Regulation of p73 by Hck through kinase-dependent and independent mechanisms

por Paliwal, Preeti, Radha, Vegesna, Swarup, Ghanshyam
Publicado 2007

Age dependent increase in the levels of osteopontin inhibits skeletal muscle regeneration

por Paliwal, Preeti, Pishesha, Novalia, Wijaya, Denny, Conboy, Irina M
Publicado 2012

A novel VSX1 mutation identified in an individual with keratoconus in India

por Paliwal, Preeti, Singh, Anuradha, Tandon, Radhika, Titiyal, Jeevan S, Sharma, Arundhati
Publicado 2009

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus

por Paliwal, Preeti, Tandon, Radhika, Dube, Divya, Kaur, Punit, Sharma, Arundhati
Publicado 2011

Combined classical cytogenetics and array Comparative Genomic Hybridisation for genomic copy number analysis

por Lall, Meena, Saviour, Pushpa, Puri, Ratna, Paliwal, Preeti, Mahajan, Surbhi, Verma, Ishwar
Publicado 2014

Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort

por Paliwal, Preeti, Sharma, Arundhati, Tandon, Radhika, Sharma, Namrata, Titiyal, Jeewan S., Sen, Seema, Nag, Tapas C., Vajpayee, Rasik B.
Publicado 2010

TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies

por Paliwal, Preeti, Sharma, Arundhati, Tandon, Radhika, Sharma, Namrata, Titiyal, Jeewan S., Sen, Seema, Kaur, Punit, Dube, Divya, Vajpayee, Rasik B.
Publicado 2010

Systemic attenuation of the TGF-β pathway by a single drug simultaneously rejuvenates hippocampal neurogenesis and myogenesis in the same old mammal

por Yousef, Hanadie, Conboy, Michael J., Morgenthaler, Adam, Schlesinger, Christina, Bugaj, Lukasz, Paliwal, Preeti, Greer, Christopher, Conboy, Irina M., Schaffer, David
Publicado 2015

A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia

por Bajracharya, Luna, Lall, Meena, Bijarnia-Mahay, Sunita, Kumar, Praveen, Mushtaq, Imran, Saviour, Pushpa, Paliwal, Preeti, Joshi, Anju, Agarwal, Shruti, Suman, Praveen
Publicado 2023

Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy

por Paliwal, Preeti, Gupta, Jaya, Tandon, Radhika, Sharma, Namrata, Titiyal, Jeewan S., Kashyap, Seema, Sen, Seema, Kaur, Punit, Dube, Divya, Sharma, Arundhati, Vajpayee, Rasik B.
Publicado 2010

Association of ZEB1 and TCF4 rs613872 changes with late onset Fuchs endothelial corneal dystrophy in patients from northern India

por Gupta, Ranjan, Kumawat, Babu Lal, Paliwal, Preeti, Tandon, Radhika, Sharma, Namrata, Sen, Seema, Kashyap, Seema, Nag, Tapas Chandra, Vajpayee, Rasik B., Sharma, Arundhati
Publicado 2015