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 *

167 related articles for article (PubMed ID: 34946872)

  • 1.
    Rudd Garces G; Knebel A; Hülskötter K; Jagannathan V; Störk T; Hewicker-Trautwein M; Leeb T; Volk HA
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946872
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlation and expansion of orodental anomalies in LTBP3-related disorders.
    Intarak N; Theerapanon T; Thaweesapphithak S; Suphapeetiporn K; Porntaveetus T; Shotelersuk V
    Mol Genet Genomics; 2019 Jun; 294(3):773-787. PubMed ID: 30887145
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in
    Flex E; Imperatore V; Carpentieri G; Bruselles A; Ciolfi A; Pizzi S; Tedesco MG; Rogaia D; Mencarelli A; Di Cara G; Verrotti A; Troiani S; Merla G; Tartaglia M; Prontera P
    Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573388
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of an ADAMTS2 frameshift variant in a cat family with Ehlers-Danlos syndrome.
    Simon R; Kiener S; Thom N; Schäfer L; Müller J; Schlohsarczyk EK; Gärtner U; Herden C; Leeb T; Lühken G
    G3 (Bethesda); 2023 Aug; 13(9):. PubMed ID: 37462293
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    Bilgen N; Çınar Kul B; Akkurt MY; Bakıcı C; Buckley RM; Lyons LA; Coghill LM; Çıldır ÖŞ; Kutlu F
    J Feline Med Surg; 2023 Oct; 25(10):1098612X231193557. PubMed ID: 37791865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.
    Huckert M; Stoetzel C; Morkmued S; Laugel-Haushalter V; Geoffroy V; Muller J; Clauss F; Prasad MK; Obry F; Raymond JL; Switala M; Alembik Y; Soskin S; Mathieu E; Hemmerlé J; Weickert JL; Dabovic BB; Rifkin DB; Dheedene A; Boudin E; Caluseriu O; Cholette MC; Mcleod R; Antequera R; Gellé MP; Coeuriot JL; Jacquelin LF; Bailleul-Forestier I; Manière MC; Van Hul W; Bertola D; Dollé P; Verloes A; Mortier G; Dollfus H; Bloch-Zupan A
    Hum Mol Genet; 2015 Jun; 24(11):3038-49. PubMed ID: 25669657
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Independent DSG4 frameshift variants in cats with hair shaft dystrophy.
    Kiener S; Rostaher A; Rüfenacht S; Jagannathan V; Sundberg JP; Welle M; Leeb T
    Mol Genet Genomics; 2022 Jan; 297(1):147-154. PubMed ID: 34878611
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus).
    Kuehn MH; Lipsett KA; Menotti-Raymond M; Whitmore SS; Scheetz TE; David VA; O'Brien SJ; Zhao Z; Jens JK; Snella EM; Ellinwood NM; McLellan GJ
    PLoS One; 2016; 11(5):e0154412. PubMed ID: 27149523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bi-allelic loss-of-function novel variants in LTBP3-related skeletal dysplasia: Report of first patient from India.
    Kaur R; Siddiqui I; Mathur V; Jana M; Kabra M; Gupta N
    Am J Med Genet A; 2020 Aug; 182(8):1944-1946. PubMed ID: 32432408
    [TBL] [Abstract][Full Text] [Related]  

  • 10.
    Rudd Garces G; Christen M; Loechel R; Jagannathan V; Leeb T
    Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205377
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enamel and dental anomalies in latent-transforming growth factor beta-binding protein 3 mutant mice.
    Morkmued S; Hemmerle J; Mathieu E; Laugel-Haushalter V; Dabovic B; Rifkin DB; Dollé P; Niederreither K; Bloch-Zupan A
    Eur J Oral Sci; 2017 Feb; 125(1):8-17. PubMed ID: 28084688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Incomplete dominant osteochondrodysplasia in heterozygous Scottish Fold cats.
    Takanosu M; Takanosu T; Suzuki H; Suzuki K
    J Small Anim Pract; 2008 Apr; 49(4):197-9. PubMed ID: 18339089
    [TBL] [Abstract][Full Text] [Related]  

  • 13. LTBP3 Pathogenic Variants Predispose Individuals to Thoracic Aortic Aneurysms and Dissections.
    Guo DC; Regalado ES; Pinard A; Chen J; Lee K; Rigelsky C; Zilberberg L; Hostetler EM; Aldred M; Wallace SE; Prakash SK; ; Leal SM; Bamshad MJ; Nickerson DA; Natowicz M; Rifkin DB; Milewicz DM
    Am J Hum Genet; 2018 Apr; 102(4):706-712. PubMed ID: 29625025
    [TBL] [Abstract][Full Text] [Related]  

  • 14. First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta.
    Nouara F; Amalou G; Bouzidi A; Charif M; Charoute H; Lenaers G; El Arabi S; Bousfiha B; Barakat A
    Arch Oral Biol; 2022 Oct; 142():105518. PubMed ID: 35998423
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia.
    McInerney-Leo AM; Le Goff C; Leo PJ; Kenna TJ; Keith P; Harris JE; Steer R; Bole-Feysot C; Nitschke P; Kielty C; Brown MA; Zankl A; Duncan EL; Cormier-Daire V
    J Med Genet; 2016 Jul; 53(7):457-64. PubMed ID: 27068007
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [IDENTIFICATION OF A NOVEL LTBP3 GENE PATHOGENIC VARIANT IN DRUZE ARAB PATIENTS PRESENTED WITH SYNDROMIC SHORT STATURE WITH BRACHYOLMIA AND AMELOGENESIS IMPERFECTA].
    Hadid Y; Daher Z; Mahroum M; Shalata A; Nakhleh Francis Y; Shalata H; Broneshter Vinter R; Ziv M; Furman C; Ali V; Levitaz J; Shalata A
    Harefuah; 2023 Jun; 162(6):352-358. PubMed ID: 37394436
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation.
    Imes DL; Geary LA; Grahn RA; Lyons LA
    Anim Genet; 2006 Apr; 37(2):175-8. PubMed ID: 16573534
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome.
    Spycher M; Bauer A; Jagannathan V; Frizzi M; De Lucia M; Leeb T
    Anim Genet; 2018 Dec; 49(6):641-644. PubMed ID: 30246406
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of a FAS ligand gene variant associated with inherited feline autoimmune lymphoproliferative syndrome in British shorthair cats in New Zealand.
    Aberdein D; Munday JS; Dittmer KE; Heathcott RW; Lyons LA
    N Z Vet J; 2017 Nov; 65(6):327-331. PubMed ID: 28814155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A
    Hug P; Kern P; Jagannathan V; Leeb T
    Genes (Basel); 2019 Oct; 10(10):. PubMed ID: 31615056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.