[PDF] Top 20 第１章 計画策定の目的 長野市歴史的風致維持向上計画 長野市ホームページ
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The -104G nucleotide of the human CYP21 gene is important for CYP21 transcription activity and protein interaction
... KK and Chang SF Abstract CYP21 gene encodes the steroid 21-hydroxylase (P450c21) that is involved in steroidogenesis in the adrenal ...on CYP21 ... 完全なドキュメントを参照
The -104G nucleotide of the human CYP21 gene is important for CYP21 transcription activity and protein interaction
... These results therefore suggest that the single G sequence of the human CYP21 gene is crucial for the expression of its basal transcription activity, and this may be influenced by the [r] ... 完全なドキュメントを参照
Transcriptional Activation of the Alpha-1 Acid Glycoprotein Gene by YY1 Is Mediated by Its Functional Interaction with a Negative Transcription Factor
... normal and LPS-treated liver. A. Western blot analysis showing the relative constant protein level of YY l in normal rat liver nuclear extract (N) and extract prepared from LPS-treated ... 完全なドキュメントを参照
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The suppression effect of DNA sequences within the C4A region on the transcription activity of human CYP21.
... SF and Cheng CL Abstract Two CYP21 genes, the active CYP21 and the pseudogene, CYP21P, also pairs of duplicated genes including the XA, ... 完全なドキュメントを参照
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Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-
... To identify the interchange region and improve detection of gene deletions and conversions in the RCCX module (10)(11)(12)(13), we have developed a novel Southern blot analysis that us[r] ... 完全なドキュメントを参照
Analysis of CYP21A1P and the duplicated CYP21A2 genes
... to the Editor Analysis of CYP21A1P and the duplicated CYP21A2 genes Li-Ping Tsai, a,b and Hsien-Hsiung Lee a,c* a Department of Pediatrics, Buddhist ... 完全なドキュメントを参照
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Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency
... (CAH) is a common autosomal recessive disorder mainly caused by defects in the steroid 21-hydroxylase (CYP21) ...NdeI and AseI digestion by Southern blot analysis indicated that ... 完全なドキュメントを参照
Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency
... (CAH) is a common autosomal recessive disorder mainly caused by defects in the steroid 21-hydroxylase (CYP21) ...NdeI and AseI digestion by Southern blot analysis indicated that ... 完全なドキュメントを参照
Analysis of the CYP21A1P pseudogene: Indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes
... t The CYP21A1P gene downstream of the XA gene, carrying 15 deteriorated mutations, is a nonfunctional pseudogene that shares 98% nucleotide sequence homology ... 完全なドキュメントを参照
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Variants of the CYP21A2 and CYP21A1P genes in congenital adrenal hyperplasia
... Therefore, CYP21A2 is considered the gene located downstream of the TNXB gene, and CYP21A1P is located downstream of the ... 完全なドキュメントを参照
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Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase
... However, the method is indirect and time-consuming, and densitometry of fragments can be prone to ...identify the interchange region and improve detection of ... 完全なドキュメントを参照
Analysis of the CYP21A2 Gene with Intergenic Recombination and Multiple Gene Deletions in the RCCX Module
... Analysis of the CYP21A2 Gene with Intergenic Recombination and Multiple Gene Deletions in the RCCX Module Shwu-Fen Chang 1 and Hsien-Hsiung Lee 2 The ... 完全なドキュメントを参照
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Characterization of the regulatory element(s) controlling the adrenal-specific expression of human CYP21(P450c21) gene.
... 人類 CYP21 基因腎上腺專一性表現之調控元素的研究 Characterization of the regulatory element(s) controlling the adrenal-specific expression of human CYP21(P450c21) ... 完全なドキュメントを参照
Difference in transcriptional activity of two homologous CYP21A genes
... report the transcriptional activities of the c21A and c21B genes have been ...that transcription derived from the c21A gene was about 5-fold lower in ... 完全なドキュメントを参照
Difference in transcriptional activity of two homologous CYP21A genes
... that transcription derived from the c21A gene was about 5-fold lower in strength than that of the c21B gene, although both sequences responded to cAMP normally in ... 完全なドキュメントを参照
High-resolution melting curve (HRM) analysis to establish CYP21A2 mutations converted from the CYP21A1P in congenital adrenal hyperplasia
... Department of Laboratory Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan 7 c Division of General Internal Medicine, Department of Internal ... 完全なドキュメントを参照
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Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency
... CHIMERIC CYP21P/CYP21; MOLECULAR DIAGNOSIS; PRENATAL-DIAGNOSIS; BRAZILIAN PATIENTS; MUTATION ANALYSIS; GENE CONVERSIONS Abstract: Congenital adrenal hyperplasia (CAH) is a common ... 完全なドキュメントを参照
Identification of the small heat shock protein, HSP21, of shrimp Penaeus monodon and the gene expression of HSP21 is inactivated after white spot syndrome virus (WSSV) infection
... apoptosis, the studies of smHSP, Mj HSP16.5, of Methanococcus jannaschii provided a reasonable construc- ...observed the crystal structure of Mj HSP16.5 and then proposed ... 完全なドキュメントを参照
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A dual function of the furanocoumarin chalepensin in inhibiting Cyp2a and inducing Cyp2b in mice: the protein stabilization and receptor-mediated activation.
... administration is the most common way for the administration of herbal ...examine the chalepensin-mediated P450 modulation in vivo, the oral effects of chalepensin ... 完全なドキュメントを参照
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CYP17;CYP1A1 and COMT polymorphisms and the risk of adenomyosis and endometriosis in Taiwanese women.
... adenomyosis and endometriosis with regard to the COMT genotypes can be partially attributed to their different ...form of endometriosis, distinct processes have been found in the two ... 完全なドキュメントを参照
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