Works matching DE "PROGERIA"
Results: 423
Molecular insights into the premature aging disease progeria.
- Published in:
- Histochemistry & Cell Biology, 2016, v. 145, n. 4, p. 401, doi. 10.1007/s00418-016-1411-1
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- Publication type:
- Article
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.
- Published in:
- Human Genetics, 2018, v. 137, n. 11/12, p. 921, doi. 10.1007/s00439-018-1957-1
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- Publication type:
- Article
Exploring the anti-aging effects of fisetin in telomerase-deficient progeria mouse model.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.16463
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- Publication type:
- Article
53. Werner Syndrome (includes Adult Progeria).
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- JNCI: Journal of the National Cancer Institute, 2008, n. 38, p. 89
- Publication type:
- Article
Premature aging effects on COVID-19 pathogenesis: new insights from mouse models.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-70612-2
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- Publication type:
- Article
Wiedemann-Rautenstrauch Syndrome: Case Report.
- Published in:
- Cumhuriyet Dental Journal, 2022, v. 25, n. 3, p. 282, doi. 10.7126/cumudj.1127344
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- Publication type:
- Article
Agrypnia excitata in a patient with progeroid short stature and pigmented Nevi (Mulvihill-Smith syndrome).
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- Journal of Sleep Research, 2005, v. 14, n. 4, p. 463, doi. 10.1111/j.1365-2869.2005.00465.x
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- Article
ELASTIC FIBRES IN UNUSUAL DERMATOSES.
- Published in:
- British Journal of Dermatology, 1955, v. 67, n. 12, p. 460
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- Publication type:
- Article
WERNER'S SYNDROME.
- Published in:
- British Journal of Dermatology, 1953, v. 65, n. 5, p. 165, doi. 10.1111/j.1365-2133.1953.tb13193.x
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- Publication type:
- Article
Progressive Early Dermatologic Changes in Hutchinson-Gilford Progeria Syndrome.
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- Pediatric Dermatology, 1991, v. 8, n. 3, p. 199, doi. 10.1111/j.1525-1470.1991.tb00859.x
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- Publication type:
- Article
Hutchinson-Gilford Syndrome.
- Published in:
- Pediatric Dermatology, 1990, v. 7, n. 4, p. 317, doi. 10.1111/j.1525-1470.1990.tb01036.x
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- Publication type:
- Article
Abstracts.
- Published in:
- Pediatric Dermatology, 1990, v. 7, n. 2, p. 158, doi. 10.1111/j.1525-1470.1990.tb00677.x
- Publication type:
- Article
Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Hutchinson-Gilford progeria syndrome: a rare case report.
- Published in:
- 2016
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- Publication type:
- Case Study
Stem Cell Models: A Guide to Understand and Mitigate Aging?
- Published in:
- 2016
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- Publication type:
- journal article
Progeria: Medical aspects, psychosocial perspectives, and intervention guidelines.
- Published in:
- Death Studies, 1995, v. 19, n. 5, p. 433, doi. 10.1080/07481189508253392
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- Publication type:
- Article
Mutations Involved in Premature-Ageing Syndromes.
- Published in:
- Application of Clinical Genetics, 2021, v. 14, p. 279, doi. 10.2147/TACG.S273525
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- Publication type:
- Article
Hutchinson–Gilford Progeria Syndrome: Clinical and Molecular Characterization.
- Published in:
- Application of Clinical Genetics, 2020, v. 13, p. 159, doi. 10.2147/TACG.S238715
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- Publication type:
- Article
A Ticking Clock.
- Published in:
- Kentucky English Bulletin, 2008, v. 58, n. 1, p. 56
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- Publication type:
- Article
From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.
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- Cellular & Molecular Life Sciences, 2007, v. 64, n. 19/20, p. 2620, doi. 10.1007/s00018-007-7123-x
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- Publication type:
- Article
Human progeroid syndromes, aging and cancer: new genetic and epigenetic insights into old questions.
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- Cellular & Molecular Life Sciences, 2007, v. 64, n. 2, p. 155, doi. 10.1007/s00018-006-6349-3
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- Publication type:
- Article
Announcement of the Editor-in-Chief.
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- Cellular & Molecular Life Sciences, 2006, v. 63, n. 14, p. 1575, doi. 10.1007/s00018-005-6001-7
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- Publication type:
- Article
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment.
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- Cellular & Molecular Life Sciences, 2005, v. 62, n. 22, p. 2669, doi. 10.1007/s00018-005-5318-6
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- Publication type:
- Article
Chromatin epigenetics and nuclear lamina keep the nucleus in shape: Examples from natural and accelerated aging.
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- Biology of the Cell (Wiley-Blackwell), 2023, v. 115, n. 1, p. 1, doi. 10.1111/boc.202200023
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- Publication type:
- Article
The Saccharomyces cerevisiae WRN homolog Sgs1p participates in telomere maintenance in cells lacking telomerase.
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- EMBO Journal, 2001, v. 20, n. 4, p. 905, doi. 10.1093/emboj/20.4.905
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- Publication type:
- Article
Involvement of xeroderma pigmentosum group A (XPA) in progeria arising from defective maturation of prelamin A.
- Published in:
- FASEB Journal, 2008, v. 22, n. 2, p. 603, doi. 10.1096/fj.07-8598com
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- Publication type:
- Article
The Werner's Syndrome RecQ Helicase/Exonuclease at the Nexus of Cancer and Aging.
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- Hawaii Medical Journal, 2011, v. 70, n. 3, p. 52
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- Publication type:
- Article
Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient.
- Published in:
- 2023
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- Publication type:
- Case Study
GFT NMR based resonance assignment for the 21 kDa human protein UFC1.
- Published in:
- Journal of Biomolecular NMR, 2005, v. 32, n. 3, p. 261, doi. 10.1007/s10858-005-7941-9
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- Publication type:
- Article
Ageing: Rushed decisions.
- Published in:
- Nature, 2008, v. 452, n. 7183, p. 39, doi. 10.1038/452039a
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- Publication type:
- Article
Research highlights.
- Published in:
- Nature, 2007, v. 446, n. 7135, p. 472, doi. 10.1038/446472a
- Publication type:
- Article
Detection of Cerebrovascular Disease in a Child with Hutchinson-Gilford Progeria Syndrome Using MR Angiography: A Case Report.
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- Journal of the Korean Society of Radiology (2951-0805), 2022, v. 83, n. 6, p. 1360, doi. 10.3348/jksr.2022.0051
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- Publication type:
- Article
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
- Published in:
- Human Genetics, 2008, v. 124, n. 4, p. 369, doi. 10.1007/s00439-008-0562-0
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- Publication type:
- Article
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference.
- Published in:
- Human Genetics, 2005, v. 118, n. 3/4, p. 444, doi. 10.1007/s00439-005-0051-7
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- Publication type:
- Article
Hyaluronan is not elevated in urine or serum in Hutchinson-Gilford Progeria Syndrome.
- Published in:
- Human Genetics, 2003, v. 113, n. 2, p. 178, doi. 10.1007/s00439-003-0958-9
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- Publication type:
- Article
Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13.
- Published in:
- Human Genetics, 2000, v. 106, n. 1, p. 66, doi. 10.1007/s004390051011
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- Publication type:
- Article
Defective nuclear import of Tpr in Progeria reflects the Ran sensitivity of large cargo transport.
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- Journal of Cell Biology, 2013, v. 201, n. 4, p. 541, doi. 10.1083/jcb.201212117
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- Publication type:
- Article
Progeria: Translational insights from cell biology.
- Published in:
- Journal of Cell Biology, 2012, v. 199, n. 1, p. 9, doi. 10.1083/jcb.201207072
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- Publication type:
- Article
Cell biology: At the center of modern biomedicine.
- Published in:
- Journal of Cell Biology, 2012, v. 199, n. 1, p. 7, doi. 10.1083/jcb.201209062
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- Publication type:
- Article
Status of treatment strategies for Hutchinson–Gilford progeria syndrome with a focus on prelamin: A posttranslational modification.
- Published in:
- Basic & Clinical Pharmacology & Toxicology, 2022, v. 131, n. 4, p. 217, doi. 10.1111/bcpt.13770
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- Publication type:
- Article
Use of Farnesyl Transferase Inhibitors in an Ageing Model in Drosophila.
- Published in:
- Journal of Developmental Biology, 2023, v. 11, n. 4, p. 40, doi. 10.3390/jdb11040040
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- Publication type:
- Article
The Activation of JAK/STAT3 Signaling and the Complement System Modulate Inflammation in the Primary Human Dermal Fibroblasts of PXE Patients.
- Published in:
- Biomedicines, 2023, v. 11, n. 10, p. 2673, doi. 10.3390/biomedicines11102673
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- Publication type:
- Article
Progeria and Aging—Omics Based Comparative Analysis.
- Published in:
- Biomedicines, 2022, v. 10, n. 10, p. N.PAG, doi. 10.3390/biomedicines10102440
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- Publication type:
- Article
In ricordo di Mauro Paradisi.
- Published in:
- European Journal of Pediatric Dermatology, 2020, v. 30, n. 2, p. 68
- Publication type:
- Article
Gene expression responses to DNA damage are altered in human aging and in Werner Syndrome.
- Published in:
- Oncogene, 2005, v. 24, n. 32, p. 5026, doi. 10.1038/sj.onc.1208692
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- Publication type:
- Article
Athena: Speciality Certificate Examination case for Paediatrics and Genetics.
- Published in:
- Clinical & Experimental Dermatology, 2022, v. 47, n. 8, p. 1595, doi. 10.1111/ced.14707
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- Publication type:
- Article
A brother and sister with Werner's syndrome demonstrating extensive tendon calcification and sacroiliitis.
- Published in:
- Clinical & Experimental Dermatology, 2006, v. 31, n. 4, p. 615, doi. 10.1111/j.1365-2230.2006.02130.x
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- Publication type:
- Article
EFFECTIVE PAIN CONTROL IN HUTCHINSON-GILFORD PROGERIA SYNDROME.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Premature aging in genetic diseases:what conclusions can be drawn for physiological aging.
- Published in:
- Frontiers in Aging Neuroscience, 2024, p. 01, doi. 10.3389/fragi.2023.1327833
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- Publication type:
- Article
Cellular and Molecular Biomarkers Indicate Premature Aging in Pseudoxanthoma Elasticum Patients.
- Published in:
- Aging & Disease, 2020, v. 11, n. 3, p. 536, doi. 10.14336/AD.2019.0610
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- Publication type:
- Article