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«Oculodentodigital

Below is an extended Oculodentodigital research listing. Click here to return to the Oculodentodigital main in depth entry.

Recent Publications on Oculodentodigital:

ODDD-linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation.
INTRODUCTION: Bone development and modeling requires precise gap...
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13th August, 2008
Department of Anatomy and Cell Biology, Schulich School of Medicine and
Fate of connexin43 in cardiac tissue harbouring a disease-linked connexin43 mutant.
AIMS: More than 40 mutations in the GJA1 gene encoding connexin43 (Cx43)...
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6th August, 2008
Department of Physiology and Pharmacology, University of Western Ontario,
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
We report a 4-generation Hispanic family with oculodentodigital dysplasia...
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29th July, 2008
Department of Neurology, Hospital Escuela, Tegucigalpa, Honduras.
Decreased levels of connexin43 result in impaired development of the mammary gland in a mouse model of oculodentodigital dysplasia.
Normal development of the mammary gland is fundamental for lactation and...
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19th June, 2008
Department of Anatomy and Cell Biology, Dental Science Building,
Cell-cell communication in the osteoblast/osteocyte lineage.
Skeletal development (bone modeling) and its maintenance in post-natal...
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12th June, 2008
Washington University in St. Louis, Department of Internal Medicine,
A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features.
Oculodentodigital dysplasia (ODDD) is an autosomal dominant disorder that...
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31st May, 2008
Research Unit, Institute of Ophthalmology Conde de Valenciana, Mexico
Report of a black South African child with oculodentodigital dysplasia and a novel GJA1 gene mutation.
Skeletal development (bone modeling) and its maintenance in post-natal...
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29th May, 2008
Department of Periodontology and Oral Medicine, School of Dentistry,
Ocular manifestations in oculodentodigital dysplasia resulting from a heterozygous missense mutation (L113P) in GJA1 (connexin 43).
PurposeTo characterize the ophthalmic findings, intrafamilial variability,...
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22nd April, 2008
1Birmingham and Midland Eye Centre, City Hospital, Birmingham, UK.
Ectopic acanthosis nigricans occurring in a child after syndactyly repair. 9th April, 2008
Naval Medical Center, San Diego, California, USA.
Closing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease.
Cells within the vast majority of human tissues communicate directly...
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1st April, 2008
Departments of Anatomy & Cell Biology and Physiology & Pharmacology,
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
Oculodentodigital dysplasia (ODDD) is a dominant negatively inherited...
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13th March, 2008
Institute of Genetics, University of Bonn, Germany.
Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels.
Oculodentodigital dysplasia (ODDD) is a dominantly inherited human...
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28th February, 2008
Institute of Genetics, University of Bonn, Roemerstrasse 164, 53117, Bonn,
Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia.
Gap junction channels are required for normal cardiac impulse propagation,...
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29th January, 2008
Leon H. Charney Division of Cardiology, New York University School of
Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene.
Oculodentodigital dysplasia (ODDD) is a rare, autosomal dominant...
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14th December, 2007
Department of Oral and Maxillofacial Surgery, University Medical Center
Connexin levels regulate keratinocyte differentiation in the epidermis.
To understand the role of connexin43 (Cx43) in epidermal differentiation,...
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6th December, 2007
Department of Anatomy and Cell Biology, The University of Western Ontario,
 

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