Zobrazeno 1 - 10
of 134
pro vyhledávání: '"IFAP"'
Autor:
Eduard T. Ambarchyan, Anastasiya D. Kuzminova, Totuy K. Eldarova, Vladislav V. Ivanchikov, Nataliya V. Zhurkova, Nato D. Vashakmadze
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 181-187 (2024)
Background. Ichthyosis follicularis with atrichia and photophobia (IFAP syndrome), type 2 is a rare hereditary disease from the group of syndromic forms of ichthyosis. It is clinically characterized by triad of non-inflammatory follicular ichthyosis,
Externí odkaz:
https://doaj.org/article/87fecd515f60437a9eed4f992bcabd47
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-16 (2021)
Abstract The MBTPS2 gene on the X-chromosome encodes the membrane-bound transcription factor protease, site-2 (MBTPS2) or site-2 protease (S2P) which cleaves and activates several signaling and regulatory proteins from the membrane. The MBTPS2 is cri
Externí odkaz:
https://doaj.org/article/2cb1e43ef48441afa70ab94f1372e457
Akademický článek
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Autor:
Paola Vallejo-Armenta, Guillermina Ferro-Flores, Clara Santos-Cuevas, Francisco Osvaldo García-Pérez, Pamela Casanova-Triviño, Bayron Sandoval-Bonilla, Blanca Ocampo-García, Erika Azorín-Vega, Myrna Luna-Gutiérrez
Publikováno v:
Pharmaceuticals, Vol 15, Iss 6, p 729 (2022)
Fibroblast activation protein (FAP) is highly expressed on the cancer-associated fibroblasts (CAF) of the tumor stroma. Recently, we reported the preclinical evaluation and clinical biokinetics of a novel 99mTc-labeled FAP inhibitor radioligand ([99m
Externí odkaz:
https://doaj.org/article/f2ad2f7d31e9443ab8f57f8657701df3
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Migliavacca, Michele Patricia, Fock, Rodrigo Ambrosio, Almeida, Nadia, Cavalcanti, Thereza, Villela, Darine, Perez, Ana Beatriz Alvarez, Valle, David, Wohler, Elizabeth, Sobreira, Nara Lygia de Macena, Raskin, Salmo
Publikováno v:
Revista Paulista de Pediatria, Volume: 41, Article number: e2022057, Published: 07 APR 2023
Objective: The classic triad, which defines IFAP syndrome, is ichthyosis follicularis, alopecia, and photophobia. It is a rare X-linked genetic disorder characterized by multiple congenital anomalies with variable severity, caused by pathogenic varia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::315402cac2ac8a6b5e1b97bef01b8efd
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822023000100605&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-05822023000100605&lng=en&tlng=en
Autor:
Diana Trujillo-Benítez, Myrna Luna-Gutiérrez, Guillermina Ferro-Flores, Blanca Ocampo-García, Clara Santos-Cuevas, Gerardo Bravo-Villegas, Enrique Morales-Ávila, Pedro Cruz-Nova, Lorenza Díaz-Nieto, Janice García-Quiroz, Erika Azorín-Vega, Antonio Rosato, Laura Meléndez-Alafort
Publikováno v:
Molecules, Vol 27, Iss 1, p 264 (2022)
Fibroblast activation protein (FAP) is expressed in the microenvironment of most human epithelial tumors. 68Ga-labeled FAP inhibitors based on the cyanopyrrolidine structure (FAPI) are currently used for the detection of the tumor microenvironment by
Externí odkaz:
https://doaj.org/article/306324e5367f4c4bb2ce0988efcde186
Autor:
Gao, Ya-sheng, Sztul, Elizabeth
Publikováno v:
The Journal of Cell Biology, 2001 Mar 01. 152(5), 877-893.
Externí odkaz:
https://www.jstor.org/stable/1620350
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 6, Iss 4, Pp 114-118 (2017)
A full term newborn small for gestational age Intra Uterine Growth Retardation (IUGR) admitted with congenital dysmorphic features with icthyosis, atrichia, microcephaly and eye abnormalities, when explored further for other congenital malformati
Externí odkaz:
https://doaj.org/article/48af48f9142b4236b76bb4150d66af2b
Autor:
Rattanavalai Nitiyarom, Wanee Wisuthsarewong, Nithiwat Vatanavicharn, Rattapon Thuangtong, Atiporn Thuangtong, Chanin Limwongse, Sunisa Sawasdichai, Jane Manonukul
Publikováno v:
Siriraj Medical Journal, Vol 69, Iss 3, Pp 156-158 (2017)
We herein describe the first reported case of Ichthyosis Follicularis with Atrichia and Photophobia (IFAP) syndrome in Thailand. A 6-year-old boy presented with a history of photophobia since 1 month of age. Then he developed widespread follicular
Externí odkaz:
https://doaj.org/article/634e67878e984bc29bb66f09bd36bc57