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    Wyświetlanie 1-12 z 12
    Tytuł:
    Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice.
    Autorzy:
    Sen P; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America.
    Dharmadhikari AV; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
    Majewski T; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
    Mohammad MA; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America.
    Kalin TV; Division of Pulmonary Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio, United States of America.
    Zabielska J; Institute of Informatics, University of Warsaw, Warsaw, Poland.
    Ren X; Division of Pulmonary Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio, United States of America.
    Bray M; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
    Brown HM; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America; Robinson Research Institute, School of Pediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
    Welty S; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America.
    Thevananther S; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
    Langston C; Department of Pathology, Baylor College of Medicine, Houston, Texas, United States of America.
    Szafranski P; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
    Justice MJ; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
    Kalinichenko VV; Division of Pulmonary Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, Ohio, United States of America.
    Gambin A; Institute of Informatics, University of Warsaw, Warsaw, Poland; Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw, Poland.
    Belmont J; Department of Pediatrics, Baylor College of Medicine, Houston, Texas, United States of America; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
    Stankiewicz P; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
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    Źródło:
    PloS one [PLoS One] 2014 Apr 10; Vol. 9 (4), pp. e94390. Date of Electronic Publication: 2014 Apr 10 (Print Publication: 2014).
    Typ publikacji:
    Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Genes, Lethal*
    Transcriptome*
    Forkhead Transcription Factors/*genetics
    Lung/*metabolism
    Persistent Fetal Circulation Syndrome/*genetics
    Pulmonary Alveoli/*abnormalities
    Pulmonary Veins/*metabolism
    Animals ; Animals, Newborn ; Female ; Forkhead Transcription Factors/deficiency ; Gene Expression Profiling ; Gene Expression Regulation ; Heterozygote ; Humans ; Infant, Newborn ; Lung/abnormalities ; Lung/blood supply ; Male ; Metabolic Networks and Pathways ; Mice ; Mice, Knockout ; Persistent Fetal Circulation Syndrome/metabolism ; Pulmonary Alveoli/blood supply ; Pulmonary Alveoli/metabolism ; Pulmonary Veins/abnormalities
    SCR Disease Name:
    Alveolar capillary dysplasia
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia.
    Autorzy:
    Szafranski, Przemyslaw (AUTHOR)
    Garimella, Rijutha P. (AUTHOR)
    Mani, Haresh (AUTHOR)
    Hartman, Ryan (AUTHOR)
    Deutsch, Gail (AUTHOR)
    Silk, Alan (AUTHOR)
    Benheim, Alan (AUTHOR)
    Stankiewicz, Paweł (AUTHOR)
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    Źródło:
    Clinical Epigenetics. 10/21/2023, Vol. 15 Issue 1, p1-6. 6p.
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    High‐level gonosomal mosaicism for a pathogenic non‐coding CNV deletion of the lung‐specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV.
    Autorzy:
    Yıldız Bölükbaşı, Esra
    Karolak, Justyna A.
    Szafranski, Przemyslaw
    Gambin, Tomasz
    Willard, Nicholas
    Abman, Steven H.
    Galambos, Csaba
    Kinsella, John P.
    Stankiewicz, Paweł
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    Temat:
    MOSAICISM
    PLANT chromosomes
    WHOLE genome sequencing
    SALIVARY glands
    GENETIC testing
    SALIVA analysis
    PULMONARY veins
    DEAD
    Źródło:
    Molecular Genetics & Genomic Medicine; Nov2022, Vol. 10 Issue 11, p1-9, 9p
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Novel parent-of-origin-specific differentially methylated loci on chromosome 16.
    Autorzy:
    Schulze, Katharina V. (AUTHOR)
    Szafranski, Przemyslaw (AUTHOR)
    Lesmana, Harry (AUTHOR)
    Hopkin, Robert J. (AUTHOR)
    Hamvas, Aaron (AUTHOR)
    Wambach, Jennifer A. (AUTHOR)
    Shinawi, Marwan (AUTHOR)
    Zapata, Gladys (AUTHOR)
    Carvalho, Claudia M. B. (AUTHOR)
    Liu, Qian (AUTHOR)
    Karolak, Justyna A. (AUTHOR)
    Lupski, James R. (AUTHOR)
    Hanchard, Neil A. (AUTHOR)
    Stankiewicz, Paweł (AUTHOR)
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    Źródło:
    Clinical Epigenetics. 4/8/2019, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p.
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
      Wyświetlanie 1-12 z 12

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