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Female Reproductive System

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Most cited protocols related to «Female Reproductive System»

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Publication 2015
alpha HML-1 Antibodies Bicarbonates BLOOD Buffers CD44 protein, human Cells Cervix Uteri Collagenase, Clostridium histolyticum Dithioerythritol Enzymes Female Reproductive System Flow Cytometry Hemoglobin, Sickle HEPES Hyperostosis, Diffuse Idiopathic Skeletal Intestines Intestines, Small isolation Kidney Lamina Propria Large Intestine Liver Lung Lymphocyte Matrix Metalloproteinase 2 Mucus Mus Needles Nodes, Lymph Nylons Pancreas Passive Immunization Percoll Polystyrenes Salivary Glands Spleen Stomach Streptavidin Syringes Thymus Plant Tissues Uterine Cornua Vagina
For immunofluorescence microscopy, tissues were frozen in 2-methylbutane surrounded by dry ice. Frozen blocks were cut into 7 μm sections, fixed in acetone, blocked in a 5% bovine serum albumin PBS solution for 1 h, and stained with DAPI (Invitrogen) and antibodies specific for Thy1.1 (OX-7), CD31 (390) and CD8β (YTS156.7.7) (Biolegend), IFN-γ (XMG12 and CD45.1 (A20) (eBioscience), CXCL9 (goat polyclonal) and CXCL11 (goat polyclonal) (R&D), CX3CL1 (rabbit polyclonal), ERTR-7, and cytokeratin 8/18 (rabbit polyclonal) (Novus Biologicals), Collagen IV (rabbit polyclonal) (Acris), or CXCL10 (rabbit polyclonal) (Peprotech). IFN-γ-PE staining was amplified using rabbit aντı–PE (Novus Biologicals). Jackson Immunoresearch secondary antibodies conjugated to various fluorochromes were used to stain unconjugated antibodies. Tiled images were acquired with an automated Leica DM5500B microscope and analysis of coronal sections was performed with ImageJ and Adobe Photoshop. Cell isolations and flow cytometry were performed as previously described30 (link).
Briefly, female reproductive tracts, including the vagina, cervix, uterine horns and ovaries, were excised and chopped into small pieces. Tissue pieces were then digested in 500 mg/L of Collagenase IV (Sigma) while stirring at 300 rpm for 1 h at 37°C with a 1 inch magnetic stir bar. Tissues were then homogenized using a gentleMACS (Miltenyi) and filtered. For chemokine staining by flow cytometry, cells were stained with antibodies specific for CD45.2 (104), CD11c (N418), CD3e (145-2C11) (Ebioscience) and Thy1.1 (HIS51) (BD). Chemokines were stained as previously described31 (link).
Publication 2013
Acetone Antibodies Biological Factors Cells Cell Separation Cervix Uteri Chemokine Collagenase Collagen Type IV CX3CL1 protein, human CXCL9 protein, human CXCL11 protein, human Cytokeratin 18 DAPI Dry Ice Female Reproductive System Flow Cytometry Fluorescent Dyes Freezing Goat Immunofluorescence Microscopy Interferon Type II isopentane Microscopy Novus Ovary Rabbits Serum Albumin Tissues Uterine Cornua Vagina
Because we sought to identify soluble, extracellular male Sfps, proteins were prepared in such a way so as to select specifically for soluble proteins. We also sought to reduce cell lysis and thus protein content from male sperm cells and female reproductive tract epithelial cells, since releasing intracellular proteins from these cells would dilute the concentration of transferred Sfps and render their identification more difficult. Female reproductive tracts were homogenized in the ammonium bicarbonate dissection buffer, which lacks any type of detergent and thus minimized cell lysis. The mixture was then centrifuged for 5 min at 18,000g. This process was repeated once, and the supernatant was retained. Protein concentration was estimated using a BCA assay (Pierce). Proteins were prepared for tandem mass spectrometry and digested with trypsin as previously described [57 (link)].
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Publication 2008
ammonium bicarbonate Biological Assay Buffers Cells Detergents Dissection Epithelial Cells Female Reproductive System Males Proteins Protoplasm Sperm Sperm Proteins spleen fibrinolytic proteinase (human) Tandem Mass Spectrometry Trypsin
To discriminate between CD8 T cells in tissue parenchyma versus tissue vasculature, i.v. injected Ab was used as previously described (28 (link)). Briefly, 3μg of anti-CD8α Ab (53-6.7, Biolegend, San Diego, CA) was injected i.v. and allowed to circulate for three minutes prior to mouse sacrifice.
Organs were harvested and digested as previously described (29 (link)). For isolation of small intestinal intraepithelial lymphocytes (IEL), Peyer’s patches were removed, the small intestine was cut longitudinally and then laterally into small pieces. Pieces were incubated for 30 minutes with stirring at 37°C with 0.154mg/mL dithioerythritol (Sigma-Aldrich, St. Louis, MO) in 10% HBSS/HEPES. Female reproductive tract (FRT), lung and salivary gland (SG) tissues were cut into small pieces in RPMI 1640 containing 5% FBS, 2 mM MgCl2, 2 mM CaCl2 and 0.5mg/mL type IV collagenase for FRT (Sigma-Aldrich, St. Louis, MO) or 100 U/mL type I collagenase for lung and SG (Worthington, Lakewood, NJ) and incubated for 1 hr at 37°C with stirring. After enzymatic digestion, the remaining tissue pieces were mechanically disrupted using a gentleMACs dissociator (Miltenyi Biotec, San Diego, CA). The liver was mechanically dissociated by pushing the tissue through a 70μm-cell strainer. Single cell suspensions of IEL, FRT, lung, liver and SG were further separated using a 44/67% Percoll (GE Healthcare Life Sciences, Pittsburgh, PA) density gradient. Spleen and lymph nodes (LN) were dissociated mechanically. Splenocytes and blood were treated with ACK lysis buffer to lyse red blood cells.
The following antibodies were used for flow cytometry: anti-KLRG1 (2F1), anti-Eomes (Dan11ma), anti-T-bet (4B10), anti-CD44 (IM7), anti-CD122 (TM-b1), anti-CD27 (LG.7F9), anti-CD69 (H1.2F3) (all from eBioscience, San Diego, CA), anti-CD8α (53-6.7, eBioscience, Biolegend, San Diego, CA), anti-CD103 (M290), anti-CD25 (PC61), anti-Bcl-2 (Bcl-2/100) and anti-CD127 (SB/199) (BD Biosciences, San Jose, CA). Cell viability was determined using Ghost DyeTM Red 780 (Tonbo Biosciences, San Diego, CA). Kb-SIINFEKL-specific CD8 T cells were identified using H-2Kb tetramers made in house containing the SIINFEKL peptide (New England Peptide, Gardener, MA). The BD Biosciences intracellular kit for cytokine staining and the eBioscience FoxP3 kit for transcription factor staining were used in accordance with manufacturer’s directions. Peptide stimulation was performed as previously described (30 (link)). Briefly, splenocytes were plated in RPMI 1640 containing 10% FBS, 1× NEAA, 2mM L-glutamine, 1mM sodium pyruvate, 1× penicillin/streptomycin and 0.05mM β-mercaptoethanol and incubated with 1ug/mL SIINFEKL peptide and 1ug/mL GolgiPlug (BD Biosciences, San Jose, CA) for four hours at 37°C. Cells were washed and stained with fixable LIVE/DEAD aqua dead cell stain (Life Technologies, San Diego, CA) before surface and intracellular staining. Samples were acquired on an LSRII flow cytometer (BD Biosciences, San Diego, CA).
Publication 2016
2-Mercaptoethanol alpha HML-1 Antibodies BCL2 protein, human BLOOD Buffers CD8-Positive T-Lymphocytes CD44 protein, human Cells Cell Survival Collagenase, Clostridium histolyticum Cytokine Digestion Dithioerythritol Enzymes Erythrocytes Female Reproductive System Flow Cytometry Glutamine Hemoglobin, Sickle HEPES IL2RA protein, human IL2RB protein, human Intestines, Small Intraepithelial Lymphocytes isolation KB Cells KLRG1 protein, human Liver Lung Lymphocyte Magnesium Chloride Matrix Metalloproteinase 2 Mus Nodes, Lymph OVA-8 Penicillins Peptides Percoll Peyer Patches Protoplasm Pyruvate Red Cell Ghost Salivary Glands Sodium Spleen Stains Streptomycin Tetrameres Thomsen-Friedenreich antibodies Tissues Transcription Factor
Patients with cervical precursor lesions and/or cancer were recruited from the West China Second Affiliated Hospital between May 2010 and January 2011. They were referred to us by their attending physicians and invited to participate in our survey on a voluntary basis. Decisions to decline the invitation were respected irrespective of the reasons. All cervical precursor lesions and cervical cancers were diagnosed based on pathologic examination. The stage of cervical cancer was further identified according to the International Federation of Gynecology and Obstetrics (FIGO) staging system based on clinical examination. Patients received standard treatments according to biopsy findings, physical conditions, and fertility requirements[13] (link). The study was approved by the Institutional Review Board of the Cancer Institute of Chinese Academy of Medical Sciences.
Publication 2014
Biopsy Cervical Cancer Chinese Ethics Committees, Research Female Reproductive System Fertility Malignant Neoplasms Neck Patients Physical Examination Physicians Staging, Cancer

Most recents protocols related to «Female Reproductive System»

The samples were processed using standard histopathological methods and evaluated by a certificated pathologist. All patients were staged according to the International Federation of Gynecology and Obstetrics (FIGO) staging system 2009 [12 (link)]. The abnormal cell percentage was calculated by selecting the area where the lesion was most representative on the slide and counting at high magnification (× 400) out of 100 cells. Only these regions with abnormal tissue were used for DNA extraction.
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Publication 2023
Cells Female Reproductive System Pathologists Patients Tissues
We retrospectively analyzed the cases of the 109 patients with early-stage
poorly-to moderately-differentiated CSCC who underwent radical cervical cancer
treatment during the period from May 2014 to December 2017 at Changzhi People’s
Hospital and Yuncheng Central Hospital in Shanxi Province, China. The ages of
the patients who underwent the treatment ranged from 27 to 71 (53.95 ± 9.6)
years.
The study’s inclusion criteria were: (1) postoperative histopathology that
revealed a diagnosis of early-stage poorly-to moderately-differentiated CSCC;
(2) no coeval tumors; (3) stage IA to IIA disease according to the 2009
International Federation of Gynecology and Obstetrics (FIGO) staging system; (4)
no treatment for CSCC was conducted within 1 week before the surgery; and (5)
complete medical records and follow-up records were available. Patient
demographics and clinical characteristics were retrieved from the patients'
medical records: age, body mass index (BMI), FIGO stage, tumor lymph node
metastasis status, vascular infiltration, and peripheral blood test results
(including routine blood tests, liver and kidney function, and the tumor marker
SCCA [squamous cell carcinoma antigen]) within 1 week before surgery. We used
these parameters to calculate the following inflammatory and nutritional
indices: the neutrophil-to-lymphocyte ratio (NLR), the platelet-to-lymphocyte
ratio (PLR), the monocyte-to-lymphocyte ratio (MLR), the OPNI, the systemic
inflammatory response index (SIRI), and the systemic immunoinflammatory index
(SII).
The patients’ overall survival (OS) was calculated from the date of the patient’s
first surgery to the date of death (or the date of last follow up). We used OS
as the end point of this study, with death as a positive event, because OS
better reflects patients’ long-term survival prognosis.
The exclusion criteria were: (1) the presence of hematologic illness, autoimmune
disease, organ dysfunction, acute or chronic infection, and other diseases that
may impact hematologic indexes; and (2) no history of other malignant
tumors.
Publication 2023
Blood Platelets Blood Vessel Chronic Infection Early Diagnosis Female Reproductive System Hematologic Tests Index, Body Mass Inflammation Kidney Liver Lymph Lymphocyte Monocytes Neck Neoplasms Neutrophil Operative Surgical Procedures Patients Prognosis Sleep Apnea, Obstructive squamous cell carcinoma antigen
A descriptive, cross-sectional study was carried out among 425 youth trainees aged 15–29 years attached to training centers of Youth Corps and National Youth Service Council which are functioning under the Ministry of Youth Affairs in Sri Lanka, to assess their knowledge, attitudes, and practices on sexual and reproductive health.
The sample of youth trainees was selected using a two-stage cluster sampling method. Six youth training centers were selected using computer-generated random numbers after listing out all the centers in which the SRH module was incorporated into the curriculum. From each center, an equal number of study subjects were selected using simple random sampling techniques. The sample of trainees were selected after listing out all eligible youth trainees who have been following a training course in a youth training center for more than 6 months. Since 80 % attendance in all modules was obligatory to sit the final examination, all trainees were included in the sample assuming that they all have 80% attendance to the module. Course attendance details were obtained from the training instructor in charge of the module. Trainees who have been following a course for less than 6 months period and those who were suffering from severe physical or mental disabilities which prevented them from attending lectures during the time of data collection or those who did not have 80% attendance to the module were excluded from the study.
The sample size was computed using the standard formula [17 ]. The anticipated proportion of trainees having satisfactory sexual and reproductive health knowledge was taken as 50% since we couldn’t come across a previous study conducted in a similar study setting.
A self-administered questionnaire that was developed with an extensive literature review and expert opinion was used for data gathering. The questionnaire contained questions that were included in the National Youth Health Survey [13 (link)] and in other Sri Lankan studies that assessed SRH knowledge and practices among young persons [18 ]. An expert panel consisted of three public health experts, two MOHs, and two youths.
The developed questionnaire was pretested among a sample of 30 youth in the same age group selected from a different youth training center. The questionnaire included questions to assess the trainee’s knowledge of male and female reproductive tract and function, family planning, pregnancy, abortion, and sexually transmitted diseases. The questionnaire also assessed the trainee’s sexual and reproductive health practices. Following the development of the questionnaire, it was tested for face, content, and consensual validity by a panel of experts using a modified Delphi technique. The Cronbach’s alpha value > 0.6 indicated fair alignment of the questions with each other. The correlation coefficient for test-retest reliability above 0.7 indicated good agreement between the responses.
Data collection was done by trained youth who were awaiting university entrance. Data collectors visited each training center to collect data from youth trainees. Data collection was conducted with minimal disturbance to the academic activities. Informed, written consent was obtained from all eligible participants before the distribution of the questionnaires.
All data were coded and entered into a database that had been created using the standard statistical package SPSS-21. Categorical variables were presented as numbers and percentages. The bivariate logistic regression model was used to determine the independent association of the selected demographic factors with youth trainees’ sexual and reproductive health knowledge. Ethical clearance was obtained from the Faculty of Medicine, University of Colombo, while administrative clearance was obtained from the Ministry of Youth Affairs and the authorities at youth training centers.
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Publication 2023
Age Groups Disabled Persons Face Faculty, Medical Female Reproductive System Induced Abortions Males Pregnancy Reproduction Sexual Health Sexually Transmitted Diseases Youth
Ultrasonography was performed following Sulikowski et al. (30 ). Briefly, an Ibex EVO II portable ultrasound (EI Medical Imaging) with a 60-mm curved linear array 2.5- to 5-MHz transducer (model 290470) capable of a 24-cm scan depth was used to obtain images of the reproductive tract of each female. Scanning was performed on the ventral surface from the pectoral to the pelvic fin in both a transverse and longitudinal orientation to obtain cross-sectional and lengthwise images, respectively. Depth of the scan ranged from 12 to 24 cm, depending on the image being obtained. Collected images and video loops were saved on the Ibex Pro at the time of sampling. Gravidity was determined on the basis of the presence or absence of embryos. Images and frozen video stills were then used to measure (via proprietary software preinstalled on the Ibex EVO II ultrasound) pup diameter (centimeters) along the transverse axis.
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Publication 2023
Embryo Epistropheus Female Reproductive System Freezing Pelvis Radionuclide Imaging Transducers Ultrasonography
Data from the Scottish Medical Record Linkage Database, held by the Scottish National Health Service (NHS Scotland), were used. This database contains annually validated data on all inpatient and day-case hospital admissions, excluding maternity-related and psychiatric admissions, as described in detail in [1 (link)]. All women having a first gynecological operation between June 2009 and June 2011, without a history of previous abdominal (including cesarean section) surgery were included. Patients were followed until December 2017, documenting migration data and deaths. All eligible women were included since data on admission and operation had no opt-out. The surgical approaches were classified as open, laparoscopic or transvaginal, using the Office of Population Censuses and Surveys Classification of Interventions and Procedures version 4 (OPCS-4) codes. The same OPCS-4 codes were used to classify subsequent reoperations.
Similar to previous SCAR (The Surgical and Clinical Adhesions Research) studies, all readmissions were screened for their potential association with adhesions [8 (link),9 (link)]. Based on International Classification of Diseases, Tenth Edition (ICD-10) codes, the association between readmission and adhesions was classified as either readmission directly related to adhesions (e.g., adhesiolysis, adhesive small bowel obstruction) or readmission possibly related to adhesions (e.g., unspecified small bowel obstruction). Readmissions unlikely to be related to adhesions were not included in the analysis.
Subgroup analyses were performed by anatomical site, such as uterus, vagina, fallopian tubes, ovaries, combined gynecological, and combined other. A procedure was categorized as ‘combined gynecological’ when multiple anatomical sites of the female reproductive tract were involved, i.e., uterus, vagina, Fallopian tubes, or ovaries. Procedures involving both the female reproductive tract and other organs (e.g., colorectal) were classified as ‘combined other’.
Specific subgroup analyses were performed for patients receiving a hysterectomy since this subgroup is large and more homogeneous.
Risk factors, based on the literature and the opinion of an expert panel, were age, surgical approach, operation site, malignancy, fertility-enhancing surgery, intra-abdominal infection, history of abdominal radiotherapy, intraperitoneal mesh placement, inflammatory bowel disease (IBD), endometriosis, and adhesiolysis.
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Publication 2023
Abdomen ARID1A protein, human Body Regions Cesarean Section Cicatrix Endometriosis Fallopian Tubes Female Reproductive System Fertility Gynecologic Surgical Procedures Health Services, National Hysterectomy Inflammatory Bowel Diseases Inpatient Intestinal Obstruction Intestines, Small Intraabdominal Infections Laparoscopy Malignant Neoplasms Operative Surgical Procedures Ovary Patients Radiotherapy Repeat Surgery Tissue Adhesions Uterus Vagina Woman

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More about "Female Reproductive System"

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Delve into the intricate mechanisms, processes, and subtopics that govern this complex biological system, including ovulation, menstruation, pregnancy, and hormonal regulation.
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