(Q36919991)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

review article

1 reference

title

Familial human hypodontia--is it all in the genes? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

Cobourne MT

series ordinal

1

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 August 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

published in

British Dental Journal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

203

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

203-208

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17721480%20AND%20SRC:MED&resulttype=core&format=json

The genetics of human tooth agenesis: New discoveries for understanding dental anomalies

4 January 2020

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The Genetics of Hypodontia

21 January 2018

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Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis

21 January 2018

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Tooth and jaw: molecular mechanisms of patterning in the first branchial arch

21 January 2018

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7 January 2021

Reiterative signaling and patterning during mammalian tooth morphogenesis

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7 January 2021

The cutting-edge of mammalian development; how the embryo makes teeth

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7 January 2021

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

The inheritance pattern of missing, peg-shaped, and strongly mesio-distally reduced upper lateral incisors

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7 January 2021

Characteristics of Incisor-Premolar Hypodontia in Families

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7 January 2021

Clinical, Radiographic, and Genetic Evaluation of a Novel Form of Autosomal-dominant Oligodontia

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7 January 2021

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

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7 January 2021

A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

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7 January 2021

Recessively inherited lower incisor hypodontia

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7 January 2021

A unifying aetiological explanation for anomalies of human tooth number and size

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7 January 2021

The restorative management of hypodontia with implants: I. Overview of alternative treatment options

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7 January 2021

The restorative management of hypodontia with implants: 2. Planning and treatment with implants.

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7 January 2021

Complete absence of the permanent dentition: an autosomal recessive disorder

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7 January 2021

The facial profile in advanced hypodontia: a mixed longitudinal study of 141 children

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7 January 2021

Symptomatology of patients with oligodontia

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7 January 2021

Gene defect in hypodontia: exclusion of EGF, EGFR, and FGF-3 as candidate genes

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7 January 2021

Interactions between Bmp-4 and Msx-1 act to restrict gene expression to odontogenic mesenchyme

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7 January 2021

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

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7 January 2021

Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation

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7 January 2021

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

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7 January 2021

The role of MSX1 in human tooth agenesis

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

A nonsense mutation in MSX1 causes Witkop syndrome

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia

1 reference

https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Novel MSX1 frameshift causes autosomal-dominant oligodontia

1 reference

https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Mutation of PAX9 is associated with oligodontia

1 reference

https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia

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7 January 2021

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia

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7 January 2021

A novel mutation in PAX9 causes familial form of molar oligodontia

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Association between PAX-9 promoter polymorphisms and hypodontia in humans

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Studies on Pax9-Msx1 protein interactions

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7 January 2021

Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer

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7 January 2021

Expression of Wnt signalling pathway genes during tooth development.

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Wnt/Shh interactions regulate ectodermal boundary formation during mammalian tooth development

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice

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7 January 2021

Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis

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7 January 2021

Homeobox genes and orofacial development.

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7 January 2021

Neural crest and tooth morphogenesis.

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7 January 2021

Two genes for missing teeth

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7 January 2021

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

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7 January 2021

TP63 gene mutation in ADULT syndrome

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7 January 2021

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

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https://api.crossref.org/works/10.1038%2FBDJ.2007.732

7 January 2021

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene

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7 January 2021

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium

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7 January 2021

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

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7 January 2021