These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 25899071)

  • 1. A late presenter and long-term survivor of alveolar capillary dysplasia with misalignment of the pulmonary veins.
    Ito Y; Akimoto T; Cho K; Yamada M; Tanino M; Dobata T; Kitaichi M; Kumaki S; Kinugawa Y
    Eur J Pediatr; 2015 Aug; 174(8):1123-6. PubMed ID: 25899071
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Novel De Novo Pathogenic Variant in FOXF1 in a Newborn with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins.
    Ma Y; Jang MA; Yoo HS; Ahn SY; Sung SI; Chang YS; Ki CS; Park WS
    Yonsei Med J; 2017 May; 58(3):672-675. PubMed ID: 28332379
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alveolar capillary dysplasia with misalignment of pulmonary [corrected] veins: concordance between pathological and molecular diagnosis.
    Castilla-Fernandez Y; Copons-Fernández C; Jordan-Lucas R; Linde-Sillo Á; Valenzuela-Palafoll I; Ferreres Piñas JC; Moreno-Galdó A; Castillo-Salinas F
    J Perinatol; 2013 May; 33(5):401-3. PubMed ID: 23624968
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De Novo mutation of FOXF1 causes alveolar capillary dysplasia with misalignment of pulmonary veins: A case report.
    Deng L; Liu X; Min J; Su Z; Yang Y; Ge L; Yang Z; Li B; Zhang X
    Medicine (Baltimore); 2021 Apr; 100(14):e25375. PubMed ID: 33832123
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel mutation in FOXF1 gene associated with alveolar capillary dysplasia with misalignment of pulmonary veins, intestinal malrotation and annular pancreas.
    Miranda J; Rocha G; Soares P; Morgado H; Baptista MJ; Azevedo I; Fernandes S; Brandão O; Sen P; Guimarães H
    Neonatology; 2013; 103(4):241-5. PubMed ID: 23407133
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A familial case of alveolar capillary dysplasia with misalignment of the pulmonary veins: the clinicopathological features and unusual glomeruloid endothelial proliferation.
    Kitano A; Nakaguro M; Tomotaki S; Hanaoka S; Kawai M; Saito A; Hayakawa M; Takahashi Y; Kawasaki H; Yamada T; Ikeda M; Onda T; Cho K; Haga H; Nakazawa A; Minamiguchi S
    Diagn Pathol; 2020 May; 15(1):48. PubMed ID: 32386508
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fast detection of FOXF1 variants in patients with alveolar capillary dysplasia with misalignment of pulmonary veins using targeted sequencing.
    Slot E; von der Thüsen JH; van Heijst A; van Marion R; Magielsen F; Dubbink HJ; Post M; Debeer A; Tibboel D; Rottier RJ; de Klein A
    Pediatr Res; 2021 Feb; 89(3):518-525. PubMed ID: 32413891
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A recurrent 8 bp frameshifting indel in FOXF1 defines a novel mutation hotspot associated with alveolar capillary dysplasia with misalignment of pulmonary veins.
    Karolak JA; Bacolla A; Liu Q; Lantz PE; Petty J; Trapane P; Panzer K; Totapally BR; Niu Z; Xiao R; Xie NG; Wu LR; Szafranski P; Zhang DY; Stankiewicz P
    Am J Med Genet A; 2019 Nov; 179(11):2272-2276. PubMed ID: 31436901
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Histopathologic and Genetic Features of Alveolar Capillary Dysplasia with Atypical Late Presentation and Prolonged Survival.
    Edwards JJ; Murali C; Pogoriler J; Frank DB; Handler SS; Deardorff MA; Hopper RK
    J Pediatr; 2019 Jul; 210():214-219.e2. PubMed ID: 30853201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.
    Sen P; Yang Y; Navarro C; Silva I; Szafranski P; Kolodziejska KE; Dharmadhikari AV; Mostafa H; Kozakewich H; Kearney D; Cahill JB; Whitt M; Bilic M; Margraf L; Charles A; Goldblatt J; Gibson K; Lantz PE; Garvin AJ; Petty J; Kiblawi Z; Zuppan C; McConkie-Rosell A; McDonald MT; Peterson-Carmichael SL; Gaede JT; Shivanna B; Schady D; Friedlich PS; Hays SR; Palafoll IV; Siebers-Renelt U; Bohring A; Finn LS; Siebert JR; Galambos C; Nguyen L; Riley M; Chassaing N; Vigouroux A; Rocha G; Fernandes S; Brumbaugh J; Roberts K; Ho-Ming L; Lo IF; Lam S; Gerychova R; Jezova M; Valaskova I; Fellmann F; Afshar K; Giannoni E; Muhlethaler V; Liang J; Beckmann JS; Lioy J; Deshmukh H; Srinivasan L; Swarr DT; Sloman M; Shaw-Smith C; van Loon RL; Hagman C; Sznajer Y; Barrea C; Galant C; Detaille T; Wambach JA; Cole FS; Hamvas A; Prince LS; Diderich KE; Brooks AS; Verdijk RM; Ravindranathan H; Sugo E; Mowat D; Baker ML; Langston C; Welty S; Stankiewicz P
    Hum Mutat; 2013 Jun; 34(6):801-11. PubMed ID: 23505205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two patients with FOXF1 mutations with alveolar capillary dysplasia with misalignment of pulmonary veins and other malformations: Two different presentations and outcomes.
    Abu-El-Haija A; Fineman J; Connolly AJ; Murali P; Judge LM; Slavotinek AM
    Am J Med Genet A; 2018 Dec; 176(12):2877-2881. PubMed ID: 30380203
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus.
    Slot E; Boers R; Boers J; van IJcken WFJ; Tibboel D; Gribnau J; Rottier R; de Klein A
    Clin Epigenetics; 2021 Jul; 13(1):148. PubMed ID: 34325731
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human.
    Sen P; Gerychova R; Janku P; Jezova M; Valaskova I; Navarro C; Silva I; Langston C; Welty S; Belmont J; Stankiewicz P
    Eur J Hum Genet; 2013 Apr; 21(4):474-7. PubMed ID: 22990143
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal mutations of FOXF1 cause alveolar capillary dysplasia despite not being imprinted.
    Alsina Casanova M; Monteagudo-Sánchez A; Rodiguez Guerineau L; Court F; Gazquez Serrano I; Martorell L; Rovira Zurriaga C; Moore GE; Ishida M; Castañon M; Moliner Calderon E; Monk D; Moreno Hernando J
    Hum Mutat; 2017 Jun; 38(6):615-620. PubMed ID: 28256047
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical Relevance of Rapid FOXF1-Targeted Sequencing in Patients Suspected of Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins.
    Edel GG; Hol JA; Slot E; von der Thüsen JH; van Bever Y; de Jonge RCJ; van Tienhoven M; Brüggenwirth HT; de Klein A; Rottier RJ
    Lab Invest; 2023 Nov; 103(11):100233. PubMed ID: 37567389
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Alveolar capillary dysplasia with misalignment of the pulmonary veins: a case report and literature review].
    Lin Y; Jiang JB; Xia B; Cao J; Yu AZ; Huang WM
    Zhonghua Er Ke Za Zhi; 2020 Oct; 58(10):838-842. PubMed ID: 32987465
    [No Abstract]   [Full Text] [Related]  

  • 17. Generation of three iPSC lines from two patients with heterozygous FOXF1 mutations associated to Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins.
    Slot E; de Klein A; Rottier RJ
    Stem Cell Res; 2020 Apr; 44():101745. PubMed ID: 32169823
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Histologic features and decreased lung FOXF1 gene expression in severe bronchopulmonary dysplasia without a genetic diagnosis of alveolar capillary dysplasia.
    Galambos C; Logan JW; Stankiewicz P; Szafranski P; Zalles C; Gonzales J; Nath S; Patel S; Abman SH
    Pediatr Pulmonol; 2023 Oct; 58(10):2746-2749. PubMed ID: 37401868
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family.
    Reiter J; Szafranski P; Breuer O; Perles Z; Dagan T; Stankiewicz P; Kerem E
    Pediatr Pulmonol; 2016 Sep; 51(9):921-7. PubMed ID: 27145217
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype.
    Szafranski P; Liu Q; Karolak JA; Song X; de Leeuw N; Faas B; Gerychova R; Janku P; Jezova M; Valaskova I; Gibbs KA; Surrey LF; Poisson V; Bérubé D; Oligny LL; Michaud JL; Popek E; Stankiewicz P
    Hum Genet; 2019 Dec; 138(11-12):1301-1311. PubMed ID: 31686214
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.