Works matching DE "WERNER'S syndrome"

Results: 356

WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil.

Published in:

Journal of Neuro-Oncology, 2008, v. 90, n. 3, p. 253

By:

France Yoshioka;
Carlos Clara;
Marcelo Santos;
JosÃ© Almeida;
Rommel Burbano;
Juan Rey;
Cacilda Casartelli

Publication type:

Article

Anaesthetic Management of a Known Case of Werner Syndrome by Peripheral Nerve Block in the Orthopaedic Surgery of Forearm.

Published in:

Turkish Journal of Anaesthesiology & Reanimation, 2020, v. 48, n. 3, p. 251, doi. 10.5152/TJAR.2020.93902

By:

Honarmand, Azim;
Mirsatari, Sayed Arash;
Zarezadeh, Abolghasem;
Safavi, Mohammadreza;
Kheirabadi, Dorna

Publication type:

Article

A Rare Cause of Acute Pancreatitis: Two Siblings With Werner Syndrome.

Published in:

2025

By:

Sakar, Kenan;
Akinci, Baris;
Simsir, Ilgin Yildirim;
Atik, Tahir;
Akbaba, Gulhan;
Cinar, Nese

Publication type:

Case Study

O-09 A rare cause of acute pancreatitis: Werner Syndrome.

Published in:

JCEM Case Reports, 2024, v. 2, p. 1, doi. 10.1210/jcemcr/luad146.026

By:

Şakar, Kenan;
Akıncı, Barış;
Yıldırım Şimşir, Ilgın;
Atik, Tahir;
Bozkurt Doğan, Ece Dilan;
Duman, Hatice;
Akbaba, Gülhan;
Çınar, Neşe

Publication type:

Article

Flame-like Calcifications in Werner Syndrome.

Published in:

JCEM Case Reports, 2023, v. 1, n. 4, p. 1, doi. 10.1210/jcemcr/luad099

By:

Tsujimoto, Yasutaka;
Bando, Hironori

Publication type:

Article

Strategies for modeling aging and age-related diseases.

Published in:

NPJ Aging, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41514-024-00161-5

By:

Jothi, D.;
Kulka, Linda Anna Michelle

Publication type:

Article

p21 Regulates Wnt-Notch balance via DREAM/MMB/Rb-E2F1 and maintains intestinal stem cell homeostasis.

Published in:

Cell Death Discovery, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41420-024-02192-z

By:

Jiang, Liangxia;
Tian, Jie;
Yang, Jun;
Luo, Ronggang;
Zhang, Yongjin;
Shao, Chihao;
Guo, Bing;
Wu, Xiaoming;
Dan, Juhua;
Luo, Ying

Publication type:

Article

Liver Aging and Pseudocapillarization in a Werner Syndrome Mouse Model.

Published in:

Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2014, v. 69, n. 9, p. 1076, doi. 10.1093/gerona/glt169

By:

Cogger, Victoria C.;
Svistounov, Dmitri;
Warren, Alessandra;
Zykova, Svetlana;
Melvin, Richard G.;
Solon-Biet, Samantha M.;
O’Reilly, Jennifer N.;
McMahon, Aisling C.;
Ballard, J. William O.;
De Cabo, Rafa;
Le Couteur, David G.;
Lebel, Michel

Publication type:

Article

Small Molecule Inhibition of p38 MAP Kinase Extends the Replicative Life Span of Human ATR-Seckel Syndrome Fibroblasts.

Published in:

Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2013, v. 68, n. 9, p. 1001, doi. 10.1093/gerona/gls336

By:

Tivey, Hannah S. E.;
Rokicki, Michal J.;
Barnacle, James R.;
Rogers, Matthew J.;
Bagley, Mark C.;
Kipling, David;
Davis, Terence

Publication type:

Article

Aging Is Accompanied by a Progressive Decrease of Expression of the WRN Gene in Human Blood Mononuclear Cells.

Published in:

Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2011, v. 66A, n. 1, p. 19, doi. 10.1093/gerona/glq162

By:

Polosak, Jacek;
Kurylowicz, Alina;
Roszkowska-Gancarz, Malgorzata;
Owczarz, Magdalena;
Puzianowska-Kuznicka, Monika

Publication type:

Article

Increased Expression of the Huntingtin Interacting Protein-1 Gene in Cells From Hutchinson Gilford Syndrome (Progeria) Patients and Aged Donors.

Published in:

Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2003, v. 58, n. 10, p. 873, doi. 10.1093/gerona/58.10.B873

By:

Chigira, Shinichi;
Sugita, Katsuo;
Kita, Kazuko;
Sugaya, Shigeru;
Arase, Yoshiko;
Ichinose, Masaharu;
Shirasawa, Hiroshi;
Suzuki, Nobuo

Publication type:

Article

Structure of the RecQ C-terminal Domain of Human Bloom Syndrome Protein.

Published in:

Scientific Reports, 2013, p. 1, doi. 10.1038/srep03294

By:

Sun-Yong Kim;
Toshio Hakoshima;
Ken Kitano

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

By:

İpek, İrem;
Derdiyok, Cansu;
Öznurhan, Fatih

Publication type:

Article

The Distinct Function of p21Waf1/Cip1 With p16Ink4a in Modulating Aging Phenotypes of Werner Syndrome by Affecting Tissue Homeostasis.

Published in:

Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.597566

By:

Zhang, Yongjin;
Shao, Chihao;
Li, Haili;
Wu, Kun;
Gong, Lixin;
Zheng, Quan;
Dan, Juhua;
Jia, Shuting;
Tang, Xiaodan;
Wu, Xiaoming;
Luo, Ying

Publication type:

Article

The Relationship between Werner Syndrome and Sinonasal Malignant Melanoma: Two Sibling Cases of Werner Syndrome with Malignant Melanoma.

Published in:

Case Reports in Otolaryngology, 2017, p. 1, doi. 10.1155/2017/9361612

By:

Kadowaki, Yoshinori;
Kodama, Satoru;
Moriyama, Munehito;
Suzuki, Masashi

Publication type:

Article

Werner syndrome: a rare cause of osteoporosis in a young female.

Published in:

2018

By:

Mahmood, Farrouq;
Helliwell, Philip S

Publication type:

Case Study

A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.

Published in:

Clinical & Experimental Dermatology, 2008, v. 33, n. 3, p. 278, doi. 10.1111/j.1365-2230.2007.02641.x

By:

Zhao, N.;
Hao, F.;
Qu, T.;
Zuo, Y.-G.;
Wang, B-X.

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

By:

Özturk, M.;
Akdeniz, N.;
Ayakta^1, H.;
Kösem, M.

Publication type:

Article

Diagnosis of Werner syndrome by immunoblot analysis.

Published in:

Clinical & Experimental Dermatology, 2002, v. 27, n. 2, p. 157, doi. 10.1046/j.1365-2230.2002.00996.x

By:

Shimizu, T;
Tateishi, Y;
Furuichi, Y;
Sugimoto, M;
Kawabe, T;
Matsumoto, T;
Shimizu, H

Publication type:

Article

Diffuse lentiginosis in a patient with Werner's syndrome--a possible association with incomplete leopard syndrome.

Published in:

Clinical & Experimental Dermatology, 1995, v. 20, n. 1, p. 46, doi. 10.1111/j.1365-2230.1995.tb01282.x

By:

Lazarov, A.;
Finkelstein, E.;
Avinoach, I.;
Kachko, L.;
Halevy, S.

Publication type:

Article

Disaccharide analysis of the skin glycosaminoglycans in patients with Werner's syndrome.

Published in:

Clinical & Experimental Dermatology, 1994, v. 19, n. 6, p. 487, doi. 10.1111/j.1365-2230.1994.tb01253.x

By:

Higuchi, T.;
Ishikawa, O.;
Hayashi, H.;
Ohnishi, K.;
Miyachi, Y.

Publication type:

Article

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

By:

Milosic, Filip;
Hengstschläger, Markus;
Osmanagic-Myers, Selma

Publication type:

Article

A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome.

Published in:

Molecular Medicine Reports, 2017, v. 15, n. 6, p. 3735, doi. 10.3892/mmr.2017.6465

By:

JI‑QIANG HE;
MIN JIN;
JU‑YU TANG;
PAN‑FENG WU;
RONG XIANG;
JIE‑YUAN JIN;
JING‑JING LI;
LIANG‑LIANG FAN;
HAO HUANG;
KUN XIA

Publication type:

Article

Werner syndrome protein positively regulates XRCC4-like factor transcription.

Published in:

Molecular Medicine Reports, 2014, v. 9, n. 5, p. 1648, doi. 10.3892/mmr.2014.2030

By:

DONGYUN LIU;
XIAOLI DENG;
CHONGZHEN YUAN;
LIN CHEN;
YUSHENG CONG;
XINGZHI XU

Publication type:

Article

Exacerbated Renal and Hematologic Toxicities to Ifosfamide and Doxorubicin-Based Chemotherapy in a Patient with Retroperitoneal Liposarcoma Harboring a Germline Mutation in the WRN Gene.

Published in:

2022

By:

Awni, Beatriz Mendes;
Holanda Lopes, Carlos Diego;
Harada, Guilherme;
Salgues, Alessandra Corte Real;
França, Gilmar de Andrade;
Testagrossa, Leonardo de Abreu;
Queiroz, Marcelo Araujo;
Gonçalves e Silva, Adriano;
Ferreira, Fabio de Oliveira;
Munhoz, Rodrigo Ramella

Publication type:

Case Study

At-Risk Populations for Osteosarcoma: The Syndromes and Beyond.

Published in:

Sarcoma, 2012, p. 1, doi. 10.1155/2012/152382

By:

Calvert, George T.;
Lor Randall, R.;
Jones, Kevin B.;
Cannon-Albright, Lisa;
Lessnick, Stephen;
Schiffman, Joshua D.

Publication type:

Article

Letter to the Editor.

Published in:

2010

By:

Nishimura, Fusanori;
Arakawa, Makoto;
Goto, Makoto

Publication type:

Letter

Enhanced intra-abdominal visceral fat accumulation in patients with Werner's syndrome.

Published in:

International Journal of Obesity & Related Metabolic Disorders, 2001, v. 25, n. 2, p. 292, doi. 10.1038/sj.ijo.0801529

By:

Mori, S;
Murano, S;
Yokote, K;
Takemoto, M;
Asaumi, S;
Take, A;
Saito, Y

Publication type:

Article

The Drosophila orthologue of progeroid human WRN exonuclease, DmWRNexo, cleaves replication substrates but is inhibited by uracil or abasic sites.

Published in:

Age (0161-9152), 2013, v. 35, n. 3, p. 793, doi. 10.1007/s11357-012-9411-0

By:

Mason, Penelope;
Boubriak, Ivan;
Robbins, Timothy;
Lasala, Ralph;
Saunders, Robert;
Cox, Lynne

Publication type:

Article

Vesieovaginal Fistula after Transurethral Resection in a Patient with Werner Syndrome.

Published in:

AUANews, 2021, v. 26, n. 12, p. 40

By:

Tomoya Fukawa

Publication type:

Article

The Saccharomyces cerevisiae WRN homolog Sgs1p participates in telomere maintenance in cells lacking telomerase.

Published in:

EMBO Journal, 2001, v. 20, n. 4, p. 905, doi. 10.1093/emboj/20.4.905

By:

Johnson, F.Brad;
Marciniak, Robert A.;
McVey, Mitch;
Stewart, Sheila A.;
Hahn, William C.;
Guarente, Leonard

Publication type:

Article

rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest.

Published in:

EMBO Journal, 1997, v. 16, n. 10, p. 2682, doi. 10.1093/emboj/16.10.2682

By:

Stewart, Elspeth;
Chapman, Carolyn Riley;
Al-Khodiary, Fahad;
Carr, Antony M.;
Enoch, Tamar

Publication type:

Article

WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts.

Published in:

BMC Cardiovascular Disorders, 2008, v. 8, p. 1, doi. 10.1186/1471-2261-8-5

By:

Castro, Elena;
Oviedo-Rodríguez, Vladimir;
Angel-Chávez, Luis I.

Publication type:

Article

Promyelocytic leukemia protein interacts with werner syndrome helicase and regulates double-strand break repair in γ-irradiation-induced DNA damage responses.

Published in:

Biochemistry (00062979), 2011, v. 76, n. 5, p. 550, doi. 10.1134/S000629791105004X

By:

Liu, Jilai;
Song, Yi;
Qian, Junjie;
Liu, Bin;
Dong, Yan;
Tian, Baolei;
Sun, Zhixian

Publication type:

Article

UBM study in spontaneous bleb formation and blebitis after cataract surgery in Werner syndrome.

Published in:

2009

By:

Moghimi, S.;
Soleimani, M.;
Soltani, R.

Publication type:

Case Study

Werner syndrome helicase (WRN), nuclear DNA helicase II (NDH II) and histone γH2AX are localized to the centrosome

Published in:

Cell Biology International, 2007, v. 31, n. 10, p. 1109, doi. 10.1016/j.cellbi.2007.03.027

By:

Zhang, Suisheng;
Hemmerich, Peter;
Grosse, Frank

Publication type:

Article

Methylation of Werner syndrome protein is associated with the occurrence and development of invasive meningioma via the regulation of Myc and p53 expression.

Published in:

Experimental & Therapeutic Medicine, 2015, v. 10, n. 2, p. 498, doi. 10.3892/etm.2015.2519

By:

PUXIAN LI;
SHUYU HAO;
ZHIYONG BI;
JUNTING ZHANG;
ZHEN WU;
XIAOHUI REN

Publication type:

Article

WRN Cys1367Arg polymorphism is not associated with skull base chordoma.

Published in:

Biomedical Reports, 2014, v. 2, n. 4, p. 521, doi. 10.3892/br.2014.275

By:

KE WANG;
LIANG WANG;
JIE FENG;
SHUYU HAO;
KAIBING TIAN;
ZHEN WU;
LIWEI ZHANG;
GUIJUN JIA;
HONG WAN;
JUNTING ZHANG

Publication type:

Article

PROTAC-mediated conditional degradation of the WRN helicase as a potential strategy for selective killing of cancer cells with microsatellite instability.

Published in:

Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-71160-5

By:

Tejwani, Vikram;
Carroll, Thomas;
Macartney, Thomas;
Bandau, Susanne;
Alabert, Constance;
Saredi, Giulia;
Toth, Rachel;
Rouse, John

Publication type:

Article

James German and the Quest to Understand Human RECQ Helicase Deficiencies.

Published in:

Cells (2073-4409), 2024, v. 13, n. 13, p. 1077, doi. 10.3390/cells13131077

By:

Monnat Jr., Raymond J.

Publication type:

Article

MUT-7 Provides Molecular Insight into the Werner Syndrome Exonuclease.

Published in:

Cells (2073-4409), 2021, v. 10, n. 12, p. 3457, doi. 10.3390/cells10123457

By:

Hsu, Tsung-Yuan;
Hsu, Ling-Nung;
Chen, Shih-Yu;
Juang, Bi-Tzen

Publication type:

Article

Cytogenetic studies in a patient with porokeratosis of Mibelli, multiple cancers and a forme fruste of Werner's syndrome.

Published in:

British Journal of Dermatology, 1984, v. 111, n. 5, p. 579, doi. 10.1111/j.1365-2133.1984.tb06628.x

By:

Machino, H.;
Miki, Y.;
Teramoto, T.;
Shiraishi, S.;
Sasaki, M. S.

Publication type:

Article

For early diagnosis of young patients with Werner syndrome: Indication for genetic testing.

Published in:

Geriatrics & Gerontology International, 2025, v. 25, n. 3, p. 468, doi. 10.1111/ggi.15094

By:

Sato, Tetta;
Maezawa, Yoshiro;
Kato, Hisaya;
Shoji, Mayumi;
Maeda, Yukari;
Kaneko, Hiyori;
Aono, Kazuto;
Kubota, Yoshitaka;
Taniguchi, Toshibumi;
Oshitari, Toshiyuki;
Motegi, Sei‐Ichiro;
Takami, Yoichi;
Nakagami, Hironori;
Taniguchi, Akira;
Watanabe, Kazuhisa;
Takemoto, Minoru;
Koshizaka, Masaya;
Kosaki, Rika;
Matsuo, Muneaki;
Kaneko, Hideo

Publication type:

Article

Efficacy of eribulin monotherapy for bone marrow carcinomatosis of breast cancer in a patient with Werner syndrome.

Published in:

2025

By:

Fujimi, Akihito;
Nagamachi, Yasuhiro;
Yamauchi, Naofumi;
Hasebe, Riku;
Onoyama, Naoki;
Hayasaka, Naotaka;
Matsuno, Teppei;
Koike, Kazuhiko;
Gotoh, Yoshiro;
Ihara, Kohji;
Kato, Junji;
Nishisato, Takuji;
Murase, Kazuyuki;
Kutomi, Goro;
Hida, Tokimasa;
Uhara, Hisashi;
Takada, Kohichi

Publication type:

Case Study

Recommendations for cancer screening and surveillance in patients with Werner syndrome.

Published in:

Geriatrics & Gerontology International, 2024, v. 24, n. 10, p. 1085, doi. 10.1111/ggi.14967

By:

Aono, Kazuto;
Maezawa, Yoshiro;
Kato, Hisaya;
Kaneko, Hiyori;
Kubota, Yoshitaka;
Taniguchi, Toshibumi;
Oshitari, Toshiyuki;
Motegi, Sei‐Ichiro;
Nakagami, Hironori;
Taniguchi, Akira;
Watanabe, Kazuhisa;
Takemoto, Minoru;
Koshizaka, Masaya;
Yokote, Koutaro

Publication type:

Article

Sex differences in symptom presentation and their impact on diagnostic accuracy in Werner syndrome.

Published in:

Geriatrics & Gerontology International, 2024, v. 24, n. 1, p. 161, doi. 10.1111/ggi.14752

By:

Kaneko, Hiyori;
Maezawa, Yoshiro;
Tsukagoshi‐Yamaguchi, Ayano;
Koshizaka, Masaya;
Takada‐Watanabe, Aki;
Nakamura, Rito;
Funayama, Shinichiro;
Aono, Kazuto;
Teramoto, Naoya;
Sawada, Daisuke;
Maeda, Yukari;
Minamizuka, Takuya;
Hayashi, Aiko;
Ide, Kana;
Ide, Shintaro;
Shoji, Mayumi;
Kitamoto, Takumi;
Takemoto, Minoru;
Kato, Hisaya;
Yokote, Koutaro

Publication type:

Article

Case of Werner syndrome complicated with Sjögren's syndrome and Hashimoto's thyroiditis presenting sclerosing panniculitis‐like symptoms.

Published in:

Geriatrics & Gerontology International, 2024, v. 24, n. 1, p. 173, doi. 10.1111/ggi.14747

By:

Nishino, Atsuna;
Adachi, Akimasa;
Koshizaka, Masaya;
Maezawa, Yoshiro;
Yokote, Kotaro;
Sawada, Yasuyuki

Publication type:

Article

Case of Werner syndrome with significant improvement of refractory skin ulcer despite fibroblast cellular senescence.

Published in:

2023

By:

Kinoshita, Daisuke;
Kato, Hisaya;
Kaneko, Hiyori;
Ishikawa, Takahiro;
Teramoto, Naoya;
Tsukagoshi, Ayano;
Maeda, Yukari;
Minamizuka, Takuya;
Hayashi, Aiko;
Shoji, Mayumi;
Sawada, Daisuke;
Funayama, Shinichiro;
Koshizaka, Masaya;
Ogata, Hideyuki;
Kubota, Yoshitaka;
Mitsukawa, Nobuyuki;
Takemoto, Minoru;
Yokote, Koutaro;
Maezawa, Yoshiro

Publication type:

Letter to the Editor

Quality of life in Werner syndrome and associated subjective foot/ankle symptoms: A cross‐sectional survey.

Published in:

Geriatrics & Gerontology International, 2023, v. 23, n. 3, p. 188, doi. 10.1111/ggi.14541

By:

Kitagawa, Yuka;
Amemiya, Ayumi;
Ogata, Hideyuki;
Koshizaka, Masaya;
Shoji, Mayumi;
Maezawa, Yoshiro;
Akita, Shinsuke;
Mitsukawa, Nobuyuki;
Yokote, Koutaro

Publication type:

Article

Corrigendum.

Published in:: 2022
Publication type:: Correction Notice