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 *

205 related articles for article (PubMed ID: 26574629)

  • 21. GNAS mutation analysis assists in differentiating chronic diffuse sclerosing osteomyelitis from fibrous dysplasia in the jaw.
    Xue J; Jia K; Li T; Zhang J; An J
    Mod Pathol; 2022 Oct; 35(10):1334-1340. PubMed ID: 35672467
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome.
    Zhadina M; Roszko KL; Geels RES; de Castro LF; Collins MT; Boyce AM
    J Clin Endocrinol Metab; 2021 Apr; 106(5):1482-1490. PubMed ID: 33512531
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of GNAS mutations in cemento-ossifying fibromas and cemento-osseous dysplasias of the jaws.
    Patel MM; Wilkey JF; Abdelsayed R; D'Silva NJ; Malchoff C; Mallya SM
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 May; 109(5):739-43. PubMed ID: 20346714
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Induced
    Khan SK; Yadav PS; Elliott G; Hu DZ; Xu R; Yang Y
    Proc Natl Acad Sci U S A; 2018 Jan; 115(3):E418-E427. PubMed ID: 29158412
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel method for PIK3CA mutation analysis: locked nucleic acid--PCR sequencing.
    Ang D; O'Gara R; Schilling A; Beadling C; Warrick A; Troxell ML; Corless CL
    J Mol Diagn; 2013 May; 15(3):312-8. PubMed ID: 23541593
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Sensitive Sequencing Analysis Suggests Thyrotropin Receptor and Guanine Nucleotide-Binding Protein G Subunit Alpha as Sole Driver Mutations in Hot Thyroid Nodules.
    Stephenson A; Eszlinger M; Stewardson P; McIntyre JB; Boesenberg E; Bircan R; Sancak S; Gozu HI; Ghaznavi S; Krohn K; Paschke R
    Thyroid; 2020 Oct; 30(10):1482-1489. PubMed ID: 32284013
    [No Abstract]   [Full Text] [Related]  

  • 27. GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation.
    Nault JC; Fabre M; Couchy G; Pilati C; Jeannot E; Tran Van Nhieu J; Saint-Paul MC; De Muret A; Redon MJ; Buffet C; Salenave S; Balabaud C; Prevot S; Labrune P; Bioulac-Sage P; Scoazec JY; Chanson P; Zucman-Rossi J
    J Hepatol; 2012 Jan; 56(1):184-91. PubMed ID: 21835143
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Two cases of Mazabraud syndrome and identification of a GNAS R201H mutation by next-generation sequencing.
    Cox JL; Cushman-Vokoun AM; McGarry SV; Kozel JA
    Virchows Arch; 2017 May; 470(5):589-593. PubMed ID: 28258512
    [No Abstract]   [Full Text] [Related]  

  • 29. GNAS is frequently mutated in both low-grade and high-grade disseminated appendiceal mucinous neoplasms but does not affect survival.
    Singhi AD; Davison JM; Choudry HA; Pingpank JF; Ahrendt SA; Holtzman MP; Zureikat AH; Zeh HJ; Ramalingam L; Mantha G; Nikiforova M; Bartlett DL; Pai RK
    Hum Pathol; 2014 Aug; 45(8):1737-43. PubMed ID: 24925222
    [TBL] [Abstract][Full Text] [Related]  

  • 30. GNAS mutations in adrenal aldosterone-producing adenomas.
    Nakajima Y; Okamura T; Horiguchi K; Gohko T; Miyamoto T; Satoh T; Ozawa A; Ishii S; Yamada E; Hashimoto K; Okada S; Takata D; Horiguchi J; Yamada M
    Endocr J; 2016; 63(2):199-204. PubMed ID: 26743443
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K-AKT pathway.
    Volckmar AL; Leichsenring J; Flechtenmacher C; Pfarr N; Siebolts U; Kirchner M; Budczies J; Bockmayr M; Ridinger K; Lorenz K; Herpel E; Noske A; Weichert W; Klauschen F; Schirmacher P; Penzel R; Endris V; Stenzinger A
    Genes Chromosomes Cancer; 2017 Jan; 56(1):11-17. PubMed ID: 27438523
    [TBL] [Abstract][Full Text] [Related]  

  • 32. McCune-Albright syndrome with acromegaly and fibrous dysplasia associated with the GNAS gene mutation identified by sensitive PNA-clamping method.
    Imanaka M; Iida K; Nishizawa H; Fukuoka H; Takeno R; Takahashi K; Kaji H; Takahashi Y; Okimura Y; Kaji H; Imanishi Y; Chihara K
    Intern Med; 2007; 46(18):1577-83. PubMed ID: 17878646
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole Exome Sequencing as an Effective Molecular Diagnosis Tool for Craniofacial Fibrous Dysplasia with Ocular Complications.
    Shen B; Fang Y; Dai Q; Xie Q; Wu W; Wang M
    Curr Eye Res; 2024 Sep; 49(9):996-1003. PubMed ID: 38708814
    [TBL] [Abstract][Full Text] [Related]  

  • 34. GNAS, GNAQ, and GNA11 alterations in patients with diverse cancers.
    Parish AJ; Nguyen V; Goodman AM; Murugesan K; Frampton GM; Kurzrock R
    Cancer; 2018 Oct; 124(20):4080-4089. PubMed ID: 30204251
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Quantitative and sensitive detection of GNAS mutations causing mccune-albright syndrome with next generation sequencing.
    Narumi S; Matsuo K; Ishii T; Tanahashi Y; Hasegawa T
    PLoS One; 2013; 8(3):e60525. PubMed ID: 23536913
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gs alpha gene: site-specific patterns and recurrent histological hallmarks.
    Riminucci M; Liu B; Corsi A; Shenker A; Spiegel AM; Robey PG; Bianco P
    J Pathol; 1999 Jan; 187(2):249-58. PubMed ID: 10365102
    [TBL] [Abstract][Full Text] [Related]  

  • 37. GNAS mutation detection is related to disease severity in girls with McCune-Albright syndrome and precocious puberty.
    Wagoner HA; Steinmetz R; Bethin KE; Eugster EA; Pescovitz OH; Hannon TS
    Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():395-400. PubMed ID: 17982386
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Searching for somatic mutations in McCune-Albright syndrome: a comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples.
    Kalfa N; Philibert P; Audran F; Ecochard A; Hannon T; Lumbroso S; Sultan C
    Eur J Endocrinol; 2006 Dec; 155(6):839-43. PubMed ID: 17132753
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A new subtype of high-grade mandibular osteosarcoma with RASAL1/MDM2 amplification.
    Guérin M; Thariat J; Ouali M; Bouvier C; Decouvelaere AV; Cassagnau E; Aubert S; Lepreux S; Coindre JM; Valmary-Degano S; Larousserie F; Meilleroux J; Projetti F; Stock N; Galant C; Marie B; Peyrottes I; de Pinieux G; Gomez-Brouchet A
    Hum Pathol; 2016 Apr; 50():70-8. PubMed ID: 26997440
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.
    Cho EK; Kim J; Yang A; Ki CS; Lee JE; Cho SY; Jin DK
    Orphanet J Rare Dis; 2016 Aug; 11(1):113. PubMed ID: 27506760
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.