Evaluation of hematopoiesis of Fanconi anemia by transcriptional analysis of active X-chromosome.

被引：0

作者：

Liu, Y

Auerbach, AD

Wagner, J

Wayne, A

Prchal, JF

Prchal, JT

机构：

[1] ROCKEFELLER UNIV,NEW YORK,NY 10021

[2] UNIV ALABAMA,BIRMINGHAM,AL

[3] UNIV MINNESOTA,MINNEAPOLIS,MN 55455

[4] UNIV S FLORIDA,ALL CHILDRENS HOSP,ST PETERSBURG,FL 33701

[5] MCGILL UNIV,MONTREAL,PQ,CANADA

来源：

BLOOD | 1995年 / 86卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1890 / 1890

页数：1

共 31 条

[11] Tradition meets high technology. Chromosome breakage analysis combined with exome sequencing in the diagnosis of Fanconi anemia
Christensen, R.
Hasle, H.
Blechingberg, J.
Thorsen, K.
Vestergaard, E.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 910 - 911
[12] Fanconi anemia: still an underdiagnosed disease? Retrospective analysis based on 25 years of cytogenetic evaluation
Porto, Beatriz
Oliveira, Claudia
Barbot, Jose
MEDICINE, 2019, 98 (26)
[13] APLASTIC-ANEMIA - ASSESSMENT OF CLONALITY BASED ON X-CHROMOSOME INACTIVATION ANALYSIS
RAGHAVACHAR, A
JANSSEN, JWG
SCHREZENMEIER, H
HEIMPEL, H
BARTRAM, CR
EXPERIMENTAL HEMATOLOGY, 1991, 19 (06) : 525 - 525
[14] CARCINOGEN-INDUCED CHROMOSOME BREAKAGE AS A MARKER FOR 1ST TRIMESTER PRENATAL-DIAGNOSIS AND COMPLEMENTATION ANALYSIS IN FANCONI ANEMIA CELLS
AUERBACH, AD
VENKATRAJ, VS
CARTER, DM
CLINICAL RESEARCH, 1985, 33 (02): : A624 - A624
[15] CARCINOGEN-INDUCED CHROMOSOME BREAKAGE AS A MARKER FOR 1ST TRIMESTER PRENATAL-DIAGNOSIS AND COMPLEMENTATION ANALYSIS IN FANCONI ANEMIA CELLS
AUERBACH, AD
VENKATRAJ, VS
CARTER, DM
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1985, 84 (04) : 338 - 338
[16] Frequencies of X-ray induced chromosome aberrations in lymphocytes of xeroderma pigmentosum and Fanconi anemia patients estimated by Giemsa and fluorescence in situ hybridization staining techniques
Saraswathy, R
Natarajan, AT
GENETICS AND MOLECULAR BIOLOGY, 2000, 23 (04) : 893 - 899
[17] Clonal analysis in MDS (refractory anemia) by fish and X-chromosome inactivation pattern using PCR.
Okada, M
Okamoto, T
Kanamaru, A
Kakishita, E
BLOOD, 1995, 86 (10) : 3183 - 3183
[18] SISTER CHROMATID EXCHANGE EVALUATION AS AN AID TO THE DIAGNOSIS AND EXCLUSION OF FANCONIS ANEMIA BY INDUCED CHROMOSOME-DAMAGE ANALYSIS
HOWELL, RT
JOURNAL OF MEDICAL GENETICS, 1991, 28 (07) : 468 - 471
[19] X-chromosome inactivation in mouse embryonic stem cells: Analysis of histone modifications and transcriptional activity using immunofluorescence and FISH
Chaumeil, J
Okamoto, I
Heard, E
CHROMATIN AND CHROMATIN REMODELING ENZYMES, PT B, 2004, 376 : 405 - +
[20] Microarray expression analysis supports upregulation of genes on the single active X chromosome, as compared to autosomal genes.
Disteche, CM
Holzman, T
Nguyen, DK
Bumgarner, R
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 472 - 472

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