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Preeti Paliwal

Showing results (11-20 of 28) with videos related to

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Molecular Human Reproduction|January 19, 2011
Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotypePreeti Paliwal, Anshul Sharma, Shweta Birla, et al.
Journal of Pediatric Genetics|August 4, 2020
Severe Polyhydramnios with Consistent Fetal Full Bladder: A Novel Sign of Antenatal Bartter's DiseaseSeema Thakur, Manisha Kumar, Supriya Malhotra, et al.
Fetal and Pediatric Pathology|August 23, 2024
Revisiting Utility of Fetal Autopsy in Genomic EraSeema Thakur, Chanchal Singh, Preeti Paliwal, et al.
Ophthalmic Research|January 21, 2012
Molecular genetic analysis of macular corneal dystrophy patients from North IndiaPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Ophthalmic Research|March 31, 2011
A novel TGFBI phenotype with amyloid deposits and Arg124Leu mutationPreeti Paliwal, Jaya Gupta, Radhika Tandon, et al.
Molecular Genetics and Metabolism|July 25, 2024
In vitro treatment with liposome-encapsulated Mannose-1-phosphate restores N-glycosylation in PMM2-CDG patient-derived fibroblastsTeppei Shirakura, Lakshmipriya Krishnamoorthy, Preeti Paliwal, et al.
The Indian Journal of Surgery|March 25, 2016
Prospective Case-Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic SignificanceVirinder Kumar Bansal, Karthik Rajan, Arundhati Sharma, et al.
Molecular Vision|January 5, 2011
Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohortPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Molecular Vision|August 4, 2010
TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophiesPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Oncotarget|May 25, 2015
Systemic attenuation of the TGF-β pathway by a single drug simultaneously rejuvenates hippocampal neurogenesis and myogenesis in the same old mammalHanadie Yousef, Michael J Conboy, Adam Morgenthaler, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Molecular Human Reproduction|January 19, 2011
Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotypePreeti Paliwal, Anshul Sharma, Shweta Birla, et al.
Journal of Pediatric Genetics|August 4, 2020
Severe Polyhydramnios with Consistent Fetal Full Bladder: A Novel Sign of Antenatal Bartter's DiseaseSeema Thakur, Manisha Kumar, Supriya Malhotra, et al.
Fetal and Pediatric Pathology|August 23, 2024
Revisiting Utility of Fetal Autopsy in Genomic EraSeema Thakur, Chanchal Singh, Preeti Paliwal, et al.
Ophthalmic Research|January 21, 2012
Molecular genetic analysis of macular corneal dystrophy patients from North IndiaPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Ophthalmic Research|March 31, 2011
A novel TGFBI phenotype with amyloid deposits and Arg124Leu mutationPreeti Paliwal, Jaya Gupta, Radhika Tandon, et al.
Molecular Genetics and Metabolism|July 25, 2024
In vitro treatment with liposome-encapsulated Mannose-1-phosphate restores N-glycosylation in PMM2-CDG patient-derived fibroblastsTeppei Shirakura, Lakshmipriya Krishnamoorthy, Preeti Paliwal, et al.
The Indian Journal of Surgery|March 25, 2016
Prospective Case-Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic SignificanceVirinder Kumar Bansal, Karthik Rajan, Arundhati Sharma, et al.
Molecular Vision|January 5, 2011
Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohortPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Molecular Vision|August 4, 2010
TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophiesPreeti Paliwal, Arundhati Sharma, Radhika Tandon, et al.
Oncotarget|May 25, 2015
Systemic attenuation of the TGF-β pathway by a single drug simultaneously rejuvenates hippocampal neurogenesis and myogenesis in the same old mammalHanadie Yousef, Michael J Conboy, Adam Morgenthaler, et al.
Pageof 3