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 *

238 related articles for article (PubMed ID: 21071979)

  • 21. Co-Occurrence of Nephronophthisis Type 1 and Alström Syndrome: A Case Report.
    Rossoni L; Lugani F; Orsi SM; Verrina EE; Ghiggeri GM; Angeletti A; Caridi G; La Porta E
    Nephron; 2024; 148(5):345-348. PubMed ID: 36746137
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report.
    Akira M; Suzuki H; Ikeda A; Iwasaki M; Honda D; Takahara H; Rinno H; Tomita S; Suzuki Y
    BMC Nephrol; 2021 Jul; 22(1):261. PubMed ID: 34246230
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Nephronophthisis.
    Wolf MT; Hildebrandt F
    Pediatr Nephrol; 2011 Feb; 26(2):181-94. PubMed ID: 20652329
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular genetics of renal ciliopathies.
    Barroso-Gil M; Olinger E; Sayer JA
    Biochem Soc Trans; 2021 Jun; 49(3):1205-1220. PubMed ID: 33960378
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development.
    Hoff S; Epting D; Falk N; Schroda S; Braun DA; Halbritter J; Hildebrandt F; Kramer-Zucker A; Bergmann C; Walz G; Lienkamp SS
    J Biol Chem; 2018 Sep; 293(39):15243-15255. PubMed ID: 30111592
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and pathological features and varied mutational spectra of pathogenic genes in 55 Chinese patients with nephronophthisis.
    Yue Z; Lin H; Li M; Wang H; Liu T; Hu M; Chen H; Tong H; Sun L
    Clin Chim Acta; 2020 Jul; 506():136-144. PubMed ID: 32173348
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Copy-number variation of the NPHP1 gene in patients with juvenile Nephronophthisis.
    Abdelwahed M; Maaloul I; Benoit V; Hilbert P; Hachicha M; Kamoun H; Keskes-Ammar L; Belguith N
    Acta Clin Belg; 2021 Feb; 76(1):16-24. PubMed ID: 31402777
    [No Abstract]   [Full Text] [Related]  

  • 28. Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome.
    Shi X; Garcia G; Van De Weghe JC; McGorty R; Pazour GJ; Doherty D; Huang B; Reiter JF
    Nat Cell Biol; 2017 Oct; 19(10):1178-1188. PubMed ID: 28846093
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Nephronophthisis-associated ciliopathies.
    Hildebrandt F; Zhou W
    J Am Soc Nephrol; 2007 Jun; 18(6):1855-71. PubMed ID: 17513324
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Ciliopathies].
    Gerth-Kahlert C; Koller S
    Klin Monbl Augenheilkd; 2018 Mar; 235(3):264-272. PubMed ID: 29534263
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Imaging centrosomes and cilia in the mouse kidney.
    Hoshi M; Wang J; Jain S; Mahjoub MR
    Methods Cell Biol; 2015; 127():1-17. PubMed ID: 25837383
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Repurposing small molecules for nephronophthisis and related renal ciliopathies.
    Benmerah A; Briseño-Roa L; Annereau JP; Saunier S
    Kidney Int; 2023 Aug; 104(2):245-253. PubMed ID: 37244473
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A family with five siblings affected with nephronophthisis.
    Albaramki J; Akl K; Hamed R; Wahbeh A
    Saudi J Kidney Dis Transpl; 2014 May; 25(3):630-3. PubMed ID: 24821164
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patient.
    Soliman NA; Hildebrandt F; Allen SJ; Otto EA; Nabhan MM; Badr AM
    Pediatr Nephrol; 2010 Oct; 25(10):2193-4. PubMed ID: 20454808
    [No Abstract]   [Full Text] [Related]  

  • 35. [Clinical features and gene mutation analysis of 13 Chinese juvenile patients with nephronophthisis].
    Sun LZ; Lin HR; Yue ZH; Wang HY; Jiang XY; Tong HJ; Li M; Wang WG; Mou YK; Yang F; Liu T; Chen HM
    Zhonghua Er Ke Za Zhi; 2016 Nov; 54(11):834-839. PubMed ID: 27806791
    [No Abstract]   [Full Text] [Related]  

  • 36. From cilia to cyst.
    Watnick T; Germino G
    Nat Genet; 2003 Aug; 34(4):355-6. PubMed ID: 12923538
    [No Abstract]   [Full Text] [Related]  

  • 37. Renal ciliopathies.
    Devlin LA; Sayer JA
    Curr Opin Genet Dev; 2019 Jun; 56():49-60. PubMed ID: 31419725
    [TBL] [Abstract][Full Text] [Related]  

  • 38. From the radiologic pathology archives: pediatric polycystic kidney disease and other ciliopathies: radiologic-pathologic correlation.
    Chung EM; Conran RM; Schroeder JW; Rohena-Quinquilla IR; Rooks VJ
    Radiographics; 2014; 34(1):155-78. PubMed ID: 24428289
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.
    Fliegauf M; Horvath J; von Schnakenburg C; Olbrich H; Müller D; Thumfart J; Schermer B; Pazour GJ; Neumann HP; Zentgraf H; Benzing T; Omran H
    J Am Soc Nephrol; 2006 Sep; 17(9):2424-33. PubMed ID: 16885411
    [TBL] [Abstract][Full Text] [Related]  

  • 40. EXPANDED PHENOTYPE OF TMEM67 GENE MUTATION (CASE REPORT).
    Tkemaladze T; Melikishvili G; Kherkheulidze V; Melikishvili A; Davitaia T
    Georgian Med News; 2017 Jun; (267):100-103. PubMed ID: 28726664
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.