Characterization of CA XV, a new GPI-anchored form of carbonic anhydrase

M Hilvo, M Tolvanen, A Clark, B Shen… - Biochemical …, 2005 - portlandpress.com
The main function of CAs (carbonic anhydrases) is to participate in the regulation of acid–
base balance. Although 12 active isoenzymes of this family had already been described …

Carbonic anhydrase II plays a major role in osteoclast differentiation and bone resorption by effecting the steady state intracellular pH and Ca2+

P Lehenkari, TA Hentunen, T Laitala-Leinonen… - Experimental cell …, 1998 - Elsevier
Carbonic anhydrase II (CA II) expression is characteristic for the early stage of osteoclast
differentiation. To study how CA II, which is crucial in proton generation in mature …

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 …

PJ Venta, RJ Welty, TM Johnson, WS Sly… - American journal of …, 1991 - ncbi.nlm.nih.gov
Abstract Carbonic anhydrase II (CA II), which has the highest turnover number and widest
tissue distribution of any of the seven CA isozymes known in humans, is absent from the red …

N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.

SE Lewis, RP Erickson, LB Barnett… - Proceedings of the …, 1988 - National Acad Sciences
Electrophoretic screening of (C57BL/6J x DBA/2J) F1 progeny of male mice treated with N-
ethyl-N-nitrosourea revealed a mouse that lacked the paternal carbonic anhydrase II (CA II) …

Differential expression of carbonic anhydrase isoenzymes in various types of anemia

WH Kuo, SF Yang, YS Hsieh, CS Tsai, WL Hwang… - Clinica chimica acta, 2005 - Elsevier
BACKGROUND: The aim of the present study was to determine the concentrations of
cytosolic carbonic anhydrase (CA) isoenzymes in erythrocytes of patients with aplastic …

[HTML][HTML] A novel renal carbonic anhydrase type III plays a role in proximal tubule dysfunction

P Gailly, F Jouret, D Martin, H Debaix, KS Parreira… - Kidney international, 2008 - Elsevier
Dysfunction of the proximal tubule (PT) is associated with variable degrees of solute wasting
and low-molecular-weight proteinuria. We measured metabolic consequences and …

Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis

A Campos-Xavier, JM Saraiva, LM Ribeiro, A Munnich… - Human genetics, 2003 - Springer
Osteopetrosis is a heterogeneous group of inherited disorders that includes a malignant
autosomal recessive form, an intermediate autosomal recessive form and autosomal …

Expression of carbonic anhydrase IX in mouse tissues

M Hilvo, M Rafajová, S Pastoreková… - … of Histochemistry & …, 2004 - journals.sagepub.com
Carbonic anhydrase IX (CA IX) is a unique member of the CA gene family. In contrast to the
other isozymes, it has been implicated in regulation of cell proliferation, adhesion, and …

Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers‐Schönberg disease (chloride channel 7 deficiency osteopetrosis) …

MP Whyte, LG Kempa, WH McAlister… - Journal of Bone and …, 2010 - academic.oup.com
Osteopetrosis (OPT) refers to the consequences of generalized failure of skeletal resorption
during growth. Most cases are explained by loss‐of‐function mutation within the genes that …

Expression of carbonic anhydrase I in motor neurons and alterations in ALS

X Liu, D Lu, R Bowser, J Liu - International journal of molecular sciences, 2016 - mdpi.com
Carbonic anhydrase I (CA1) is the cytosolic isoform of mammalian α-CA family members
which are responsible for maintaining pH homeostasis in the physiology and pathology of …