Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Marci Laudenslager"'
Autor:
Kacey Chae, Jashalynn German, Karla Kendrick, Sean Tackett, Paul O’Rourke, Kimberly A. Gudzune, Marci Laudenslager
Publikováno v:
Obesity Science & Practice, Vol 10, Iss 2, Pp n/a-n/a (2024)
Abstract Objective Despite the rising prevalence of people living with obesity, physicians are providing suboptimal care to these individuals, which may be a consequence of inadequate education in weight management and negative attitudes toward peopl
Externí odkaz:
https://doaj.org/article/0807d14a9dbd4fc8b10346310aeccde8
Autor:
James S. Pankow, Jeanne M. Clark, Marci Laudenslager, Elizabeth Selvin, Dan Wang, Po Hung Chen, Mariana Lazo
Publikováno v:
Dig Liver Dis
Background Inflammation is key in the pathogenesis of Nonalcoholic Fatty Liver Disease (NAFLD) – a common progressive liver disease. The soluble receptor for advanced glycation end products (sRAGE) attenuates inflammatory signaling; low levels of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f819dfb56657672a7bf818d8c565589
https://doi.org/10.1016/j.dld.2021.02.005
https://doi.org/10.1016/j.dld.2021.02.005
Publikováno v:
Curr Obes Rep
PURPOSE OF REVIEW: Comprehensive lifestyle programs are cornerstones of obesity management, but clinician referrals may be limited by program availability. Commercial weight-loss programs may be an alternative, but clinicians may be unaware of their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45aa04294e9653d9fc6ad98a14c2d9be
https://doi.org/10.1007/s13679-021-00428-y
https://doi.org/10.1007/s13679-021-00428-y
Autor:
John M. Maris, Kristopher R. Bosse, Cynthia Winter, Rachel Sennett, Michael P. LaQuaglia, Jonathan Huggins, Patrick A. Mayes, Kristina A. Cole, Sharon J. Diskin, Edward F. Attiyeh, Marci Laudenslager, Chase Hulderman, Yael P. Mosse, Andrew C. Wood, Geoffrey T. Norris, Jayanti Jagannathan, Mike R. Russell
Publikováno v:
Proceedings of the National Academy of Sciences. 108:3336-3341
Neuroblastoma is a childhood cancer that is often fatal despite intense multimodality therapy. In an effort to identify therapeutic targets for this disease, we performed a comprehensive loss-of-function screen of the protein kinome. Thirty kinases s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c52e6367a3299a0a5146a4dab87c468
https://doi.org/10.1073/pnas.1012351108
https://doi.org/10.1073/pnas.1012351108
Autor:
Luca Longo, Yael P. Mosse, Marcella Devoto, Claudia Specchia, Hakon Hakonarson, Marci Laudenslager, John M. Maris
Publikováno v:
Human Heredity. 71:135-139
Background: Neuroblastoma (NB) is an important childhood cancer with a strong genetic component related to disease susceptibility. Approximately 1% of NB cases have a positive family history. Following a genome-wide linkage analysis and sequencing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52a14f607b1688e56ca3b3429978caa3
https://doi.org/10.1159/000324843
https://doi.org/10.1159/000324843
Autor:
Kai Wang, Cecilia Kim, Kristina A. Cole, Jill E. Lynch, Jonathan P. Bradfield, Alexandra I. F. Blakemore, Patrick McGrady, Maura Diamond, Kristopher R. Bosse, Katlyn Pecor, Hakon Hakonarson, Marci Laudenslager, Sharon J. Diskin, Hongzhe Li, Cuiping Hou, Edward F. Attiyeh, John M. Maris, Cynthia Winter, Andrew Wood, Wendy B. London, Marcella Devoto, Yael P. Mosse, Tamim H. Shaikh, Struan F.A. Grant, Elizabeth A. Geiger, E. Rappaport, Joseph T. Glessner
Publikováno v:
Nature. 459:987-991
Copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) are two important potential sources of phenotypic variation in humans. Until now, only SNPs have been associated with cancer, but the increasing recognition that germline DNA do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a201763cbc7dd0802a8345812a88f8c
https://doi.org/10.1038/nature08035
https://doi.org/10.1038/nature08035
Autor:
Wendy B. London, Shahab Asgharzadeh, Nazneen Rahman, Sharon J. Diskin, Robert C. Seeger, Edward F. Attiyeh, Struan F.A. Grant, Marcella Devoto, Hongzhe Li, Carmel McConville, Cynthia Winter, Richard H Scott, Jonathan P. Bradfield, Maria Garris, Marci Laudenslager, Yael P. Mosse, Jayanti Jagannathan, Kristina A. Cole, Cecilia Kim, Kristopher R. Bosse, Eric F. Rappaport, John M. Maris, Mario Capasso, Joseph T. Glessner, Cuiping Hou, Hakon Hakonarson, Maura Diamond
Publikováno v:
Nature genetics
We conducted a SNP-based genome-wide association study (GWAS) focused on the high-risk subset of neuroblastoma. As our previous unbiased GWAS showed strong association of common 6p22 SNP alleles with aggressive neuroblastoma, we restricted our analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63a2dda868eb99e0cbcd250f8718e4fe
http://europepmc.org/articles/PMC2753610
http://europepmc.org/articles/PMC2753610
Autor:
Cecilia Kim, Robert C. Seeger, Stefano Monni, Richard H Scott, Edward F. Attiyeh, Shahab Asgharzadeh, Joseph T. Glessner, Eric F. Rappaport, Edward C. Frackelton, Cynthia Winter, Hongzhe Li, Mario Capasso, Carmel McConville, Hakon Hakonarson, Marcella Devoto, John M. Maris, Sharon J. Diskin, Kristina A. Cole, Marci Laudenslager, Wendy B. London, Nazneen Rahman, Jonathan P. Bradfield, Andrew W. Eckert, Cuiping Hou, Tracy Casalunovo, Struan F.A. Grant, Yael P. Mosse
Neuroblastoma is a malignant condition of the developing sympathetic nervous system that most commonly affects young children and is often lethal. Its cause is not known.We performed a genomewide association study by first genotyping blood DNA sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfc1fbf1555e07373041a7acf0eaf97a
http://hdl.handle.net/11573/50401
http://hdl.handle.net/11573/50401
Autor:
Devoto, Marcella, Claudia, Specchia, Marci, Laudenslager, Luca, Longo, Hakon, Hakonarson, John, Maris, Yael, Mosse
Publikováno v:
Human heredity. 71(2)
Neuroblastoma (NB) is an important childhood cancer with a strong genetic component related to disease susceptibility. Approximately 1% of NB cases have a positive family history. Following a genome-wide linkage analysis and sequencing of candidate g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b6e6915e29b05af7e7cee2b73225a60a
https://pubmed.ncbi.nlm.nih.gov/21734404
https://pubmed.ncbi.nlm.nih.gov/21734404
Autor:
Nora Wasserman, John M. Maris, Yael P. Mosse, D J Maris, Marci Laudenslager, Cynthia Winter, Eric H. Raabe, Kristina A. Cole, Michael J. Laquaglia
Publikováno v:
Oncogene. 27(4)
PHOX2B is a homeodomain-containing protein that is involved in the development of the peripheral nervous system and is the major disease gene for the rare congenital breathing disorder congenital central hypoventilation syndrome (CCHS). Germline PHOX
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a852e9dec2aa3b90d347be67a30aa2f8
https://pubmed.ncbi.nlm.nih.gov/17637745
https://pubmed.ncbi.nlm.nih.gov/17637745