Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Vineeta, Bajaj"'
Autor:
Evelyn M Mrozek, Vineeta Bajaj, Yanan Guo, Izabela A Malinowska, Jianming Zhang, David J Kwiatkowski
Publikováno v:
PLoS ONE, Vol 16, Iss 4, p e0248380 (2021)
Inactivating mutations in either TSC1 or TSC2 cause Tuberous Sclerosis Complex, an autosomal dominant disorder, characterized by multi-system tumor and hamartoma development. Mutation and loss of function of TSC1 and/or TSC2 also occur in a variety o
Externí odkaz:
https://doaj.org/article/909a6fb01eae496fab917357e7b74006
Autor:
Yuichi Ichikawa, Caitlin F Connelly, Alon Appleboim, Thomas CR Miller, Hadas Jacobi, Nebiyu A Abshiru, Hsin-Jung Chou, Yuanyuan Chen, Upasna Sharma, Yupeng Zheng, Paul M Thomas, Hsuiyi V Chen, Vineeta Bajaj, Christoph W Müller, Neil L Kelleher, Nir Friedman, Daniel NA Bolon, Oliver J Rando, Paul D Kaufman
Publikováno v:
eLife, Vol 6 (2017)
The repeating subunit of chromatin, the nucleosome, includes two copies of each of the four core histones, and several recent studies have reported that asymmetrically-modified nucleosomes occur at regulatory elements in vivo. To probe the mechanisms
Externí odkaz:
https://doaj.org/article/24b6ece5ed4441b78cfba5f0e8e8b723
Autor:
Yanan Guo, Izabela A. Malinowska, Evelyn M Mrozek, David J. Kwiatkowski, Vineeta Bajaj, Jianming Zhang
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 4, p e0248380 (2021)
PLoS ONE, Vol 16, Iss 4, p e0248380 (2021)
Inactivating mutations in either TSC1 or TSC2 cause Tuberous Sclerosis Complex, an autosomal dominant disorder, characterized by multi-system tumor and hamartoma development. Mutation and loss of function of TSC1 and/or TSC2 also occur in a variety o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb9d62b479f7eb2b0d9ddea22dc2dc9
http://europepmc.org/articles/PMC8064564
http://europepmc.org/articles/PMC8064564
Autor:
Wei Qin, Vineeta Bajaj, Izabela Malinowska, Xin Lu, Laura MacConaill, Chin-Lee Wu, David J Kwiatkowski
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24919 (2011)
Renal angiomyolipoma are part of the PEComa family of neoplasms, and occur both in association with Tuberous Sclerosis Complex (TSC) and independent of that disorder. Previous studies on the molecular genetic alterations that occur in angiomyolipoma
Externí odkaz:
https://doaj.org/article/20c6ba53d2e14e1e9937d6b9a9db5743
Autor:
Neil L. Kelleher, Christoph W. Müller, Caitlin F. Connelly, Yuanyuan Chen, Hsin-Jung Chou, Vineeta Bajaj, Oliver J. Rando, Thomas C. Miller, Daniel N. Bolon, Upasna Sharma, Paul M. Thomas, Nir Friedman, Hadas Jacobi, Hsuiyi V Chen, Yuichi Ichikawa, Paul D. Kaufman, Alon Appleboim, Yupeng Zheng, Nebiyu Abshiru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceade51f3bf2bf8d2a4ec6a77f684617
https://doi.org/10.7554/elife.28836.019
https://doi.org/10.7554/elife.28836.019
The histone acetyltransferase Rtt109 is the sole enzyme responsible for acetylation of histone H3 lysine 56 (H3K56) in fungal organisms. Loss of Rtt109 renders fungal cells extremely sensitive to genotoxic agents, and prevents pathogenesis in several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63d4a224e2f62a766adb75daca012e05
https://europepmc.org/articles/PMC3654155/
https://europepmc.org/articles/PMC3654155/
Autor:
Vineeta Bajaj, Xin Lu, Wei Qin, Izabela A. Malinowska, David J. Kwiatkowski, Laura E. MacConaill, Chin-Lee Wu
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24919 (2011)
PLoS ONE
PLoS ONE
Renal angiomyolipoma are part of the PEComa family of neoplasms, and occur both in association with Tuberous Sclerosis Complex (TSC) and independent of that disorder. Previous studies on the molecular genetic alterations that occur in angiomyolipoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1294acd1f70ea479fbd7ebbe0d9c658
http://europepmc.org/articles/PMC3174984?pdf=render
http://europepmc.org/articles/PMC3174984?pdf=render
Publikováno v:
Gene. 429(1-2)
SLC22A18, a poly-specific organic cation transporter, is paternally imprinted in humans and mice. It shows loss-of-heterozygosity in childhood and adult tumors, and gain-of-imprinting in hepatocarcinomas and breast cancers. Despite the importance of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5491e01711905176cfcff62ed4f1789a
https://pubmed.ncbi.nlm.nih.gov/18996451
https://pubmed.ncbi.nlm.nih.gov/18996451
Publikováno v:
Gene. 424(1-2)
The SLC22A18/SLC22A18AS genes are a sense–antisense pair located at human chromosome segment 11p15.5. These genes are paternally imprinted: paternal alleles are silenced and maternal alleles are expressed. Although SLC22A18 is a well-characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc5b0968ad54d7e7cc657ad2246966fa
https://pubmed.ncbi.nlm.nih.gov/18721868
https://pubmed.ncbi.nlm.nih.gov/18721868
Autor:
Arun, Kumar, Manjunath G, Basavaraj, Santosh K, Gupta, Imteyaz, Qamar, Abdullah Mahmood, Ali, Vineeta, Bajaj, T K, Ramesh, D Ravi, Prakash, Jyoti S, Shetty, Syril K, Dorairaj
Publikováno v:
Molecular Vision
Purpose Mutations in the CYP1B1, MYOC, OPTN, and WDR36 genes result in glaucoma. Given its expression in the optic nerve, it is likely a mutation in the OPTC gene is also involved in initiating glaucoma. This study was designed to evaluate the involv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::824e8d392d53152c9bbc1c21ae8d0627
https://pubmed.ncbi.nlm.nih.gov/17563717
https://pubmed.ncbi.nlm.nih.gov/17563717