Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Gayatri R Iyer"'
Autor:
Mina Darooei, Subhadra Poornima, Bibi Umae Salma, Gayatri R Iyer, Akhilesh N Pujar, Srirambhatla Annapurna, Ashwin Shah, Srinivas Maddali, Qurratulain Hasan
Publikováno v:
Tumor Biology, Vol 39 (2017)
Global burden of breast cancer is expected to increase to >2 million new cases every year by 2030 and 10% of these are likely to have hereditary breast and ovarian cancer syndrome. Identifying these individuals by pedigree and BRCA1/2 mutation analys
Externí odkaz:
https://doaj.org/article/33c2df15250d437ba06a386644edff4e
Autor:
Gayatri R. Iyer, Roshan Kumar, Subhadra Poornima, Aruna Priya Kamireddy, Keerthi Konda Juturu, Lekhangda Bhatnagar, Srinka Arora, Vaishnavi Suresh, Prashant R. Utage, Sarah Bailur, Akhilesh N. Pujar, Qurratulain Hasan
Publikováno v:
Journal of Orthopaedic Surgery and Research, Vol 17, Iss 1, Pp 1-10 (2022)
Abstract Background Disorders involving the musculoskeletal system are often identified with short stature and a range of orthopedic problems. The clinical and genetic heterogeneity of these diseases along with several characteristic overlaps makes d
Externí odkaz:
https://doaj.org/article/fb701ff063da4fd0a62b5fcb39629272
Autor:
Gayatri R. Iyer, Sayani Samajder, Syeda Zubeda, Devi Soorya Narayana S, Vishakha Mali, Sharath Krishnan PV, Anuradha Sharma, Neyha Zainab Abbas, Nandini Shyamali Bora, Amulya Narravula, Qurratulain Hasan
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Introduction: Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) has spread around the globe. Susceptibility has been associated with age, biological sex, and other prior existing health conditions. However, host genes are involved in viral
Externí odkaz:
https://doaj.org/article/740d9b9f98df462981fff3b0f4faca3e
Aim: Renal disorders (RDs) are heterogeneous in nature with different ages of onset ranging from in-utero to adults that arise as independent disease and also as syndromes. RDs are of both heritable and acquired type. The aim of this study was to uti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6fbc6305177ecf408297b3a601b59e0
https://doi.org/10.21203/rs.3.rs-1313278/v1
https://doi.org/10.21203/rs.3.rs-1313278/v1
Publikováno v:
Annals of human geneticsREFERENCES. 86(2)
Angelman syndrome (AS) (OMIM#105830) is an imprinting disorder caused due to alterations in the maternal chr 15q11-13 region. Majority of cases can be diagnosed by methylation-specific polymerase chain reaction (MS-PCR) of SNRPN gene and by UBE3A seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bbf12d368a8da7e873fddd85b880ea3
https://pubmed.ncbi.nlm.nih.gov/34779508
https://pubmed.ncbi.nlm.nih.gov/34779508
Autor:
Alla Karnovsky, Charles F. Burant, Gayatri R Iyer, Joyce M. Lee, Emily Hirschfeld, Jennifer L LaBarre, William H. Herman, Karen E. Peterson
Publikováno v:
Curr Dev Nutr
OBJECTIVES: To reveal alterations in metabolic pathways in response to an oral glucose tolerance test (OGTT) underlying the development of insulin resistance during the pubertal transition. METHODS: Participants were recruited as healthy controls (HC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ea76eb77d6cc91f9bc78de9f23c9f7b
https://europepmc.org/articles/PMC8181935/
https://europepmc.org/articles/PMC8181935/
Autor:
Aruna Priya, Lekhanga Bhatnagar, Gayatri R Iyer, Qurratulain Hasan, Srinka Arora, Subhadra Poornima, Prashanth Utage, Vaishnavi Suresh, Roshan Kumar, Akhilesh N Pujar, Sarah Bailur, Keerthi Konda Juturu
Background: Disorders involving the musculoskeletal system are often identified with short stature and a range of orthopedic problems. The clinical and genetic heterogeneity of these diseases, with several characteristic overlaps, makes specific diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96c52b8c4bb1dd1c2ecdc36cfd53dab6
https://doi.org/10.21203/rs.3.rs-431437/v1
https://doi.org/10.21203/rs.3.rs-431437/v1
Autor:
Gayatri R Iyer, Qurratulain Hasan
Publikováno v:
Environmental and molecular mutagenesisREFERENCES. 61(8)
DNA methylation is an epigenetic mechanism that regulates gene expression, which also facilitates genomic imprinting. Genomic imprinting is responsible for differential expression of genes based on parent of origin. Altered methylation of parental al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f5a1d5a2017ff96ed6b77ec9856938
https://pubmed.ncbi.nlm.nih.gov/32649027
https://pubmed.ncbi.nlm.nih.gov/32649027
Autor:
Sarah Bailur, Annapurna Srirambhatla, Gayatri R Iyer, Aparna Utage, Qurratulain Hasan, Prashant Utage
Publikováno v:
Journal of child neurology. 35(6)
Infection-induced acute encephalopathies (IIAEs) are a group of neurologic disorders caused post infection. They are of 8 types, 6 of which are herpes specific, whereas IIAE3 and IIAE4 can be triggered by infections additional to herpeslike influenza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a2399d937ba0bc08251d3e5fcf3d72
https://pubmed.ncbi.nlm.nih.gov/32102593
https://pubmed.ncbi.nlm.nih.gov/32102593