PMC Articles for MedGen (Select 11449) - PMC

Ariana Ellis, Steven D. Billings, Urmi Khanna, Christine B. Warren, Melissa Piliang, Alok Vij, Jennifer S. Ko, Wilma F. Bergfeld, Anthony P. Fernandez

J Cutan Pathol. 2020 Apr; 47(4): 346–356. Published online 2019 Dec 26. doi: 10.1111/cup.13628

PMCID:: PMC9291190

Article PDF–7.1M

Select item 88633584.

Melanoma in the Blink of an Eye: Pathologists’ Rapid Detection, Classification, and Localization of Skin Abnormalities

Tad T. Brunyé, Trafton Drew, Manob Jyoti Saikia, Kathleen F. Kerr, Megan M. Eguchi, Annie C. Lee, Caitlin May, David E. Elder, Joann G. Elmore

Vis cogn. Author manuscript; available in PMC 2022 Jun 16.

Published in final edited form as: Vis cogn. 2021; 29(6): 386–400. Published online 2021 Jun 16. doi: 10.1080/13506285.2021.1943093

PMCID:: PMC8863358

Article PDF–1.8M

Select item 79876915.

Skin abnormalities in disorders with DNA repair defects, premature aging, and mitochondrial dysfunction

Mansoor Hussain, Sudarshan Krishnamurthy, Jaimin Patel, Edward Kim, Beverly A. Baptiste, Deborah L. Croteau, Vilhelm A. Bohr

J Invest Dermatol. Author manuscript; available in PMC 2022 Apr 1.

Published in final edited form as: J Invest Dermatol. 2021 Apr; 141(4 Suppl): 968–975. Published online 2021 Jan 19. doi: 10.1016/j.jid.2020.10.019

PMCID:: PMC7987691

Article PDF–546K

Select item 59673176.

Correction to: Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice

Eric Press, Katanya C Alaga, Kevin Barr, Qing Shao, Felicitas Bosen, Klaus Willecke, Dale W Laird

Cell Death Dis. 2018 Jun; 9(6): 630. Published online 2018 May 24. doi: 10.1038/s41419-018-0639-1

Corrects:: Cell Death Dis. 2017 Jun; 8(6): e2845.

PMCID:: PMC5967317

Correction PDF–199K

Select item 55208937.

Disease-linked connexin26 S17F promotes volar skin abnormalities and mild wound healing defects in mice

Eric Press, Katanya C Alaga, Kevin Barr, Qing Shao, Felicitas Bosen, Klaus Willecke, Dale W Laird

Cell Death Dis. 2017 Jun; 8(6): e2845. Published online 2017 Jun 1. doi: 10.1038/cddis.2017.234

Correction in:: Cell Death Dis. 2018 Jun; 9(6): 630.

PMCID:: PMC5520893

Article PDF–6.1M

Select item 40579448.

Loss of Mpzl3 Function Causes Various Skin Abnormalities and Greatly Reduced Adipose Depots

Angel G. Leiva, Anne L. Chen, Priyadharshini Devarajan, Zhibin Chen, Shadi Damanpour, Jessica A. Hall, Antonio C. Bianco, Jie Li, Evangelos V. Badiavas, Julia Zaias, Mariya Miteva, Paolo Romanelli, Keyvan Nouri, Tongyu Cao Wikramanayake

J Invest Dermatol. Author manuscript; available in PMC 2015 Jan 1.

Published in final edited form as: J Invest Dermatol. 2014 Jul; 134(7): 1817–1827. Published online 2014 Feb 14. doi: 10.1038/jid.2014.94

PMCID:: PMC4057944

Article PDF–2.3M

Select item 38887779.

CHARACTERIZATION OF SKIN ABNORMALITIES IN A MOUSE MODEL OF OSTEOGENESIS IMPERFECTA USING HIGH RESOLUTION MAGNETIC RESONANCE IMAGING AND FOURIER TRANSFORM INFRARED IMAGING SPECTROSCOPY

Holly C. Canuto, Kenneth W. Fishbein, Alice Huang, Stephen B. Doty, Ron A. Herbert, John Peckham, Nancy Pleshko, Richard G. Spencer

NMR Biomed. Author manuscript; available in PMC 2014 Jan 12.

Published in final edited form as: NMR Biomed. 2012 Jan; 25(1): 169–176. Published online 2011 Aug 15. doi: 10.1002/nbm.1732

PMCID:: PMC3888777

Article PDF–3.6M

Select item 325528810.

55-Week Treatment of Mice with the Unani and Ayurvedic Medicine Pomegranate Flower Ameliorates Ageing-Associated Insulin Resistance and Skin Abnormalities

Jianwei Wang, Xianglu Rong, Irene S. I. Um, Johji Yamahara, Yuhao Li

Evid Based Complement Alternat Med. 2012; 2012: 350125. Published online 2011 Dec 28. doi: 10.1155/2012/350125

PMCID:: PMC3255288

Article PDF–4.4M

Select item 1044913211.

Hyperglycemia alters retinoic acid catabolism in embryos exposed to a maternal diabetic milieu

Leo Man Yuen Lee, Yun-chung Leung, Alisa Sau Wun Shum

PLoS One. 2023; 18(8): e0287253. Published online 2023 Aug 24. doi: 10.1371/journal.pone.0287253

PMCID:: PMC10449132

Article PDF–1.6M

Select item 1036404112.

Síndrome de rotura de Varsovia: una causa de microcefalia congénita y sordera neurosensorial

Ignacio Arroyo-Carrera, María Solo de Zaldívar-Tristancho, Verónica D. García Navas-Núñez, Alba Ramajo-Polo, Marta Gutiérrez-Agujetas

Rev Neurol. 2023; 76(3): 111–115. Spanish. Published online 2023 Feb 1. doi: 10.33588/rn.7603.2022165

PMCID:: PMC10364041

Article PDF–791K

Select item 964880213.

Lamin A to Z in normal aging

Stanley R. Primmer, Chen-Yu Liao, Oona M.P. Kummert, Brian K. Kennedy

Aging (Albany NY) 2022 Oct 31; 14(20): 8150–8166. Published online 2022 Oct 17. doi: 10.18632/aging.204342

PMCID:: PMC9648802

Article PDF–699K

Select item 836623914.

PCR-RFLP molecular confirmation of color dilution alopecia in dogs in Brazil

Silvana M. Caramalac, Simone M. Caramalac, Veronica J. Babo-Terra, Carlos A. N. Ramos, Mariana I. P. Palumbo

J Vet Diagn Invest. 2021 Sep; 33(5): 984–986. Published online 2021 Jun 4. doi: 10.1177/10406387211022309

PMCID:: PMC8366239

Article PDF–508K

Select item 798267815.

High Glucose Causes Distinct Expression Patterns of Primary Human Skin Cells by RNA Sequencing

Shan Zhang, Zunxiang Ke, Chao Yang, Peng Zhou, Huanzong Jiang, Lei Chen, Yiqing Li, Qin Li

Front Endocrinol (Lausanne) 2021; 12: 603645. Published online 2021 Mar 8. doi: 10.3389/fendo.2021.603645

PMCID:: PMC7982678

Article PDF–2.4M

Select item 735423416.

Gating of human TRPV3 in a lipid bilayer

Zengqin Deng, Grigory Maksaev, Michael Rau, Zili Xie, Hongzhen Hu, James A.J. Fitzpatrick, Peng Yuan

Nat Struct Mol Biol. Author manuscript; available in PMC 2020 Dec 22.

Published in final edited form as: Nat Struct Mol Biol. 2020 Jul; 27(7): 635–644. Published online 2020 Jun 22. doi: 10.1038/s41594-020-0428-2

PMCID:: PMC7354234

Article PDF–3.5M

Select item 714497817.

Phenogenon: Gene to phenotype associations for rare genetic diseases

Nikolas Pontikos, Cian Murphy, Ismail Moghul, Gavin Arno, Kaoru Fujinami, Yu Fujinami, Dayyanah Sumodhee, Susan Downes, Andrew Webster, Jing Yu, UK Inherited Retinal Dystrophy Consortium, Phenopolis Consortium

PLoS One. 2020; 15(4): e0230587. Published online 2020 Apr 9. doi: 10.1371/journal.pone.0230587

PMCID:: PMC7144978

Article PDF–972K

Select item 641669718.

Novel desmoplakin mutations in familial Carvajal syndrome

DANAT YERMAKOVICH, LARYSA SIVITSKAYA, TATIYANA VAIKHANSKAYA, NINA DANILENKO, IRYNA MOTUK

Acta Myol. 2018 Dec; 37(4): 263–266. Published online 2018 Dec 1.

PMCID:: PMC6416697

Article PDF–270K

Select item 637859219.

Utility of systematic TSHR gene testing in adults with hyperthyroidism lacking overt autoimmunity and diffuse uptake on thyroid scintigraphy

Kashyap A. Patel, Bridget Knight, Aftab Aziz, Tarig Babiker, Avades Tamar, Joanna Findlay, Sue Cox, Ioannis Dimitropoulos, Carolyn Tysoe, Vijay Panicker, Bijay Vaidya

Clin Endocrinol (Oxf) 2019 Feb; 90(2): 328–333. Published online 2018 Nov 27. doi: 10.1111/cen.13892