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 *

120 related articles for article (PubMed ID: 38277988)

  • 1. PCYT2 deficiency in Saarlooswolfdogs with progressive retinal, central, and peripheral neurodegeneration.
    Christen M; Oevermann A; Rupp S; Vaz FM; Wever EJM; Braus BK; Jagannathan V; Kehl A; Hytönen MK; Lohi H; Leeb T
    Mol Genet Metab; 2024 Mar; 141(3):108149. PubMed ID: 38277988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs.
    Hitti-Malin RJ; Burmeister LM; Ricketts SL; Lewis TW; Pettitt L; Boursnell M; Schofield EC; Sargan D; Mellersh CS
    BMC Genet; 2020 Sep; 21(1):100. PubMed ID: 32894063
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Complex Structural
    Murgiano L; Becker D; Torjman D; Niggel JK; Milano A; Cullen C; Feng R; Wang F; Jagannathan V; Pearce-Kelling S; Katz ML; Leeb T; Aguirre GD
    G3 (Bethesda); 2019 Feb; 9(2):425-437. PubMed ID: 30541930
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes
    Hitti RJ; Oliver JAC; Schofield EC; Bauer A; Kaukonen M; Forman OP; Leeb T; Lohi H; Burmeister LM; Sargan D; Mellersh CS
    Genes (Basel); 2019 May; 10(5):. PubMed ID: 31117272
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Axonal Polyneuropathy in 2 Brothers With a Homozygous Missense Variant in the First Catalytic Domain of
    Leonardis L; Skrjanec Pusenjak M; Maver A; Jaklic H; Ozura Brecko A; Koritnik B; Peterlin B; Writzl K
    Neurol Genet; 2022 Apr; 8(2):e658. PubMed ID: 35243002
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (
    Hitti-Malin RJ; Burmeister LM; Lingaas F; Kaukonen M; Pettinen I; Lohi H; Sargan D; Mellersh CS
    Genes (Basel); 2021 Nov; 12(11):. PubMed ID: 34828377
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis.
    Schmutz I; Jagannathan V; Bartenschlager F; Stein VM; Gruber AD; Leeb T; Katz ML
    Mol Genet Metab; 2019 May; 127(1):95-106. PubMed ID: 30956123
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Missense Variant in
    Letko A; Dietschi E; Nieburg M; Jagannathan V; Gurtner C; Oevermann A; Drögemüller C
    Genes (Basel); 2019 May; 10(5):. PubMed ID: 31083464
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole genome sequencing identifies a homozygous nonsense mutation in the JPH2 gene in Shih Tzu dogs with progressive retinal atrophy.
    Urkasemsin G; Pongpanich M; Sariya L; Kongcharoen A; Buddhirongawatr R; Rungarunlert S; Ferreira JN; Chetruengchai W; Phokaew C; Srichomthong C; Shotelersuk V
    Anim Genet; 2021 Oct; 52(5):714-719. PubMed ID: 34231238
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs.
    Murgiano L; Becker D; Spector C; Carlin K; Santana E; Niggel JK; Jagannathan V; Leeb T; Pearce-Kelling S; Aguirre GD; Miyadera K
    Sci Rep; 2020 Dec; 10(1):21162. PubMed ID: 33273526
    [TBL] [Abstract][Full Text] [Related]  

  • 11.
    Ludwig-Peisker O; Ansel E; Schweizer D; Jagannathan V; Loechel R; Leeb T
    Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs.
    Hahn K; Rohdin C; Jagannathan V; Wohlsein P; Baumgärtner W; Seehusen F; Spitzbarth I; Grandon R; Drögemüller C; Jäderlund KH
    PLoS One; 2015; 10(11):e0141824. PubMed ID: 26555167
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    Christen M; Booij-Vrieling H; Oksa-Minalto J; de Vries C; Kehl A; Jagannathan V; Leeb T
    Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680893
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs.
    Christen M; Högler S; Kleiter M; Leschnik M; Weber C; Thaller D; Jagannathan V; Leeb T
    PLoS Genet; 2021 Aug; 17(8):e1009716. PubMed ID: 34339417
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Gurtner C; Hug P; Kleiter M; Köhler K; Dietschi E; Jagannathan V; Leeb T
    Genes (Basel); 2020 Mar; 11(3):. PubMed ID: 32183361
    [TBL] [Abstract][Full Text] [Related]  

  • 16. cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog.
    Petersen-Jones SM; Entz DD; Sargan DR
    Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1637-44. PubMed ID: 10393029
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Christen M; Rupp S; Van Soens I; Bhatti SFM; Matiasek K; von Klopmann T; Jagannathan V; Madden I; Batcher K; Bannasch D; Leeb T
    Genes (Basel); 2022 Jul; 13(7):. PubMed ID: 35886006
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A putative silencer variant in a spontaneous canine model of retinitis pigmentosa.
    Kaukonen M; Quintero IB; Mukarram AK; Hytönen MK; Holopainen S; Wickström K; Kyöstilä K; Arumilli M; Jalomäki S; Daub CO; Kere J; Lohi H;
    PLoS Genet; 2020 Mar; 16(3):e1008659. PubMed ID: 32150541
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery.
    Kyöstilä K; Cizinauskas S; Seppälä EH; Suhonen E; Jeserevics J; Sukura A; Syrjä P; Lohi H
    PLoS Genet; 2012; 8(6):e1002759. PubMed ID: 22719266
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of canine photoreceptor phosducin cDNA and identification of a sequence variant in dogs with photoreceptor dysplasia.
    Zhang Q; Acland GM; Parshall CJ; Haskell J; Ray K; Aguirre GD
    Gene; 1998 Jul; 215(2):231-9. PubMed ID: 9714819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.