| scholarly article | Q13442814 |
| case report | Q2782326 |
| P2093 | author name string | Andre Megarbane | |
| Eliane Chouery | |||
| Philippe de Mazancourt | |||
| Salman Mroueh | |||
| Hanen Belguith | |||
| Hala Megarbane | |||
| Valerie Delague | |||
| Elsa Nicolas | |||
| Lynn Adaimy | |||
| P2860 | cites work | Expression of Wnt signalling pathway genes during tooth development. | Q52175657 |
| Further delineation of the odonto-onycho-dermal dysplasia syndrome | Q59526297 | ||
| Hair changes in ectodermal dysplasia associated with multiple anomalies | Q70515893 | ||
| Odonto-onycho-dermal dysplasia | Q70883188 | ||
| Variant of odontoonychodermal dysplasia? | Q70969768 | ||
| Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia | Q71699525 | ||
| New form of hidrotic ectodermal dysplasia in a Lebanese family | Q74122587 | ||
| Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome | Q24296426 | ||
| A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman | Q24301616 | ||
| Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy | Q24304241 | ||
| Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family | Q24307763 | ||
| Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair | Q24318751 | ||
| Wnt4 overexpression disrupts normal testicular vasculature and inhibits testosterone synthesis by repressing steroidogenic factor 1/beta-catenin synergy | Q24319025 | ||
| Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer | Q24319963 | ||
| Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene. | Q24538706 | ||
| Continuous tooth generation in mouse is induced by activated epithelial Wnt/beta-catenin signaling | Q24675013 | ||
| A comprehensive genetic map of the human genome based on 5,264 microsatellites | Q27860812 | ||
| FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice | Q28505123 | ||
| Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis | Q28591573 | ||
| Wnt-beta-catenin signaling initiates taste papilla development | Q28592063 | ||
| Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth | Q28592767 | ||
| Wnt signaling: a common theme in animal development | Q29547527 | ||
| Mechanisms of Wnt signaling in development | Q29547537 | ||
| Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children | Q29615807 | ||
| WNT signals are required for the initiation of hair follicle development | Q29619115 | ||
| Wnt signaling in oncogenesis and embryogenesis--a look outside the nucleus | Q29620188 | ||
| Autosomal recessive hydrotic ectodermal dysplasia | Q33587476 | ||
| WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells | Q33946452 | ||
| Ectodermal dysplasias: a new clinical-genetic classification | Q34090412 | ||
| Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait | Q34205334 | ||
| Ectodermal dysplasias: a clinical classification and a causal review | Q34318645 | ||
| R-spondin1 is essential in sex determination, skin differentiation and malignancy. | Q34573938 | ||
| The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia | Q34573951 | ||
| Towards a new classification of ectodermal dysplasias. | Q35161176 | ||
| Ectodermal dysplasias | Q35910647 | ||
| Selected conditions with ectodermal dysplasia | Q39532794 | ||
| A previously undescribed condition: tricho-odonto-onycho-dermal syndrome. A review of the tricho-odonto-onychial subgroup of ectodermal dysplasias | Q40355771 | ||
| WNT signaling in the control of hair growth and structure. | Q41610142 | ||
| Murine Wnt10a and Wnt10b: cloning and expression in developing limbs, face and skin of embryos and in adults | Q46856339 | ||
| Wnt10a is involved in AER formation during chick limb development. | Q52054171 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | skin development | Q14599571 |
| ectodermal dysplasia | Q1323713 | ||
| Odonto-onycho-dermal dysplasia | Q55782160 | ||
| Wnt family member 10A | Q21123978 | ||
| P304 | page(s) | 821-8 | |
| P577 | publication date | 2007-10-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia | |
| P478 | volume | 81 |
| Q39211878 | "Ant-egg" cataract revisited. |
| Q40422847 | A 190 base pair, TGF-β responsive tooth and fin enhancer is required for stickleback Bmp6 expression |
| Q35755034 | A Comprehensive Overview of Skeletal Phenotypes Associated with Alterations in Wnt/β-catenin Signaling in Humans and Mice |
| Q36202800 | Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency |
| Q37654079 | Almost Unilateral Focal Dermal Hypoplasia |
| Q42468054 | Altered expression of cell-cell adhesion molecules β-catenin/E-cadherin and related Wnt-signaling pathway in sporadic and syndromal keratocystic odontogenic tumors |
| Q57264068 | Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology |
| Q31133813 | Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations |
| Q48359905 | Case report of Schöpf-Schulz-Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A. |
| Q53637908 | Common polymorphisms in WNT10A affect tooth morphology as well as hair shape. |
| Q24657996 | Common variants in the trichohyalin gene are associated with straight hair in Europeans |
| Q55111743 | Critical in vivo roles of WNT10A in wound healing by regulating collagen expression/synthesis in WNT10A-deficient mice. |
| Q45840369 | Current understanding of the process of tooth formation: transfer from the laboratory to the clinic |
| Q59792061 | DLX3 Inhibits the Proliferation of Human Dental Pulp Cells Through Inactivation of Canonical Wnt/β-Catenin Signaling Pathway |
| Q64274948 | Depletion of WNT10A Prevents Tumor Growth by Suppressing Microvessels and Collagen Expression |
| Q37352236 | Developmental disorders of the dentition: an update |
| Q41887923 | Distinct functions for Wnt/β-catenin in hair follicle stem cell proliferation and survival and interfollicular epidermal homeostasis |
| Q37296773 | Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients |
| Q39883776 | Epithelium-Derived Wnt Ligands Are Essential for Maintenance of Underlying Digit Bone |
| Q34977220 | Establishment of intestinal identity and epithelial-mesenchymal signaling by Cdx2. |
| Q33949717 | Expression of Gpr177, a Wnt trafficking regulator, in mouse embryogenesis |
| Q50676358 | Expression patterns of WNT/β-CATENIN signaling molecules during human tooth development. |
| Q38784827 | FGF signaling refines Wnt gradients to regulate the patterning of taste papillae. |
| Q51829567 | FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia. |
| Q28508503 | Frizzled6 deficiency disrupts the differentiation process of nail development |
| Q39023016 | Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis |
| Q38058973 | Genetic pathways in disorders of epidermal differentiation |
| Q36279817 | Genetic prediction of male pattern baldness. |
| Q38950667 | Genetics of syndromic and non-syndromic hereditary nail disorders |
| Q60953217 | Hypermethylated and its clinical significance in colorectal cancer |
| Q90481510 | Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis |
| Q39307002 | Impact of next generation sequencing on diagnostics in a genetic skin disease clinic |
| Q49406691 | Impacted Lower Second Permanent Molars at the Ramus and Coronoid Process: A New Clinical Symptom of the WNT10A Mutation in Ectodermal Dysplasia |
| Q35060281 | Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population |
| Q43507937 | Late diagnosis of ectodermal dysplasia syndrome. |
| Q21145702 | Macrophages contribute to the cyclic activation of adult hair follicle stem cells |
| Q26796229 | Molecular basis of hypohidrotic ectodermal dysplasia: an update |
| Q39450241 | Molecular genetics and targeted therapy of WNT-related human diseases (Review). |
| Q41641043 | Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families |
| Q51701612 | Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements. |
| Q35039924 | Mutations in Frizzled 6 cause isolated autosomal-recessive nail dysplasia. |
| Q36162463 | Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. |
| Q55843640 | Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia |
| Q55059336 | Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation. |
| Q44540307 | Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis. |
| Q34509578 | Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I). |
| Q46895103 | Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. |
| Q35953110 | Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation |
| Q50335958 | Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases |
| Q50934692 | Oral phenotype and variation in focal dermal hypoplasia. |
| Q64038719 | Pathophysiology of pachyonychia congenita-associated palmoplantar keratoderma: New insight into skin epithelial homeostasis and avenues for treatment |
| Q51925038 | Patterns of Wnt pathway activity in the mouse incisor indicate absence of Wnt/beta-catenin signaling in the epithelial stem cells. |
| Q24299785 | Phenotypic variability associated with WNT10A nonsense mutations |
| Q35600613 | Polymorphisms in WNT6 and WNT10A and colorectal adenoma risk |
| Q48174705 | Rare and Common Variants Conferring Risk of Tooth Agenesis. |
| Q28586747 | Reciprocal requirements for EDA/EDAR/NF-kappaB and Wnt/beta-catenin signaling pathways in hair follicle induction |
| Q39241874 | Role of the Wnt signaling molecules in the tooth. |
| Q64105061 | Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate |
| Q42554864 | Roles of heparan sulfate sulfation in dentinogenesis |
| Q34855927 | SMAD4-mediated WNT signaling controls the fate of cranial neural crest cells during tooth morphogenesis |
| Q59810214 | Schopf-Schulz-Passarge Syndrome |
| Q28256055 | Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds |
| Q47983362 | The Biology Underlying Abnormalities of Tooth Number in Humans |
| Q53958309 | The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis. |
| Q55647515 | The WNT10A gene in ectodermal dysplasias and selective tooth agenesis. |
| Q40572562 | The association between WNT10A variants and dental development in patients with isolated oligodontia. |
| Q39216023 | The biology and genetics of curly hair |
| Q34734363 | The molecular basis of hereditary enamel defects in humans |
| Q36885744 | To Control Site-Specific Skin Gene Expression, Autocrine Mimics Paracrine Canonical Wnt Signaling and Is Activated Ectopically in Skin Disease |
| Q37705212 | To grow or not to grow: hair morphogenesis and human genetic hair disorders |
| Q35587798 | Topical application of lithium chloride on the pulp induces dentin regeneration. |
| Q34055758 | Variability in dentofacial phenotypes in four families with WNT10A mutations |
| Q92422653 | WNT Signaling in Disease |
| Q48247471 | WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI). |
| Q24599707 | WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome |
| Q33786543 | WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation |
| Q54336553 | WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations. |
| Q54483083 | WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity. |
| Q24339460 | WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes |
| Q35583076 | WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma |
| Q43488766 | WNT10A variants are associated with non-syndromic tooth agenesis in the general population |
| Q90568544 | WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population |
| Q60054218 | WNT6 is an effective marker for osteosarcoma diagnosis and prognosis |
| Q21092440 | Web-based, participant-driven studies yield novel genetic associations for common traits |
| Q47945688 | Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis. |
| Q34037153 | Wnt activation in nail epithelium couples nail growth to digit regeneration. |
| Q37724188 | Wnt and the Wnt signaling pathway in bone development and disease |
| Q24618567 | Wnt modulators in the biotech pipeline |
| Q34658275 | Wnt signaling and the control of human stem cell fate. |
| Q36555217 | Wnt signaling in skin development, homeostasis, and disease |
| Q35119945 | Wnt/beta-catenin signaling in oral tissue development and disease |
| Q24630938 | Wnt/beta-catenin signaling: components, mechanisms, and diseases |
| Q36740274 | Wnt/β-Catenin Regulates the Activity of Epiprofin/Sp6, SHH, FGF, and BMP to Coordinate the Stages of Odontogenesis |
| Q26823272 | Wnt/β-catenin signaling and disease |
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