Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Karen, Swisshelm"'
Autor:
Jeanine Ruggeri, Billie Carstens, Veronica McDaniel, Christine Henderson, Hala Nijmeh, Patricia Trevisan, Sudabeh Balakhani, Kimberly Harding, Aline Murakami-Walter, Alexandra Ohene-Mobley, Karen Swisshelm, Stephen Wicks, Laura Schultz-Rogers, Mary Haag
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101004- (2024)
Externí odkaz:
https://doaj.org/article/1926f52cb097426a85850f245ac057d6
Autor:
Emily M. Kudalkar, Changlee Pang, Mary M. Haag, Daniel A. Pollyea, Manali Kamdar, Gang Xu, Meng Su, Billie Carstens, Karen Swisshelm, Liming Bao
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-9 (2022)
Abstract Background 21q22 amplification is a rare cytogenetic aberration in acute myeloid leukemia (AML). So far, the cytogenomic and molecular features and clinical correlation of 21q22 amplification in AML have not been well-characterized. Case pre
Externí odkaz:
https://doaj.org/article/d5c884544b7a49b19e6e0e52fa8bb4f5
Autor:
Martha R. Stampfer, Andrew J. Wyrobek, Heidi S. Feiler, Karen Swisshelm, Ekaterina Bassett, Batul Merchant, Sanchita Bhattacharya, James C. Garbe
Supplementary Figure 3 from Molecular Distinctions between Stasis and Telomere Attrition Senescence Barriers Shown by Long-term Culture of Normal Human Mammary Epithelial Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12b2990dbbc5dd4611c29c25ac74803d
https://doi.org/10.1158/0008-5472.22377812.v1
https://doi.org/10.1158/0008-5472.22377812.v1
Autor:
Martha R. Stampfer, Andrew J. Wyrobek, Heidi S. Feiler, Karen Swisshelm, Ekaterina Bassett, Batul Merchant, Sanchita Bhattacharya, James C. Garbe
Supplementary Tables 1- 4 from Molecular Distinctions between Stasis and Telomere Attrition Senescence Barriers Shown by Long-term Culture of Normal Human Mammary Epithelial Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34a4f94aa2aef82cc24293e07713571b
https://doi.org/10.1158/0008-5472.22377809.v1
https://doi.org/10.1158/0008-5472.22377809.v1
Autor:
Martha R. Stampfer, Andrew J. Wyrobek, Heidi S. Feiler, Karen Swisshelm, Ekaterina Bassett, Batul Merchant, Sanchita Bhattacharya, James C. Garbe
Supplementary Figure 1 from Molecular Distinctions between Stasis and Telomere Attrition Senescence Barriers Shown by Long-term Culture of Normal Human Mammary Epithelial Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdfb1f47a713865f979cc0b7aa523450
https://doi.org/10.1158/0008-5472.22377818.v1
https://doi.org/10.1158/0008-5472.22377818.v1
Autor:
Martha R. Stampfer, Andrew J. Wyrobek, Heidi S. Feiler, Karen Swisshelm, Ekaterina Bassett, Batul Merchant, Sanchita Bhattacharya, James C. Garbe
Supplementary Figure 2 from Molecular Distinctions between Stasis and Telomere Attrition Senescence Barriers Shown by Long-term Culture of Normal Human Mammary Epithelial Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6159094d1fbaa5be2fdea43ebdd18641
https://doi.org/10.1158/0008-5472.22377815.v1
https://doi.org/10.1158/0008-5472.22377815.v1
Autor:
Jamie LeRoux, Meng Su, Stephanie Page, Karen Swisshelm, Deborrah Hennerich, Liming Bao, Shayna Svihovec, Sharon L. Graw, Peter Brzeskiewicz, Mary Haag
Publikováno v:
Journal of Genetic Counseling. 31:364-374
Chromosomal microarray (CMA) is now widely used as first-tier testing for the detection of copy number variants (CNVs) and absence of heterozygosity (AOH) in patients with multiple congenital anomalies (MCA), autism spectrum disorder (ASD), developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6ee013aaf63190efb9c9f2ebe54b7fe
https://doi.org/10.1002/jgc4.1496
https://doi.org/10.1002/jgc4.1496
Autor:
Emily Kudalkar, Changlee Pang, Mary M. Haag, Daniel A. Pollyea, Manali Kamdar, Gang Xu, Meng Su, Billie Carstens, Karen Swisshelm, Liming Bao
Background: 21q22 amplification is a rare cytogenetic aberration in acute myeloid leukemia (AML). So far, the cytogenomic and molecular features and clinical correlation of 21q22 amplification in AML have not been well-characterized. Case Presentatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9413b3d36775cf0c994df868c9f47906
https://doi.org/10.21203/rs.3.rs-1630638/v1
https://doi.org/10.21203/rs.3.rs-1630638/v1
Autor:
Beth A. Pitel, Madina Sukhanova, Hui Chen, Xiaolin Hu, Deborah Ritter, Ashwini Yenamandra, Tracy Tucker, Francesc Sole, Jennelle C. Hodge, Shashirekha Shetty, Rashmi Kanagal-Shamanna, M. Anwar Iqbal, Rajyasree Emmadi, Gloria T. Haskell, Yajuan J. Liu, XinYan Lu, Karen Swisshelm, Patricia T. Greipp, Gordana Raca, Katherine B. Geiersbach, Xinjie Xu
Publikováno v:
Cancer Genetics. :5-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6775f3c72f0e4e620e9e5c763c75458f
https://doi.org/10.1016/j.cancergen.2021.05.029
https://doi.org/10.1016/j.cancergen.2021.05.029
Autor:
Emily Kudalkar, Meng Su, Liming Bao, Mary Haag, Billie Carstens, Changlee Pang, Daniel Pollyea, Manali Kamdar, Gang Xu, Karen Swisshelm
Publikováno v:
Genetics in Medicine. 24:S32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7ef4ff6023fbc6d1be1b17d4648d0ee
https://doi.org/10.1016/j.gim.2022.01.089
https://doi.org/10.1016/j.gim.2022.01.089