Results 21 to 30 of about 188,907 (313)
International Journal of Reproductive BioMedicine, 2021 Background: Lymphoid-tyrosine-phosphatase which is encoded by the protein tyrosine phosphatase non-receptor 22 (PTPN22) gene plays a pivotal role in the regulation of immune responses by dephosphorylating several signaling intermediates of immune cells ...
Fateme Khanbarari +3 more
doaj +1 more source
International Journal of Reproductive BioMedicine, 2022 Background: Primary ovarian insufficiency (POI) is a rare disease clinically characterized by ovarian follicles depletion or dysfunction and menopause before the age of 40 yr as the cut-off age for POI.
Farzaneh Sadat Eshaghi +3 more
doaj +1 more source
Histopathological and molecular study of Neospora caninum infection in bovine aborted fetuses
Asian Pacific Journal of Tropical Biomedicine, 2014 Objective: To estimate the extent to which abortion in dairy cows was associated with of Neospora caninum (N. caninum) and to determine the risk factors of neosporosis in dairy farms from 9 provinces in Iran. Methods: Polymerase chain reaction (PCR) test
Amir Kamali +4 more
doaj +1 more source
Veterinary Medicine and Science, 2022 Background Many studies in dairy cows are towards calcium homeostasis and there is a lack of knowledge about the effect of vitamin D in preventing insulin resistance and improving energy balance in the transition period of dairy cows.
Morteza Hassanabadi +2 more
doaj +1 more source
Human Reproduction, 2017 Abortion is common. Data on abortion rates are inexact but can be used to explore trends. Globally, the estimated rate in the period 2010-2014 was 35 abortions per 1000 women (aged 15-44 years), five points less than the rate of 40 for the period 1990-1994.
S. Cameron +12 more
openaire +3 more sources
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Annals of Clinical and Translational Neurology, EarlyView.Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao +34 more
wiley +1 more source
International Journal of Reproductive BioMedicine, 2022 Background: Premature ovarian failure (POF), is menopause occurring before the age of 40, affecting 1-3% of women worldwide. The risk of POF increases with altered immunological parameters such as FAS and FASL genes, which play a fundamental role in ...
Zhima Akhavansales +8 more
doaj +1 more source
Frontiers in Global Women's Health, 2022 Telehealth, one of the newest health innovations, has been promoted as a tool to enhance access to health care services in ways that center patient needs. However, integrating telehealth within an inequitable health system undermines its potential.
Terri-Ann Thompson +2 more
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Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT MRPS14 (uS14m) is a nuclear‐encoded ribosomal protein important for mitochondria‐specific translation. To date, only a single individual with a recessive MRPS14‐related disorder (also known as COXPD38) has been reported. We report an additional subject possessing novel compound heterozygous MRPS14 variants (p.Asp37Asn, p.Asn60Asp). The subject
Maria Gabriela Otero +15 more
wiley +1 more source
Evaluation of NF1 and RASA1 gene expression in endometriosis
European Journal of Obstetrics & Gynecology and Reproductive Biology: X, 2022 Background: Endometrios affecting 6–10% of women of reproductive ages around the globe. Important pathways, including the MAPK and PI3K / Akt pathways, have been identified in the disease.
Ghafour Yarahmadi +5 more
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