BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 30799240)

  • 1. Tulp3 Is a Ciliary Trafficking Gene that Regulates Polycystic Kidney Disease.
    Legué E; Liem KF
    Curr Biol; 2019 Mar; 29(5):803-812.e5. PubMed ID: 30799240
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tulp3 Regulates Renal Cystogenesis by Trafficking of Cystoproteins to Cilia.
    Hwang SH; Somatilaka BN; Badgandi H; Palicharla VR; Walker R; Shelton JM; Qian F; Mukhopadhyay S
    Curr Biol; 2019 Mar; 29(5):790-802.e5. PubMed ID: 30799239
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease.
    Jafari Khamirani H; Palicharla VR; Dastgheib SA; Dianatpour M; Imanieh MH; Tabei SS; Besse W; Mukhopadhyay S; Liem KF
    Front Genet; 2022; 13():1021037. PubMed ID: 36276950
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Interactions between TULP3 tubby domain and ARL13B amphipathic helix promote lipidated protein transport to cilia.
    Palicharla VR; Hwang SH; Somatilaka BN; Legué E; Shimada IS; Familiari NE; Tran VM; Woodruff JB; Liem KF; Mukhopadhyay S
    Mol Biol Cell; 2023 Mar; 34(3):ar18. PubMed ID: 36652335
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic reduction of cilium length by targeting intraflagellar transport 88 protein impedes kidney and liver cyst formation in mouse models of autosomal polycystic kidney disease.
    Shao L; El-Jouni W; Kong F; Ramesh J; Kumar RS; Shen X; Ren J; Devendra S; Dorschel A; Wu M; Barrera I; Tabari A; Hu K; Haque N; Yambayev I; Li S; Kumar A; Behera TR; McDonough G; Furuichi M; Xifaras M; Lu T; Alhayaza RM; Miyabayashi K; Fan Q; Ajay AK; Zhou J
    Kidney Int; 2020 Nov; 98(5):1225-1241. PubMed ID: 32610050
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pkd2 Deficiency in Embryonic Aqp2 + Progenitor Cells Is Sufficient to Cause Severe Polycystic Kidney Disease.
    Tsilosani A; Gao C; Chen E; Lightle AR; Shehzad S; Sharma M; Tran PV; Bates CM; Wallace DP; Zhang W
    J Am Soc Nephrol; 2024 Apr; 35(4):398-409. PubMed ID: 38254271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. XBP1 Activation Reduces Severity of Polycystic Kidney Disease due to a Nontruncating Polycystin-1 Mutation in Mice.
    Krappitz M; Bhardwaj R; Dong K; Staudner T; Yilmaz DE; Pioppini C; Westergerling P; Ruemmele D; Hollmann T; Nguyen TA; Cai Y; Gallagher AR; Somlo S; Fedeles S
    J Am Soc Nephrol; 2023 Jan; 34(1):110-121. PubMed ID: 36270750
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ttc21b deficiency attenuates autosomal dominant polycystic kidney disease in a kidney tubular- and maturation-dependent manner.
    Wang W; Silva LM; Wang HH; Kavanaugh MA; Pottorf TS; Allard BA; Jacobs DT; Dong R; Cornelius JT; Chaturvedi A; Swenson-Fields KI; Fields TA; Pritchard MT; Sharma M; Slawson C; Wallace DP; Calvet JP; Tran PV
    Kidney Int; 2022 Sep; 102(3):577-591. PubMed ID: 35644283
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cilia-Localized Counterregulatory Signals as Drivers of Renal Cystogenesis.
    Walker RV; Maranto A; Palicharla VR; Hwang SH; Mukhopadhyay S; Qian F
    Front Mol Biosci; 2022; 9():936070. PubMed ID: 35832738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pkd1 and Nek8 mutations affect cell-cell adhesion and cilia in cysts formed in kidney organ cultures.
    Natoli TA; Gareski TC; Dackowski WR; Smith L; Bukanov NO; Russo RJ; Husson H; Matthews D; Piepenhagen P; Ibraghimov-Beskrovnaya O
    Am J Physiol Renal Physiol; 2008 Jan; 294(1):F73-83. PubMed ID: 17928412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cilia and polycystic kidney disease.
    Ma M
    Semin Cell Dev Biol; 2021 Feb; 110():139-148. PubMed ID: 32475690
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Large deletion of Wdr19 in developing renal tubules disrupts primary ciliogenesis, leading to polycystic kidney disease in mice.
    Yu SS; Wang E; Chiang CY; Cheng PH; Yeh YS; Wu YY; Chiou YY; Jiang ST
    J Pathol; 2022 May; 257(1):5-16. PubMed ID: 35007346
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
    Claus LR; Chen C; Stallworth J; Turner JL; Slaats GG; Hawks AL; Mabillard H; Senum SR; Srikanth S; Flanagan-Steet H; Louie RJ; Silver J; Lerner-Ellis J; Morel C; Mighton C; Sleutels F; van Slegtenhorst M; van Ham T; Brooks AS; Dorresteijn EM; Barakat TS; Dahan K; Demoulin N; Goffin EJ; Olinger E; ; Larsen M; Hertz JM; Lilien MR; Obeidová L; Seeman T; Stone HK; Kerecuk L; Gurgu M; Yousef Yengej FA; Ammerlaan CME; Rookmaaker MB; Hanna C; Rogers RC; Duran K; Peters E; Sayer JA; van Haaften G; Harris PC; Ling K; Mason JM; van Eerde AM; Steet R
    Kidney Int; 2023 Nov; 104(5):995-1007. PubMed ID: 37598857
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cell-Autonomous Hedgehog Signaling Is Not Required for Cyst Formation in Autosomal Dominant Polycystic Kidney Disease.
    Ma M; Legué E; Tian X; Somlo S; Liem KF
    J Am Soc Nephrol; 2019 Nov; 30(11):2103-2111. PubMed ID: 31451534
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The master regulators Myc and p53 cellular signaling and functions in polycystic kidney disease.
    Kurbegovic A; Trudel M
    Cell Signal; 2020 Jul; 71():109594. PubMed ID: 32145315
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functions of the primary cilium in the kidney and its connection with renal diseases.
    Clearman KR; Haycraft CJ; Croyle MJ; Collawn JF; Yoder BK
    Curr Top Dev Biol; 2023; 155():39-94. PubMed ID: 38043952
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The exocyst protein Sec10 interacts with Polycystin-2 and knockdown causes PKD-phenotypes.
    Fogelgren B; Lin SY; Zuo X; Jaffe KM; Park KM; Reichert RJ; Bell PD; Burdine RD; Lipschutz JH
    PLoS Genet; 2011 Apr; 7(4):e1001361. PubMed ID: 21490950
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reduced ciliary polycystin-2 in induced pluripotent stem cells from polycystic kidney disease patients with PKD1 mutations.
    Freedman BS; Lam AQ; Sundsbak JL; Iatrino R; Su X; Koon SJ; Wu M; Daheron L; Harris PC; Zhou J; Bonventre JV
    J Am Soc Nephrol; 2013 Oct; 24(10):1571-86. PubMed ID: 24009235
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia.
    Mukhopadhyay S; Wen X; Chih B; Nelson CD; Lane WS; Scales SJ; Jackson PK
    Genes Dev; 2010 Oct; 24(19):2180-93. PubMed ID: 20889716
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tubby family proteins are adapters for ciliary trafficking of integral membrane proteins.
    Badgandi HB; Hwang SH; Shimada IS; Loriot E; Mukhopadhyay S
    J Cell Biol; 2017 Mar; 216(3):743-760. PubMed ID: 28154160
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.