Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kari Boardman"'
Autor:
Erica B. Esrick, Amy Federico, Daniela Abriss, Myriam Armant, Kari Boardman, Christian Brendel, Marioara-Felicia Ciuculescu, Heather Daley, Colleen Dansereau, Augustine Fernandes, Matthew M. Heeney, David G. Justus, Pei-Chi Kao, Annette S. Kim, Donald B. Kohn, Leslie E. Lehmann, Donghui Liu, Wendy B. London, John P Manis, Theodore B. Moore, Emily Morris, Danilo Pellin, Ellen Proeung, Shanna Richard, Gavin D. Roach, Kit L. Shaw, Dayna Terrazas, Shanna L White, David A. Williams
Publikováno v:
Blood. 140:10665-10667
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e828f889a6fcfac4de9b7fcb45370915
https://doi.org/10.1182/blood-2022-169089
https://doi.org/10.1182/blood-2022-169089
Autor:
Erica B, Esrick, Leslie E, Lehmann, Alessandra, Biffi, Maureen, Achebe, Christian, Brendel, Marioara F, Ciuculescu, Heather, Daley, Brenda, MacKinnon, Emily, Morris, Amy, Federico, Daniela, Abriss, Kari, Boardman, Radia, Khelladi, Kit, Shaw, Helene, Negre, Olivier, Negre, Sarah, Nikiforow, Jerome, Ritz, Sung-Yun, Pai, Wendy B, London, Colleen, Dansereau, Matthew M, Heeney, Myriam, Armant, John P, Manis, David A, Williams
Publikováno v:
The New England journal of medicine. 384(3)
Sickle cell disease is characterized by hemolytic anemia, pain, and progressive organ damage. A high level of erythrocyte fetal hemoglobin (HbF) comprising α- and γ-globins may ameliorate these manifestations by mitigating sickle hemoglobin polymer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a54e613c2a9b45852cee621477397c3b
https://pubmed.ncbi.nlm.nih.gov/33471981
https://pubmed.ncbi.nlm.nih.gov/33471981
Autor:
Leslie B. Smoot, Dita Obler, Mary P. Mullen, Doff B. McElhinney, Bai-Lin Wu, Va Lip, Kari Boardman
Publikováno v:
Archives of Disease in Childhood. 94:506-511
Background: Pulmonary arterial hypertension (PAH) has been linked to mutations in genes encoding two members of the transforming growth factor-β family, BMPR2 and ALK1 , the latter of which is also associated with hereditary haemorrhagic telangiecta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9ac90770f4dcfa4da59ef110dbf0ea
https://doi.org/10.1136/adc.2007.133082
https://doi.org/10.1136/adc.2007.133082
Autor:
Ani Manichaikul, Vidu Garg, Qing Ma, Satish Rajagopal, Dita Obler, Leslie B. Smoot, Kari Boardman, Christine Briggs, D. Woodrow Benson, Karl W. Broman, Aoy Tomita-Mitchell, Deepak Srivastava, William T. Pu, Jie Shen, Elizabeth Goldmuntz
Publikováno v:
Journal of Molecular and Cellular Cardiology. 43:677-685
The transcription factor GATA4 is essential for heart morphogenesis. Heterozygous mutation of GATA4 causes familial septal defects. However, the phenotypic spectrum of heterozygous GATA4 mutation is not known. In this study, we defined the cardiac ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8ba82621647798177d4694a516addf1
https://doi.org/10.1016/j.yjmcc.2007.06.004
https://doi.org/10.1016/j.yjmcc.2007.06.004
Autor:
Jane E. Wilkinson, Craig DeLoughery, Ron Caspi, Terry Shea, Kari Boardman, Aresa Toukdarian, Vic Knauf, Tracy J. Mincer, Donald R. Helinski, Zhenping Zhong
Publikováno v:
Plasmid. 47:1-9
A 50,709-bp cryptic plasmid isolated from a marine Micrococcus has been sequenced and found to contain a number of putative mobile genetic elements. The coding regions for 11 putative transposases comprise approximately 17% of the total plasmid seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17fbe98d88c1660b170df857f1852d3f
https://doi.org/10.1006/plas.2001.1550
https://doi.org/10.1006/plas.2001.1550