V. Ananthapur

发表

Endothelin 1 gene as a modifier in dilated cardiomyopathy.

S. R. Sagurthi, P. Nallari, Lova Satyanarayana Matsa, 2014, Gene.

Synergistic Effects of Andrographolide on DNA Damage Repair Mechanism and Apoptosis in Breast Cancer Cells

P. Nallari, V. Ananthapur, Pushpanjali Pendyala, 2019 .

Association of estrogen receptor alpha gene polymorphisms with BMD and their affect on estradiol levels in pre- and postmenopausal women in south Indian population from Andhra Pradesh.

A. Munshi, V. Kolla, Jyothy Akka, 2010, Clinica chimica acta; international journal of clinical chemistry.

Association of ER-α gene PvuII polymorphism with ovarian cancer.

P. Nallari, Jyothy Akka, V. Ananthapur, 2018, Cancer treatment and research communications.

Heat shock protein 70 polymorphism in hypertrophic cardiomyopathy of South Indian cohort

P. Nallari, C. Narasimhan, V. Ananthapur, 2013 .

Novel mutations of KCNQ1 in Long QT syndrome.

K. Thangaraj, P. Nallari, M. P. Jayakrishnan, 2013, Indian heart journal.

A Case Report of Family with Congenital NonSyndromic Hearing Loss (NSHL) with Variants of Uncertain Significance (VUS) in GATA3 and COLA43 Genes

P. Nallari, Sujatha Madireddy, V. Ananthapur, 2021 .

Recurrent Pregnancy Loss (RPL): An overview

P. Nallari, V. Ananthapur, Shehnaz Sultana, 2020 .

miRNA regulation during cardiac development and remodeling in cardiomyopathy

P. Nallari, V. Ananthapur, K. Ulaganathan, 2013, EXCLI journal.

The Genetic Bases of Uterine Fibroids; A Review

P. Nallari, M. Deenadayal, V. Ananthapur, 2011, Journal of reproduction & infertility.

Role of Genetic Factors in the Causation of Non-Syndromic Hearing Loss (NSHL) in Indian Population

P. Nallari, V. Ananthapur, Shehnaz Sultana, 2020 .

Detection and evaluation of estrogen DNA‐adducts and their carcinogenic effects in cultured human cells using biotinylated estradiol

K. Tripathi, Chinnadurai Mani, Komaraiah Palle, 2017, Molecular carcinogenesis.

Inherited Robertsonian translocation (13;14) in a child with Down Syndrome

Sujatha Madireddy, V. Ananthapur, N. Mishra, 2020, Journal of Biochemical and Clinical Genetics.

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

P. Nallari, Jyothy Akka, V. Ananthapur, 2012, Journal of Assisted Reproduction and Genetics.

Covid-19 Infection and its Adverse Effects on Multiorgan

V. Ananthapur, P. Pardhanandana Reddy, Shehnaz Sultana, 2022, Archives of Internal Medicine Research.

Non‐Robertsonian translocation t (2;11) is associated with infertility in an oligospermic man

A. Jyothy, V. Ananthapur, M. Sujatha, 2014, Andrologia.

Role of Proteases and Antiprotease in the Etiology of Chronic Pancreatitis

P. Nallari, B. Nagalla, Jyothy Akka, 2012, Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association.

Haplotypes of NOS3 Gene Polymorphisms in Dilated Cardiomyopathy

P. Nallari, Lova Satyanarayana Matsa, V. Ananthapur, 2013, PloS one.

COVID-19 and its impact on neurological manifestations and mental health: the present scenario

V. Ananthapur, Shehnaz Sultana, 2020, Neurological Sciences.

Are Altered Expression of Vascular Endothelial Growth Factor and Placental Growth Factor Associated with Placental Angiogenesis in Recurrent Pregnancy Loss?

V. Ananthapur, Shehnaz Sultana, P. Reddy, 2023, Indian Journal of Clinical Biochemistry.

Role of Interstitial Collagenase Gene Promoter Polymorphism in the Etiology of Gastric Cancer

P. Nallari, Jyothy Akka, V. Ananthapur, 2014, Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association.

Maternal TCN1 (rs526934) G>A Gene Polymorphism and its Association with Congenital Heart Disease (CHD)

Jyothy Akka, V. Ananthapur, Shehnaz Sultana, 2020 .

A Dysmorphic Child with a Pericentric Inversion of Chromosome 8

P. Nallari, Jyothy Akka, V. Ananthapur, 2012, Case reports in pediatrics.

miRNA regulation during cardiac development and remodeling in cardiomyopathy

P. Nallari, V. Ananthapur, Chaitra Kl, 2013, EXCLI journal.

Identification of key functional pathways: arginine biosynthesis and IL-17 signalling in placental decidua of unexplained recurrent pregnancy loss through RNA sequencing—a case series

V. Ananthapur, Shehnaz Sultana, B. D. Bhanu, 2024, Middle East Fertility Society Journal.

Epidermolysis Bullosa: A Report of Three Cases with Novel Heterozygous Deletions in PLEC and Homozygous Non sense Mutations in COL7A1 Genes

P. Nallari, Sujatha Madireddy, V. Ananthapur, 2022, Indian journal of dermatology.