Identification and characterization of the human long form of Sox5 (L-SOX5) gene
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Tensor GSVD of patient- and platform-matched tumor and normal DNA copy-number profiles uncovers chromosome arm-wide patterns of tumor-exclusive platform-consistent alterations encoding for cell transformation and predicting ovarian cancer survivalConcerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphomaTranscriptional regulation of an axonemal central apparatus gene, sperm-associated antigen 6, by a SRY-related high mobility group transcription factor, S-SOX5Genome-wide map of quantified epigenetic changes during in vitro chondrogenic differentiation of primary human mesenchymal stem cells.SOX5 is a candidate gene for chronic obstructive pulmonary disease susceptibility and is necessary for lung development.High levels of SOX5 decrease proliferative capacity of human B cells, but permit plasmablast differentiation.Transcriptional regulation of human sperm-associated antigen 16 gene by S-SOX5Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.Modulation of IL-6 induced RANKL expression in arthritic synovium by a transcription factor SOX5Expression and function of a novel isoform of Sox5 in malignant B cells.Sox6, jack of all trades: a versatile regulatory protein in vertebrate developmentExpressions of Sox9, Sox5, and Sox13 transcription factors in mice testis during postnatal development.SOX5-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral Abnormalities.Silencing of the Drosophila ortholog of SOX5 leads to abnormal neuronal development and behavioral impairment.SOX5 interacts with YAP1 to drive malignant potential of non-small cell lung cancer cells.A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novoSOX5deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic featuresExome sequencing expands the mechanism of SOX5-associated intellectual disability: A case presentation with review of sox-related disorders
P2860
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P2860
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
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2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
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name
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@ast
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@en
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@nl
type
label
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@ast
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@en
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@nl
prefLabel
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@ast
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@en
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@nl
P2093
P3181
P1433
P1476
Identification and characterization of the human long form of Sox5 (L-SOX5) gene
@en
P2093
Akihiko Mabuchi
Akira Fukuda
Hiroshi Kawaguchi
Junwei Zhang
Kozo Nakamura
Shiro Ikegawa
Tokuhiro Chano
Toshiyuki Ikeda
P3181
P356
10.1016/S0378-1119(02)00927-7
P407
P577
2002-09-18T00:00:00Z