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Relevant Topics
- Biomarkers and Molecular Diagnosis of all Gynaecologic Cancers
- Cervical Erosin
- Clinical Gynecologic Oncology
- Cysts and Ovaries
- Diarrhea in Pregnancy
- Endometreosis in Pregnancy
- Epidemiology of Gynecologic Cancers
- Fallopian Tube Cancer
- Gestational Trophoplastic Tumors
- Gynecological Oncology
- HIV and Pregnancy
- High Risk Pregnancy
- Nausea Pregnancy
- Neuroblastoma Cancer
- Omentum Cancer
- Ovarian Cancer
- Ovarian Cancer Prognosis
- Ovarian Tumors
- Pathological aspects and molecular pathology of all Gynecologic Cancers
- Preclampsia in Pregnancy
- Pregnancy Care
- Pregnancy Constipation
- Pregnancy Fitness
- Pregnancy Nutrition
- Primary Peritoneal Cancer
- Quality of Life of Patients with Gynecologic Cancers
- Reproductive Cancer
- Smoking in Pregnancy
- Socio- Psychological Aspects of Gynecological Cancers
- Stress in Pregnancy
- Targeted Molecular Therapy for all Gynaecologic Cancers
- Termination of Pregnancy
- Ultrasound Pregnancy
- Uterine Cancer
- Vaginal Cancer
- Vulva Cancer
- Womb Cancer
Double Uterus
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Instead, each one develops into a separate structure. This condition is called double uterus (uterus didelphys). A double uterus may have one opening (cervix) into one vagina, or each uterine cavity may have a cervix. There may even be two vaginas. Double uterus is rare and sometimes never diagnosed. The percentage of women with a double uterus is likely higher in those with a history of miscarriage or premature birth. The cause of double uterus is unknown.
Expert PPTs
- Ioan Magyar
Introduction to Clinical Pharmacology
PPT Version | PDF Version
Speaker PPTs
- Yosef Yarden
Classically, the 3âuntranslated region (3âUTR) is that region in eukaryotic protein-coding genes from the translation termination codon to the polyA signal. It is transcribed as an integral part of the mRNA encoded by the gene. However, there exists another kind of RNA, which consists of the 3âUTR alone, without all other elements in mRNA such as 5âUTR and coding region. The importance of independent 3âUTR RNA (referred as I3âUTR) was prompted by results of artificially introducing such RNA species into malignant mammalian cells. Since 1991, we found that the middle part of the 3âUTR of the human nuclear factor for interleukin-6 (NF-IL6) or C/EBP gene exerted tumor suppression effect in vivo. Our subsequent studies showed that transfection of C/EBP 3âUTR led to down-regulation of several genes favorable for malignancy and to up-regulation of some genes favorable for phenotypic reversion. Also, it was shown that the sequences near the termini of the C/EBP 3âUTR were important for its tumor suppression activity. Then, the C/EBP 3âUTR was found to directly inhibit the phosphorylation activity of protein kinase CPKC in SMMC-7721, a hepatocarcinoma cell line. Recently, an AU-rich region in the C/EBP 3âUTR was found also to be responsible for its tumor suppression. Recently we have also found evidence that the independent C/EBP 3âUTR RNA is actually exists in human tissues, such as fetal liver and heart, pregnant uterus, senescent fibroblasts etc. Through 1990âs to 2000âs, world scientists found several 3âUTR RNAs that functioned as artificial independent RNAs in cancer cells and resulted in tumor suppression. Interestingly, majority of genes for these RNAs have promoter-like structures in their 3âUTR regions, although the existence of their transcribed products as independent 3âUTR RNAs is still to be confirmed. Our studies indicate that the independent 3âUTR RNA is a novel non-coding RNA species whose function should be the regulation not of the expression of their original mRNA, but of some essential life activities of the cell as a whole.
PPT Version | PDF Version - Ramesh T Subramaniam
Development of Nanocomposite Polymer Electrolytes (NCPEs) in Electric Double Layer Capacitors (EDLCs) Application
PPT Version | PDF Version - Vladimir Pak
Double Targeting as an Effective Anti-Cancer Strategy
PPT Version | PDF Version