Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sheila Mohan"'
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227603 (2020)
In-vitro studies with different Fanconi anemia (FA) cell lines and FANC gene silenced cell lines indicating involvement of mitochondria function in pathogenesis of FA have been reported. However, in-vivo studies have not been studied so far to unders
Externí odkaz:
https://doaj.org/article/57e4ea4b92b4451681d6ee8150390d95
Autor:
Josephine C. Dorsman, Marieke Levitus, Davy Rockx, Martin A. Rooimans, Anneke B. Oostra, Anneke Haitjema, Sietske T. Bakker, Jûrgen Steltenpool, Dezsö Schuler, Sheila Mohan, Detlev Schindler, Fré Arwert, Gerard Pals, Christopher G. Mathew, Quinten Waisfisz, Johan P. de Winter, Hans Joenje
Publikováno v:
Cellular Oncology, Vol 29, Iss 3, Pp 211-218 (2007)
To identify the gene underlying Fanconi anemia (FA) complementation group I we studied informative FA-I families by a genome-wide linkage analysis, which resulted in 4 candidate regions together encompassing 351 genes. Candidates were selected via bi
Externí odkaz:
https://doaj.org/article/1d446edcb77d4052afe9b566c074090a
Autor:
Sheila Mohan, Merin George, Aruna Rajendran, Babu Rao Vundinti, Avani Solanki, Purvi Mohanty, Somprakash Dhangar
Publikováno v:
Molecular Biology Reports. 48:2519-2525
Fanconi anemia (FA) occurs due to genomic instability with predisposition to bone marrow failure, phenotypic abnormalities and cancers. Though mutations in 22 genes leading to DNA repair defect have been identified, the cellular factor such as oxidat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ba243e388c4de394a6d5c865eb6ee59
https://doi.org/10.1007/s11033-021-06293-1
https://doi.org/10.1007/s11033-021-06293-1
Autor:
Sheila Mohan, Anjali Shah, Merin George, Babu Rao Vundinti, Somprakash Dhangar, Aruna Rajendran
Publikováno v:
Molecular Biology Reports. 48:585-593
Fanconi Anemia (FA) is a rare genetic disease with the incidence of 1 in 360,000 and is characterised by bone marrow failure, physical abnormalities, pancytopenia, and high frequency of chromosomal breakage and increased risk of evolving into maligna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18afdd71fdc6cac5b0752f214f1c774a
https://doi.org/10.1007/s11033-020-06101-2
https://doi.org/10.1007/s11033-020-06101-2
Autor:
Binita Zipporah E, Pavithra Shyamsunder, Kavitha Govarthanan, Rajesh Yadav, Sheila Mohan, Rama Shanker Verma, Bamadeb Patra
Publikováno v:
Genomics. 112:4628-4639
Fanconi Anemia (FA) is an inherited bone marrow failure syndrome caused by mutation in FA pathway proteins, involved in Interstrand Cross Link (ICL) repair. FA cells exhibit in vitro proliferation arrest due to accumulated DNA damage, hence understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb3a3caccca33faabfc937e89418e4f
https://doi.org/10.1016/j.ygeno.2020.08.009
https://doi.org/10.1016/j.ygeno.2020.08.009
Autor:
Chandrakala Shanmukhaiah, Revathi Raj, Sowmyashree Ramesh, Sunil Bhat, Merin George, Shailesh Kanvinde, Nita Radhakrishnan, Avani Solanki, Niranjan Chavan, Sheila Mohan, Aruna Rajendran, Deendayalan Munirathnam, Pritesh Junagade, Sandeep Nemani, Anchu Anna Cherian, Mamta Manglani, Harsha Prasada Lashkari, Radha Gulati Ghildhiyal, Sudha Rao, Babu Rao Vundinti
Publikováno v:
Human mutationREFERENCES. 42(12)
Fanconi anemia (FA) is a rare autosomal or X-linked genetic disorder characterized by chromosomal breakages, congenital abnormalities, bone marrow failure (BMF), and cancer. There has been a discovery of 22 FANC genes known to be involved in the FA p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94cdd9e4daca6faddb9ccf86bd09dcc5
https://pubmed.ncbi.nlm.nih.gov/34585473
https://pubmed.ncbi.nlm.nih.gov/34585473
Autor:
Frank X. Donovan, Kenichi Yoshida, Minoru Takata, Agata Smogorzewska, Babu Rao Vundinti, Avani Solanki, Akifumi Takaori-Kondo, Niranjan Chavan, Yusuke Okuno, Selvaa Kumar C, Minako Mori, Settara C. Chandrasekharappa, Seiji Kojima, Merin George, Hiromasa Yabe, Seishi Ogawa, Sheila Mohan, Arleen D. Auerbach, Aruna Rajendran, Miharu Yabe, Hideki Muramastsu, Ramanagouda Ramanagoudr-Bhojappa, Akira Shimamoto
Publikováno v:
Hum Mutat
Fanconi anemia (FA) is a rare genetic disorder characterized by bone marrow failure, predisposition to cancer, and congenital abnormalities. FA is caused by pathogenic variants in any of 22 genes involved in the DNA repair pathway responsible for rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0cf1057a5d78838591eeaf71993515
https://doi.org/10.1002/humu.23914
https://doi.org/10.1002/humu.23914
Autor:
Merin, George, Avani, Solanki, Purvi, Mohanty, Somprakash, Dhangar, Aruna, Rajendran, Sheila, Mohan, Babu Rao, Vundinti
Publikováno v:
Molecular biology reports. 48(3)
Fanconi anemia (FA) occurs due to genomic instability with predisposition to bone marrow failure, phenotypic abnormalities and cancers. Though mutations in 22 genes leading to DNA repair defect have been identified, the cellular factor such as oxidat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::efd26c716263d39b20200818b838c593
https://pubmed.ncbi.nlm.nih.gov/33778919
https://pubmed.ncbi.nlm.nih.gov/33778919
Autor:
Anjali, Shah, Merin, George, Somprakash, Dhangar, Aruna, Rajendran, Sheila, Mohan, Babu Rao, Vundinti
Publikováno v:
Molecular biology reports. 48(1)
Fanconi Anemia (FA) is a rare genetic disease with the incidence of 1 in 360,000 and is characterised by bone marrow failure, physical abnormalities, pancytopenia, and high frequency of chromosomal breakage and increased risk of evolving into maligna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::678eb3eda46621c9dab4d72bfcc44f07
https://pubmed.ncbi.nlm.nih.gov/33394227
https://pubmed.ncbi.nlm.nih.gov/33394227
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 1, p e0227603 (2020)
PLoS ONE, Vol 15, Iss 1, p e0227603 (2020)
In-vitro studies with different Fanconi anemia (FA) cell lines and FANC gene silenced cell lines indicating involvement of mitochondria function in pathogenesis of FA have been reported. However, in-vivo studies have not been studied so far to unders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca1d84ecad687a2839271035256df1b
http://europepmc.org/articles/PMC6961948
http://europepmc.org/articles/PMC6961948