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Julie Plaisancie et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2013)
Modeling Recent Human Evolution in Mice by Expression of a Selected EDAR Variant
Yana G. Kamberov et al.
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Tooth shape formation and tooth renewal: evolving with the same signals
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Mutations in WNT10A are present in more than half of isolated hypodontia cases
Marie-Jose van den Boogaard et al.
JOURNAL OF MEDICAL GENETICS (2012)
Structural Basis of Wnt Recognition by Frizzled
Claudia Y. Janda et al.
SCIENCE (2012)
Isolated Oligodontia Associated With Mutations in EDARADD, AXIN2, MSX1, and PAX9 Genes
Birgitta Bergendal et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Schopf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A
Gabriela Petrof et al.
AUSTRALASIAN JOURNAL OF DERMATOLOGY (2011)
Only Four Genes (EDA1, EDAR, EDARADD, and WNT10A) Account for 90% of Hypohidrotic/Anhidrotic Ectodermal Dysplasia Cases
Celine Cluzeau et al.
HUMAN MUTATION (2011)
Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis
Gabriele Mues et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
An Arginine Stretch Limits ADAM10 Exit from the Endoplasmic Reticulum
Elena Marcello et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
Axel Bohring et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
A Common Variation in EDAR Is a Genetic Determinant of Shovel-Shaped Incisors
Ryosuke Kimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction
Yuhang Zhang et al.
DEVELOPMENTAL CELL (2009)
Agenesis of permanent teeth in 8138 Danish schoolchildren: prevalence and intra-oral distribution according to gender
Steen Rolling et al.
INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY (2009)
EDA Gene Mutations Underlie Non-syndromic Oligodontia
S. Song et al.
JOURNAL OF DENTAL RESEARCH (2009)
Genetic Basis of Tooth Agenesis
Pekka Nieminen
JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION (2009)
Dental agenesis: genetic and clinical perspectives
P. J. De Coster et al.
JOURNAL OF ORAL PATHOLOGY & MEDICINE (2009)
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia
Annemarie H. van der Hout et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Non-Syndromic Tooth Agenesis in Two Chinese Families Associated with Novel Missense Mutations in the TNF Domain of EDA (Ectodysplasin A)
Shufeng Li et al.
PLOS ONE (2008)
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia:: The odonto-onycho-dermal dysplasia
Lynn Adaimy et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
E. Bal et al.
HUMAN MUTATION (2007)
A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia
Patrick Tarpey et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Anomalies of tooth formation in hypohidrotic ectodermal dysplasia
Michala O. Lexner et al.
INTERNATIONAL JOURNAL OF PAEDIATRIC DENTISTRY (2007)
Novel MSX1 frameshift causes autosomal-dominant oligodontia
JW Kim et al.
JOURNAL OF DENTAL RESEARCH (2006)
Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis
A Mostowska et al.
JOURNAL OF HUMAN GENETICS (2006)
Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia
R Kist et al.
HUMAN MOLECULAR GENETICS (2005)
Association between PAX-9 promoter polymorphisms and hypodontia in humans
RCR Peres et al.
ARCHIVES OF ORAL BIOLOGY (2005)
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer
L Lammi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
A meta-analysis of the prevalence of dental agenesis of permanent teeth
BJ Polder et al.
COMMUNITY DENTISTRY AND ORAL EPIDEMIOLOGY (2004)
Ectodysplasin A1 promotes placodal cell fate during early morphogenesis of ectodermal appendages
T Mustonen et al.
DEVELOPMENT (2004)
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia
L Lammi et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Gene defect in ectodermal dysplasia implicates a death domain adapter in development
DJ Headon et al.
NATURE (2001)
Identification of a nonsense mutation in the PAX9 gene in molar oligodontia
P Nieminen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Recessively inherited lower incisor hypodontia
S Pirinen et al.
JOURNAL OF MEDICAL GENETICS (2001)
Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A
P Schneider et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Characteristics of incisor-premolar hypodontia in families
S Arte et al.
JOURNAL OF DENTAL RESEARCH (2001)
TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
J Laurikkala et al.
DEVELOPMENTAL BIOLOGY (2001)
Mutation of PAX9 is associated with oligodontia
DW Stockton et al.
NATURE GENETICS (2000)
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