Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Michael G. FitzGerald"'
Autor:
Margaret E. Brousseau, Ernst J. Schaefer, Josee Dupuis, Brenda Eustace, Paul Van Eerdewegh, Allison L. Goldkamp, Lisa M. Thurston, Michael G. FitzGerald, Diane Yasek-McKenna, Gilmore O'Neill, Gretchen P. Eberhart, Barbara Weiffenbach, Jose M. Ordovas, Mason W. Freeman, Robert H. Brown, Jr., Jessie Z. Gu
Publikováno v:
Journal of Lipid Research, Vol 41, Iss 3, Pp 433-441 (2000)
Abstract: Tangier disease (TD) is an autosomal co-dominant disorder in which homozygotes have a marked deficiency of high density lipoprotein (HDL) cholesterol and, in some cases, peripheral neuropathy and premature coronary heart disease (CHD). Homo
Externí odkaz:
https://doaj.org/article/fd9cecdea07e49dd948151a1774c02e1
Autor:
Marc P Hoeppner, Andrew Lundquist, Mono Pirun, Jennifer R S Meadows, Neda Zamani, Jeremy Johnson, Görel Sundström, April Cook, Michael G FitzGerald, Ross Swofford, Evan Mauceli, Behrooz Torabi Moghadam, Anna Greka, Jessica Alföldi, Amr Abouelleil, Lynne Aftuck, Daniel Bessette, Aaron Berlin, Adam Brown, Gary Gearin, Annie Lui, J Pendexter Macdonald, Margaret Priest, Terrance Shea, Jason Turner-Maier, Andrew Zimmer, Eric S Lander, Federica di Palma, Kerstin Lindblad-Toh, Manfred G Grabherr
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91172 (2014)
The domestic dog, Canis familiaris, is a well-established model system for mapping trait and disease loci. While the original draft sequence was of good quality, gaps were abundant particularly in promoter regions of the genome, negatively impacting
Externí odkaz:
https://doaj.org/article/a00dababd8554f008848530283adc7b5
Publikováno v:
Journal of the American Academy of Orthopaedic Surgeons. 25:304-313
Background The ideal method for management of the subscapularis tendon during anatomic total shoulder arthroplasty (TSA) remains controversial. Methods In a retrospective cohort study, primary anatomic TSA procedures performed with either a subscapul
Publikováno v:
The Journal of hand surgery, European volume. 43(9)
The purpose of this study was to better define an ideal tendon transfer suture construct to allow for early active range of motion. A side-to-side tendon construct was used to test suture technique (cross stich vs. Krackow stitch), number of suture t
Autor:
Chad, Nusbaum, Michael C, Zody, Mark L, Borowsky, Michael, Kamal, Chinnappa D, Kodira, Todd D, Taylor, Charles A, Whittaker, Jean L, Chang, Christina A, Cuomo, Ken, Dewar, Michael G, FitzGerald, Xiaoping, Yang, Amr, Abouelleil, Nicole R, Allen, Scott, Anderson, Toby, Bloom, Boris, Bugalter, Jonathan, Butler, April, Cook, David, DeCaprio, Reinhard, Engels, Manuel, Garber, Andreas, Gnirke, Nabil, Hafez, Jennifer L, Hall, Catherine Hosage, Norman, Takehiko, Itoh, David B, Jaffe, Yoko, Kuroki, Jessica, Lehoczky, Annie, Lui, Pendexter, Macdonald, Evan, Mauceli, Tarjei S, Mikkelsen, Jerome W, Naylor, Robert, Nicol, Cindy, Nguyen, Hideki, Noguchi, Sinéad B, O'Leary, Keith, O'Neill, Bruno, Piqani, Cherylyn L, Smith, Jessica A, Talamas, Kerri, Topham, Yasushi, Totoki, Atsushi, Toyoda, Hester M, Wain, Sarah K, Young, Qiandong, Zeng, Andrew R, Zimmer, Asao, Fujiyama, Masahira, Hattori, Bruce W, Birren, Yoshiyuki, Sakaki, Eric S, Lander
Publikováno v:
Nature. 437:551-555
Chromosome 18 appears to have the lowest gene density of any human chromosome and is one of only three chromosomes for which trisomic individuals survive to term. There are also a number of genetic disorders stemming from chromosome 18 trisomy and an
Autor:
Charis Eng, Andreas von Deimling, Patricia L. M. Dahia, Zimu Zheng, Daniel A. Haber, Frank G. Haluska, Xue Zhang, Torsten Pietsch, Michael G. FitzGerald, Deborah J. Marsh
Publikováno v:
Oncogene. 16:2403-2406
PTEN/MMAC1/TEP1, encoding a dual-specificity phosphatase, is a tumor suppressor gene which has recently been cloned and mapped to chromosome 10q23.3. We have shown that germline mutations of PTEN are present in individuals with two hamartoma syndrome
Autor:
Michael Krainer, Kanamaru R, Kurt J. Isselbacher, Daniel A. Haber, Chikashi Ishioka, Michael G. FitzGerald, Akira Shimada, Anne M. Bowcock, Sandra Silva-Arrieta, Hilal Unsal, Dianne M. Finkelstein, Deborah J. MacDonald
Publikováno v:
New England Journal of Medicine. 336:1416-1422
Background Germ-line mutations in the BRCA1 and BRCA2 genes predispose women to breast cancer. BRCA1 mutations are found in approximately 12 percent of women with breast cancer of early onset, and the specific mutation causing a deletion of adenine a
Autor:
Daniel A. Haber, Kathleen A. Mayzel, Peggy Beer-Romero, Dianne M. Finkelstein, Erin O'Neil, Michael Krainer, Kurt J. Isselbacher, Jerry Younger, Stephen H. Friend, Christoph Englert, Hilal Unsal, Dennis C. Sgroi, Rosemary B. Duda, Barbara L. Smith, Michael G. FitzGerald, Deborah J. MacDonald, Ingrid Hoover, Sandra Silva-Arrieto, Judy Garber
Publikováno v:
New England Journal of Medicine. 334:143-149
Background Mutations in a germ-line allele of the BRCA1 gene contribute to the familial breast cancer syndrome. However, the prevalence of these mutations is unknown in women with breast cancer who do not have the features of this familial syndrome.
Autor:
M. Khan, Michael G. FitzGerald, Mark Raymond Adams, W. R. McCombie, Teresa Utterback, Mark Dubnick, Jenny M. Kelley, J. C. Venter, Chris Fields, Anthony R. Kerlavage
Publikováno v:
Nature Genetics. 1:124-131
A database containing mapped partial cDNA sequences from Caenorhabdhitis elegans will provide a ready starting point for identifying nematode homologues of important human genes and determining their functions in C. elegans. A total of 720 expressed
Autor:
Mirek Gorski, Michael G. FitzGerald, Carl R. Merril, Ruben F. Moreno, Mihael H. Polymeropoulos, Mark Raymond Adams, Hong Xiao, Anna Glodek, J. Craig Venter
Publikováno v:
Genomics. 12:492-496
Expressed sequence tags (ESTs) have been obtained from several hundred brain cDNAs as an initial effort to characterize expressed brain genes. These ESTs will become tools for human genome mapping and they will also provide candidate causative genes