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 *

122 related articles for article (PubMed ID: 16416775)

  • 21. Minireview: GNAS: normal and abnormal functions.
    Weinstein LS; Liu J; Sakamoto A; Xie T; Chen M
    Endocrinology; 2004 Dec; 145(12):5459-64. PubMed ID: 15331575
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Albright hereditary osteodystrophy: identification of a novel mutation in a family].
    Bastida Eizaguirre M; Iturbe Ortiz De Urbina R; Arto Urzainqui M; Ezquerra Larreina R; Escalada San Martín J
    An Esp Pediatr; 2001 Jun; 54(6):598-600. PubMed ID: 11412411
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Albright hereditary osteodystrophy].
    Tohma T
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):131-2. PubMed ID: 11057167
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. "A rare disorder, yes; an unimportant one, never".
    Olsen BR
    J Clin Invest; 1998 Apr; 101(8):1545-6. PubMed ID: 9541481
    [No Abstract]   [Full Text] [Related]  

  • 27. Pegvisomant for the treatment of gsp-mediated growth hormone excess in patients with McCune-Albright syndrome.
    Akintoye SO; Kelly MH; Brillante B; Cherman N; Turner S; Butman JA; Robey PG; Collins MT
    J Clin Endocrinol Metab; 2006 Aug; 91(8):2960-6. PubMed ID: 16720661
    [TBL] [Abstract][Full Text] [Related]  

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

  • 29. Rare bone disorders reveal a key metabolic gene.
    Senior K
    Trends Mol Med; 2001 Feb; 7(2):45-6. PubMed ID: 11286735
    [No Abstract]   [Full Text] [Related]  

  • 30. Ovarian dysfunction by activating mutation of GS alpha: McCune-Albright syndrome as a model.
    Chanson P; Salenave S; Young J
    Ann Endocrinol (Paris); 2010 May; 71(3):210-3. PubMed ID: 20362972
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gnathodiaphyseal dysplasia presenting as polyostotic fibrous dysplasia.
    Vengoechea J; Carpenter L
    Am J Med Genet A; 2015 Jun; 167(6):1421-2. PubMed ID: 25866257
    [No Abstract]   [Full Text] [Related]  

  • 32. Genes and chromosomes. Part 4--Genetic anomalies and disorders.
    Nigam Y; Bexfield A
    Nurs Times; 2008 Jul 1-7; 104(26):24-5. PubMed ID: 18669399
    [No 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. A maternal epimutation of GNAS leads to Albright osteodystrophy and parathyroid hormone resistance.
    Mariot V; Maupetit-Méhouas S; Sinding C; Kottler ML; Linglart A
    J Clin Endocrinol Metab; 2008 Mar; 93(3):661-5. PubMed ID: 18182455
    [TBL] [Abstract][Full Text] [Related]  

  • 35. "Mistakes happen": somatic mutation and disease.
    Qian F; Germino GG
    Am J Hum Genet; 1997 Nov; 61(5):1000-5. PubMed ID: 9345111
    [No Abstract]   [Full Text] [Related]  

  • 36. Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.
    de Sanctis L; Romagnolo D; Greggio N; Genitori L; Lala R; de Sanctis C
    J Pediatr Endocrinol Metab; 2002; 15 Suppl 3():883-9. PubMed ID: 12199346
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Fibrous dysplasia: overview].
    Akasbi N; Abourazzak FE; Talbi S; Tahiri L; Harzy T
    Pan Afr Med J; 2015; 21():21. PubMed ID: 26401215
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37.
    Sakaguchi H; Sanke T; Ohagi S; Iiri T; Nanjo K
    J Clin Endocrinol Metab; 1998 May; 83(5):1563-5. PubMed ID: 9589656
    [TBL] [Abstract][Full Text] [Related]  

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