| 1 |
28409923 | The Catalase Activity of Catalase-Peroxidases Is Modulated by Changes in the pKa of the Distal Histidine. | 2017 May 2 |
2 |
| 2 |
29058294 | A novel gene mutation of Runx2 in cleidocranial dysplasia. | 2017 Oct |
1 |
| 3 |
24412336 | Stabilisation of proteins via mixtures of amino acids during spray drying. | 2014 Mar 10 |
1 |
| 4 |
23871971 | Potential toxicity of sarafloxacin to catalase: spectroscopic, ITC and molecular docking descriptions. | 2013 Nov |
1 |
| 5 |
19199251 | [Molecular diagnosis of a Chinese pedigree with osteogenesis imperfecta type I]. | 2009 Feb |
1 |
| 6 |
16417235 | UVA-induced modification of catalase charge properties in the epidermis is correlated with the skin phototype. | 2006 Jan |
1 |
| 7 |
16450583 | Genetic analysis of a family with 46,XY "female" associated with infertility. | 2006 Jan |
2 |
| 8 |
16513636 | On the relationship of coral allene oxide synthase to catalase. A single active site mutation that induces catalase activity in coral allene oxide synthase. | 2006 May 5 |
2 |
| 9 |
16309371 | Simple PCR heteroduplex, SSCP mutation screening methods for the detection of novel catalase mutations in Hungarian patients with type 2 diabetes mellitus. | 2005 |
1 |
| 10 |
11270626 | Singlet oxygen generation from phosphatidylcholine hydroperoxide in the presence of copper. | 2001 Mar 2 |
1 |
| 11 |
9189046 | Friedreich-like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the alpha-tocopherol transfer protein gene. | 1997 Jun |
1 |
| 12 |
7566022 | Adult-onset spinocerebellar dysfunction caused by a mutation in the gene for the alpha-tocopherol-transfer protein. | 1995 Nov 16 |
1 |
| 13 |
8593088 | [The property of tetracyclines to induce methemoglobin formation in erythrocytes and to inactivate catalase when exposed to radiation in the visible range]. | 1995 Jun |
1 |
| 14 |
7866410 | Marked zinc activation of ester hydrolysis by a mutation, 67-His (CAT) to Arg (CGT), in the active site of human carbonic anhydrase I. | 1994 |
1 |
| 15 |
7913773 | Genetic analysis of a large kindred exhibiting type I protein C deficiency and associated thrombosis. | 1994 May 1 |
1 |
| 16 |
8205256 | Single amino acid substitution (840Arg-->His) in the hormone-binding domain of the androgen receptor leads to incomplete androgen insensitivity syndrome associated with a thermolabile androgen receptor. | 1994 Jun |
1 |
| 17 |
8400271 | Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion. | 1993 Oct 1 |
1 |
| 18 |
2349545 | Antithrombin Padua. I: Impaired heparin binding caused by an Arg47 to his (CGT to CAT) substitution. | 1990 Apr 15 |
1 |
| 19 |
12142 | The chemical modification of beef liver catalase. V. Ethoxyformylation of histidine and tyrosine residues of catalase with diethylpyrocarbonate. | 1976 Aug |
4 |