نتائج البحث

m6A-modified circXPO1 accelerates colorectal cancer progression via interaction with FMRP to promote WWC2 mRNA decay.

• Authors : Zhu X; Key laboratory of Microecology-immune Regulatory Network and Related Diseases, School of Basic Medicine, Jiamusi University, No. 258 Xuefu Road, Xiangyang District, Jiamusi, 154000, Heilongjiang Province, P. R. China.; General surgery, The first Affiliated Hospital of Jiamusi University, Jiamusi, 154000, Heilongjiang Province, P. R. China.

Subjects: Colorectal Neoplasms*/Colorectal Neoplasms*/Colorectal Neoplasms*/genetics ; Colorectal Neoplasms*/Colorectal Neoplasms*/Colorectal Neoplasms*/pathology ; Colorectal Neoplasms*/Colorectal Neoplasms*/Colorectal Neoplasms*/metabolism

• Source: Journal of translational medicine [J Transl Med] 2024 Oct 14; Vol. 22 (1), pp. 931. Date of Electronic Publication: 2024 Oct 14.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium:

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Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy.

• Authors : Montanaro FAM; Child & Adolescent Neuropsychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, 00165, Italy.; Department of Education, Psychology, Communication, University of Bari Aldo Moro, Bari, 70122, Italy.

Subjects: Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/therapy ; Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/geneticsFragile X Tremor Ataxia Syndrome

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Jul 12; Vol. 19 (1), pp. 264. Date of Electronic Publication: 2024 Jul 12.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

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FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea.

• Authors : Rodrigues B; Molecular Genetics Laboratory, Laboratory Genetics Service, Genetics and Pathology Clinic, Unidade Local de Saúde de Santo António (ULSSA), Porto, Portugal.; UMIB - Unit for Multidisciplinary Research in Biomedicine, ICBAS - School of Medicine and Biomedical Sciences, UPorto - University of Porto, Porto, Portugal.

Subjects: Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Amenorrhea*/Amenorrhea*/Amenorrhea*/genetics ; Alleles*

• Source: Reproductive biology and endocrinology : RB&E [Reprod Biol Endocrinol] 2024 Jun 21; Vol. 22 (1), pp. 71. Date of Electronic Publication: 2024 Jun 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101153627 Publication Model: Electronic Cited Medium:

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miR-142 downregulation alleviates rat PTSD-like behaviors, reduces the level of inflammatory cytokine expression and apoptosis in hippocampus, and upregulates the expression of fragile X mental retardation protein.

• Authors : Nie PY; Department of Anatomy, College of Basic Medical Sciences, China Medical University, Shenyang, China.; Tong L

Subjects: Apoptosis/Apoptosis/Apoptosis/*physiology ; Cytokines/Cytokines/Cytokines/*biosynthesis ; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*biosynthesis

• Source: Journal of neuroinflammation [J Neuroinflammation] 2021 Jan 06; Vol. 18 (1), pp. 17. Date of Electronic Publication: 2021 Jan 06.Publisher: BioMed Central Country of Publication: England NLM ID: 101222974 Publication Model: Electronic Cited Medium:

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Mxc, a Drosophila homolog of mental retardation-associated gene NPAT, maintains neural stem cell fate.

• Authors : Sang, Rong^1,2 (AUTHOR); Wu, Cheng¹ (AUTHOR); Xie, Shanshan¹ (AUTHOR)

• Source: Cell & Bioscience. 5/31/2022, Vol. 12 Issue 1, p1-16. 16p.

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Genetic analysis of a pedigree with MECP2 duplication syndrome in China.

• Authors : Zeng L; Department of Medical Genetics and Prenatal Diagnosis, Sichuan Provincial Maternity and Child Health Care Hospital, Chengdu, Sichuan, China.; Zhu H

Subjects: DNA Copy Number Variations* ; Gene Duplication* ; Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/geneticsLubs X-linked mental retardation syndrome

• Source: BMC medical genomics [BMC Med Genomics] 2024 Feb 19; Vol. 17 (1), pp. 54. Date of Electronic Publication: 2024 Feb 19.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium:

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Development and validation of parent-reported gastrointestinal health scale in MECP2 duplication syndrome.

• Authors : Pehlivan D; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, 77030, USA. .; Blue Bird Circle Rett Center, Texas Children's Hospital, Houston, TX, 77030, USA. .

Subjects: Parents* ; Mental Retardation, X-Linked*; Humans Lubs X-linked mental retardation syndrome

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Feb 09; Vol. 19 (1), pp. 52. Date of Electronic Publication: 2024 Feb 09.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium:

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Neurovascular unit disruption and blood-brain barrier leakage in MCT8 deficiency.

• Authors : Guillén-Yunta M; Laboratory of Thyroid Hormones and CNS, Department of Endocrine and Nervous System Pathophysiology, Instituto de Investigaciones Biomédicas 'Alberto-Sols', Consejo Superior de Investigaciones Científicas (CSIC), Universidad Autónoma de Madrid (UAM), C/ Arturo Duperier 4, 28029, Madrid, Spain.; Valcárcel-Hernández V

Subjects: Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/diagnosis ; Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/genetics ; Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/Mental Retardation, X-Linked*/pathology Allan-Herndon-Dudley syndrome

• Source: Fluids and barriers of the CNS [Fluids Barriers CNS] 2023 Nov 03; Vol. 20 (1), pp. 79. Date of Electronic Publication: 2023 Nov 03.Publisher: Biomed Central Country of Publication: England NLM ID: 101553157 Publication Model: Electronic Cited Medium:

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Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome.

• Authors : Schenkel LC; Department of Pathology and Lab Medicine, Western University, London, ON Canada.; Kernohan KD

Subjects: Epigenesis, Genetic*; Mental Retardation, X-Linked/Mental Retardation, X-Linked/Mental Retardation, X-Linked/*genetics ; alpha-Thalassemia/alpha-Thalassemia/alpha-Thalassemia/*geneticsATR-X syndrome

• Source: Epigenetics & chromatin [Epigenetics Chromatin] 2017 Mar 10; Vol. 10, pp. 10. Date of Electronic Publication: 2017 Mar 10 (Print Publication: 2017).Publisher: BioMed Central Country of Publication: England NLM ID: 101471619 Publication Model: eCollection Cited Medium:

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Fragile X mental retardation protein knockdown in the developing Xenopus tadpole optic tectum results in enhanced feedforward inhibition and behavioral deficits.

• Authors : Truszkowski TL; Department of Neuroscience, Brown University, Box G-LN, 60 Olive St., 02912, Providence, RI, USA.; James EJ

Subjects: Behavior, Animal* ; Neural Inhibition*; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*physiology

• Source: Neural development [Neural Dev] 2016 Aug 08; Vol. 11 (1), pp. 14. Date of Electronic Publication: 2016 Aug 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101286574 Publication Model: Electronic Cited Medium:

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