Genetic variation in exon 5 of troponin - I gene in hypertrophic cardiomyopathy cases

Por Annapurna, S. D., Reena, T. R., Nallari, Pratibha, Calambur, Narasimhan
Publicado em 2007

t-plasminogen activator inhibitor-1 polymorphism in idiopathic pulmonary arterial hypertension

Por Katta, Sujana, Vadapalli, Shivani, Sastry, B. K. S., Nallari, Pratibha
Publicado em 2008

Endothelin-1 and endothelial nitric oxide polymorphisms in idiopathic pulmonary arterial hypertension

Por Vadapalli, Shivani, Rani, H Surekha, Sastry, BKS, Nallari, Pratibha
Publicado em 2010

Paternally derived translocation t(8;18)(q22.1;q22)pat associated in a patient with developmental delay: Case report and review

Por Rao, Lakshmi, Kanakavalli, Murthy, Padmalatha, Venkata, Nallari, Pratibha, Singh, Lalji
Publicado em 2010

A Dysmorphic Child with a Pericentric Inversion of Chromosome 8

Por Ananthapur, Venkateshwari, Avvari, Srilekha, Madireddi, Sujatha, Nallari, Pratibha, Akka, Jyothy
Publicado em 2012

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

Por Tanjore, Reena R, Rangaraju, Advithi, Kerkar, PG, Calambur, Narsimhan, Nallari, Pratibha
Publicado em 2008

Plasma TGF-β1, MMP-1 and MMP-3 Levels in Chronic Pancreatitis

Por Sri Manjari, K., Nallari, Pratibha, Vidyasagar, A., Jyothy, A., Venkateshwari, A.
Publicado em 2011

The Genetic Bases of Uterine Fibroids; A Review

Por Medikare, Veronica, Kandukuri, Lakshmi Rao, Ananthapur, Venkateshwari, Deenadayal, Mamata, Nallari, Pratibha
Publicado em 2011

A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)

Por Rani, Deepa Selvi, Dhandapany, Perundurai S., Nallari, Pratibha, Narasimhan, Calambur, Thangaraj, Kumarasamy
Publicado em 2014

miRNA regulation during cardiac development and remodeling in cardiomyopathy

Por Chaitra, K.L., Ulaganathan, Kayalvili, James, Anita, Ananthapur, Venkateshwari, Nallari, Pratibha
Publicado no EXCLI J (2013)

A novel chromosomal translocation and heteromorphism in a female with recurrent pregnancy loss—a case study

Por Ananthapur, Venkateshwari, Avvari, Srilekha, Cingeetham, Vinod, Maddireddi, Sujatha, Nallari, Pratibha, Akka, Jyothy
Publicado em 2012

Evaluation of Interleukin-10 (G-1082A) Promoter Polymorphism in Preeclampsia

Por Sowmya, Sabnavis, Ramaiah, Aruna, Sunitha, Tella, Nallari, Pratibha, Jyothy, Akka, Venkateshwari, Ananthapur
Publicado em 2013

A functional polymorphism in the promoter region of interleukin-10 gene increases the risk for spontaneous abortions—a triad study

Por Vidyadhari, M., Sujatha, M., Krupa, P., Jyothy, A., Nallari, Pratibha, Venkateshwari, A.
Publicado no J Assist Reprod Genet (2015)

Linkage analysis of three families with arrythmogenic right ventricular cardiomyopathy in India

Por Dokuparthi, Maithili V.N., Pamuru, Pranathi R, Oruganti, Sai S, Calambur, Narsimhan, Nallari, Pratibha
Publicado em 2009

Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy

Por Tanjore, Reena, RangaRaju, Advithi, Vadapalli, Shivani, Remersu, Sushant, Narsimhan, Calambur, Nallari, Pratibha
Publicado em 2010

Role of Plasma MMP 9 levels in the Pathogenesis of Chronic Pancreatitis

Por Venkateshwari, A., Sri Manjari, K., Krishnaveni, D., Nallari, Pratibha, Vidyasagar, A., Jyothy, A.
Publicado em 2011

Novel mutations in arrhythmogenic right ventricular cardiomyopathy from Indian population

Por Pamuru, Pranathi Rao, Maithili, D. V. N., Mohiuddin, Khalid, Calambur, Narasimhan, Nallari, Pratibha
Publicado em 2011

Genetic variations of α-cardiac actin and cardiac muscle LIM protein in hypertrophic cardiomyopathy in South India

Por Rangaraju, Advithi, Rani, Deepa Selvi, Satyanarayana, ML, Calambur, Narasimhan, Swapna, Nalla, Nallari, Pratibha
Publicado em 2012

High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians

Por Rani, Deepa Selvi, Nallari, Pratibha, Priyamvada, Singh, Narasimhan, Calambur, Singh, Lalji, Thangaraj, Kumarasamy
Publicado em 2012

Transferrin (rs3811647) gene polymorphism in iron deficiency anemia

Por Manjari, K Sri, Teja, KSPS, Sujatha, M, Jyothy, A, Nallari, Pratibha, Venkateshwari, A
Publicado em 2014