(Q48300723)

10 February 2018

title

FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome (English)

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10 February 2018

1 reference

Abrams MT

1

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10 February 2018

Kaufmann WE

2

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10 February 2018

Rousseau F

3

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10 February 2018

Oostra BA

4

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10 February 2018

Wolozin B

5

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10 February 2018

Taylor CV

6

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10 February 2018

Lishaa N

7

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10 February 2018

Morel ML

8

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10 February 2018

Hoogeveen A

9

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10 February 2018

Reiss AL

10

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10 February 2018

publication date

1 January 1999

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10 February 2018

American Journal of Medical Genetics Part A

published in

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10 February 2018

volume

82

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10 February 2018

issue

1

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10 February 2018

page(s)

25-30

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10 February 2018

Molecular-neurobehavioral associations in females with the fragile X full mutation.

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Thymidine incorporation in the olfactory epithelium of mice: early exponential response induced by olfactory neurectomy

21 January 2018

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Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients

21 January 2018

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The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

21 January 2018

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Quantitative comparison of FMR1 gene expression in normal and premutation alleles

21 January 2018

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Regeneration in the olfactory system of vertebrates

21 January 2018

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Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

21 January 2018

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Two new cases of FMR1 deletion associated with mental impairment.

21 January 2018

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COX-2, a synaptically induced enzyme, is expressed by excitatory neurons at postsynaptic sites in rat cerebral cortex

21 January 2018

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Transmitting males and carrier females in fragile X--revisited.

21 January 2018

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A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood

21 January 2018

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Characterization of the full fragile X syndrome mutation in fetal gametes

21 January 2018

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Autistic behaviors among girls with fragile X syndrome.

21 January 2018

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A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

21 January 2018

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Mosaicism in fragile X affected males.

21 January 2018

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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

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Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

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Neurodevelopmental effects of the FMR-1 full mutation in humans.

21 January 2018

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Neuroanatomy of fragile X syndrome: the posterior fossa

21 January 2018

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Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

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Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children

21 January 2018

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Neuroanatomy of fragile X syndrome: the temporal lobe

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

1 reference

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Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

1 reference

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Pathological changes in olfactory neurons in patients with Alzheimer's disease.

21 January 2018

1 reference

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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Characterization of FMR1 proteins isolated from different tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

21 January 2018

1 reference

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Genotype mosaicism in fragile X fetal tissues

21 January 2018

1 reference

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Continuous culture of neuronal cells from adult human olfactory epithelium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

A.E. Bennett Research Award 1993. Olfactory neuroblasts from Alzheimer donors: studies on APP processing and cell regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation

21 January 2018

1 reference

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Protein alterations in olfactory neuroblasts from Alzheimer donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990101%2982%3A1%3C25%3A%3AAID-AJMG5%3E3.0.CO%3B2-Y

10.1002/(SICI)1096-8628(19990101)82:1<25::AID-AJMG5>3.0.CO;2-Y

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

1 reference

10 February 2018