BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 19329231)

  • 21. A 3-month-old girl with failure to thrive.
    Listernick R
    Pediatr Ann; 2011 Apr; 40(4):181-4. PubMed ID: 21485992
    [No Abstract]   [Full Text] [Related]  

  • 22. [McCune-Albright syndrome].
    Yamada N; Tatsuno I
    Nihon Rinsho; 2006 Jun; Suppl 2():126-30. PubMed ID: 16817366
    [No Abstract]   [Full Text] [Related]  

  • 23. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.
    Lietman SA; Ding C; Levine MA
    J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Pseudopseudohypoparathyroidism and genomic imprinting].
    Minagawa M
    Clin Calcium; 2007 Aug; 17(8):1229-33. PubMed ID: 17660620
    [TBL] [Abstract][Full Text] [Related]  

  • 25. McCune-Albright syndrome: radiological and MR findings.
    Yongjing G; Huawei L; Zilai P; Bei D; Hao J; Kemin C
    JBR-BTR; 2001; 84(6):250-2. PubMed ID: 11817476
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Different genotype of periosteal and endosteal cells of a patient with polyostotic fibrous dysplasia.
    Kitoh H; Yamada Y; Nogami H
    J Med Genet; 1999 Sep; 36(9):724-5. PubMed ID: 10507737
    [No Abstract]   [Full Text] [Related]  

  • 27. A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency.
    Thiele S; Werner R; Ahrens W; Hoppe U; Marschke C; Staedt P; Hiort O
    J Clin Endocrinol Metab; 2007 May; 92(5):1764-8. PubMed ID: 17299070
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type Ia.
    Thiele S; Werner R; Ahrens W; Hübner A; Hinkel KG; Höppner W; Igl B; Hiort O
    Exp Clin Endocrinol Diabetes; 2010 Feb; 118(2):127-32. PubMed ID: 19658058
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gs alpha mutation at codon 201 in pituitary adenoma causing gigantism in a 6-year-old boy with McCune-Albright syndrome.
    Dötsch J; Kiess W; Hänze J; Repp R; Lüdecke D; Blum WF; Rascher W
    J Clin Endocrinol Metab; 1996 Nov; 81(11):3839-42. PubMed ID: 8923825
    [No Abstract]   [Full Text] [Related]  

  • 30. Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations.
    Collins MT; Sarlis NJ; Merino MJ; Monroe J; Crawford SE; Krakoff JA; Guthrie LC; Bonat S; Robey PG; Shenker A
    J Clin Endocrinol Metab; 2003 Sep; 88(9):4413-7. PubMed ID: 12970318
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Picture of the month. Albright hereditary osteodystrophy.
    Eronocodelu Y; Böber E; Tunnessen WW
    Arch Pediatr Adolesc Med; 1997 Dec; 151(12):1263-4. PubMed ID: 9412606
    [No Abstract]   [Full Text] [Related]  

  • 32. Undifferentiated Pleomorphic Sarcoma Arising in a Fibrous Dysplasia Confirmed by GNAS Mutation Analysis: A Case Report.
    Okuda M; Kobayashi S; Gabata T; Yamamoto N; Nojima T
    JBJS Case Connect; 2020 Oct; 10(4):e20.00157. PubMed ID: 33438968
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune-Albright syndrome.
    Rey RA; Venara M; Coutant R; Trabut JB; Rouleau S; Lahlou N; Sultan C; Limal JM; Picard JY; Lumbroso S
    Hum Mol Genet; 2006 Dec; 15(24):3538-43. PubMed ID: 17101633
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Albright's hereditary osteodystrophy (pseudohypoparathyroidism type Ia): clinical case with a novel mutation of GNAS1.
    Garavelli L; Pedori S; Zanacca C; Caselli G; Loiodice A; Mantovani G; Ammenti A; Virdis R; Banchini G
    Acta Biomed; 2005 Apr; 76(1):45-8. PubMed ID: 16116826
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.
    Aldred MA; Aftimos S; Hall C; Waters KS; Thakker RV; Trembath RC; Brueton L
    Am J Med Genet; 2002 Nov; 113(2):167-72. PubMed ID: 12407707
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation analysis of GNAS1 and overlapping transcripts in Silver-Russell syndrome patients.
    Eggermann T; Meyer E; Schönherr N; Flick F; Chauvistré H; Mavany M; Wollmann HA
    Mol Genet Metab; 2007 Feb; 90(2):224-6. PubMed ID: 17056291
    [No Abstract]   [Full Text] [Related]  

  • 38. Hypocalcemia, prolonged QT interval and massive brain calcifications in an Iranian Jewish woman with APECED.
    Buber J; Goldenberg S; Eyal A; Mouallem M; Farfel Z
    Isr Med Assoc J; 2008 Dec; 10(12):899-900. PubMed ID: 19160953
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleeding.
    Freson K; Hoylaerts MF; Jaeken J; Eyssen M; Arnout J; Vermylen J; Van Geet C
    Thromb Haemost; 2001 Sep; 86(3):733-8. PubMed ID: 11583302
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.