(Q24532132)

2

0 references

Paula Tabares

3

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Fengli Zhang

4

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Martina Durner

5

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David A Greenberg

American Journal of Human Genetics

6

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language of work or name

English

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publication date

August 2003

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published in

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volume

73

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issue

2

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page(s)

261-70

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cites work

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RING3 kinase transactivates promoters of cell cycle regulatory genes through E2F

24 March 2017

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Channelopathies as a genetic cause of epilepsy

24 March 2017

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Reproductive cycle regulation of nuclear import, euchromatic localization, and association with components of Pol II mediator of a mammalian double-bromodomain protein

24 March 2017

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A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions

24 March 2017

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First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene

24 March 2017

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Activation-induced nuclear translocation of RING3

24 March 2017

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Chromosomal localization, gene structure and transcription pattern of the ORFX gene, a homologue of the MHC-linked RING3 gene

24 March 2017

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Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy

24 March 2017

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Parametric and nonparametric linkage analysis: a unified multipoint approach

24 March 2017

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Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

24 March 2017

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Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy

27 September 2017

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Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and why.

27 September 2017

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Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.

27 September 2017

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Genes induced in programmed cell death of neuronal PC12 cells and developing sympathetic neurons in vivo

27 September 2017

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27 September 2017

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Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region

27 September 2017

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The role of dosage of the region 7D1-7D5-6 of the X chromosome in the production of homeotic transformations in Drosophila melanogaster

27 September 2017

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Evidence for multiple gene loci in the expression of the common generalized epilepsies

27 September 2017

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Isolation and characterization of sex-linked female-sterile mutants in Drosophila melanogaster

27 September 2017

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Mechanisms underlying neuronal migration disorders and epilepsy.

27 September 2017

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Expression and potential role of Fsrg1, a murine bromodomain-containing homologue of the Drosophila gene female sterile homeotic

27 September 2017

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Genetic and molecular analysis of fs(1)h, a maternal effect homeotic gene in Drosophila.

30 May 2018

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Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

30 May 2018

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Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

30 May 2018

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30 May 2018

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Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

30 May 2018

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Abnormal cerebral structure in juvenile myoclonic epilepsy demonstrated with voxel-based analysis of MRI

29 November 2018

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12 December 2020

Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type

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12 December 2020

On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands

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12 December 2020

Neuropathological findings in primary generalized epilepsy: a study of eight cases

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12 December 2020

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

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12 December 2020

Segregation analysis of juvenile myoclonic epilepsy

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12 December 2020

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

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12 December 2020

https://api.crossref.org/works/10.1086%2F377006

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7 January 2021