Zobrazeno 1 - 10
of 240
pro vyhledávání: '"Brian R, Davis"'
Autor:
Melissa Pille, John M. Avila, So Hyun Park, Cuong Q. Le, Haipeng Xue, Filomeen Haerynck, Lavanya Saxena, Ciaran Lee, Elizabeth J. Shpall, Gang Bao, Bart Vandekerckhove, Brian R. Davis
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 1, Pp 101208- (2024)
Wiskott-Aldrich syndrome (WAS) is a severe X-linked primary immunodeficiency resulting from a diversity of mutations distributed across all 12 exons of the WAS gene. WAS encodes a hematopoietic-specific and developmentally regulated cytoplasmic prote
Externí odkaz:
https://doaj.org/article/c869b7adf0164810aa0dd2b9dccebba3
Publikováno v:
Gastrointestinal Disorders, Vol 3, Iss 1, Pp 44-50 (2021)
Median arcuate ligament syndrome (MALS), otherwise called celiac artery compression syndrome (CACS), is an uncommon disorder that results from an anatomical compression of the celiac axis and/or celiac ganglion by the MAL. Patients typically present
Externí odkaz:
https://doaj.org/article/7074ea1f1e9b4905876b3bd4817438b6
Publikováno v:
Frontiers in Genome Editing, Vol 4 (2022)
Cystic Fibrosis (CF) is caused by a diverse set of mutations distributed across the approximately 250 thousand base pairs of the CFTR gene locus, of which at least 382 are disease-causing (CFTR2.org). Although a variety of editing tools are now avail
Externí odkaz:
https://doaj.org/article/c70b35dd032144e4b943a9a2064bf1b6
Autor:
Shingo Suzuki, Finn J. Hawkins, Cristina Barillà, Mary Lou Beermann, Darrell N. Kotton, Brian R. Davis
Publikováno v:
STAR Protocols, Vol 2, Iss 3, Pp 100683- (2021)
Summary: Airway basal cells play an essential role in the maintenance of the airway epithelium. Here, we provide a detailed directed differentiation protocol to generate ‘‘induced basal cells (iBCs)’’ from human pluripotent stem cells. iBCs r
Externí odkaz:
https://doaj.org/article/248c5d3ddf434c6a951fd66ad7c2e66e
Autor:
Tamara J. Laskowski, Yasmine Van Caeneghem, Rasoul Pourebrahim, Chao Ma, Zhenya Ni, Zita Garate, Ana M. Crane, Xuan Shirley Li, Wei Liao, Manuel Gonzalez-Garay, Jose Carlos Segovia, David E. Paschon, Edward J. Rebar, Michael C. Holmes, Dan Kaufman, Bart Vandekerckhove, Brian R. Davis
Publikováno v:
Stem Cell Reports, Vol 7, Iss 2, Pp 139-148 (2016)
Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency disease caused by mutations in the gene encoding the WAS protein (WASp). Here, induced pluripotent stem cells (iPSCs) were derived from a WAS patient (WAS-iPSC) and the endogenous
Externí odkaz:
https://doaj.org/article/676abc2202b146eb97e086edfc92f229
Publikováno v:
The AFS Textbook of Foregut Disease ISBN: 9783031196706
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::835264c88d5d780a31e8e09f3ca38fa4
https://doi.org/10.1007/978-3-031-19671-3_44
https://doi.org/10.1007/978-3-031-19671-3_44
Autor:
Zita Garate, Oscar Quintana-Bustamante, Ana M. Crane, Emmanuel Olivier, Laurent Poirot, Roman Galetto, Penelope Kosinski, Collin Hill, Charles Kung, Xabi Agirre, Israel Orman, Laura Cerrato, Omaira Alberquilla, Fatima Rodriguez-Fornes, Noemi Fusaki, Felix Garcia-Sanchez, Tabita M. Maia, Maria L. Ribeiro, Julian Sevilla, Felipe Prosper, Shengfang Jin, Joanne Mountford, Guillermo Guenechea, Agnes Gouble, Juan A. Bueren, Brian R. Davis, Jose C. Segovia
Publikováno v:
Stem Cell Reports, Vol 5, Iss 6, Pp 1053-1066 (2015)
Pyruvate kinase deficiency (PKD) is a rare erythroid metabolic disease caused by mutations in the PKLR gene. Erythrocytes from PKD patients show an energetic imbalance causing chronic non-spherocytic hemolytic anemia, as pyruvate kinase defects impai
Externí odkaz:
https://doaj.org/article/c4e6f66da3a7499d96a1b9ff98b4f2e1
Autor:
Ana M. Crane, Philipp Kramer, Jacquelin H. Bui, Wook Joon Chung, Xuan Shirley Li, Manuel L. Gonzalez-Garay, Finn Hawkins, Wei Liao, Daniela Mora, Sangbum Choi, Jianbin Wang, Helena C. Sun, David E. Paschon, Dmitry Y. Guschin, Philip D. Gregory, Darrell N. Kotton, Michael C. Holmes, Eric J. Sorscher, Brian R. Davis
Publikováno v:
Stem Cell Reports, Vol 4, Iss 4, Pp 569-577 (2015)
Recently developed reprogramming and genome editing technologies make possible the derivation of corrected patient-specific pluripotent stem cell sources—potentially useful for the development of new therapeutic approaches. Starting with skin fibro
Externí odkaz:
https://doaj.org/article/3bd18eafc9e34d40b5c4fab5ff9e7a11
Autor:
Katsutsugu Umeda, Hirotsugu Oda, Qing Yan, Nadine Matthias, Jiangang Zhao, Brian R. Davis, Naoki Nakayama
Publikováno v:
Stem Cell Reports, Vol 4, Iss 4, Pp 712-726 (2015)
Here we report the successful generation and long-term expansion of SOX9-expressing CD271+PDGFRα+CD73+ chondrogenic ectomesenchymal cells from the PAX3/SOX10/FOXD3-expressing MIXL1−CD271hiPDGFRαloCD73− neural crest-like progeny of human pluripo
Externí odkaz:
https://doaj.org/article/7a68c48ec3a1400d8b03d78eb8d80020
Autor:
Jisoo Kim, Samuel Grasso, Brittany Harper, Christopher Dodoo, Brian R. Davis, Christian Castro, Marah Hamdan, Benjamin Clapp
Publikováno v:
Surgery for Obesity and Related Diseases. 17:555-561
Background Magnetic sphincter augmentation (MSA) has gained popularity as a treatment for gastroesophageal reflux disease (GERD). The role of MSA in treating GERD in metabolic and bariatric surgery (MBS) patients at the time of primary MBS is unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4675d1f517f0fb8c1dd008544e6a5439
https://doi.org/10.1016/j.soard.2020.10.024
https://doi.org/10.1016/j.soard.2020.10.024