Works matching Progeria

Results: 914

Progeria: A brief review.

Published in:

International Journal of Pharmacy & Life Sciences, 2013, v. 4, n. 9, p. 2965

By:

Negi, Seema;
Shah, Dharti;
Naik, Puja;
Shivmore, Komal;
Atre, Kavita;
Chandra, Shruti;
Chaudhary, Prashant;
Bhosle, Deepak

Publication type:

Article

Anesthetic considerations in children with Hutchinson‐Gilford progeria syndrome: A narrative review.

Published in:

Pediatric Anesthesia, 2020, v. 30, n. 5, p. 537, doi. 10.1111/pan.13847

By:

Nijs, Kristof;
Van de Velde, Marc;
Hoogma, Danny;
Veyckemans, Francis

Publication type:

Article

Ocular manifestations in the Hutchinson-Gilford progeria syndrome.

Published in:

Indian Journal of Ophthalmology, 2011, v. 59, n. 6, p. 509, doi. 10.4103/0301-4738.86327

By:

Chandravanshi, Shivcharan L;
Rawat, Ashok Kumar;
Dwivedi, Prem Chand;
Choudhary, Pankaj

Publication type:

Article

Cancer Drug and Progeria.

Published in:

JAMA: Journal of the American Medical Association, 2005, v. 294, n. 16, p. 2016, doi. 10.1001/jama.294.16.2016-a

By:

Hampton, Tracy

Publication type:

Article

Small-Molecule Therapeutic Perspectives for the Treatment of Progeria.

Published in:

International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 7190, doi. 10.3390/ijms22137190

By:

Macicior, Jon;
Marcos-Ramiro, Beatriz;
Ortega-Gutiérrez, Silvia

Publication type:

Article

Anesthetic management of a patient with Progeria.

Published in:

International Student Journal of Nurse Anesthesia, 2011, v. 10, n. 2, p. 43

By:

Payne, Bridgette

Publication type:

Article

The Molecular and Cellular Basis of Hutchinson–Gilford Progeria Syndrome and Potential Treatments.

Published in:

Genes, 2023, v. 14, n. 3, p. 602, doi. 10.3390/genes14030602

By:

Batista, Noelle J.;
Desai, Sanket G.;
Perez, Alexis M.;
Finkelstein, Alexa;
Radigan, Rachel;
Singh, Manrose;
Landman, Aaron;
Drittel, Brian;
Abramov, Daniella;
Ahsan, Mina;
Cornwell, Samantha;
Zhang, Dong

Publication type:

Article

Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells.

Published in:

Nucleus (1949-1034), 2015, v. 6, n. 1, p. 66, doi. 10.1080/19491034.2015.1004256

By:

Bercht Pfleghaar, Katrin;
Taimen, Pekka;
Butin-Israeli, Veronika;
Shimi, Takeshi;
Langer-Freitag, Sabine;
Markaki, Yolanda;
Goldman, Anne E;
Wehnert, Manfred;
Goldman, Robert D

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

By:

Pachajoa, Harry;
Claros-Hulbert, Angelica;
García-Quintero, Ximena;
Perafan, Lina;
Ramirez, Andres;
Zea-Vera, Andres F

Publication type:

Article

Progeria: A rare genetic premature ageing disorder.

Published in:

Indian Journal of Medical Research, 2014, v. 139, n. 5, p. 667

By:

Sinha, Jitendra Kumar;
Ghosh, Shampa;
Raghunath, Manchala

Publication type:

Article

Hutchinson-Gilford progeria syndrome.

Published in:

2010

By:

Agarwal, Uma Shankar;
Sitaraman, S.;
Mehta, Sharad;
Panse, Gauri

Publication type:

Case Study

Sex-specific preservation of neuromuscular function and metabolism following systemic transplantation of multipotent adult stem cells in a murine model of progeria.

Published in:

GeroScience, 2024, v. 46, n. 1, p. 1285, doi. 10.1007/s11357-023-00892-5

By:

Thompson, Seth D.;
Barrett, Kelsey L.;
Rugel, Chelsea L.;
Redmond, Robin;
Rudofski, Alexia;
Kurian, Jacob;
Curtin, Jodi L.;
Dayanidhi, Sudarshan;
Lavasani, Mitra

Publication type:

Article

Pharmacotherapy to gene editing: potential therapeutic approaches for Hutchinson–Gilford progeria syndrome.

Published in:

GeroScience, 2020, v. 42, n. 2, p. 467, doi. 10.1007/s11357-020-00167-3

By:

Saxena, Saurabh;
Kumar, Sanjeev

Publication type:

Article

Hutchinson-Gilford progeria syndrome: a rare case report.

Published in:

2016

By:

Deepadarshan, Kalegowda;
Gangadhar, Bugude;
Mallikarjun, Mallaiah

Publication type:

Case Study

Treatment Considerations in Hutchinson-Gilford Progeria Syndrome: A Case Report.

Published in:

2015

By:

Hazan-Molina, Hagai;
Aizenbud, Dror

Publication type:

Case Study

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

By:

Yiyong liu;
Youjie Wang;
Rusinol, Antonio E.;
Sinensky, Michael S.;
Ji liu;
Shell, Steven M.;
Yue Zou

Publication type:

Article

Progeria—a Rare Genetic Condition with Accelerated Ageing Process.

Published in:

Applied Biochemistry & Biotechnology, 2023, v. 195, n. 4, p. 2587, doi. 10.1007/s12010-021-03514-y

By:

Talukder, Pratik;
Saha, Arunima;
Roy, Sohini;
Ghosh, Gargi;
Dutta Roy, Debshikha;
Barua, Snejuti

Publication type:

Article

Premature ageing in children: a rare genetic disorder called progeria.

Published in:

International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 3, p. 31, doi. 10.31838/ijpr/2020.12.03.005

By:

ANANDU H.;
SUGUNAN, AADHARSA;
K. N., ANILA;
NAIR, GAYATHRI VASANTHA SASIDHARAN

Publication type:

Article

Microbiome at sites of gingival recession in children with Hutchinson-Gilford progeria syndrome.

Published in:

2018

By:

Bassir, Seyed Hossein;
Chase, Isabelle;
Paster, Bruce J.;
Gordon, Leslie B.;
Kleinman, Monica E.;
Kieran, Mark W.;
Kim, David M.;
Sonis, Andrew

Publication type:

journal article

Aortic Calcification in a Patient With Hutchinson–Gilford Progeria Syndrome.

Published in:

Pediatric Cardiology, 2010, v. 31, n. 6, p. 925, doi. 10.1007/s00246-010-9711-z

By:

Salamat, Mehrdad;
Dhar, Pradip K.;
Neagu, Daniela L.;
Lyon, Jane B.

Publication type:

Article

Progeria: an extremely unusual disorder.

Published in:

2017

By:

Chawla, Gurnihal;
Agrawal, Purva;
Dhok, Avinash;
Chawla, Gurnihal Singh;
Agrawal, Purva Mahesh

Publication type:

journal article

Progeria: report of a case and review of the literature.

Published in:

1991

By:

Yu Qin-Xi, Lars Olov;
Zeng Ling-Hua, Lars Olov;
Yu, Q X;
Zeng, L H

Publication type:

journal article

Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.

Published in:

European Heart Journal, 2021, v. 42, n. 42, p. 4352, doi. 10.1093/eurheartj/ehab547

By:

Mojiri, Anahita;
Walther, Brandon K;
Jiang, Chongming;
Matrone, Gianfranco;
Holgate, Rhonda;
Xu, Qiu;
Morales, Elisa;
Wang, Guangyu;
Gu, Jianhua;
Wang, Rongfu;
Cooke, John P

Publication type:

Article

Extradural hematoma surgery in a child with Hutchinson--Gilford progeria syndrome: Perioperative concerns.

Published in:

Journal of Pediatric Neurosciences, 2013, v. 8, n. 2, p. 165, doi. 10.4103/1817-1745.117860

By:

Hansda, Upendra;
Agarwal, Jyotsna;
Patra, Chitralekha;
Ganjoo, Pragati

Publication type:

Article

Early Onset Diabetes in Two Children due to Progeria, a Monogenic Disease of DNA Repair.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 315, doi. 10.4274/jcrpe.galenos.2019.2019.0126

By:

Holder, Martin;
Schwitzgebel, Valerie

Publication type:

Article

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment.

Published in:

Cellular & Molecular Life Sciences, 2005, v. 62, n. 22, p. 2669, doi. 10.1007/s00018-005-5318-6

By:

Columbaro, M.;
Capanni, C.;
Mattioli, E.;
Novelli, G.;
Parnaik, V.;
Squarzoni, S.;
Maraldi, N.;
Lattanzi, G.

Publication type:

Article

A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndrome.

Published in:

Pediatric Radiology, 2012, v. 42, n. 9, p. 1089, doi. 10.1007/s00247-012-2423-1

By:

Cleveland, Robert;
Gordon, Leslie;
Kleinman, Monica;
Miller, David;
Gordon, Catherine;
Snyder, Brian;
Nazarian, Ara;
Giobbie-Hurder, Anita;
Neuberg, Donna;
Kieran, Mark

Publication type:

Article

Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient.

Published in:

2023

By:

Siddiqi, Saima;
Ain, Noor ul;
Kauser, Mehran;
Mukhtar, Zahra;
Ansar, Muhammad;
Umair, Muhammad

Publication type:

Case Study

Mesenchymal Stem Cell Therapy for Hutchinson–Gilford Progeria: Improvements in Arterial Stiffness and Bone Mineral Density in a Single Case.

Published in:

Children, 2025, v. 12, n. 4, p. 523, doi. 10.3390/children12040523

By:

Joo, Eun-Young;
Park, Ji-Sun;
Shin, Hyun-Tae;
Yoo, Myungji;
Kim, Su-Jin;
Lee, Ji-Eun;
Choi, Gwang-Seong

Publication type:

Article

Acute Coronary Syndrome Treated with Percutaneous Coronary Intervention in Hutchinson–Gilford Progeria.

Published in:

Children, 2023, v. 10, n. 3, p. 526, doi. 10.3390/children10030526

By:

De Simone, Luciano;
Chiellino, Serena;
Spaziani, Gaia;
Porcedda, Giulio;
Calabri, Giovan Battista;
Berti, Sergio;
Favilli, Silvia;
Stefani, Laura;
Santoro, Giuseppe

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

By:

Caliskan, Aylin;
Crouch, Samantha A. W.;
Giddins, Sara;
Dandekar, Thomas;
Dangwal, Seema

Publication type:

Article

Molecular elucidations of hutchinson-gilford progeria syndrome: A hope for managing horrors of premature aging in children.

Published in:

Pakistan Journal of Pharmaceutical Sciences, 2020, v. 33, n. 3, p. 1179, doi. 10.36721/PJPS.2020.33.3.REG.1179-1182.1

By:

Ahmed, Bilal;
Basheer, Ruby;
Irfan, Muhammad;
Akash, Muhammad Sajid Hamid;
Muhammad, Syed Aun;
Qadir, Muhammad Imran

Publication type:

Article

Non-syndromic cardiac progeria in a patient with the rare pathogenic p.Asp300Asn variant in the LMNA gene.

Published in:

2017

By:

Marian, Ali J.

Publication type:

Case Study

Detection of Cerebrovascular Disease in a Child with Hutchinson-Gilford Progeria Syndrome Using MR Angiography: A Case Report.

Published in:

Journal of the Korean Society of Radiology (2951-0805), 2022, v. 83, n. 6, p. 1360, doi. 10.3348/jksr.2022.0051

By:

Jae Ho Lee;
Ha Young Lee;
Myung Kwan Lim;
Young Hye Kang

Publication type:

Article

Mechanisms of A-Type Lamin Targeting to Nuclear Ruptures Are Disrupted in LMNA- and BANF1- Associated Progerias.

Published in:

Cells (2073-4409), 2022, v. 11, n. 5, p. 865, doi. 10.3390/cells11050865

By:

Sears, Rhiannon M.;
Roux, Kyle J.

Publication type:

Article

Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.

Published in:

British Journal of Dermatology, 2007, v. 156, n. 6, p. 1308, doi. 10.1111/j.1365-2133.2007.07897.x

By:

Mazereeuw-Hautier, J.;
Wilson, L. C.;
Mohammed, S.;
Smallwood, D.;
Shackleton, S.;
Atherton, D. J.;
Harper, J. I.

Publication type:

Article

Modelling premature cardiac aging with induced pluripotent stem cells from a hutchinson-gilford Progeria Syndrome patient.

Published in:

Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.1007418

By:

Monnerat, Gustavo;
Kasai-Brunswick, Tais Hanae;
Asensi, Karina Dutra;
dos Santos, Danubia Silva;
Quintanilha Barbosa, Raiana Andrade;
Paccola Mesquita, Fernanda Cristina;
Calvancanti Albuquerque, Joao Paulo;
Ferreira Raphaela, Pires;
Wendt, Camila;
Miranda, Kildare;
Barbosa Domont, Gilberto;
Sousa Nogueira, Fábio César;
Bastos Carvalho, Adriana;
Campos de Carvalho, Antonio Carlos

Publication type:

Article

An Analysis of Hearing Outcomes in Children with Hutchinson-Gilford Progeria Syndrome.

Published in:

British Journal of Hospital Medicine (17508460), 2024, v. 85, n. 11, p. 1, doi. 10.12968/hmed.2024.0449

By:

Sun, Jing;
Wang, Jingjing;
Bi, Jing

Publication type:

Article

Aging Model for Analyzing Drug-Induced Proarrhythmia Risks Using Cardiomyocytes Differentiated from Progeria-Patient-Derived Induced Pluripotent Stem Cells.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 15, p. 11959, doi. 10.3390/ijms241511959

By:

Daily, Neil;
Elson, Julian;
Wakatsuki, Tetsuro

Publication type:

Article

Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model.

Published in:

Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1481985

By:

Beeram, Indeevar;
Cubria, Maria Belen;
Kamalapathy, Pramod;
Yeritsyan, Diana;
Dubose, Amanda J.;
Razavi, Ahmad Hedayatzadeh;
Nafisi, Nazanin;
Erdos, Michael R.;
Snyder, Brian D.;
Cabral, Wayne A.;
Collins, Francis S.;
Nazarian, Ara

Publication type:

Article

Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T.

Published in:

Cell & Tissue Research, 2023, v. 394, n. 1, p. 189, doi. 10.1007/s00441-023-03813-2

By:

Perales, Selene;
Sigamani, Vinoth;
Rajasingh, Sheeja;
Czirok, Andras;
Rajasingh, Johnson

Publication type:

Article

A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI).

Published in:

American Journal of Case Reports, 2021, p. 1, doi. 10.12659/AJCR.928969

By:

Pongbangli, Natnicha;
Pitipakorn, Kannika;
Jai-aue, Sasivimon;
Sirijanchune, Piyaporn;
Pongpittayut, Sorawit;
Wongcharoen, Wanwarang

Publication type:

Article

Simultaneous Shoulder and Hip Dislocation in a 12-Year-Old Girl with Hutchinson-Gilford Progeria Syndrome.

Published in:

Acta Medica Iranica, 2012, v. 50, n. 6, p. 439

By:

Espandar, Ramin;
Eraghi, Amir Sobhani;
Mardookhpour, Shirin

Publication type:

Article

Néstor-Guillermo Progeria Syndrome: a biochemical insight into Barrier-to-Autointegration Factor 1, alanine 12 threonine mutation.

Published in:

BMC Molecular Biology, 2014, v. 15, n. 1, p. 1, doi. 10.1186/s12867-014-0027-z

By:

Paquet, Nicolas;
Box, Joseph K.;
Ashton, Nicholas W.;
Suraweera, Amila;
Croft, Laura V.;
Urquhart, Aaron J.;
Bolderson, Emma;
Shu-Dong Zhang;
O'Byrne, Kenneth J.;
Richard, Derek J.

Publication type:

Article

Baricitinib and Lonafarnib Synergistically Target Progerin and Inflammation, Improving Lifespan and Health in Progeria Mice.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 10, p. 4849, doi. 10.3390/ijms26104849

By:

Krüger, Peter;
Schroll, Moritz;
Fenzl, Felix Quirin;
Hartinger, Ramona;
Lederer, Eva-Maria;
Görlach, Agnes;
Gordon, Leslie B.;
Cavalcante, Paola;
Iacomino, Nicola;
Rathkolb, Birgit;
Pimentel, Juan Antonio Aguilar;
Östereicher, Manuela;
Spielmann, Nadine;
Wolf, Cordula Maria;
de Angelis, Martin Hrabe;
Djabali, Karima

Publication type:

Article

Splicing Variants, Protein-Protein Interactions, and Drug Targeting in Hutchinson-Gilford Progeria Syndrome and Small Cell Lung Cancer.

Published in:

Genes, 2022, v. 13, n. 2, p. 165, doi. 10.3390/genes13020165

By:

Kim, Bae-Hoon;
Woo, Tae-Gyun;
Kang, So-Mi;
Park, Soyoung;
Park, Bum-Joon

Publication type:

Article

Impairment of nuclear F-actin formation and its relevance to cellular phenotypes in Hutchinson-Gilford progeria syndrome.

Published in:

Nucleus (1949-1034), 2020, v. 11, n. 1, p. 250, doi. 10.1080/19491034.2020.1815395

By:

Takahashi, Yuto;
Hiratsuka, Shogo;
Machida, Nanako;
Takahashi, Daisuke;
Matsushita, Junpei;
Hozak, Pavel;
Misteli, Tom;
Miyamoto, Kei;
Harata, Masahiko

Publication type:

Article

Vascular smooth muscle cell loss underpins the accelerated atherosclerosis in Hutchinson-Gilford progeria syndrome.

Published in:

Nucleus (1949-1034), 2019, v. 10, n. 1, p. 48, doi. 10.1080/19491034.2019.1589359

By:

Hamczyk, Magda R.;
Andrés, Vicente

Publication type:

Article

Progeria Research Day at Brunel University.

Published in:

Nucleus (1949-1034), 2011, v. 2, n. 6, p. 517, doi. 10.4161/nucl.2.6.17605

By:

Bridger, Joanna M.;
Eskiw, Christopher H.;
Makarov, Evgeny M.;
Tree, David;
Kill, Ian R.

Publication type:

Article

Hutchinson-Gilford progeria syndrome with severe calcific aortic valve stenosis.

Published in:

Annals of Pediatric Cardiology, 2011, v. 4, n. 2, p. 204, doi. 10.4103/0974-2069.84670

By:

Hanumanthappa, Natesh B.;
Madhusudan, Ganigara;
Mahimarangaiah, Jayaranganath;
Manjunath, Cholenahally N.

Publication type:

Article