Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mohammad Parwez Alam"'
Autor:
Eric D. Wieben, Vinod Kumar Yadav, Ram Krishna Thakur, Aradhita Baral, Tapas K. Kundu, Raj K. Pandita, Bruce W. Eckloff, Shantanu Chowdhury, Tej K. Pandita, Ankita Singh, Rashi Halder, Akinchan Kumar, Mohammad Parwez Alam
Publikováno v:
Nucleic Acids Research
Previous studies have analyzed patterns of transcription, transcription factor (TF) binding or mapped nucleosome occupancy across the genome. These suggest that the three aspects are genetically connected but the cause and effect relationships are st
Autor:
Vinod Scaria, Mohammad Parwez Alam, Beena Pillai, Shivani Gupta, Meghna Singh, Manali Garg, Tamer Ali, Ramya Purkanti, Rhishikesh Bargaje, Sridhar Sivasubbu, Ashok Patowary, Vani Brahmachari, Maharnob Sarkar
Publikováno v:
Nucleic Acids Research
Nucleosome positioning maps of several organisms have shown that Transcription Start Sites (TSSs) are marked by nucleosome depleted regions flanked by strongly positioned nucleosomes. Using genome-wide nucleosome maps and histone variant occupancy in
Autor:
Abhishek Kumar Mehta, Sonal Datta, Vani Brahmachari, Subeer S. Majumdar, Sujatha Baskaran, Mohammad Parwez Alam, Neerja Gulati
Publikováno v:
Epigenetics. 5:241-248
Methylation of CpG sequences in and around CGG triplet repeats in FMR1 gene has strong correlation with manifestation of the fragile X syndrome in human patients. In contrast, we have observed a lack of correlation between repeat instability and DNA
Autor:
Jinfeng Zhang, Hank W. Bass, Gregg G. Hoffman, Jonathan D J Labonne, S.B. Girimurugan, Karen M. McGinnis, Thelma F. Madzima, Mohammad Parwez Alam, Jonathan H. Dennis, Daniel L. Vera
The eukaryotic genome is organized into nucleosomes, the fundamental units of chromatin. The positions of nucleosomes on DNA regulate protein-DNA interactions and in turn influence DNA-templated events. Despite the increasing number of genome-wide ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7389fa8d0b516085a74c962cd3c52a4
https://europepmc.org/articles/PMC4247582/
https://europepmc.org/articles/PMC4247582/
Autor:
Vani Brahmachari, Sonal Datta, Subeer S. Majumdar, Abhishek Kumar Mehta, Mohammad Parwez Alam, Neerja Wadhwa, Souvik Maiti
Publikováno v:
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 19(4)
The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the molecular basis of fragile X syndrome in most of the patients. The nature of the flanking sequences in addition to the length and interruption pattern of repeats i
Autor:
Yadav, Vinod Kumar, Thakur, Ram Krishna, Eckloff, Bruce, Baral, Aradhita, Singh, Ankita, Halder, Rashi, Akinchan Kumar, Mohammad Parwez Alam, Kundu, Tapas K., Pandita, Raj, Pandita, Tej K., Wieben, Eric D., Chowdhury, Shantanu
Publikováno v:
Nucleic Acids Research; Sep2014, Vol. 42 Issue 15, p9602-9611, 10p, 1 Diagram, 4 Graphs