Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maria Celestina Vanaja"'
Autor:
Veronica Arora, Nitika Setia, Ashwin Dalal, Maria Celestina Vanaja, Deepti Gupta, Tinku Razdan, Shubha R. Phadke, Renu Saxena, Anshu Rohtagi, Ishwar C. Verma, Ratna Dua Puri
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 22, Iss , Pp - (2020)
Sialidosis, an autosomal recessive disorder, is characterized by progressive lysosomal storage of sialylated glycopeptides and oligosaccharides. It occurs as a result of biallelic mutations in the NEU1 gene. Sialidosis is traditionally classified as
Externí odkaz:
https://doaj.org/article/c585e0f01cc24b8ea61b7c8bc29accae
Autor:
Maheshwar Lakkireddy, Vijaykrishna Chilakamarri, Prajnya Ranganath, Abhishek Jagdishchander Arora, Maria Celestina Vanaja
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 8, Pp RD01-RD03 (2015)
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by congenital malformation of the great toes and disabling heterotopic ossification in specific anatomic locations with a world wide prevalence of 1 in 2 million po
Externí odkaz:
https://doaj.org/article/c750a9527258453ba267515ad1fd45aa
Publikováno v:
Global Journal of Computer Science and Technology. :19-20
Artificial Neural Networks Field (ANN Field) is an exciting field of research. ANN field took its inspiration from Human Brain. The heart and Brain are very important for the survival of Humans. Research Scientists published many articles by giving i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c855255eea77ed4c4fe3d54cb0e5c187
https://doi.org/10.34257/gjcstdvol21is1pg19
https://doi.org/10.34257/gjcstdvol21is1pg19
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 36:825-831
Aim: To investigate whether the interferon-γ (IFNG) gene dinucleotide (CA)-repeat polymorphism is responsible in part for genetic susceptibility to endometriosis in South Indian women. Methods: Following extraction of genomic DNA, genotyping of inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64dc688575670079385869364b56c313
https://doi.org/10.1111/j.1447-0756.2010.01201.x
https://doi.org/10.1111/j.1447-0756.2010.01201.x
Autor:
Prajnya Ranganath, Vijaykrishna Chilakamarri, Maheshwar Lakkireddy, Maria Celestina Vanaja, Abhishek J. Arora
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 8, Pp RD01-RD03 (2015)
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by congenital malformation of the great toes and disabling heterotopic ossification in specific anatomic locations with a world wide prevalence of 1 in 2 million pop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0959adb116c107bd8594657cc69eb547
https://doi.org/10.7860/jcdr/2015/15160.6393
https://doi.org/10.7860/jcdr/2015/15160.6393
Publikováno v:
Frontiers in bioscience (Elite edition). 5(2)
The present study was designed to explore the association between the SNP +405GC of the VEGF gene with the risk of endometriosis, and endometriosis associated with adenomyosis and chocolate cysts. Following extraction of genomic DNA, genotyping of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7589bc164f09be8d9ad94235280b3afa
https://pubmed.ncbi.nlm.nih.gov/23277029
https://pubmed.ncbi.nlm.nih.gov/23277029
Publikováno v:
The journal of obstetrics and gynaecology research. 36(4)
To investigate whether the interferon-gamma (IFNG) gene dinucleotide (CA)-repeat polymorphism is responsible in part for genetic susceptibility to endometriosis in South Indian women.Following extraction of genomic DNA, genotyping of interferon-gamma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da6a6f3462eed551b21bd2aef5cba4a0
https://pubmed.ncbi.nlm.nih.gov/20666952
https://pubmed.ncbi.nlm.nih.gov/20666952
Objectives To evaluate the efficacy of in vitro fertilization (IVF) and intra-uterine insemination (IUI) in couples with unexplained and mild male factor infertility.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8b0aaf33038770fba608a4635b547f
https://europepmc.org/articles/PMC3394493/
https://europepmc.org/articles/PMC3394493/
Publikováno v:
Journal of Obstetrics & Gynaecology Research; Oct2010, Vol. 36 Issue 5, p1149-1149, 1p