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 *

183 related articles for article (PubMed ID: 33924028)

  • 1. A Homozygous Dab1
    Racetin A; Filipović N; Lozić M; Ogata M; Gudelj Ensor L; Kelam N; Kovačević P; Watanabe K; Katsuyama Y; Saraga-Babić M; Glavina Durdov M; Vukojević K
    Biomolecules; 2021 Apr; 11(4):. PubMed ID: 33924028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Immunohistochemical Expression Pattern of FGFR1, FGFR2, RIP5, and HIP2 in Developing and Postnatal Kidneys of
    Kelam N; Racetin A; Katsuyama Y; Vukojević K; Kostić S
    Int J Mol Sci; 2022 Feb; 23(4):. PubMed ID: 35216141
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression and localization of DAB1 and Reelin during normal human kidney development.
    Racetin A; Jurić M; Filipović N; Šolić I; Kosović I; Glavina Durdov M; Kunac N; Zekić Tomaš S; Saraga M; Šoljić V; Martinović V; Petričević J; Restović I; Lasić V; Kostić S; Kablar B; Watanabe K; Katsuyama Y; Saraga Babić M; Vukojević K
    Croat Med J; 2019 Dec; 60(6):521-531. PubMed ID: 31894918
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Immunoexpression Pattern of Autophagy Markers in Developing and Postnatal Kidneys of
    Maglica M; Kelam N; Haque E; Perutina I; Racetin A; Filipović N; Katsuyama Y; Vukojević K
    Biomolecules; 2023 Feb; 13(3):. PubMed ID: 36979337
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Histological study in the brain of the reelin/Dab1-compound mutant mouse.
    Yamamoto T; Setsu T; Okuyama-Yamamoto A; Terashima T
    Anat Sci Int; 2009 Sep; 84(3):200-9. PubMed ID: 19221860
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aberrant fragment of Dab1 protein is present in yotari mouse.
    Onoue A; Takeuchi M; Kohno T; Hattori M
    Neurosci Res; 2014 Nov; 88():23-7. PubMed ID: 25149914
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disturbances in Switching between Canonical and Non-Canonical Wnt Signaling Characterize Developing and Postnatal Kidneys of
    Perutina I; Kelam N; Maglica M; Racetin A; Ogorevc M; Filipović N; Katsuyama Y; Mišković J; Vukojević K
    Biomedicines; 2023 Apr; 11(5):. PubMed ID: 37238991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Immunoexpression Pattern of Autophagy-Related Proteins in Human Congenital Anomalies of the Kidney and Urinary Tract.
    Maglica M; Kelam N; Perutina I; Racetin A; Rizikalo A; Filipović N; Kuzmić Prusac I; Mišković J; Vukojević K
    Int J Mol Sci; 2024 Jun; 25(13):. PubMed ID: 38999938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Defective Reelin/Dab1 signaling pathways associated with disturbed hippocampus development of homozygous yotari mice.
    Arimitsu N; Mizukami Y; Shimizu J; Takai K; Suzuki T; Suzuki N
    Mol Cell Neurosci; 2021 Apr; 112():103614. PubMed ID: 33845123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
    Saygili S; Atayar E; Canpolat N; Elicevik M; Kurugoglu S; Sever L; Caliskan S; Ozaltin F
    Clin Genet; 2020 Oct; 98(4):390-395. PubMed ID: 32666543
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Alteration of Cx37, Cx40, Cx43, Cx45, Panx1, and Renin Expression Patterns in Postnatal Kidneys of Dab1-/- (
    Lozić M; Filipović N; Jurić M; Kosović I; Benzon B; Šolić I; Kelam N; Racetin A; Watanabe K; Katsuyama Y; Ogata M; Saraga-Babić M; Vukojević K
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33525532
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
    Kohl S; Hwang DY; Dworschak GC; Hilger AC; Saisawat P; Vivante A; Stajic N; Bogdanovic R; Reutter HM; Kehinde EO; Tasic V; Hildebrandt F
    J Am Soc Nephrol; 2014 Sep; 25(9):1917-22. PubMed ID: 24700879
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel neurological mutant mouse, yotari, which exhibits reeler-like phenotype but expresses CR-50 antigen/reelin.
    Yoneshima H; Nagata E; Matsumoto M; Yamada M; Nakajima K; Miyata T; Ogawa M; Mikoshiba K
    Neurosci Res; 1997 Nov; 29(3):217-23. PubMed ID: 9436647
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
    Neirijnck Y; Reginensi A; Renkema KY; Massa F; Kozlov VM; Dhib H; Bongers EMHF; Feitz WF; van Eerde AM; Lefebvre V; Knoers NVAM; Tabatabaei M; Schulz H; McNeill H; Schaefer F; Wegner M; Sock E; Schedl A
    Kidney Int; 2018 May; 93(5):1142-1153. PubMed ID: 29459093
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Secreted Glycoprotein Reelin Suppresses the Proliferation and Regulates the Distribution of Oligodendrocyte Progenitor Cells in the Embryonic Neocortex.
    Ogino H; Nakajima T; Hirota Y; Toriuchi K; Aoyama M; Nakajima K; Hattori M
    J Neurosci; 2020 Sep; 40(40):7625-7636. PubMed ID: 32913108
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Importance of Reelin C-terminal region in the development and maintenance of the postnatal cerebral cortex and its regulation by specific proteolysis.
    Kohno T; Honda T; Kubo K; Nakano Y; Tsuchiya A; Murakami T; Banno H; Nakajima K; Hattori M
    J Neurosci; 2015 Mar; 35(11):4776-87. PubMed ID: 25788693
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice.
    Sheldon M; Rice DS; D'Arcangelo G; Yoneshima H; Nakajima K; Mikoshiba K; Howell BW; Cooper JA; Goldowitz D; Curran T
    Nature; 1997 Oct; 389(6652):730-3. PubMed ID: 9338784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modulation of Reelin signaling by Cyclin-dependent kinase 5.
    Ohshima T; Suzuki H; Morimura T; Ogawa M; Mikoshiba K
    Brain Res; 2007 Apr; 1140():84-95. PubMed ID: 16529723
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare RELN variants affect Reelin-DAB1 signal transduction in autism spectrum disorder.
    Sánchez-Sánchez SM; Magdalon J; Griesi-Oliveira K; Yamamoto GL; Santacruz-Perez C; Fogo M; Passos-Bueno MR; Sertié AL
    Hum Mutat; 2018 Oct; 39(10):1372-1383. PubMed ID: 29969175
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.
    van der Ven AT; Kobbe B; Kohl S; Shril S; Pogoda HM; Imhof T; Ityel H; Vivante A; Chen J; Hwang DY; Connaughton DM; Mann N; Widmeier E; Taglienti M; Schmidt JM; Nakayama M; Senguttuvan P; Kumar S; Tasic V; Kehinde EO; Mane SM; Lifton RP; Soliman N; Lu W; Bauer SB; Hammerschmidt M; Wagener R; Hildebrandt F
    PLoS One; 2018; 13(1):e0191224. PubMed ID: 29351342
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.