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1. Epigenetic Regulation and Neurodevelopmental Disorders: From MeCP2 to the TCF20/PHF14 Complex.

2. Case Report: A Case of a Patient with Smith–Magenis Syndrome and Early-Onset Parkinson's Disease.

3. Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.

4. Comparative analyses of the Smith−Magenis syndrome protein RAI1 in mice and common marmoset monkeys.

5. Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation.

6. Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome.

7. RAI1 Regulates Activity-Dependent Nascent Transcription and Synaptic Scaling

8. RAI1 gene mutations: mechanisms of Smith–Magenis Syndrome

9. Importance of OsRac1 and RAI1 in signalling of nucleotide‐binding site leucine‐rich repeat protein‐mediated resistance to rice blast disease.

10. Psychiatric and neurological manifestations in adults with Smith-Magenis syndrome: A scoping review.

11. Twenty‐four‐hour motor activity and body temperature patterns suggest altered central circadian timekeeping in Smith–Magenis syndrome, a neurodevelopmental disorder.

12. Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice.

13. A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation

14. Retinoic acid-induced 1 gene haploinsufficiency alters lipid metabolism and causes autophagy defects in Smith-Magenis syndrome

15. First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation.

16. Delayed diagnosis in a house of correction: Smith-Magenis syndrome due to a de novo nonsense RAI1 variant.

17. A de novo mutation (p.S1419F) of Retinoic acid induced 1 is responsible for a patient with Smith-Magenis syndrome exhibiting schizophrenia.

18. Copy number loss upstream of RAI1 uncovers gene expression regulatory region that may impact Potocki-Lupski syndrome diagnosis.

19. Phenotypic and Molecular Convergence of 2q23.1 Deletion Syndrome with Other Neurodevelopmental Syndromes Associated with Autism Spectrum Disorder.

20. Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus.

21. mRNA quality control at the 5′ end.

22. Inherited dup(17)(p11.2p11.2): Expanding the phenotype of the Potocki-Lupski syndrome.

23. Clinical and cytogenetic features of a Potocki–Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1.

24. Distorted Mendelian transmission as a function of genetic background in Rai1-haploinsufficient mice

25. A functional network module for Smith–Magenis syndrome.

26. How much is too much? Phenotypic consequences of Rai1 overexpression in mice.

27. Smith–Magenis syndrome.

28. Gender, genotype, and phenotype differences in Smith–Magenis syndrome: a meta-analysis of 105 cases.

29. Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb

30. Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder

31. Transcriptome Sequencing Reveals Potential Mechanisms of the Maternal Effect on Egg Diapause Induction of Locusta migratoria

32. Recent insights into noncanonical 5' capping and decapping of RNA.

33. Smith-Magenis Syndrome—Clinical Review, Biological Background and Related Disorders.

34. Transcriptome Sequencing Reveals Potential Mechanisms of the Maternal Effect on Egg Diapause Induction of

35. A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation

36. Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy

37. Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior

38. Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.

39. Transcriptome Sequencing Reveals Potential Mechanisms of the Maternal Effect on Egg Diapause Induction of Locusta migratoria.

40. Copy number loss upstream of RAI1 uncovers gene expression regulatory region that may impact Potocki–Lupski syndrome diagnosis

41. A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation.

42. CapZyme-Seq Comprehensively Defines Promoter-Sequence Determinants for RNA 5′ Capping with NAD+.

43. RAI1 Overexpression Promotes Altered Circadian Gene Expression and Dyssomnia in Potocki-Lupski Syndrome.

44. Yin-yang actions of histone methylation regulatory complexes in the brain.

45. Rare Syndromes and Common Variants of the Brain-Derived Neurotrophic Factor Gene in Human Obesity.

46. Molecular characterization of near-complete trisomy 17p syndrome from inverted duplication in association with cryptic deletion of 17pter.

47. Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions.

48. Structures of 5'-3' Exoribonucleases.

49. Normal and Aberrantly Capped mRNA Decapping.

50. Rat1 and Xrn2: The Diverse Functions of the Nuclear Rat1/Xrn2 Exonuclease.

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