Illegitimate transcription: its use in the study of inherited disease.
about
Detection of circulating tumor cells in prostate cancer patients: methodological pitfalls and clinical relevanceA novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 yearsTruncated mutants of the putative Wnt receptor LRP6/Arrow can stabilize beta-catenin independently of Frizzled proteinsMolecular detection of minimal residual disease in colorectal and breast cancer.Minimal residual marrow disease: detection and significance of isolated tumour cells in bone marrow.Detection and clinical significance of occult tumour cells in colorectal cancer.Molecular detection and characterization of circulating tumor cells and micrometastases in prostatic, urothelial, and renal cell carcinomas.New best1 mutations in autosomal recessive bestrophinopathy.Circulating tumor cells: detection, molecular profiling and future prospects.Roles of Fas and Fas ligand during mammary gland remodeling.Modifications of RNA processing modulate the expression of hemoglobin genesNew technologies for the detection of circulating tumour cells.Biomarkers in cancer micrometastasis: where are we at?Diagnostic strategy for the detection of dystrophin gene mutations in asian patients and carriers using immortalized cell lines.Ectopic (illegitimate) transcription: new possibilities for the analysis and diagnosis of human genetic disease.Rescue of human RET gene expression by sodium butyrate: a novel powerful tool for molecular studies in Hirschsprung diseaseSplice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome.
P2860
Q24646761-608AA4B1-EEFF-44AE-BD10-ED43B91822DBQ28239316-64A3731B-82B6-4D1C-A5EC-39CF92CE6EE3Q28509118-2E3B9A00-360B-4AE7-AD88-1526C930DA33Q33609814-E96E7416-9E49-477A-BA80-86046133D3E7Q34284347-CB31D368-3753-423B-A5DC-1CEDF7A6974AQ34385776-23963EF6-5430-4765-B54D-EFB8B3E352F2Q34465200-FD50C2E5-9BC9-4FDE-8B6C-9A0DBB3C99EDQ35588708-19514F95-9932-4A36-BE50-07B880D511D2Q37027492-D496DA89-0075-47E4-809A-6280E1B88300Q37271091-A7DE26D4-D3F7-44BA-9375-1A105B201914Q37549347-43B36DB1-1C77-4357-A6C3-2D2641814107Q37736981-158492FB-B748-412B-ACC5-003A43E3E3DEQ37810222-136233C0-7A1D-47B5-B922-EB79F38AED1AQ40299495-290392FD-E818-4605-9A39-55C96460B9C1Q40744835-9082DA22-9D00-408F-8B3B-48CAA00F8A33Q41895307-BDB570FA-86AC-49E9-ABAC-5E601E2D414AQ50499115-C7478BBC-C006-4317-B93E-C15FA8FD85D5
P2860
Illegitimate transcription: its use in the study of inherited disease.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Illegitimate transcription: its use in the study of inherited disease.
@ast
Illegitimate transcription: its use in the study of inherited disease.
@en
type
label
Illegitimate transcription: its use in the study of inherited disease.
@ast
Illegitimate transcription: its use in the study of inherited disease.
@en
prefLabel
Illegitimate transcription: its use in the study of inherited disease.
@ast
Illegitimate transcription: its use in the study of inherited disease.
@en
P2093
P356
P1433
P1476
Illegitimate transcription: its use in the study of inherited disease.
@en
P2093
P304
P356
10.1002/HUMU.1380010502
P577
1992-01-01T00:00:00Z