BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 35563209)

  • 1. Etonogestrel Administration Reduces the Expression of PHOX2B and Its Target Genes in the Solitary Tract Nucleus.
    Cardani S; Janes TA; Saini JK; Di Lascio S; Benfante R; Fornasari D; Pagliardini S
    Int J Mol Sci; 2022 Apr; 23(9):. PubMed ID: 35563209
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Serotonin and the ventilatory effects of etonogestrel, a gonane progestin, in a murine model of congenital central hypoventilation syndrome.
    Casciato A; Bianchi L; Reverdy M; Joubert F; Delucenay-Clarke R; Parrot S; Ramanantsoa N; Sizun E; Matrot B; Straus C; Similowski T; Cayetanot F; Bodineau L
    Front Endocrinol (Lausanne); 2023; 14():1077798. PubMed ID: 36896185
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Desogestrel down-regulates PHOX2B and its target genes in progesterone responsive neuroblastoma cells.
    Cardani S; Di Lascio S; Belperio D; Di Biase E; Ceccherini I; Benfante R; Fornasari D
    Exp Cell Res; 2018 Sep; 370(2):671-679. PubMed ID: 30036539
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Knockdown of PHOX2B in the retrotrapezoid nucleus reduces the central CO
    Cardani S; Janes TA; Betzner W; Pagliardini S
    Elife; 2024 May; 13():. PubMed ID: 38727716
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome.
    Di Lascio S; Bachetti T; Saba E; Ceccherini I; Benfante R; Fornasari D
    Neurobiol Dis; 2013 Feb; 50():187-200. PubMed ID: 23103552
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alanine Expansions Associated with Congenital Central Hypoventilation Syndrome Impair PHOX2B Homeodomain-mediated Dimerization and Nuclear Import.
    Di Lascio S; Belperio D; Benfante R; Fornasari D
    J Biol Chem; 2016 Jun; 291(25):13375-93. PubMed ID: 27129232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital central hypoventilation syndrome.
    Ramanantsoa N; Gallego J
    Respir Physiol Neurobiol; 2013 Nov; 189(2):272-9. PubMed ID: 23692929
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Activation of Phox2b-Expressing Neurons in the Nucleus Tractus Solitarii Drives Breathing in Mice.
    Fu C; Shi L; Wei Z; Yu H; Hao Y; Tian Y; Liu Y; Zhang Y; Zhang X; Yuan F; Wang S
    J Neurosci; 2019 Apr; 39(15):2837-2846. PubMed ID: 30626698
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Etonogestrel promotes respiratory recovery in an in vivo rat model of central chemoreflex impairment.
    Janes TA; Cardani S; Saini JK; Pagliardini S
    Acta Physiol (Oxf); 2024 Apr; 240(4):e14093. PubMed ID: 38258900
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene.
    Klaskova E; Drabek J; Hobzova M; Smolka V; Seda M; Hyjanek J; Slavkovsky R; Stranska J; Prochazka M
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2016 Dec; 160(4):495-498. PubMed ID: 27485184
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Respiratory and autonomic dysfunction in congenital central hypoventilation syndrome.
    Moreira TS; Takakura AC; Czeisler C; Otero JJ
    J Neurophysiol; 2016 Aug; 116(2):742-52. PubMed ID: 27226447
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndrome.
    Wang TC; Su YN; Lai MC
    Pediatr Neonatol; 2014 Feb; 55(1):68-70. PubMed ID: 23597545
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea.
    Amimoto Y; Okada K; Nakano H; Sasaki A; Hayasaka K; Odajima H
    J Clin Sleep Med; 2014 Mar; 10(3):327-9. PubMed ID: 24634632
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chemosensitive Phox2b-expressing neurons are crucial for hypercapnic ventilatory response in the nucleus tractus solitarius.
    Fu C; Xue J; Wang R; Chen J; Ma L; Liu Y; Wang X; Guo F; Zhang Y; Zhang X; Wang S
    J Physiol; 2017 Jul; 595(14):4973-4989. PubMed ID: 28488367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non-cell autonomous developmental mechanisms.
    Alzate-Correa D; Mei-Ling Liu J; Jones M; Silva TM; Alves MJ; Burke E; Zuñiga J; Kaya B; Zaza G; Aslan MT; Blackburn J; Shimada MY; Fernandes-Junior SA; Baer LA; Stanford KI; Kempton A; Smith S; Szujewski CC; Silbaugh A; Viemari JC; Takakura AC; Garcia AJ; Moreira TS; Czeisler CM; Otero JJ
    Brain Pathol; 2021 Jan; 31(1):84-102. PubMed ID: 32654284
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital central hypoventilation syndrome: diagnosis and management.
    Maloney MA; Kun SS; Keens TG; Perez IA
    Expert Rev Respir Med; 2018 Apr; 12(4):283-292. PubMed ID: 29486608
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medico-legal investigation in an explicable case of congenital central hypoventilation syndrome due to a rare variant of the PHOX2B gene.
    Ventura F; Barranco R; Bachetti T; Nozza P; Fulcheri E; Palmieri A; Ceccherini I
    J Forensic Leg Med; 2018 Aug; 58():1-5. PubMed ID: 29679838
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Novel c.676_677insG
    Ye G; Han D; Jiang Y; Wang Z; Zhou Y; Lin X; Chen W; Chen M; Xu J; Yang Y; Guo Q
    J Clin Sleep Med; 2019 Mar; 15(3):509-513. PubMed ID: 30853048
    [No Abstract]   [Full Text] [Related]  

  • 19. A respiratory/Hirschsprung phenotype in a three-generation family associated with a novel pathogenic PHOX2B splice donor mutation.
    Pace NP; Pace Bardon M; Borg I
    Mol Genet Genomic Med; 2020 Dec; 8(12):e1528. PubMed ID: 33047879
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation.
    Meylemans A; Depuydt P; De Baere E; Hertegonne K; Derom E; Dermaut B; Hemelsoet D
    Acta Neurol Belg; 2021 Feb; 121(1):23-35. PubMed ID: 32335870
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.