Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Anupam Kaur"'
Publikováno v:
Heliyon, Vol 10, Iss 13, Pp e33494- (2024)
The etiology of PCOS is complex and frequently mis or undiagnosed, which may enhance morbidity and reduce the quality of life. Attenuated total reflection- Fourier transform infrared (ATR-FTIR) spectroscopy examines the structural fingerprints of the
Externí odkaz:
https://doaj.org/article/5bf5c97a86e049bdb740d22ef6edf425
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract This study was conducted to analyze the association of Luteinizing Hormone/Choriogonadotropin Receptor (LHCGR) gene rs4953616 and rs7371084 polymorphisms with the risk of polycystic ovary syndrome (PCOS) in Punjab, India. A total of 823 wome
Externí odkaz:
https://doaj.org/article/8f92b521fb43483985f752066c38be4e
Publikováno v:
Journal of Ovarian Research, Vol 16, Iss 1, Pp 1-13 (2023)
Abstract Background Two polymorphisms, rs6165 and rs6166 located in the intracellular domain of FSHR has been reported to affect folliculogenesis, steroidogenesis and oocyte maturation. Several studies have highlighted the role of FSHR polymorphisms
Externí odkaz:
https://doaj.org/article/8948d3e11e994b02ba55ea19cdd9ae31
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Polycystic ovary syndrome (PCOS) is an endocrine-metabolic disorder that affects women at their child bearing age. The exact etiology is uncertain, however the involvement of multiple genes and environmental interactions has been
Externí odkaz:
https://doaj.org/article/ab011c3482f647e1a743805f9d5de359
Publikováno v:
Korean Journal of Clinical Laboratory Science, Vol 54, Iss 4, Pp 316-324 (2022)
Polycystic ovary syndrome (PCOS) is a complex endocrinopathy in women of reproductive age. The genetics of PCOS is heterogeneous with the involvement of number of genes in the steroid synthesis pathway. The CYP11B2 encodes aldosterone synthase and th
Externí odkaz:
https://doaj.org/article/87477bc1f4d746548b8091d95ff97f33
Autor:
Avinash Sharma, Pooja Chauhan, Khushboo Sharma, Vishali Kalotra, Anupam Kaur, Pooja Chadha, Sukhraj Kaur, Amarjeet Kaur
Publikováno v:
BMC Microbiology, Vol 22, Iss 1, Pp 1-17 (2022)
Abstract Background Oxidative stress is responsible for the onset of several chronic and degenerative diseases. Exogenous supply of antioxidants is reported to neutralize the effects of oxidative stress. Several synthetic antioxidants suffer from var
Externí odkaz:
https://doaj.org/article/7203d6c8786b495dbbce45c5bee030aa
Publikováno v:
Indian Journal of Public Health, Vol 67, Iss 3, Pp 477-479 (2023)
Heavy metals are capable of inducing toxicity even at lower levels and the contamination adversely impact humans, animals, and plants thus, resulting in variety of health issues. Thus, the present study investigated the presence of metals in the seru
Externí odkaz:
https://doaj.org/article/c7ba6d7ef85c4e50bebd0d5209a78480
Publikováno v:
Korean Journal of Clinical Laboratory Science, Vol 54, Iss 1, Pp 1-8 (2022)
Erythrocyte sedimentation rate (ESR) evaluation is a useful tool for monitoring disease activity in various inflammatory and non-inflammatory conditions. ESR is known to be influenced by a multitude of confounding factors. The present study aimed t
Externí odkaz:
https://doaj.org/article/5127f2e5fc6945408b3e6e6a0627a9f5
Autor:
Amandeep Kaur, Anupam Kaur
Publikováno v:
Tzu-Chi Medical Journal, Vol 34, Iss 4, Pp 456-461 (2022)
Objectives: Folates are essential nutrients required for the synthesis of DNA/RNA in cell division and segregation. Folates are reduced and methylated in the liver with the help of enzymes such as methylenetetrahydrofolate reductase (MTHFR), MTR MTRR
Externí odkaz:
https://doaj.org/article/0d5f9ad8ea534b3ab0d404b145a06dd2
Publikováno v:
Journal of Human Reproductive Sciences, Vol 10, Iss 4, Pp 302-309 (2017)
Background: About 15%–20% of couples get affected by recurrent miscarriages (RM) and chromosomal abnormality in one partner affects 3%–6% of RM couples. Aims: The present study aimed to determine the prevalence of cytogenetic anomalies in couples
Externí odkaz:
https://doaj.org/article/a83201aeac904b089ef0b77fd24c4dfc