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Literature DB >> 22105961

Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families.

O Zilina¹, T Reimand, P Zjablovskaja, K Männik, M Männamaa, A Traat, H Puusepp-Benazzouz, A Kurg, K Ounap.

Abstract

Entities: Gene Mutation

Mesh：

Substances：

Year: 2011 PMID： 22105961 DOI： 10.1002/ajmg.a.34378

Source DB: PubMed Journal: Am J Med Genet A ISSN： 1552-4825 Impact factor: 2.802

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12 in total

1. Monoallelic expression of the human FOXP2 speech gene.

Authors: Abidemi A Adegbola; Gerald F Cox; Elizabeth M Bradshaw; David A Hafler; Alexander Gimelbrant; Andrew Chess
Journal: Proc Natl Acad Sci U S A Date: 2014-11-24 Impact factor: 11.205

2. Single-Cell RNA Sequencing Reveals Novel Markers of Male Pituitary Stem Cells and Hormone-Producing Cell Types.

Authors: Leonard Y M Cheung; Akima S George; Stacey R McGee; Alexandre Z Daly; Michelle L Brinkmeier; Buffy S Ellsworth; Sally A Camper
Journal: Endocrinology Date: 2018-12-01 Impact factor: 4.736

3. The butterfly pattern in a patient with chromosome 7 deletion.

Authors: Suji Velayuthan; Amber Dawson; Rosario Maria S Riel-Romero; Eduardo Gonzalez-Toledo
Journal: J Neurosci Rural Pract Date: 2014-11

4. Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System.

Authors: Ezequiel Mendoza; Constance Scharff
Journal: Front Mol Neurosci Date: 2017-05-01 Impact factor: 5.639

5. A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer.

Authors: Martin Becker; Paolo Devanna; Simon E Fisher; Sonja C Vernes
Journal: Mol Cytogenet Date: 2015-08-20 Impact factor: 2.009

Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families.

1. Monoallelic expression of the human FOXP2 speech gene.

2. Single-Cell RNA Sequencing Reveals Novel Markers of Male Pituitary Stem Cells and Hormone-Producing Cell Types.

3. The butterfly pattern in a patient with chromosome 7 deletion.

4. Protein-Protein Interaction Among the FoxP Family Members and their Regulation of Two Target Genes, VLDLR and CNTNAP2 in the Zebra Finch Song System.

5. A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer.

6. Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

7. Assessing the effects of common variation in the FOXP2 gene on human brain structure.

8. FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways.

9. Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development.

10. Retinoic Acid Signaling: A New Piece in the Spoken Language Puzzle.