Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Emily L. Niemitz"'
Autor:
Emily L. Niemitz, Andrew P. Feinberg, Paul E. Grundy, Sheri A. Brandenburg, Michael R. DeBaun
Publikováno v:
The American Journal of Human Genetics. 77(5):887-891
Idiopathic hemihypertrophy (IH) is a congenital overgrowth syndrome associated with an increased risk of embryonal cancers in childhood. A related developmental disorder is Beckwith-Wiedemann syndrome (BWS), which increases risk for embryonal cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b790f453df43f6e8a12c83573097030
Publikováno v:
The American Journal of Human Genetics. 72(1):156-160
Recent data in humans and animals suggest that assisted reproductive technology (ART) might affect the epigenetics of early embryogenesis and might cause birth defects. We report the first evidence, to our knowledge, that ART is associated with a hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1e0dfc571477be3f701a03009c7c751
Autor:
Andrew P. Feinberg, Emily L. Niemitz, D. Elizabeth McNeil, Sheri A. Brandenburg, Maxwell P. Lee, Michael R. DeBaun
Publikováno v:
The American Journal of Human Genetics. 70:604-611
Beckwith-Wiedemann syndrome (BWS) is a congenital cancer-predisposition syndrome associated with embryonal cancers, macroglossia, macrosomia, ear pits or ear creases, and midline abdominal-wall defects. The most common constitutional abnormalities in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97b0fad90fe86fde14990b9ccace9791
https://doi.org/10.1086/338934
https://doi.org/10.1086/338934
Autor:
Mousumi Mutsuddi, Emily L Niemitz, Yanping Gao, Jack Mosher, Wayne A. Johnson, Stephen T. Crews, Yue Ma, John R. Nambu, Ashim Mukherjee, Kaan Certel, Neda Huseinovic
Publikováno v:
The Journal of Neuroscience. 20:4596-4605
DuringDrosophilaembryogenesis the CNS midline cells have organizing activities that are required for proper elaboration of the axon scaffold and differentiation of neighboring neuroectodermal and mesodermal cells. CNS midline development is dependent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c06bd63a0bdaadac9db92fd3e5183a6d
https://doi.org/10.1523/jneurosci.20-12-04596.2000
https://doi.org/10.1523/jneurosci.20-12-04596.2000
Autor:
Emily L. Niemitz, Jonathan Fallon, Michael R. DeBaun, Mitsuo Oshimura, Hiroyuki Kugoh, Kazuhiro Murakami, Andrew P. Feinberg
Beckwith-Wiedemann syndrome (BWS), which causes prenatal overgrowth, midline abdominal wall defects, macroglossia, and embryonal tumors, is a model for understanding the relationship between genomic imprinting, human development, and cancer. The caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eded1a74817e709722df990d1e32617f
https://europepmc.org/articles/PMC1182113/
https://europepmc.org/articles/PMC1182113/
Autor:
Dmitri I. Loukinov, Elena Pugacheva, Sergei Vatolin, Svetlana D. Pack, Hanlim Moon, Igor Chernukhin, Poonam Mannan, Erik Larsson, Chandrasekhar Kanduri, Alexander A. Vostrov, Hengmi Cui, Emily L. Niemitz, John E. J. Rasko, France M. Docquier, Malathi Kistler, Joseph J. Breen, Zhengping Zhuang, Wolfgang W. Quitschke, Rainer Renkawitz, Elena M. Klenova, Andrew P. Feinberg, Rolf Ohlsson, Herbert C. Morse, Victor V. Lobanenkov
CTCF, a conserved, ubiquitous, and highly versatile 11-zinc-finger factor involved in various aspects of gene regulation, forms methylation-sensitive insulators that regulate X chromosome inactivation and expression of imprinted genes. We document he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6438bc128662b2751f3b6373ff0d6f1b
https://europepmc.org/articles/PMC124484/
https://europepmc.org/articles/PMC124484/
Autor:
Hiroshi Uejima, Tilanthi M. Jayawardena, Karl W. Broman, Andrew P. Feinberg, Daniel A. Haber, Jason D. Ravenel, Elizabeth J. Perlman, Daphne W. Bell, Emily L. Niemitz
Publikováno v:
Journal of the National Cancer Institute. 93(22)
Background: Loss of imprinting (LOI) of the insulin-like growth factor-II (IGF2) gene, an epigenetic alteration associated with expression of the normally silent maternal allele, was observed first in Wilms tumor. Although LOI has subsequently been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6858496fc9aa4dbb6140f1e861001bc
https://pubmed.ncbi.nlm.nih.gov/12464656
https://pubmed.ncbi.nlm.nih.gov/12464656
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 14(14)
A crucial aspect of the inflammatory response is the recruitment of activated neutrophils (PMN) to the site of damage. Lytic enzymes and oxygen radicals released by PMN are important in clearing an infection or cellular debris, but can also produce h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07887cb7f84400419bc41601181b76e
https://pubmed.ncbi.nlm.nih.gov/11053246
https://pubmed.ncbi.nlm.nih.gov/11053246