Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5

por Bajaj, Vineeta, Markandaya, Manjunath, Krishna, Lingegowda, Kumar, Arun
Publicado 2004

Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient cancer

por Mrozek, Evelyn M., Bajaj, Vineeta, Guo, Yanan, Malinowska, Izabela A., Zhang, Jianming, Kwiatkowski, David J.
Publicado 2021

Angiomyolipoma Have Common Mutations in TSC2 but No Other Common Genetic Events

por Qin, Wei, Bajaj, Vineeta, Malinowska, Izabela, Lu, Xin, MacConaill, Laura, Wu, Chin-Lee, Kwiatkowski, David J.
Publicado 2011

Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients

por Kumar, Arun, Basavaraj, Manjunath G., Gupta, Santosh K., Qamar, Imteyaz, Ali, Abdullah Mahmood, Bajaj, Vineeta, Ramesh, T.K., Prakash, D. Ravi, Shetty, Jyoti S., Dorairaj, Syril K.
Publicado 2007

A synthetic biology approach to probing nucleosome symmetry

por Ichikawa, Yuichi, Connelly, Caitlin F, Appleboim, Alon, Miller, Thomas CR, Jacobi, Hadas, Abshiru, Nebiyu A, Chou, Hsin-Jung, Chen, Yuanyuan, Sharma, Upasna, Zheng, Yupeng, Thomas, Paul M, Chen, Hsuiyi V, Bajaj, Vineeta, Müller, Christoph W, Kelleher, Neil L, Friedman, Nir, Bolon, Daniel NA, Rando, Oliver J, Kaufman, Paul D
Publicado 2017