P. Paliwal

发表

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

P. Kaur, D. Dube, R. Tandon, 2011, Molecular vision.

Inhibitors of tyrosine phosphatases and apoptosis reprogram lineage-marked differentiated muscle to myogenic progenitor cells.

I. Conboy, P. Paliwal, 2011, Chemistry & biology.

Prospective Case–Control Study to Evaluate the Role of Glutathione S Transferases (GSTT1 and GSTM1) Gene Deletion in Breast Carcinoma and Its Prognostic Significance

M. Misra, K. Kucheria, V. Bansal, 2015, Indian Journal of Surgery.

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

I. Conboy, P. Paliwal, Novalia Pishesha, 2012, Aging.

Outcome of Prenatally-Detected Fetal Ventriculomegaly

P. Paliwal, S. Bijarnia-Mahay, I. Verma, 2015, Journal of Fetal Medicine.

Relevance of Molecular Diagnosis of Corneal Dystrophies

P. Paliwal, Arundhati Sharma, 2011 .

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

R. Tandon, Ranjan Gupta, N. Sharma, 2015, Molecular vision.

Molecular Genetic Analysis of Macular Corneal Dystrophy Patients from North India

R. Tandon, N. Sharma, R. Vajpayee, 2012, Ophthalmic Research.

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

R. Tandon, N. Sharma, R. Vajpayee, 2010, Molecular vision.

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

P. Kaur, D. Dube, R. Tandon, 2010, Molecular vision.

FISH is not Suitable as a Standalone Test for Detecting Fetal Chromosomal Abnormalities

P. Paliwal, I. Verma, M. Lall, 2015, Journal of Fetal Medicine.

BMC Molecular Biology BioMed Central Research article Regulation of p73 by Hck through kinase-dependent and

V. Radha, G. Swarup, P. Paliwal, 2007 .

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

R. Tandon, P. Paliwal, Arundhati Sharma, 2009, Molecular vision.

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

P. Kaur, D. Dube, R. Tandon, 2010, Molecular vision.

Spinal Myxopapillary Ependymoma With Down Syndrome: Exploring an Unusual Association

P. Julka, G. Rath, V. Suri, 2010, Journal of pediatric hematology/oncology.

Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype.

R. Khadgawat, A. Kriplani, P. Paliwal, 2011, Molecular human reproduction.

The changing scenario in prenatal diagnosis of genetic disorders: Genetics to genomics

S. Agarwal, R. Saxena, P. Paliwal, 2018, Current Medicine Research and Practice.

Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience

S. Agarwal, P. Paliwal, S. Bijarnia-Mahay, 2021, The Journal of Obstetrics and Gynecology of India.

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

D. Schaffer, H. Yousef, I. Conboy, 2015, Oncotarget.

Rare finding of 2n/4n mixoploidy in mother and fetus with severe immune hydrops

A. Sharma, P. Paliwal, V. Dadhwal, 2009, Cytogenetic and Genome Research.

Molecular characterization of supernumerary marker chromosomes found as unexpected chromosome abnormalities in nine prenatal and nine postnatal samples

S. Agarwal, P. Paliwal, I. Verma, 2019, Obstetrics & Gynecology International Journal.

A Novel TGFBI Phenotype with Amyloid Deposits and Arg124Leu Mutation

R. Tandon, S. Kashyap, S. Sen, 2011, Ophthalmic Research.

Clinical and genetic profile of Avellino corneal dystrophy in 2 families from north India.

R. Tandon, R. Vajpayee, P. Paliwal, 2009, Archives of ophthalmology.

Genetic Testing in Pediatric Ophthalmology

Kanika Singh, P. Paliwal, I. Verma, 2018, The Indian Journal of Pediatrics.

Abstract 332: Pharmacologic Characterization of the Cardiac Myosin Inhibitor, CK-3773274: A Potential Therapeutic Approach for Hypertrophic Cardiomyopathy

E. Chin, D. Hwee, B. Morgan, 2019, Circulation Research.

Severe Polyhydramnios with Consistent Fetal Full Bladder: A Novel Sign of Antenatal Bartter's Disease

S. Thakur, S. Malhotra, P. Paliwal, 2020, Journal of Pediatric Genetics.

A Good Family History , the First Step in Reaching a Diagnosis

Kanika Singh, P. Paliwal, I. Verma, 2017 .

Phosphofurin Acidic Cluster Sorting Protein 1 Syndrome: Insights Gained on the Multisystem Involvement Reviewing Encoded Protein Interactions?

P. Paliwal, Rajni Farmania, V. Garg, 2022, Journal of Pediatric Genetics.

Characterization of the Cardiac Myosin Inhibitor CK-3773274: a Potential Therapeutic Approach for Hypertrophic Cardiomyopathy

E. Chin, D. Hwee, T. Ewing, 2020 .

Practical Applications of Chromosomal Microarray in Prenatal Diagnosis

Vineet Sethia, P. Paliwal, C. Singh, 2023, Journal of Fetal Medicine.

An unusual association of hypospadias with partial deletion of chromosome 1q.

P. Paliwal, Arundhati Sharma, Jayaprakash Sahoo, 2010, Fertility and sterility.

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

I. Conboy, P. Paliwal, Novalia Pishesha, 2012, Aging.

Inhibitors of tyrosine phosphatases and apoptosis reprogram lineage-marked differentiated muscle to myogenic progenitor cells.

I. Conboy, P. Paliwal, 2011, Chemistry & biology.