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 *

149 related articles for article (PubMed ID: 26070936)

  • 21. [Pseudohypoparathyroidism].
    Yasuda T
    Nihon Rinsho; 2005 Oct; 63 Suppl 10():352-6. PubMed ID: 16279661
    [No Abstract]   [Full Text] [Related]  

  • 22. [The activating GNAS mutation : A survey of fibrous dysplasia, its associated syndromes, and other skeletal and extraskeletal lesions].
    Ostertag H; Glombitza S
    Pathologe; 2018 Mar; 39(2):146-153. PubMed ID: 29488004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Increased proliferation of osteoblastic cells expressing the activating Gs alpha mutation in monostotic and polyostotic fibrous dysplasia.
    Marie PJ; de Pollak C; Chanson P; Lomri A
    Am J Pathol; 1997 Mar; 150(3):1059-69. PubMed ID: 9060842
    [TBL] [Abstract][Full Text] [Related]  

  • 24. McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient.
    Tinschert S; Gerl H; Gewies A; Jung HP; Nürnberg P
    Am J Med Genet; 1999 Mar; 83(2):100-8. PubMed ID: 10190480
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel GNAS1 mutation, R201G, in McCune-albright syndrome.
    Riminucci M; Fisher LW; Majolagbe A; Corsi A; Lala R; De Sanctis C; Robey PG; Bianco P
    J Bone Miner Res; 1999 Nov; 14(11):1987-9. PubMed ID: 10571700
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. [Genetic counseling in osteodystrophy Albright's syndrome. Part II. GNAS1 gene and encoded protein function, genetic forecast and treatment].
    Janusz L; Morawska J; Wasilewska E; Sierakowski S; Midro AT
    Przegl Lek; 2010; 67(7):527-31. PubMed ID: 21387769
    [TBL] [Abstract][Full Text] [Related]  

  • 28. An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome.
    Shenker A; Weinstein LS; Sweet DE; Spiegel AM
    J Clin Endocrinol Metab; 1994 Sep; 79(3):750-5. PubMed ID: 8077356
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene.
    Germain-Lee EL; Schwindinger W; Crane JL; Zewdu R; Zweifel LS; Wand G; Huso DL; Saji M; Ringel MD; Levine MA
    Endocrinology; 2005 Nov; 146(11):4697-709. PubMed ID: 16099856
    [TBL] [Abstract][Full Text] [Related]  

  • 30. McCune-Albright syndrome in a discordant monozygotic twin.
    Peleg R; Luba A; Eliakim A; Israeli-Shani L; Manor E; Birk R; Parvari R
    Isr Med Assoc J; 2009 Jun; 11(6):343-7. PubMed ID: 19697584
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation.
    Klaassens M; Blom EW; Schrander JJ; Ris-Stalpers C; Nieuwenhuijzen Kruseman AC; van Steensel MA; Schrander-Stumpel CT
    Br J Dermatol; 2010 Mar; 162(3):690-4. PubMed ID: 19863504
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cutaneous and superficial soft tissue lesions associated with Albright hereditary osteodystrophy: clinicopathological and molecular genetic study of 4 cases, including a novel mutation of the GNAS gene.
    Kacerovska D; Nemcova J; Pomahacova R; Michal M; Kazakov DV
    Am J Dermatopathol; 2008 Oct; 30(5):417-24. PubMed ID: 18806481
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

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

  • 37. Albright hereditary osteodystrophy: a rare case report.
    Goswami M; Verma M; Singh A; Grewal H; Kumar G
    J Indian Soc Pedod Prev Dent; 2009; 27(3):184-8. PubMed ID: 19841552
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutations in the Gs alpha gene causing hormone resistance.
    Mantovani G; Spada A
    Best Pract Res Clin Endocrinol Metab; 2006 Dec; 20(4):501-13. PubMed ID: 17161328
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Unusual phenotypical variations in a boy with McCune-Albright syndrome.
    Mamkin I; Philibert P; Anhalt H; Ten S; Sultan C
    Horm Res Paediatr; 2010; 73(3):215-22. PubMed ID: 20197676
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.