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Academic Journal

Therapeutic Approaches to Tuberous Sclerosis Complex: From Available Therapies to Promising Drug Targets.

Authors : Conte E; Department of Pharmacy-Drug Sciences, University of Bari 'Aldo Moro', 70125 Bari, Italy.; Boccanegra B

Subjects: Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/drug therapy ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/genetics ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/metabolism

Source: Biomolecules [Biomolecules] 2024 Sep 21; Vol. 14 (9). Date of Electronic Publication: 2024 Sep 21.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101596414 Publication Model: Electronic Cited Medium: Internet ISSN: 2218-273X

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Academic Journal

miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1.

Authors : Chen Y; Hainan Eye Hospital and Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, No.19 Xiuhua Road, Xiuying District, Haikou, 570311, Hainan, China. .; Li S

Subjects: Endophthalmitis*/Endophthalmitis*/Endophthalmitis*/metabolism ; Endophthalmitis*/Endophthalmitis*/Endophthalmitis*/genetics ; Endophthalmitis*/Endophthalmitis*/Endophthalmitis*/pathology

Source: Scientific reports [Sci Rep] 2024 Aug 21; Vol. 14 (1), pp. 19353. Date of Electronic Publication: 2024 Aug 21.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" Cohort.

Authors : Chung CWT; Centre for Clinical Genetics, Sydney Children's Hospital, Randwick, New South Wales, Australia.; Tuberous Sclerosis Management Clinic, Sydney Children's Hospital, Randwick, New South Wales, Australia.

Subjects: Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/genetics ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/pathology ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/diagnosis

Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Oct; Vol. 12 (10), pp. e70017.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Deep phenotyping reveals movement phenotypes in mouse neurodevelopmental models.

Authors : Klibaite U; Department of Organismic and Evolutionary Biology, Harvard University, 52 Oxford St, 02138, Cambridge, MA, USA. .; Kislin M

Subjects: Autism Spectrum Disorder*/Autism Spectrum Disorder*/Autism Spectrum Disorder*/genetics ; Membrane Proteins*/Membrane Proteins*/Membrane Proteins*/genetics ; Nerve Tissue Proteins*/Nerve Tissue Proteins*/Nerve Tissue Proteins*/genetics

Source: Molecular autism [Mol Autism] 2022 Mar 12; Vol. 13 (1), pp. 12. Date of Electronic Publication: 2022 Mar 12.Publisher: BioMed Central Country of Publication: England NLM ID: 101534222 Publication Model: Electronic Cited Medium: Internet ISSN: 2040-2392

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Academic Journal

Role of TSC1 in physiology and diseases.

Authors : Mallela K; Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore, 560012, India.; Kumar A

Subjects: Gene Expression Regulation, Neoplastic* ; Signal Transduction*; Neoplasms/Neoplasms/Neoplasms/*metabolism

Source: Molecular and cellular biochemistry [Mol Cell Biochem] 2021 Jun; Vol. 476 (6), pp. 2269-2282. Date of Electronic Publication: 2021 Feb 11.Publisher: Springer Country of Publication: Netherlands NLM ID: 0364456 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

The m6A Reader IGF2BP2 Regulates Macrophage Phenotypic Activation and Inflammatory Diseases by Stabilizing TSC1 and PPAR γ .

Authors : Wang X; Department of Physiology School of Basic Medical Sciences Cheeloo College of Medicine Shandong University Jinan Shandong 250012 China.; Ji Y

Subjects: Inflammation/Inflammation/Inflammation/*genetics ; Inflammation/Inflammation/Inflammation/*metabolism ; Macrophage Activation/Macrophage Activation/Macrophage Activation/*genetics

Source: Advanced science (Weinheim, Baden-Wurttemberg, Germany) [Adv Sci (Weinh)] 2021 May 03; Vol. 8 (13), pp. 2100209. Date of Electronic Publication: 2021 May 03 (Print Publication: Publisher: WILEY-VCH Country of Publication: Germany NLM ID: 101664569 Publication Model: eCollection Cited Medium: Internet ISSN: 2198-3844

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Academic Journal

Malignant tumors in tuberous sclerosis complex: a case report and review of the literature.

Authors : Liu C; Disivion of Surgical Oncology, Department of Surgery, Fred and Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE, USA.; Lele SM

Subjects: Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/genetics ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/complications ; Tuberous Sclerosis*/Tuberous Sclerosis*/Tuberous Sclerosis*/diagnosis

Source: BMC medical genomics [BMC Med Genomics] 2024 May 27; Vol. 17 (1), pp. 144. Date of Electronic Publication: 2024 May 27.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Academic Journal

Carbonic Anhydrase 2 Deletion Delays the Growth of Kidney Cysts Whereas Foxi1 Deletion Completely Abrogates Cystogenesis in TSC.

Authors : Barone S; Research Services, New Mexico Veterans Health Care System, Albuquerque, NM 87108, USA.; Department of Medicine, Division of Nephrology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.

Subjects: Carbonic Anhydrase II*/Carbonic Anhydrase II*/Carbonic Anhydrase II*/genetics ; Carbonic Anhydrase II*/Carbonic Anhydrase II*/Carbonic Anhydrase II*/metabolism ; Forkhead Transcription Factors*/Forkhead Transcription Factors*/Forkhead Transcription Factors*/genetics

Source: International journal of molecular sciences [Int J Mol Sci] 2024 Apr 27; Vol. 25 (9). Date of Electronic Publication: 2024 Apr 27.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Methylation of Hypothalamic Tsc1-mTOR Signaling in Regulation of Obesity and Obesity Resistance.

Authors : Wang Y; Department of Endocrinology and Metabolism, Zigong First People's Hospital, Sichuan Province, China.; Chengdu University of Traditional Chinese Medicine, Sichuan Province, China.

Subjects: Signal Transduction*; DNA Methylation/DNA Methylation/DNA Methylation/*genetics ; Hypothalamus/Hypothalamus/Hypothalamus/*metabolism

Source: BioMed research international [Biomed Res Int] 2020 Dec 30; Vol. 2020, pp. 8723869. Date of Electronic Publication: 2020 Dec 30 (Print Publication: 2020).Publisher: Hindawi Pub. Co Country of Publication: United States NLM ID: 101600173 Publication Model: eCollection Cited Medium: Internet ISSN:

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Academic Journal

A novel TSC1 frameshift mutation c.1550_1551del causes tuberous sclerosis complex by aberrant splicing and nonsense-mediated mRNA degradation (NMD) simultaneously in a Chinese family.

Authors : Qiu C; Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.; Li C

Subjects: Nonsense Mediated mRNA Decay* ; RNA Splicing*; Tuberous Sclerosis/Tuberous Sclerosis/Tuberous Sclerosis/*genetics

Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Oct; Vol. 8 (10), pp. e1410. Date of Electronic Publication: 2020 Jul 31.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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نتائج البحث

فلترة النتائج

Therapeutic Approaches to Tuberous Sclerosis Complex: From Available Therapies to Promising Drug Targets.

miR-27a-3p promotes inflammatory response in infectious endophthalmitis via targeting TSC1.

Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" Cohort.

Deep phenotyping reveals movement phenotypes in mouse neurodevelopmental models.

Role of TSC1 in physiology and diseases.

The m6A Reader IGF2BP2 Regulates Macrophage Phenotypic Activation and Inflammatory Diseases by Stabilizing TSC1 and PPAR γ .

Malignant tumors in tuberous sclerosis complex: a case report and review of the literature.

Carbonic Anhydrase 2 Deletion Delays the Growth of Kidney Cysts Whereas Foxi1 Deletion Completely Abrogates Cystogenesis in TSC.

Methylation of Hypothalamic Tsc1-mTOR Signaling in Regulation of Obesity and Obesity Resistance.

A novel TSC1 frameshift mutation c.1550_1551del causes tuberous sclerosis complex by aberrant splicing and nonsense-mediated mRNA degradation (NMD) simultaneously in a Chinese family.

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