| 1 |
22391343 | Description and molecular modeling of a novel human leukocyte antigen allele: A*32:22. | 2012 May |
1 |
| 2 |
22880226 | [Functional analysis for dysfibrinogenemias, Toyama and Adachi, which have a mutation of Aalpha16Arg-->His (CGT-->CAT) with aberrant fibrinopeptide A release]. | 2012 Jun |
1 |
| 3 |
16511838 | Evidence that variation in the peripheral benzodiazepine receptor (PBR) gene influences susceptibility to panic disorder. | 2006 Apr 5 |
2 |
| 4 |
12561067 | p53 alteration is not an independent prognostic indicator, but affects the efficacy of adjuvant chemotherapy in human pancreatic cancer. | 2003 Feb |
1 |
| 5 |
8769716 | Point mutation of the p53 gene is an infrequent event in untreated prostate cancer. | 1996 |
1 |
| 6 |
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 |
| 7 |
8187056 | A novel p53 mutant in human breast cancer revealed by multiple SSCP analysis. | 1994 Apr 29 |
1 |
| 8 |
8556514 | Genetic diversity in human Fc receptor II for immunoglobulin G: Fc gamma receptor IIA ligand-binding polymorphism. | 1994 Nov |
1 |
| 9 |
8320037 | Protein and gene structure analysis of an albumin genetic variant: proalbumin Wu Yang (-2 Arg-->His). | 1993 May |
1 |
| 10 |
8445019 | Point mutation in a family with hyperproinsulinemia detected by single stranded conformational polymorphism. | 1993 Mar |
1 |
| 11 |
2043465 | Occurrence of the alpha I 22 Arg----His (CGT----CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis. | 1991 May |
1 |
| 12 |
2196279 | Two unrelated patients with familial hyperproinsulinemia due to a mutation substituting histidine for arginine at position 65 in the proinsulin molecule: identification of the mutation by direct sequencing of genomic deoxyribonucleic acid amplified by polymerase chain reaction. | 1990 Jul |
1 |
| 13 |
2328319 | Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain. | 1990 Apr 15 |
1 |