Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Joannah Kim"'
Autor:
Friedrich Kueppers, Mark D. Andrake, Qifang Xu, Roland L. Dunbrack, Joannah Kim, Christopher L. Sanders
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-19 (2019)
Abstract Background Alpha 1 Antitrypsin (AAT) is a key serum proteinase inhibitor encoded by SERPINA1. Sequence variants of the gene can cause Alpha 1 Antitrypsin Deficiency (AATD), a condition associated with lung and liver disease. The majority of
Externí odkaz:
https://doaj.org/article/d32b605cb01a47899ade581892491c43
Autor:
Kimberly E. Foil, M. Gwen Blanton, Chris Sanders, Joannah Kim, Haitham S. Al Ashry, Suchit Kumbhare, Charlie Strange
Publikováno v:
Pulmonary Medicine, Vol 2018 (2018)
Rationale. Individuals with a single Z mutation in the SERPINA1 gene that codes for alpha-1 antitrypsin (AAT) are at increased risk for COPD if they have ever-smoked. Whether additional variants alter the risk for COPD in this population remains unkn
Externí odkaz:
https://doaj.org/article/ae8f975dedd540fe84b9d1c8789c9848
Autor:
Roland L. Dunbrack, Qifang Xu, Friedrich Kueppers, Mark Andrake, Joannah Kim, Christopher Sanders
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-19 (2019)
BMC Medical Genetics
BMC Medical Genetics
Background Alpha 1 Antitrypsin (AAT) is a key serum proteinase inhibitor encoded by SERPINA1. Sequence variants of the gene can cause Alpha 1 Antitrypsin Deficiency (AATD), a condition associated with lung and liver disease. The majority of AATD case
Autor:
Christopher Sanders, Joannah Kim
Publikováno v:
Chest. 150:1131A
Autor:
Kueppers, Friedrich, Andrake, Mark, Qifang Xu, Dunbrack, Roland, Joannah Kim, Sanders, Christopher
Protein modeling to assess the pathogenicity of rare variants of SERPINA1 in patients suspected of having Alpha 1 Antitrypsin Deficiency (DOCX 25 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f85e3922a703569face770fdee8eb4b1
Autor:
Kueppers, Friedrich, Andrake, Mark, Qifang Xu, Dunbrack, Roland, Joannah Kim, Sanders, Christopher
Protein modeling to assess the pathogenicity of rare variants of SERPINA1 in patients suspected of having Alpha 1 Antitrypsin Deficiency (DOCX 25 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cdddf1e01f8068f8fb26fc189755be2
Autor:
Foil, Kimberly E.1, Blanton, M. Gwen1, Sanders, Chris2, Kim, Joannah2, Al Ashry, Haitham S.1, Kumbhare, Suchit1, Strange, Charlie1
Publikováno v:
Pulmonary Medicine. 9/5/2018, p1-6. 6p.
Autor:
Kueppers, Friedrich1 Friedrich.Kueppers@tuhs.temple.edu, Andrake, Mark D.2 Mark.Andrake@fccc.edu, Xu, Qifang2 Qifang.Xu@fccc.edu, Dunbrack, Roland L.2 rolanddunbrack@gmail.com, Kim, Joannah3 joannah_kim@biocerna.com, Sanders, Christopher L.3 csanders@biocerna.com
Publikováno v:
BMC Medical Genetics. 7/15/2019, Vol. 20 Issue 1, pN.PAG-N.PAG. 1p.