Zobrazeno 1 - 10
of 122
pro vyhledávání: '"M Peter Marinkovich"'
Autor:
Amy S. Paller, Shireen V. Guide, Diego Ayala, Mercedes E. Gonzalez, Anne W. Lucky, Isin Sinem Bagci, M. Peter Marinkovich
Publikováno v:
Journal of Dermatological Treatment, Vol 35, Iss 1 (2024)
AbstractBackground/purpose Dystrophic epidermolysis bullosa (DEB), a rare genetic skin disease caused by loss-of-function mutations in COL7A1, the gene encoding type VII collagen (COL7), is characterized by skin blistering, scarring, and extracutaneo
Externí odkaz:
https://doaj.org/article/4d22581de2c841f09a639f4a31802fdc
Autor:
Tracy L Adair-Kirk, Gail L Griffin, Michelle J Meyer, Diane G Kelley, Jeffrey H Miner, Douglas R Keene, M Peter Marinkovich, J Michael Ruppert, Jouni Uitto, Robert M Senior
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45546 (2012)
Laminin-332 is a heterotrimeric basement membrane component comprised of the α3, ß3, and γ2 laminin chains. Laminin-332 modulates epithelial cell processes, such as adhesion, migration, and differentiation and is prominent in many embryonic and ad
Externí odkaz:
https://doaj.org/article/0d0b7f25a524459b96d7840d807b0f76
Autor:
Jemima E. Mellerio, MD, Dimitra Kiritsi, MD, PhD, M. Peter Marinkovich, MD, Natividad Romero Haro, RN, Kellie Badger, RN, Meena Arora, MSc, Marc A. Dziasko, PhD, Mansi Vithlani, PhD, Anna E. Martinez
Publikováno v:
JAAD International, Vol 11, Iss , Pp 224-232 (2023)
Background: The pathophysiological processes underlying the phenotypic spectrum of severe forms of epidermolysis bullosa (EB) are complex and poorly understood. Objective: To use burden mapping to explore relationships between primary pathomechanisms
Externí odkaz:
https://doaj.org/article/e4ae6b17e7704c7d9028491aded80452
Autor:
Thinh Chau, MD, Joseph Wu, PhD, Benjamin Kahn, MD, Christopher Elco, MD, M. Peter Marinkovich, MD, Kerri E. Rieger, MD, PhD, Leslie Robinson-Bostom, MD, Elnaz F. Firoz, MD
Publikováno v:
JAAD Case Reports, Vol 34, Iss , Pp 7-9 (2023)
Externí odkaz:
https://doaj.org/article/f3e6874edefc494eb3ca5d8838313a65
Autor:
Jodi Y. So, Jaron Nazaroff, Chinonso V. Iwummadu, Nicki Harris, Emily S. Gorell, Shivali Fulchand, Irene Bailey, Daniel McCarthy, Zurab Siprashvili, M. Peter Marinkovich, Jean Y. Tang, Albert S. Chiou
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-13 (2022)
Abstract Background Recessive dystrophic epidermolysis bullosa (RDEB) is a rare, devastating blistering genodermatosis caused by mutations in the COL7A1 gene, which encodes for type VII collagen and is necessary for dermal-epidermal adhesion and inte
Externí odkaz:
https://doaj.org/article/a959db06942649538593eea193c20f13
Autor:
Jean Yuh Tang, M. Peter Marinkovich, Eleanor Lucas, Emily Gorell, Albert Chiou, Ying Lu, Jodie Gillon, Dipen Patel, Dan Rudin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-25 (2021)
Abstract Background/objective Recessive dystrophic epidermolysis bullosa (RDEB) is a genetic collagen disorder characterized by skin fragility leading to blistering, wounds, and scarring. There are currently no approved curative therapies. The object
Externí odkaz:
https://doaj.org/article/9335d467f94b4495ba644a2dd5de792e
Autor:
Shireen V. Guide, Mercedes E. Gonzalez, I. Sinem Bağcı, Brittani Agostini, Hubert Chen, Gloria Feeney, Molly Steimer, Binoy Kapadia, Kunju Sridhar, Lori Quesada Sanchez, Franshesca Gonzalez, Matthew Van Ligten, Trevor J. Parry, Surya Chitra, Lisa A. Kammerman, Suma Krishnan, M. Peter Marinkovich
Publikováno v:
New England Journal of Medicine. 387:2211-2219
Dystrophic epidermolysis bullosa is a rare genetic blistering skin disease caused by mutations inWe conducted a phase 3, double-blind, intrapatient randomized, placebo-controlled trial involving patients 6 months of age or older with genetically conf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d053a942c03e819a50c9d47264492443
https://doi.org/10.1056/nejmoa2206663
https://doi.org/10.1056/nejmoa2206663
Publikováno v:
Clinical Advances in Periodontics. 13:38-41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56010ea65447b24b88a22820aa8cce29
https://doi.org/10.1002/cap.10210
https://doi.org/10.1002/cap.10210
Autor:
M. Peter Marinkovich, Paul A. Khavari, Susana Ortiz-Urda, Clara N. Dey, Dallas P. Veitch, Basil A.J. Horst, Ngon T. Nguyen, Noriyasu Sakai, Elizabeth A. Waterman
Supplementary Information, Figure 1, Table 1 from A Laminin-Collagen Complex Drives Human Epidermal Carcinogenesis through Phosphoinositol-3-Kinase Activation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69974dda75d435d18131ced6afe2b76a
https://doi.org/10.1158/0008-5472.22370988.v1
https://doi.org/10.1158/0008-5472.22370988.v1
Autor:
Irina Gurevich, Pooja Agarwal, PeiPei Zhang, John A. Dolorito, Stacie Oliver, Henry Liu, Nicholas Reitze, Nikhil Sarma, Isin Sinem Bagci, Kunju Sridhar, Visesha Kakarla, Vamsi K. Yenamandra, Mark O’Malley, Marco Prisco, Sara F. Tufa, Douglas R. Keene, Andrew P. South, Suma M. Krishnan, M. Peter Marinkovich
Publikováno v:
Nature Medicine. 28:780-788
Recessive dystrophic epidermolysis bullosa (RDEB) is a lifelong genodermatosis associated with blistering, wounding, and scarring caused by mutations in COL7A1, the gene encoding the anchoring fibril component, collagen VII (C7). Here, we evaluated b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce9c26f71edbe1ea4feaf5906f51c6c4
https://doi.org/10.1038/s41591-022-01737-y
https://doi.org/10.1038/s41591-022-01737-y