Citations for
1CA2, CTCF, LDB1
The LDB1 Complex Co-opts CTCF for Erythroid Lineage-Specific Long-Range Enhancer Interactions.
Lee J, Krivega I, Dale RK, Dean A.
Cell Rep 19(12):2490-2502. doi: 10.1016/j.celrep.2017.05.072. 2017
2CA2, FASL, FASLG, OSCAR
The effect of rotative stress on CAII, FAS, FASL, OSCAR, and TRAP gene expression in osteoclasts.
Qing Hong Z, Meng Tao L, Yi Z, Wei L, Ju Xiang S, Li L.
J Cell Biochem 114(2):388-97. doi: 10.1002/jcb.24372. 2013
3CA12, CA2
Carbonic anhydrases II and XII are up-regulated in osteoclast-like cells in advanced human atherosclerotic plaques-Tampere Vascular Study.
Oksala N, Levula M, Pelto-Huikko M, Kytömäki L, Soini JT, Salenius J, Kähönen M, Karhunen PJ, Laaksonen R, Parkkila S, Lehtimäki T.
Ann Med 42(5):360-70.PMID: 20509747 2010
4CA2
Autoimmunity against carbonic anhydrase II affects retinal cell functions in autoimmune retinopathy.
Adamus G, Karren L.
J Autoimmun 32(2):133-9. Epub 2009 Mar 6. 2009
5CA2
Small-molecule suppression of misfolding of mutated human carbonic anhydrase II linked to marble brain disease.
Almstedt K, Rafstedt T, Supuran CT, Carlsson U, Hammarström P.
Biochemistry 48(23):5358-64. 2009
6CA2
Potential for differential diagnosis of autoimmune pancreatitis and pancreatic cancer using carbonic anhydrase II antibody.
Hosoda H, Okawa-Takatsuji M, Shinmura W, Hasimoto N, Ozaki Y, Ikeda Y.
Pancreas 37(1):e1-7. 2008
7CA2, SLC9A1
A novel carbonic anhydrase II binding site regulates NHE1 activity.
Li X, Liu Y, Alvarez BV, Casey JR, Fliegel L.
Biochemistry 45(7):2414-24. 2006
8CA2
Carbonic anhydrase II in the developing and adult human brain.
Kida E, Palminiello S, Golabek AA, Walus M, Wierzba-Bobrowicz T, Rabe A, Albertini G, Wisniewski KE.
J Neuropathol Exp Neurol 65(7):664-74. 2006
9CA2
Carbonic anhydrase inhibitors. Zonisamide is an effective inhibitor of the cytosolic isozyme II and mitochondrial isozyme V: solution and X-ray crystallographic studies.
De Simone G, Di Fiore A, Menchise V, Pedone C, Antel J, Casini A, Scozzafava A, Wurl M, Supuran CT.
Bioorg Med Chem Lett 15(9):2315-20. 2005
10CA2
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds.
Puccetti L, Fasolis G, Cecchi A, Winum JY, Gamberi A, Montero JL, Scozzafava A, Supuran CT.
Bioorg Med Chem Lett 15(9):2359-64. 2005
11CA2, CRABP1, CRABP2, PAPSS2, MATN1
Identification of proteins differentially expressed during chondrogenesis of mesenchymal cells.
Lee SJ, Jeon HB, Lee JH, Yoo JS, Chun JS, Yoo YJ.
FEBS Lett 563(1-3):35-40. 2004
12CA2
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 40(2):115-21. 2003
13CA2
Osteopetrosis, renal tubular acidosis without urinary concentration abnormality, cerebral calcification and severe mental retardation in three Turkish brothers.
Ocal G, Berberoglu M, Adiyaman P, Cetinkaya E, Ekim M, Aycan Z, Evliyaoglu O.
J Pediatr Endocrinol Metab 14(9):1671-7. Review. 2001
14CA1, CA2
Carbonic anhydrase I and II as a differentiation marker of human and rat colonic enterocytes.
Bekku S, Mochizuki H, Takayama E, Shinomiya N, Fukamachi H, Ichinose M, Tadakuma T, Yamamoto T.
Res Exp Med (Berl) 198(4):175-85. 1998
15CA2
Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: evidence for founder effect and genomic recombination at the CA II locus.
Fathallah DM, Bejaoui M, Lepaslier D, Chater K, Sly WS, Dellagi K.
Hum Genet 99(5):634-7. 1997
16CA2
Seven novel mutations in carbonic anhydrase II deficiency syndrome identified by SSCP and direct sequencing analysis.
Hu PY, et al.
Hum Mutat 9 : 383-387. 1997
17CA2
A point mutation in exon 3 (His 107-Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement.
Soda H, et al.
Hum Genet 97 : 435-437. 1996
18CA1, CA2, CA3
Human carbonic anhydrases and carbonic anhydrase deficiencies.
Sly WS, Hu PY.
Annu Rev Biochem 64:375-401. Review. 1995
19CA2
Carbonic anhydrase II deficiency : single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patients.
Hu PY, et al.
Am J Hum Genet 54 : 602-608. 1994
20CA2
A unique mutation underlying carbonic anhydrase II deficiency syndrome in patients of Arab descent.
Fathallah DM, et al.
Hum Genet 94 : 581-582. 1994
21CA2
Molecular basis of human carbonic anhydrase II deficiency.
Roth DE, et al.
Proc Natl Acad Sci U S A 89 : 1804-1808. 1992
22CA2
PCR detection of a BstNI RSP in exon 6 of the human carbonic anydrase II locus, CA2.
Venta PJ, et al.
Nucleic Acids Res 19 : 4795. 1991
23CA2
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His-Tyr): complete structure of the normal human CA II gene.
Venta PJ, et al.
Am J Hum Genet 49 : 1082-1090. 1991
24CA2
PCR detection of the TAQ1 polymorphism at the CA2 locus.
Venta PJ, et al.
Nucleic Acids Res 18 : 5585. 1990
25CA2
The gene for human carbonic anhydrase II(CA2) is located at chromosome 8q22.
Nakai H, et al.
Cytogenet Cell Genet 44 : 234-235. 1987
26CA2
Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
Sly WS, et al.
N Engl J Med 313 : 139-145. 1985
27CA2
DNA polymorphism in the 5' flanking region of the flanking region of the human carbonic anhydrase II gene on chromosome 8.
Lee BL, et al.
Hum Genet 69 : 337-339. 1985
28CA2
Polymorphic gene for carbonic anhydrase II : a molecular disease marker located on chromosome 8.
Venta PJ, et al.
Proc Natl Acad Sci U S A 80 : 4437-4440. 1983
29CA2
OstŽopŽtrose et acidose rŽnale tubulaire. Deux cas de cette association dans une fratrie.
Guibaud P, et al.
Arch Fr Pediatr 29 : 269-286. 1972