1.Effect of N-tosyl-L-phenylalnylchloromethyl ketone and dexamethasone on expression of nuclear transcription factor-kappaB in childhood acute lymphoblastic leukemia and its significance.
Qig AN ; Tian-Yang XUE ; Wei XU ; Ji-Zhao GAO ; Yi WU ; Chun-Pin XU
Journal of Experimental Hematology 2007;15(2):399-403
In order to investigate the effect of N-tosyl-L-phenylalnylchloromethyl ketone (TPCK) and dexamethasone (Dex) on expression of nuclear transcription factor-kappaB (NF-kappaB) in childhood acute lymphoblastic leukemia (ALL) and its significance, so as to provide the experimental basis for corresponding clinical treatment of ALL, in which NF-kappaB is taken as a target. The biotin-streptavidin method was used to detect the expression of NF-kappaB P65 protein and the effects of TPCK and Dex at clinically relevant dosage on activity of NF-kappaB P65 protein in 20 childhood ALL patients. The results indicated that the expression of NF-kappaB P65 protein was strongly diminished and reached to negative level at 2 hours by treatment with 40 micromol/L TPCK, the positive expression of NF-kappaB P65 protein was (2.5 +/- 1.6)%. TPCK had a time-dependent inhibitory effect on ALL cells cultured in vitro. The expression of NF-kappaB P65 protein in ALL cells was strongly inhibited by clinically relevant concentration of dexamethasone 5.0 microg/ml for 24 hours in vitro. The positive expression was (25.0 +/- 3.0)%, there was significant difference, as compared with untreated ALL cells (T=55, P<0.01). It is concluded that TPCK and Dex can inhibit NF-kappaB activity. Inhibition of NF-kappaB activity may be one of the effect mechanism of dexamethasone on ALL cells. Inhibition of NF-kappaB conduction pathway may have a significant value in childhood ALL treatment.
Bone Marrow Cells
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pathology
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Cells, Cultured
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Child
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Child, Preschool
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Dexamethasone
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pharmacology
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Female
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Humans
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Infant
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Leukocytes, Mononuclear
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pathology
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Male
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NF-kappa B
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biosynthesis
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genetics
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Precursor Cell Lymphoblastic Leukemia-Lymphoma
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metabolism
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pathology
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Protein Synthesis Inhibitors
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pharmacology
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Tosylphenylalanyl Chloromethyl Ketone
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pharmacology
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Tumor Cells, Cultured
2.Urban-Rural Comparison of Nutrient Intake by Adult Women in Shaanxi Province, China
NAKATSUKA HARUO ; ZUo-WEN ZHANG ; JtANc-BIN QU ; WEI-PIN GAO ; YI-JUAN DENG ; SHIMBO SHINICHIRO ; WATANABE TAKAO ; INOGUCHI-MATSUDA NAOKO ; HIGASHIKAWA KAE ; IKEDA MASAYUKI
Biomedical and Environmental Sciences 1999;12(4):270-284
Triplet surveys were conducted in the city of Xi' an and two villages (one in the vicinity and the other at a distance) in Shaanxi Province in China in October-November (when agricultural activitis were low), 1997, to elucidate nutrient intakes with a focus on possible urban-rural differences. Total food duplicate samples were collected from non-smoking and non-habitually drinking adult healthy women (about 50 subjects per site and 149 in total). The nutrient intakes were estimated from the weight of food items in reference to national food composition tables. On average, the women took 1873 kcal energy, 54 g protein and 37 g lipid per day, with a lipid energy ratio of18.4%. Both excess and insufficient energy intake was observed as a result of food intake analysis and body mass index determination. With regard to minor nutrient intakes, insufficiency was serious in the case of calcium, vitamin A and vitamin B2, but not with iron. Whereas dependency on plant foods for sources of energy and protein was common to the three regions, Xi' an people consumed more animal foods than those in the villages. Intake of fish and shellfish was quite low throughout the three regions. Among the four types of cereals, wheat was consumed most substantially in the three regions and in three meals (except for the village where people essentially did not take lunch in reflection of low agricultural activities), whereas rice was consumed more in Xi' an than in the two villages. Maize consumption was higher in the two villages (especially for breakfast) than in the city.In contrast, foxtail millet (although in small amounts) was taken primarily in Xi'an and only at the time of breakfast.
3.Comparison of exosome extracting methods from human umbilical cord mesenchymal stem cells
Ying GUO ; Xiu-Wei WANG ; Yu-Hu NIU ; Li WANG ; Nan ZHOU ; Bai-Yi LI ; Zhen-Dong WANG ; Pin ZHANG ; Ya-Jie GAO ; Bo NIU
Chinese Journal of Tissue Engineering Research 2018;22(9):1382-1388
BACKGROUND: Cell-free stem cell therapy has been an issue of concern, but there is no conclusion on how to extract high-quality exosomes. OBJECTIVE: To extract exosomes from human umbilical cord mesenchymal stem cells by using three different methods, and then to screen the optimal method. METHODS: Exosomes were extracted from human umbilical cord mesenchymal stem cells by using the Total Exosome Isolation test kit, Exo Quick test kit and differential ultracentrifugation method, respectively. Then, transmission electron microscopy was used for morphological observations, BCA was utilized to quantify the protein, and western blot assay was applied to detect surface markers CD9, CD81 and CD63. RESULTS AND CONCLUSION: Extraction of exosomes was completed by all the three methods, and round or oval membranous vesicles were observed under the transmission electron microscope. The protein content and purity of exosomes was highest in the differential ultracentrifugation group, followed by the Exobiology Quick kit group, and lowest in the Total Exosome Isolation kit group, and there were significant differences among the three groups (P < 0.05). Under the same protein concentration, surface specific markers, CD81, CD63 and CD9, were expressed highest in the differential ultracentrifugation group, followed by the Exobiology Quick kit group, and lowest in the Total Exosome Isolation kit group. The operating time was significantly lower in the Exobiology Quick kit group compared with the other two groups (P < 0.05). To conclude, despite a longer operating time, the differential ultracentrifugation method is a rational method to extract enough exosomes with relative high purity.
4.Isolation of cytotoxic compounds from the seeds of Crataegus pinnatifida.
Ling-Zhi LI ; Ying PENG ; Chao NIU ; Pin-Yi GAO ; Xiao-Xiao HUANG ; Xin-Liang MAO ; Shao-Jiang SONG
Chinese Journal of Natural Medicines (English Ed.) 2013;11(4):411-414
AIM:
To study the chemical constituents and bioactivity of the seeds of Crataegus pinnatifida.
METHODS:
The chemical constituents were isolated and purified by macroporous adsorptive resin D101, silica gel, and ODS column chromatography, and preparative HPLC. Their structures were elucidated on the basis of spectroscopic methods. In addition, the cytotoxic activities of compounds 1-4 were investigated on OPM2 and RPMI-8226 cells.
RESULTS:
Four compounds were obtained and their structures were identified as (7S, 8S)-4-[2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-(hydroxymethyl)ethoxy]-3, 5-dimethoxybenzaldehyde (1), (+)-balanophonin (2), erythro-guaiacylglycerol-β-coniferyl aldehyde ether (3), buddlenol A (4).
CONCLUSION
Compound 1 is a novel norlignan, while compounds 1-4 exhibited marginal inhibition on the proliferation of OPM2 and RPMI-8226 cells.
Cell Line
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Cell Proliferation
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drug effects
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Crataegus
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chemistry
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Humans
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Molecular Structure
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Nerve Tissue Proteins
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chemistry
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isolation & purification
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toxicity
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Plant Extracts
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chemistry
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isolation & purification
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toxicity
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Seeds
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chemistry
5.Prophylaxsis against recurrance of hepatitis B virus after liver transplantation
Ju-Shan WU ; Shi-Chun LU ; Meng-Long WANG ; Ren-Pin XIA ; Qing-Liang GUO ; Da-Ming GAO ; Yi ZHANG ; Yuan LIU ; Ning LI
Chinese Journal of Experimental and Clinical Virology 2008;22(5):367-369
Objective To summarize the clinical data in preventing HBV recurrence after liver transplantation and explore a optimal individual protocol in prophylaxis of HBV recurrence. Methods We retrospected outcomes in 195 recipients who underwent a liver transplantation for HBV-related liver disease between June 2004 and July 2008. According to the anti-virus protocol these recipients are divided into two groups as following: group A received a protocol of combination treatment of lamivudine with HBIG, and group B with combination treatment of adefovir with HBIG. With mean follow-up of 23.7 months, HBV recurrent rate was observed in overall and each group separately. Results A total of 195 liver transplant recipients were identified that met the study criteria. At the sixth and eleventh month after operation, HBV recurrence appeared in 2 recipients, each in two groups, which were due to LAM cessation and HBV mutation respectively. Recurrent rate was 0.6% in group A, 3.7% in group B and 1% in total. There was no significant difference in HBV recurrent rate between group A and B. Conclusion Lamivudine combined with HBIg should be considered as a reliable method in preventing HBV recurrence after liver transplantation. Better outcomes can be achieved by individual anti-virus protocol and HBIg administration according to HBV stares in recipient.
6.Phase II multicenter clinical trial of nedaplatin in the treatment of malignant tumors.
Pin ZHANG ; Feng-yi FENG ; Ling-ying WU ; Yi HU ; Ji-wei LIU ; Ya-jie GAO ; Xiao-qian GUAN ; Ke-jun NAN ; Ai-li SUO ; Xiu-wen WANG ; Mao-hong ZHANG ; Wen-dong ZHANG ; Chao-wu LI ; Yang ZHANG ; Jin-bo ZHAO
Chinese Journal of Oncology 2006;28(3):230-234
OBJECTIVETo evaluate and compare the efficacy and safety of Nedaplatin (NDP)-based regimen and cisplatin (DDP)-based regimen for head and neck squamous cell carcinoma (HNSCC), non-small cell lung cancer (NSCLC), esophageal cancer and ovary epithelial cell carcinoma.
METHODSSingle agent group: NDP was administered at a dose of 100 mg/m(2) on D1, every 3 weeks for at least 2 cycles. Combination chemotherapy group: combined with 5-Fu, NVB, VDS + 5-Fu, PTX or CTX respectively, NDP 80 mg/m(2) on D1 or DDP 30 mg/m(2) on D1-3, every 3 weeks for at least 2 cycles was given.
RESULTSOf 237 patients in this trial, 37 were treated by single Nedaplatin, 139 by NDP-based regimen, 61 by DDP-based regimen in the control group. The response rate of single Nedaplatin chemotherapy for advanced NSCLC was 10.5% (2/19), for ovary carcinoma (1/3) and HNSCC (1/1). For NSCLC and ovary carcinoma patients who had failed in the previous DDP-based chemotherapy, the response rates by single NDP chemotherapy were still 9.1% and 33.3%. The response rate of NDP-based combination regimen for NSCLC, ovary carcinoma, HNSCC and esophageal cancer was 33.9% (21/62), 44.8% (13/29), 20.0% (3/15) and 18.2% (4/22), respectively, which was not statistically different from the rate of controlled group treated by DDP-based regimen. For chemonaive NSCLC, the effect of NDP-based combination regimen (35.7%) was significantly superior to the effect of DDP-based regimen (17.1%) (P = 0.045). The most common adverse events of nedaplatin were myelosuppression (leukopenia, thrombocytopenia, anemia), nausea and vomiting. The myelosuppression and renal toxicity of NDP-based regimen were similar to that of DDP-based regimen, but vomiting was milder than that of DDP-based regimen (54% vs. 75.4%), and grade I/II liver toxicity was more common in the NDP-based regimen than in DDP-based regimen (10.8% vs. 0).
CONCLUSIONNedaplatin is effective in the treatment for HNSCC, NSCLC and ovary carcinoma. Compared with the control group treated by DDP-based regimen, nedaplatin-based combination chemotherapy has similar effect on HNSCC, NSCLC, ovary carcinoma and esophageal cancer. Gastrointestinal reaction of nedaplatin is milder than that of cisplatin but the liver function during chemotherapy must be monitored closely.
Adolescent ; Adult ; Aged ; Antineoplastic Agents ; therapeutic use ; Antineoplastic Combined Chemotherapy Protocols ; adverse effects ; therapeutic use ; Carcinoma, Non-Small-Cell Lung ; drug therapy ; Cisplatin ; administration & dosage ; Esophageal Neoplasms ; drug therapy ; Female ; Fluorouracil ; administration & dosage ; Head and Neck Neoplasms ; drug therapy ; Humans ; Leukopenia ; chemically induced ; Lung Neoplasms ; drug therapy ; Lymphatic Metastasis ; Male ; Middle Aged ; Nausea ; chemically induced ; Organoplatinum Compounds ; administration & dosage ; therapeutic use ; Ovarian Neoplasms ; drug therapy ; Vinblastine ; administration & dosage ; analogs & derivatives
7.Late-onset noninfectious pulmonary complications after allogeneic peripheral blood stem cell transplantation.
Yi-Zhuo ZHANG ; Chun-Ji GAO ; Bo-Long ZHANG ; Wan-Ming DA ; Xiao-Pin HAN ; Hong-Hua LI ; Yu JING ; Wen-Rong HUANG ; Jian BO ; Shu-Hong WANG ; Hai-Yan ZHU ; Hai-Jie JIN ; Li YU
Journal of Experimental Hematology 2007;15(3):632-635
The aim of study was to explore the incidence, risk factors, outcome and efficacious treatment of late-onset noninfectious pulmonary complications (LNIPC) after allogeneic peripheral blood stem cell transplantation (allo-PBSCT). Seventy patients received allo-PBSCT were analyzed retrospectively. The results showed that 9 out of 63 patients surviving more than 3 months occurred late-onset noninfectious pulmonary complications (14.3%). Five out of the 9 patients developed secondary pulmonary infections. In 4 patients, LNIPC caused death directly. Advanced stage of disease at transplantation and extensive chronic graft-versus-host disease (GVHD) happened in association with LNIPC. However, other transplantation-related factors including age at transplantation, gender of patient, conditioning regimen, HLA matching and GVHD prophylaxis were not significantly correlated with the incidence of LNIPC. It is concluded that performing pulmonary function test (PFT) and thoracic computer tomography should be taken routinely after transplantation. Most patients who get correct and early diagnosis for LNIPC will show a positive response to prednisone with or without CsA.
Adolescent
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Adult
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Cyclosporine
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therapeutic use
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Female
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Graft vs Host Disease
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prevention & control
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Humans
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Incidence
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Leukemia
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therapy
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Lung Diseases, Interstitial
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classification
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drug therapy
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etiology
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Male
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Peripheral Blood Stem Cell Transplantation
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adverse effects
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Prednisone
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therapeutic use
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Retrospective Studies
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Risk Factors
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Transplantation, Homologous
8.Clinical study on pulmonary complications after allogeneic peripheral blood stem cell transplantation.
Yi-zhuo ZHANG ; Wan-ming DA ; Bo-Long ZHANG ; Chun-Ji GAO ; Xiao-pin HAN ; Wen-rong HUANG ; Yu JING ; Hong-hua LI ; Yu ZHAO ; Jian BO ; Shu-hong WANG ; Hai-yan ZHU ; Hai-jie JIN
Chinese Journal of Hematology 2006;27(6):366-369
OBJECTIVETo explore the incidence, pathogenesis, risk factors and effective treatment of pulmonary complications after allogeneic peripheral blood stem cell transplantation (allo-PBSCT).
METHODSPulmonary complications in 70 patients received allo-PBSCT were analyzed.
RESULTSThirty one episodes were observed in 26 patients. Among them episodes were infectious complications, including bacteria pneumonia, pulmonary fungus disease, CMV interstitial pneumonia and tuberculosis, some cases were caused by two pathogens, and 11 episodes were noninfectious complications, including late-onset noninfectious pulmonary complications (LONIPCs) (n=9), pulmonary edema (n=1) and interstitial pneumonia (n=1). The overall mortality was 12.9%. Graft-versus-host disease (GVHD) prophylaxis without MTX, severe acute GVHD and extensive chronic GVHD were high risk factors for pulmonary complications and advanced disease at transplantation, extensive chronic GVHD were significantly associated with the incidence of LONIPCs.
CONCLUSIONPulmonary disease is the main complication occurred in patients undergoing allo-PBSCT. It is of greatly importance to treat pathogens specifically and diagnose LONIPCs in its early stage.
Adolescent ; Adult ; Female ; Graft vs Host Disease ; prevention & control ; Hematologic Diseases ; surgery ; Humans ; Lung Diseases ; etiology ; Male ; Middle Aged ; Peripheral Blood Stem Cell Transplantation ; adverse effects
9.Effect of Intelligent Rehabilitation Training System on Upper Limb and Hand Function of Patients with Stroke
Pin-cao GAO ; Fang TANG ; Yi YANG ; Bin YU
Chinese Journal of Rehabilitation Theory and Practice 2020;26(10):1198-1203
Objective:To explore the effect of intelligent rehabilitation training system on upper limb and hand function in patients with stroke. Methods:From December, 2018 to December, 2019, 68 stroke patients were randomly divided into control group (
10.Talin1 is highly expressed in the fallopian tube and chorionic villi to promote trophoblast invasion in tubal pregnancy.
Pin QIU ; Xin Yi LIN ; Gao Pi DENG
Journal of Southern Medical University 2022;42(4):610-617
OBJECTIVE:
To investigate the expression of Talin1 in the fallopian tube and chorionic villi in patients with tubal pregnancy and its role in regulating invasion and migration of trophoblasts.
METHODS:
Immunohistochemistry and Western blotting were used to detect the localization and expression level of Talin1 in the fallopian tube and chorionic villi in patients with tubal pregnancy and in women with normal pregnancy. In the cell experiment, HTR-8/SVneo cells was transfected with Talin1 siRNA and the changes in cell invasion and migration were assessed using scratch assay and Transwell assay. The expressions of MMP-2, MMP-9, N-cadherin and Snail in the transfected cells were detected by qRT-PCR and Western blotting.
RESULTS:
Positive expression of Talin1 was detected in both normal fallopian tube tissues and tissues from women tubal pregnancy, and its expression was localized mainly in the cytoplasm of cilia cells. The expression level of Talin1 was significantly higher in both the fallopian tube and chorionic villi in women with tubal pregnancy than in normal fallopian tube and chorionic villi samples (P < 0.01). In HTR-8/SVneo cells, transfection with Talin1 siRNA significantly inhibited cell invasion (P < 0.01) and migration (P < 0.05), down-regulated the expression of N-cadherin, MMP-2 and Snail (P < 0.05), and up-regulated the expression of MMP-9 in the cells (P < 0.05).
CONCLUSION
The expression of Talin1 in the fallopian tube and chorionic villi is significantly increased in women with tubal pregnancy, suggesting the association of Talin1-regulated trophoblast cell invasion with the occurrence of tubal pregnancy.
Cadherins/metabolism*
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Cell Movement
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Chorionic Villi/metabolism*
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Fallopian Tubes/metabolism*
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Female
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Humans
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Matrix Metalloproteinase 2/metabolism*
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Matrix Metalloproteinase 9/metabolism*
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Pregnancy
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Pregnancy, Tubal/metabolism*
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RNA, Small Interfering/metabolism*
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Talin/metabolism*
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Trophoblasts/metabolism*