Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Venkateshwari Ananthapur"'
Publikováno v:
Middle East Fertility Society Journal, Vol 29, Iss 1, Pp 1-10 (2024)
Abstract Background Three or more consecutive pregnancy losses before the 20th week of gestation constitute recurrent pregnancy loss (RPL), and about half of these cases are still unsolved despite routine screening tests. The purpose of the current s
Externí odkaz:
https://doaj.org/article/7907901443174da1a3032426cc914269
Autor:
Sunitha Tella, Shehnaz Sultana, Sujatha Madireddy, Pratibha Nallari, Venkateshwari Ananthapur
Publikováno v:
Indian Journal of Dermatology, Vol 67, Iss 1, Pp 45-49 (2022)
Epidermolysis bullosa (EB) is a group of rare inherited conditions that results in blistering of the skin and mucous membranes. Mutations in the PLEC gene cause epidermolysis bullosa simplex (EBS). Mutations in type VII collagen, encoded by COL7A1 le
Externí odkaz:
https://doaj.org/article/4589e7971df648c89c6a186dedf8e80c
Autor:
Shilpa Reddy, Sailaja Maddhuri, Pratibha Nallari, Venkateshwari Ananthapur, Srinivas Kalyani, Murali Krishna, Nirmala Cherkuri, Sireesha Patibandala
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-11 (2021)
Abstract Background Type 1 diabetes mellitus (TIDM) is a polygenic disorder with the involvement of several genetic and environmental risk factors. Mutation in genes namely ABCC8 and KCNJ11 disrupt the potentiality of KATP channel and regulates the s
Externí odkaz:
https://doaj.org/article/c48c1a6b15ac42bb8e21574b29aca806
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 3, Iss 2, Pp 113-117 (2020)
Background: Down Syndrome is a genetic disorder caused by abnormal cell division, resulting in extra genetic material from chromosome 21. Non-homologous Robertsonian translocation (RT) between chromosomes 13 and 14 is a common genetic abnormality see
Externí odkaz:
https://doaj.org/article/a48559d242de4c1aa509f269c883cce0
Autor:
Krishnaveni Devulapalli, Amar Chand Bhayal, Shravan Kumar Porike, Ramanna Macherla, Jyothy Akka, Pratibha Nallari, Venkateshwari Ananthapur
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 20, Iss 5, Pp 309-314 (2014)
Background/Aims: Gastric cancer (GC) is a multifactorial disorder mediated by genetic, epigenetic, and environmental risk factors. GC is the most common cancer in India and it is the third prominent cause of cancer death worldwide. A single nucleotid
Externí odkaz:
https://doaj.org/article/c0d7f3b57ef143849ea73645ae2a17c4
Autor:
Sameera F. Qureshi, Altaf Ali, Venkateshwari Ananthapur, M.P. Jayakrishnan, Narasimhan Calambur, Kumarasamy Thangaraj, Pratibha Nallari
Publikováno v:
Indian Heart Journal, Vol 65, Iss 5, Pp 552-560 (2013)
Background: Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends on mutations in K+ channel genes. A family of a Long QT syndrome proband from India has been identified with novel ind
Externí odkaz:
https://doaj.org/article/a0fe3c91cae94a15aa3fd47ea66fc488
Autor:
Srimanjari Kavutharapu, Balakrishna Nagalla, Vidyasagar Abbagani, Shravan K Porika, Jyothy Akka, Pratibha Nallari, Venkateshwari Ananthapur
Publikováno v:
The Saudi Journal of Gastroenterology, Vol 18, Iss 6, Pp 364-368 (2012)
Background/Aim: Chronic pancreatitis (CP) is the progressive and irreversible destruction of the pancreas characterized by the permanent loss of endocrine and exocrine function. Trypsin, the most important digestive enzyme plays a central role in the
Externí odkaz:
https://doaj.org/article/c083fb3da5c44b6d99c435b828cfefc9
Autor:
Lova Satyanarayana Matsa, Advithi Rangaraju, Viswamitra Vengaldas, Mona Latifi, Hossein Mehraban Jahromi, Venkateshwari Ananthapur, Pratibha Nallari
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e70523 (2013)
Dilated Cardiomyopathy (DCM) is characterized by systolic dysfunction, followed by heart failure necessitating cardiac transplantation. The genetic basis is well established by the identification of mutations in sarcomere and cytoskeleton gene/s. Mod
Externí odkaz:
https://doaj.org/article/a68a723b80a24037bf7fc1035198b1fe
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
An 8-year-old boy was referred to our institute with dysmorphic features such as mild lupus, micrognathia, low hair line, hypoplasia, hemi atrophy of left side of the face, abnormal size of ears, hypothenar, hypoplasia of chin, and tongue tie. MRI sc
Externí odkaz:
https://doaj.org/article/bf18dbbd24e54d10abea79e2e8344d4f
Autor:
Kumar, C. Sandeep, Ali, Altaf, Manchineela, Sairam, Venkateshwari, Ananthapur, Narasimhan, Calambur, Nallari, Pratibha
Publikováno v:
In Journal of Indian College of Cardiology September 2018 8(3):127-131