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Sex reversal by loss of the C–terminal transactivation domain of human SOX9

Data up to Jan 2025

Published1996
Citations208
References21

Total Citations Per Year

Abstract

References (21)

Rapid detection of octamer binding proteins with ‘mini extracts’, prepared from a small number of cells

1989 • 4,279 citations

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

1994 • 1,573 citations

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

1994 • 1,521 citations

Biochemical transfer of single-copy eucaryotic genes using total cellular DNA as donor

1978 • 1,284 citations

Transcriptional activation: A complex puzzle with few easy pieces

1994 • 1,112 citations

HMG domain proteins: architectural elements in the assembly of nucleoprotein structures

1994 • 813 citations

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

1994 • 683 citations

The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos

1995 • 648 citations

Transcriptional Activation Modulated by Homopolymeric Glutamine and Proline Stretches

1994 • 598 citations

Identification and cloning of TCF-1, a T lymphocyte-specific transcription factor containing a sequence-specific HMG box.

1991 • 545 citations

The oncoprotein Bcl-3 directly transactivates through κB motifs via association with DNA-binding p50B homodimers

1993 • 506 citations

DNA Binding Activity of Recombinant SRY from Normal Males and XY Females

1992 • 454 citations

SRY, like HMG1, recognizes sharp angles in DNA.

1992 • 439 citations

Sox-4, an Sry-like HMG box protein, is a transcriptional activator in lymphocytes.

1993 • 340 citations

A transferable silencing domain is present in the thyroid hormone receptor, in the v-erbA oncogene product and in the retinoic acid receptor.

1992 • 302 citations

DNA-binding properties of the HMG domain of the lymphoid-specific transcriptional regulator LEF-1.

1991 • 265 citations

Direct interaction between the transcriptional activation domain of human p53 and the TATA box-binding protein.

1993 • 209 citations

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

1995 • 199 citations

A general mechanism for transcriptional synergy by eukaryotic activators

1995 • 185 citations

Transactivation Domain 2 (TA2) of p65 NF-κB

1995 • 161 citations

Mutations in the coding region of c-MYC in AIDS-associated and other aggressive lymphomas.

1994 • 71 citations

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Sex reversal by loss of the C–terminal transactivation domain of human SOX9 (1996) – Nature Genetics | Metascience Observatory Explorer