BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 36826034)

  • 1. Carbonic Anhydrase II Activators in Osteopetrosis Treatment: A Review.
    Alkhayal Z; Shinwari Z; Gaafar A; Alaiya A
    Curr Issues Mol Biol; 2023 Feb; 45(2):1373-1386. PubMed ID: 36826034
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fluconazole-Induced Protein Changes in Osteogenic and Immune Metabolic Pathways of Dental Pulp Mesenchymal Stem Cells of Osteopetrosis Patients.
    Alkhayal Z; Shinwari Z; Gaafar A; Alaiya A
    Int J Mol Sci; 2023 Sep; 24(18):. PubMed ID: 37762144
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carbonic anhydrase II deficiency.
    Whyte MP
    Bone; 2023 Apr; 169():116684. PubMed ID: 36709914
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
    Sly WS; Whyte MP; Sundaram V; Tashian RE; Hewett-Emmett D; Guibaud P; Vainsel M; Baluarte HJ; Gruskin A; Al-Mosawi M
    N Engl J Med; 1985 Jul; 313(3):139-45. PubMed ID: 3925334
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evaluation of carbonic anhydrase isozymes in disorders involving osteopetrosis and/or renal tubular acidosis.
    Sly WS; Sato S; Zhu XL
    Clin Biochem; 1991 Aug; 24(4):311-8. PubMed ID: 1959222
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carbonic anhydrase II deficiency syndrome: recessive osteopetrosis with renal tubular acidosis and cerebral calcification.
    Ohlsson A; Cumming WA; Paul A; Sly WS
    Pediatrics; 1986 Mar; 77(3):371-81. PubMed ID: 3081869
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of carbonic anhydrase in autosomal dominant osteopetrosis.
    Bollerslev J; Mondrup MP
    Scand J Clin Lab Invest; 1989 Feb; 49(1):93-5. PubMed ID: 2499032
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification.
    Cotter M; Connell T; Colhoun E; Smith OP; McMahon C
    J Pediatr Hematol Oncol; 2005 Feb; 27(2):115-7. PubMed ID: 15701991
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The neurology of carbonic anhydrase type II deficiency syndrome.
    Bosley TM; Salih MA; Alorainy IA; Islam MZ; Oystreck DT; Suliman OS; al Malki S; Suhaibani AH; Khiari H; Beckers S; van Wesenbeeck L; Perdu B; AlDrees A; Elmalik SA; Van Hul W; Abu-Amero KK
    Brain; 2011 Dec; 134(Pt 12):3502-15. PubMed ID: 22120147
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recent developments in the understanding of the pathophysiology of osteopetrosis.
    Felix R; Hofstetter W; Cecchini MG
    Eur J Endocrinol; 1996 Feb; 134(2):143-56. PubMed ID: 8630510
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Osteopetrosis with carbonic anhydrase II deficiency: report of 24 cases].
    Sonia HL; Mohamed F; Mohamed B; Rafika A; Dehmani F; Kossay D; Azza H
    Tunis Med; 2005 Jul; 83(7):409-13. PubMed ID: 16220698
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
    Sly WS; Hewett-Emmett D; Whyte MP; Yu YS; Tashian RE
    Proc Natl Acad Sci U S A; 1983 May; 80(9):2752-6. PubMed ID: 6405388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Proteomic Profiling of the First Human Dental Pulp Mesenchymal Stem/Stromal Cells from Carbonic Anhydrase II Deficiency Osteopetrosis Patients.
    Alkhayal Z; Shinwari Z; Gaafar A; Alaiya A
    Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33396517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Osteopetrosis.
    Kocher MS; Kasser JR
    Am J Orthop (Belle Mead NJ); 2003 May; 32(5):222-8. PubMed ID: 12772872
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Carbonic anhydrase isozymes of osteoclasts and erythrocytes of osteopetrotic microphthalmic mice.
    Jilka RL; Rogers JI; Khalifah RG; Vaananen HK
    Bone; 1985; 6(6):445-9. PubMed ID: 3938292
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Case report 718. Osteopetrosis with carbonic anhydrase II deficiency.
    Eddy R; Resendes M; Genant H
    Skeletal Radiol; 1992; 21(2):135-6. PubMed ID: 1566113
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Case Report of Clinical Vignette: Osteopetrosis.
    Moore JB; Hoang TD; Shwayhat AF
    Mil Med; 2017 Mar; 182(3):e1886-e1888. PubMed ID: 28290981
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Carbonic Anhydrase II Deficiency: A Rare Case of Severe Obstructive Sleep Apnea.
    di Palmo E; Gallucci M; Tronconi E; Bergamaschi R; Cazzato S; La Scola C; Ricci G; Pession A
    Front Pediatr; 2018; 6():213. PubMed ID: 30109220
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome.
    McMahon C; Will A; Hu P; Shah GN; Sly WS; Smith OP
    Blood; 2001 Apr; 97(7):1947-50. PubMed ID: 11264157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.
    Borthwick KJ; Kandemir N; Topaloglu R; Kornak U; Bakkaloglu A; Yordam N; Ozen S; Mocan H; Shah GN; Sly WS; Karet FE
    J Med Genet; 2003 Feb; 40(2):115-21. PubMed ID: 12566520
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.