Related references
Note: Only part of the references are listed.Over-expression of DMRT1 induces the male pathway in embryonic chicken gonads
Luke S. Lambeth et al.
DEVELOPMENTAL BIOLOGY (2014)
Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene
Bala Bhagavath et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2014)
Enhancer biology and enhanceropathies
Edwin Smith et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2014)
A rare case of 46, XX SRY-negative male with a ∼74-kb duplication in a region upstream of SOX9
Bing Xiao et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2013)
Gene Mutations Associated with Anomalies of Human Gonad Formation
A. Bashamboo et al.
SEXUAL DEVELOPMENT (2013)
Fine Time Course Expression Analysis Identifies Cascades of Activation and Repression and Maps a Putative Regulator of Mammalian Sex Determination
Steven C. Munger et al.
PLOS GENETICS (2013)
XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication
Sharon Moalem et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Steroidogenic Factor-1 and Human Disease
Ranna El-Khairi et al.
SEMINARS IN REPRODUCTIVE MEDICINE (2012)
Setting up and maintaining differential insulators and boundaries for genomic imprinting
Adele Murrell
BIOCHEMISTRY AND CELL BIOLOGY (2011)
Identification of SOX3 as an XX male sex reversal gene in mice and humans
Edwina Sutton et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
XX males SRY negative: a confirmed cause of infertility
Annalisa Vetro et al.
JOURNAL OF MEDICAL GENETICS (2011)
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
Sabina Benko et al.
JOURNAL OF MEDICAL GENETICS (2011)
DMRT1 prevents female reprogramming in the postnatal mammalian testis
Clinton K. Matson et al.
NATURE (2011)
A SOX9 Duplication and Familial 46,XX Developmental Testicular Disorder.
James J. Cox et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Clinical traits and molecular findings in 46,XX males
Marisol López et al.
CLINICAL GENETICS (2010)
Histone H3 lysine 4 (H3K4) methylation in development and differentiation
Joel C. Eissenberg et al.
DEVELOPMENTAL BIOLOGY (2010)
Sex determination and disorders of sex development according to the revised nomenclature and classification in 46,XX individuals
Eleni Kousta et al.
HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM (2010)
Sox10 gain-of-function causes XX sex reversal in mice: implications for human 22q-linked disorders of sex development
Juan Carlos Polanco et al.
HUMAN MOLECULAR GENETICS (2010)
Genome-wide analysis of DNA binding and transcriptional regulation by the mammalian Doublesex homolog DMRT1 in the juvenile testis
Mark W. Murphy et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Mutations of the SRY-Responsive Enhancer of SOX9 Are Uncommon in XY Gonadal Dysgenesis
I. Georg et al.
SEXUAL DEVELOPMENT (2010)
Smad3 activates the Sox9-dependent transcription on chromatin
Takayuki Furumatsu et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2009)
Long-range regulation at the SOX9 locus in development and disease
C. T. Gordon et al.
JOURNAL OF MEDICAL GENETICS (2009)
The avian Z-linked gene DMRT1 is required for male sex determination in the chicken
Craig A. Smith et al.
NATURE (2009)
Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia
Ingo Kurth et al.
NATURE GENETICS (2009)
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
Sabina Benko et al.
NATURE GENETICS (2009)
SERKAL syndrome: An autosomal-recessive disorder caused by a loss-of-function mutation in WNT4
Hannah Mandel et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Sex determination involves synergistic action of SRY and SF1 on a specific Sox9 enhancer
Ryohei Sekido et al.
NATURE (2008)
R-spondin1 is essential in sex determination, skin differentiation and malignancy
Pietro Parma et al.
NATURE GENETICS (2006)
Long-range upstream and downstream enhancers control distinct subsets of the complex spatiotemporal Sox9 expression pattern
S Bagheri-Fam et al.
DEVELOPMENTAL BIOLOGY (2006)
Position effects due to chromosome breakpoints that map ∼900 Kb upstream and ∼1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia
GVN Velagaleti et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Pbx1 is essential for adrenal development and urogenital differentiation
CA Schnabel et al.
GENESIS (2003)
Deletions of 9p and the quest for a conserved mechanism of sex determination
C Ottolenghi et al.
MOLECULAR GENETICS AND METABOLISM (2000)
Share Paper
