression of a dominant negative FGF receptor blocks branching morphogenesis and epithelial differentiation of the mouse lung.

S. Werner, J. Whitsett, L. Williams, 1994, The EMBO journal.

Expression of Thyroid Transcription Factor-1, Surfactant Proteins, Type I Cell–associated Antigen, and Clara Cell Secretory Protein in Pulmonary Hypoplasia

J. Whitsett, C. Langston, S. Wert, 2001, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

A Molecular atlas of Xenopus respiratory system development

A. Zorn, S. Rankin, S. Wert, 2015, Developmental dynamics : an official publication of the American Association of Anatomists.

A nonredundant role for mouse Serpinb3a in the induction of mucus production in asthma.

J. Whitsett, M. Wills-Karp, G. Silverman, 2011, The Journal of allergy and clinical immunology.

Immunohistochemical localization of Foxa1 and Foxa2 in mouse embryos and adult tissues.

J. Whitsett, V. Besnard, S. Wert, 2004, Gene expression patterns : GEP.

Acrolein-induced MUC5ac expression in rat airways.

G. Leikauf, M. Borchers, S. Wert, 1998, American journal of physiology. Lung cellular and molecular physiology.

Acrolein-induced MUC5ac expression in rat airways.

G. Leikauf, M. Borchers, S. Wert, 1998, The American journal of physiology.

Keratinocyte growth factor stimulates transduction of the respiratory epithelium by retroviral vectors.

C. Halbert, A. Miller, J. Whitsett, 1999, Human gene therapy.

FGF-10 disrupts lung morphogenesis and causes pulmonary adenomas in vivo.

J. Tichelaar, J. Whitsett, J. C. Clark, 2001, American journal of physiology. Lung cellular and molecular physiology.

Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR.

J. Whitsett, R. Frizzell, S. Wert, 1994, Science.

Conditional deletion of Pten causes bronchiolar hyperplasia.

A. R. Thitoff, J. Whitsett, V. Davé, 2008, American journal of respiratory cell and molecular biology.

Comprehensive anatomic ontologies for lung development: A comparison of alveolar formation and maturation within mouse and human lung

Huaqin Pan, Gail H Deutsch, Susan E Wert, 2019, Journal of Biomedical Semantics.

Sox17 is required for normal pulmonary vascular morphogenesis.

P. Thurner, J. Whitsett, Yan Xu, 2014, Developmental biology.

Foxm1 transcription factor is critical for proliferation and differentiation of Clara cells during development of conducting airways.

Susan E Wert, Jeffrey A Whitsett, J. Whitsett, 2012, Developmental biology.

Sox2 activates cell proliferation and differentiation in the respiratory epithelium.

J. Whitsett, V. Besnard, M. Bruno, 2011, American journal of respiratory cell and molecular biology.

Kruppel-like factor 5 is required for perinatal lung morphogenesis and function

J. Whitsett, Yan Xu, H. Wan, 2008, Development.

In situ localization of sodium-potassium ATPase mRNA in developing mouse lung epithelium.

J. Lingrel, S. Wert, G. R. Askew, 1995, The American journal of physiology.

ABCA3 gene mutations in newborns with fatal surfactant deficiency.

J. Whitsett, M. Dean, S. Wert, 2004, The New England journal of medicine.

Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease.

Susan E Wert, Jeffrey A Whitsett, J. Whitsett, 2010, Annual review of medicine.

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA

B. Rubin, J. Whitsett, T. Smolarek, 2008, The Journal of experimental medicine.

Interleukin-4 alters epithelial cell differentiation and surfactant homeostasis in the postnatal mouse lung.

J. Whitsett, J. Rankin, S. Wert, 1997, American journal of respiratory cell and molecular biology.

Conditional deletion of Abca3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice.

J. Whitsett, Yan Xu, V. Besnard, 2010, American journal of physiology. Lung cellular and molecular physiology.

Conditional deletion of Abca 3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice

J. Whitsett, Yan Xu, V. Besnard, 2010 .

Expression of ABCA3 in Developing Lung and Other Tissues

J. Whitsett, Yan Xu, V. Besnard, 2007, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Immunoregulatory effects of regulated, lung-targeted expression of IL-10 in vivo.

T. Shanley, Bin Zhao, S. Wert, 2005, American journal of physiology. Lung cellular and molecular physiology.

Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1.

J. Rosenfeld, A. Halbower, A. Hamvas, 2013, Chest.

Pulmonary Nodules in a Newborn With ATP-Binding Cassette Transporter A3 (ABCA3) Mutations

S. Wert, L. Nogee, Derek A. Uchida, 2011, Pediatrics.

Fibroblast Growth Factor 18 Influences Proximal Programming during Lung Morphogenesis*

J. Tichelaar, J. Whitsett, N. Itoh, 2002, The Journal of Biological Chemistry.

Stat-3 is required for pulmonary homeostasis during hyperoxia.

S. Akira, K. Takeda, J. Whitsett, 2004, The Journal of clinical investigation.

Unexplained neonatal respiratory distress due to congenital surfactant deficiency.

R. Boldrini, M. Ferrari, O. Danhaive, 2007, The Journal of pediatrics.

Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.

J. Whitsett, S. Wert, L. Nogee, 2000, American journal of respiratory and critical care medicine.

Deficiency of lamellar bodies in alveolar type II cells associated with fatal respiratory disease in a full-term infant.

A. Moore, E. Cutz, S. Wert, 2000, American journal of respiratory and critical care medicine.

CDC42 is required for structural patterning of the lung during development.

J. Whitsett, W. Xu, Yi Zheng, 2013, Developmental biology.

Reversal of lung lesions in transgenic transforming growth factor alpha mice by expression of mutant epidermal growth factor receptor.

J. Whitsett, W. Hardie, K. Huelsman, 1996, American journal of respiratory cell and molecular biology.

SPDEF regulates goblet cell hyperplasia in the airway epithelium.

Kwon-Sik Park, J. Whitsett, H. Wan, 2007, The Journal of clinical investigation.

Ultrastructure of Highly Ordered Granules in Alveolar Type II Cells in Several Species

Aleksey A. Porollo, A. Porollo, Marian L Miller, 2018, Anatomical record.

Genetic element from human surfactant protein SP-C gene confers bronchiolar-alveolar cell specificity in transgenic mice.

J. Whitsett, M. Bruno, T. Korfhagen, 1991, The American journal of physiology.

Stat3 Is Required for Cytoprotection of the Respiratory Epithelium during Adenoviral Infection1

Kwon-Sik Park, J. Whitsett, Yan Xu, 2006, The Journal of Immunology.

Safety of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator cDNA to the lungs of nonhuman primates.

G. Boivin, J. Whitsett, B. Trapnell, 1996, Human gene therapy.

Partial SP-B deficiency perturbs lung function and causes air space abnormalities.

J. Whitsett, K. Melton, M. Ikegami, 2005, American journal of physiology. Lung cellular and molecular physiology.

Hereditary surfactant protein B deficiency resulting from a novel mutation

A. Colombo, S. Wert, L. Nogee, 2000, Intensive Care Medicine.

Surfactant Protein-D Regulates Surfactant Phospholipid Homeostasis in Vivo *

Susan E. Wert, James H. Fisher, Jeffrey A. Whitsett, 1998, The Journal of Biological Chemistry.

Transcriptional Programs Controlling Perinatal Lung Maturation

Susan E. Wert, Leah Rae Donahue, Jeffrey A. Whitsett, 2012, PloS one.

Expression of a Human Surfactant Protein C Mutation Associated with Interstitial Lung Disease Disrupts Lung Development in Transgenic Mice*

Susan E Wert, J. Bridges, S. Wert, 2003, Journal of Biological Chemistry.

Calcineurin/Nfat signaling is required for perinatal lung maturation and function.

J. Neilson, G. Crabtree, J. Whitsett, 2006, The Journal of clinical investigation.

Deletion of Scap in Alveolar Type II Cells Influences Lung Lipid Homeostasis and Identifies a Compensatory Role for Pulmonary Lipofibroblasts*

J. Whitsett, Yan Xu, V. Besnard, 2009, Journal of Biological Chemistry.

Surfactant Protein B Corrects Oxygen-Induced Pulmonary Dysfunction in Heterozygous Surfactant Protein B–Deficient Mice

J. Whitsett, J. Baatz, M. Ikegami, 1999, Pediatric Research.

Preferential uptake of small-aggregate fraction of pulmonary surfactant in vitro.

J. Whitsett, M. Ikegami, S. Wert, 1997, The American journal of physiology.

Transgenic models for study of lung morphogenesis and repair: Parker B. Francis lecture.

J. Tichelaar, J. Whitsett, J. C. Clark, 2001, Chest.

Increased expression of thyroid transcription factor-1 (TTF-1) in respiratory epithelial cells inhibits alveolarization and causes pulmonary inflammation.

Susan E Wert, Shioko Kimura, Jeffrey A Whitsett, 2002, Developmental biology.

Congenital Malformations of the Lung

A. Jobe, J. Whitsett, K. Wikenheiser-Brokamp, 2016 .

An En Bloc Staining Protocol Improves The Preservation of Lamellar Bodies in Alveolar Type II Epithelial Cells for Transgenic Mice Expressing Modified Pulmonary Surfactant Protein B

S. Wert, D. Beck, J. S. Breslin, 1998, Microscopy and Microanalysis.

Surfactant peptides stimulate uptake of phosphatidylcholine by isolated cells.

J. Whitsett, J. Baatz, S. Wert, 1989, Biochimica et biophysica acta.

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic mice

B. Stripp, J. Whitsett, James M. Wilson, 1992, Nature genetics.

Maternal Synchronization of Gestational Length and Lung Maturation

S. Murray, L. Donahue, J. Whitsett, 2011, PloS one.

Pulmonary Alveolar Proteinosis (PAP) Reproduced in Non-Human Primates.

B. Trapnell, K. Nakata, R. Wood, 2009, ATS 2009.

Surfactant proteins and cell markers in the respiratory epithelium of the amphibian, Ambystoma mexicanum.

J. Whitsett, S. Wert, L. D. Miller, 2001, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

Plasminogen Did Not Affect Lung Function in Surfactant-Treated Preterm Lambs

A. Jobe, M. Ikegami, S. Wert, 2000, Neonatology.

Forkhead box M1 transcriptional factor is required for smooth muscle cells during embryonic development of blood vessels and esophagus.

Yan Xu, J. Lessard, T. Kalin, 2009, Developmental biology.

Conditional Deletion Of Abca3 In Alveolar Type II Cells Alters Surfactant Homeostasis In Newborn And Adult Mice

J. Whitsett, Yan Xu, V. Besnard, 2010, ATS 2010.

Expression of Thyroid Transcription Factor-1 in Congenital Cystic Adenomatoid Malformation of the Lung

F. Askin, J. Whitsett, S. Wert, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

In vivo evaluation of the safety of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator cDNA to the lung.

J. Whitsett, B. Trapnell, J. Whitsett, 1994, Human gene therapy.

Ontology-guided segmentation and object identification for developmental mouse lung immunofluorescent images

Anna Maria Masci, Scott White, Ben Neely, 2020, bioRxiv.

Surfactant protein B deficiency: Clinical, histological and molecular evaluation

J. Christodoulou, S. Wert, L. Nogee, 1999, Journal of paediatrics and child health.

SURFACTANT PROTEIN (SP) B DEFICIENCY IN NEONATES WITH SEVERE RESPIRATORY FAILURE. • 2044

J. Whitsett, S. Wert, L. Nogee, 1996, Pediatric Research.

Does adiponectin play a role in pulmonary emphysema?

S. Wert, 2008, American journal of physiology. Lung cellular and molecular physiology.

SPDEF is required for mouse pulmonary goblet cell differentiation and regulates a network of genes associated with mucus production.

H. Clevers, J. Whitsett, Yan Xu, 2009, The Journal of clinical investigation.