Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chen G. Han"'
Autor:
Shachar Abudi-Sinreich, Steven P. Bodine, Tadafumi Yokoyama, Nathanial J. Tolman, Michal Tyrlik, Lauren C. Testa, Chen G. Han, Heidi M. Dorward, Stephen M. Wincovitch, Yair Anikster, William A. Gahl, Resat Cinar, Bernadette R. Gochuico, May Christine V. Malicdan
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background HPS-1 is a genetic type of Hermansky-Pudlak syndrome (HPS) with highly penetrant pulmonary fibrosis (HPSPF), a restrictive lung disease that is similar to idiopathic pulmonary fibrosis (IPF). Hps1 ep/ep (pale ear) is a naturally o
Externí odkaz:
https://doaj.org/article/eac6fc1a82114d36a07a67ff3d28be6a
Autor:
Kim M, Keppler-Noreuil, Jasmine, Burton-Akright, David E, Kleiner, Julie C, Sapp, Marjorie J, Lindhurst, Chen G, Han, Leslie G, Biesecker, Bernadette R, Gochuico
Publikováno v:
Annals of the American Thoracic Society. 19:1871-1880
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8064bcf55a6c99c163a659a1af1f09e8
https://doi.org/10.1513/annalsats.202111-1214oc
https://doi.org/10.1513/annalsats.202111-1214oc
Autor:
Shachar Abudi-Sinreich, Steven P. Bodine, Tadafumi Yokoyama, Nathanial J. Tolman, Michal Tyrlik, Lauren C. Testa, Chen G. Han, Heidi M. Dorward, Stephen M. Wincovitch, Yair Anikster, William A. Gahl, Resat Cinar, Bernadette R. Gochuico, May Christine V. Malicdan
Publikováno v:
Respiratory research. 23(1)
Background HPS-1 is a genetic type of Hermansky-Pudlak syndrome (HPS) with highly penetrant pulmonary fibrosis (HPSPF), a restrictive lung disease that is similar to idiopathic pulmonary fibrosis (IPF). Hps1ep/ep (pale ear) is a naturally occurring H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab353aba05178dbc109e320cf8058edc
https://pubmed.ncbi.nlm.nih.gov/35509004
https://pubmed.ncbi.nlm.nih.gov/35509004
Autor:
Bernadette R. Gochuico, Koyamangalath Krishnan, Dong Chen, Nagabhishek Moka, Wendy J. Introne, Sara G. Haroutunian, Ellen Macnamara, Chen G. Han, William A. Gahl, Kevin J. O'Brien, Lea M. Coon, May Christine V. Malicdan, Laryssa A. Huryn, Julie A. Majerus
Publikováno v:
American Journal of Medical Genetics Part A. 176:2819-2823
Heřmanský-Pudlak syndrome (HPS), a rare autosomal recessive disorder, manifests with oculocutaneous albinism and a bleeding diathesis. However, severity of disease can be variable and is typically related to the genetic subtype of HPS; HPS type 6 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fbee90e10fa3ea7a7b6bfc27436efa
https://doi.org/10.1002/ajmg.a.40514
https://doi.org/10.1002/ajmg.a.40514