Recent Publications on : |  |
Modulation of neuritogenesis by a protein implicated in X-linked mental retardation.
Posttranscriptional regulation is an important control mechanism governing...
Direct Link | 9th October, 2009
| Department of Cell Biology and Neuroscience, Rutgers University,
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A phase advance of the light-dark cycle stimulates production of BDNF, but not of other neurotrophins, in the adult rat cerebral cortex: association with the activation of CREB.
Circadian variation in the expression of brain-derived neurotrophic factor...
Direct Link | 4th November, 2008
| Department of Perinatology, Institute for Developmental Research, Aichi
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Identification of methylation-silenced genes in colorectal cancer cell lines: genomic screening using oligonucleotide arrays.
OBJECTIVE: Aberrant methylation of promoter CpG islands is associated with...
Direct Link | 18th June, 2008
| Department of General Surgery, Chiba University Graduate School of
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Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes.
Xp22.3 deletion in males can be associated with short stature (SHOX),...
Direct Link | 7th June, 2008
| INSERM U679, Hopital de la Salpetriere, Paris, France.
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A shared promoter region suggests a common ancestor for the human VCX/Y, SPANX, and CSAG gene families and the murine CYPT family.
Many testis-specific genes from the sex chromosomes are subject to rapid...
Direct Link | 6th May, 2008
| Department of Growth and Reproduction, Rigshospitalet, Copenhagen
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Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis.
BACKGROUND: X-linked ichthyosis (XLI), an inborn error of metabolism, is...
Direct Link | 29th April, 2008
| Servicio de Genetica, Hospital General de Mexico, Facultad de Medicina,
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First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation.
We report here on a 6-year-old boy referred to the laboratory for...
Direct Link | 4th August, 2007
| AP-HP, Hopital Cochin, Service Histologie Embryologie Cytogenetique,
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Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.
BACKGROUND: Patients with Xp22.3 interstitial and terminal deletions have...
Direct Link | 4th July, 2007
| Department of Human Genetics, Hebrew University-Hadassah Medical School
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| Comparative analysis of human masculinity.
| 6th April, 2007
| School of Advanced Sciences, The Graduate University for Advanced Studies,
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Deletion of distal promoter of VCXA in a patient with X-linked ichthyosis associated with borderline mental retardation.
BACKGROUND: X-linked ichthyosis (XLI) is caused by deficiency of steroid...
Direct Link | 21st March, 2007
| Division of Dermatology, Kashiwara Municipal Hospital, Kashiwara, Japan.
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Identification of an mRNA-decapping regulator implicated in X-linked mental retardation.
Two major decapping enzymes are involved in the decay of eukaryotic mRNA,...
Direct Link | 12th January, 2007
| Department of Cell Biology and Neuroscience, Rutgers University,
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Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers.
We describe a familial interstitial deletion of 7.7-Mb involving...
Direct Link | 31st May, 2006
| Abteilung Humangenetik, Universitat Ulm, Ulm, Germany.
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Projected valve area at normal flow rate improves the assessment of stenosis severity in patients with low-flow, low-gradient aortic stenosis: the multicenter TOPAS (Truly or Pseudo-Severe Aortic Stenosis) study.
BACKGROUND: We sought to investigate the use of a new parameter, the...
Direct Link | 11th March, 2006
| Research Center of Laval Hospital/Quebec Heart Institute, Laval
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Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.
X-linked ichthyosis (XLI) is often associated with a recurrent...
Direct Link | 12th October, 2005
| Department of Human Genetics, University Hospital Gasthuisberg, Leuven,
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Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation.
X-linked ichthyosis (XLI) is often associated with a recurrent...
Direct Link | 17th June, 2005
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