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 *

127 related articles for article (PubMed ID: 33377691)

  • 1. [A complicated case of calcium urolithiasis in a carrier of SLC7A9 gene mutation responsible for cystinuria].
    Litvinova MM; Filippova TV; Khafizov KF; Svetlichnaya DV; Ahmedzyanova DA; Rudenko VI; Gadzhieva ZK; Shumikhina MV
    Urologiia; 2020 Dec; (6):126-130. PubMed ID: 33377691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and genetic characterization of Chinese pediatric cystine stone patients.
    Shen L; Cong X; Zhang X; Wang N; Zhou P; Xu Y; Zhu Q; Gu X
    J Pediatr Urol; 2017 Dec; 13(6):629.e1-629.e5. PubMed ID: 28689648
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular and genetic technologies for the diagnosis of monogenic forms of urinary stone disease: clinical cases].
    Litvinova MM; Filippova TV; Svetlichnaya DV; Morozov SL; Chugunov IS; Nuralieva SZ; Rudenko VI; Gadzhieva ZK; Subbotina TI; Shumikhina MV
    Urologiia; 2020 Jun; (3):81-86. PubMed ID: 32597591
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis.
    Feliubadaló L; Arbonés ML; Mañas S; Chillarón J; Visa J; Rodés M; Rousaud F; Zorzano A; Palacín M; Nunes V
    Hum Mol Genet; 2003 Sep; 12(17):2097-108. PubMed ID: 12915471
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cystinuria: an inborn cause of urolithiasis.
    Eggermann T; Venghaus A; Zerres K
    Orphanet J Rare Dis; 2012 Apr; 7():19. PubMed ID: 22480232
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterozygous cystinuria and calcium oxalate urolithiasis.
    Resnick MI; Goodman HO; Boyce WH
    J Urol; 1979 Jul; 122(1):52-4. PubMed ID: 458988
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SLC3A1 and SLC7A9 mutations in autosomal recessive or dominant canine cystinuria: a new classification system.
    Brons AK; Henthorn PS; Raj K; Fitzgerald CA; Liu J; Sewell AC; Giger U
    J Vet Intern Med; 2013; 27(6):1400-8. PubMed ID: 24001348
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and genetic analysis of patients with cystinuria in the United Kingdom.
    Rhodes HL; Yarram-Smith L; Rice SJ; Tabaksert A; Edwards N; Hartley A; Woodward MN; Smithson SL; Tomson C; Welsh GI; Williams M; Thwaites DT; Sayer JA; Coward RJ
    Clin J Am Soc Nephrol; 2015 Jul; 10(7):1235-45. PubMed ID: 25964309
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of early onset cystinuria in a 4-month-old girl.
    Ikeyama S; Kanda S; Sakamoto S; Sakoda A; Miura K; Yoneda R; Nogi A; Ariji S; Shimoda M; Ono M; Kanda S; Yokoyama S; Takahashi K; Yokoyama Y; Hattori M
    CEN Case Rep; 2022 May; 11(2):216-219. PubMed ID: 34669168
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cystinuria caused by a SLC7A9 missense mutation in Siamese-crossbred littermates in Germany].
    Hilton S; Mizukami K; Giger U
    Tierarztl Prax Ausg K Kleintiere Heimtiere; 2017 Aug; 45(4):265-272. PubMed ID: 28585658
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical profile of a Polish cohort of children and young adults with cystinuria.
    Tkaczyk M; Gadomska-Prokop K; Załuska-Leśniewska I; Musiał K; Zawadzki J; Jobs K; Porowski T; Rogowska-Kalisz A; Jander A; Kirolos M; Haliński A; Krzemień A; Sobieszczańska-Droździel A; Zachwieja K; Beck BB; Sikora P; Zaniew M
    Ren Fail; 2021 Dec; 43(1):62-70. PubMed ID: 33349102
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical Characteristics and In Silico Analysis of Cystinuria Caused by a Novel
    Liu L; Xu Z; Guan Y; Zhang Y; Li X; Ren Y; Hu L; Yan X
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421847
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic analysis of SLC3A1 and SLC7A9 genes in Czech and Slovak cystinuric patients.
    Skopková Z; Hrabincová E; Stástná S; Kozák L; Adam T
    Ann Hum Genet; 2005 Sep; 69(Pt 5):501-7. PubMed ID: 16138908
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [From gene to disease; SLC3A1, SLC7A9 and cystinuria].
    Breuning MH; Hamdy NA
    Ned Tijdschr Geneeskd; 2003 Feb; 147(6):245-7. PubMed ID: 12621979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [SLC7A9 gene variation: impact of 13 frequent mutations in the etiology of cystinuria in a Spanish Mediterranean population].
    Francés F; Portolés O; Corella D; Sorlí JV; Sabater A; Carrasco P; Guillén M
    Med Clin (Barc); 2006 Jul; 127(5):161-6. PubMed ID: 16834950
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Novel Mutation in SLC7A9 Gene in Cystinuria.
    Fazaeli S; Ashouri S; Kheirollahi M; Mohammadi M; Fazilati M
    Iran J Kidney Dis; 2017 Mar; 11(2):138-141. PubMed ID: 28270646
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for association of SLC7A9 gene haplotypes with cystinuria manifestation in SLC7A9 mutation carriers.
    Chatzikyriakidou A; Sofikitis N; Kalfakakou V; Siamopoulos K; Georgiou I
    Urol Res; 2006 Oct; 34(5):299-303. PubMed ID: 16838140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Twenty-four novel mutations identified in a cohort of 85 patients by direct sequencing of the SLC3A1 and SLC7A9 cystinuria genes.
    Di Perna M; Louizou E; Fischetti L; Dedoussis GV; Stanziale P; Michelakakis H; Zelante L; Pras E; Bisceglia L
    Genet Test; 2008 Sep; 12(3):351-5. PubMed ID: 18752446
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of SLC7A9 in cystinuria patients in Sweden.
    Harnevik L; Fjellstedt E; Molbaek A; Denneberg T; Söderkvist P
    Genet Test; 2003; 7(1):13-20. PubMed ID: 12820697
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria.
    Yuen YP; Lam CW; Lai CK; Tong SF; Li PS; Tam S; Kwan EY; Chan SY; Tsang WK; Chan KY; Mak WL; Cheng CW; Chan YW
    Kidney Int; 2006 Jan; 69(1):123-8. PubMed ID: 16374432
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.