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1,665 Possible Causes for chromatid, cohesion, female, meiosis, sister

Did you mean: chromatid, cohesion, female, miosis, spinster

  • Premature Ovarian Failure

    Such a breakdown/arrest of meiosis could lead to oligomenorrhea seen in our patient. [2] The recently identified gene MATER, which is mapped at 19q13.4, could be the causative[ncbi.nlm.nih.gov] STAG3 encodes a meiosis-specific subunit of the cohesin ring, which ensures correct sister chromatid cohesion.[ncbi.nlm.nih.gov] Women with premature ovarian failure and age-matched controls were evaluated through the Female Sexual Function Index and the Female Sexual Distress Scale-Revised, and their[ncbi.nlm.nih.gov] Oocytes donated by her dizygotic twin sister were used for IVF.[ncbi.nlm.nih.gov] PATIENT(S): A 33-year-old Japanese female with POF and proximal symphalangism. INTERVENTION(S): Direct sequence analysis of the NOG gene.[ncbi.nlm.nih.gov]

  • Microcephaly

    The cohesin complex is an evolutionarily conserved multi-subunit protein complex which regulates sister chromatid cohesion during mitosis and meiosis.[ncbi.nlm.nih.gov] This novel mutation has resulted in different phenotypes in affected male and female patients of this family.[ncbi.nlm.nih.gov] By investigating GPKOW transcripts in lymphoblastoid cell lines (LCLs) of three carrier females, we show that the GPKOW c.331 5G A variant disrupts normal splicing of its[ncbi.nlm.nih.gov] […] linear growth retardation, poor weight gain, microcephaly, characteristic facial features, cutaneous syndactyly of the toes, high myopia, and intellectual disability in two sisters[ncbi.nlm.nih.gov] Lima, 35, says her daughters both lead normal lives now—they attend school, play with their younger sister, and participate in family events.[fortune.com]

  • Lindane

    Also cofinanced by the Cohesion Funds, the station was constructed near the stockpiles to limit the risks of transporting the product.[ec.europa.eu] In a face-to-face interview, job history and reproductive history of 398 female teachers were ascertained.[ncbi.nlm.nih.gov] Also, lindane was assessed for its potential to induce sister chromatid exchanges in vivo in the bone marrow of Chinese hamsters.[ncbi.nlm.nih.gov] Since both estrogen receptors (ER-alpha and -beta) have shown to be target for endocrine disruption, we investigated the role of gamma-HCH on the development of female reproductive[ncbi.nlm.nih.gov] […] data on the effects of the organochlorine pesticides DDT, its metabolites, TCPM, methoxychlor and lindane on folliculogenesis, ovulation, fertilization, and implantation of female[ncbi.nlm.nih.gov]

    Missing: meiosis
  • Fanconi Anemia

    Studies have showed that FA genes play significant functions in promoting the proliferation of primordial germ cell, maintaining normal meiosis of the oocytes, participating[ncbi.nlm.nih.gov] In addition, defective sister chromatid cohesion was observed in five HNSCC cell lines.[cancerres.aacrjournals.org] The donor, a now 14-yr-old female, was recently reported healthy. 2011 John Wiley & Sons A/S.[ncbi.nlm.nih.gov] This is the report of an 18- and her 28-year old sister who developed a post-HSCT oral squamous cell carcinoma.[ncbi.nlm.nih.gov] FANC proteins. [28] This finding suggests that recombinational repair processes mediated by the FANC proteins are active during germ cell development, particularly during meiosis[en.wikipedia.org]

  • Phocomelia

    […] in establishing sister chromatid cohesion during S phase.[ncbi.nlm.nih.gov] We report the case of a 33 year-old female affected with the association of ectrodactyly and phocomelia.[ncbi.nlm.nih.gov] In each experiment, only the patient's metaphase spreads revealed chromatid repulsion.[ncbi.nlm.nih.gov] The older sister also had phocomelia of the left upper extremity with 5 finger rays; she died immediately after birth.[ncbi.nlm.nih.gov] Abstract We report a female fetus of 20 weeks gestation with severe symmetrical deformity affecting all four limbs.[ncbi.nlm.nih.gov]

    Missing: meiosis
  • Saccharomyces Cerevisiae

    "Meiosis and the Paradox of Sex in Nature". Meiosis . doi : 10.5772/56542 .[en.wikipedia.org] Chromosome loss was enhanced, accompanied by a delay in the completion of replication and a modest defect in sister chromatid cohesion, in nse1-103.[ncbi.nlm.nih.gov] Abstract We report a very rare case of acute pyelonephritis in a 51-year-old female with a history of chronic kidney disease (CKD) and diabetes caused by a normally benign[ncbi.nlm.nih.gov] We describe the cases of two adult females with vulvovaginal infections caused by itraconazole-resistant S. cerevisiae who made a full recovery after oral fluconazole therapy[ncbi.nlm.nih.gov] However, S. cerevisiae has a very closely related sister species, S. paradoxus , which has little to no association with human influences.[microbewiki.kenyon.edu]

  • Pelizaeus-Merzbacher Disease

    However, family cohesion (73.3 vs 72.3,[ncbi.nlm.nih.gov] Conversely, mutations causing severe disease in males rarely cause clinical signs in carrier females.[ncbi.nlm.nih.gov] We suggest repair of a double-stranded break (DSB) by one-sided homologous strand invasion of a sister chromatid, followed by DNA synthesis and nonhomologous end joining with[ncbi.nlm.nih.gov] Abstract We report on a brother and sister with the connatal form of Pelizaeus-Merzbacher disease.[ncbi.nlm.nih.gov] The elder sister showed a prolonged central motor conduction time.[ncbi.nlm.nih.gov]

    Missing: meiosis
  • Werner Syndrome

    Meiotic recombination was not increased in sgs1 Δ mutants, although meiosis I chromosome missegregation has been shown to be elevated. sgs1 Δ suppresses the slow growth of[genetics.org] Here we report a 29-year-old female patient who displayed cataracts, hair graying, and tendinous calcinosis. Her parents were first cousins.[ncbi.nlm.nih.gov] Abstract An analysis of the baseline and mitomycin-C-induced sister chromatid exchange (SCE) frequencies in peripheral lymphocytes derived from three patients with progeria[ncbi.nlm.nih.gov] However, there have been reports in the literature confirming that some affected males and females have reproduced.[rarediseases.org] Decatenation Checkpoint Assay As a consequence of DNA replication, the DNA strands of sister chromatids become intimately entangled, or catenated.[frontiersin.org]

    Missing: cohesion
  • Flurbiprofen

    CONCLUSIONS: Topical nepafenac has been shown to be a more effective inhibitor of meiosis during SICS and provides a more stable mydriatic effect compared to topical flurbiprofen[ncbi.nlm.nih.gov] The purpose of the study was to explore the genotoxic and cytotoxic effects of flurbiprofen in human cultured lymphocytes by sister chromatid exchange, chromosome aberration[ncbi.nlm.nih.gov] METHODS: A total of 201 osteoarthritis patients (mean age; 66.3, 151 females, mean estimated glomerular filtration rate; 74.6 mL/min/1.73 mm 2 ) were applied 40 or 80 mg SFPP[ncbi.nlm.nih.gov] METHODS: After obtaining Institutional Ethics Committee approval, a series of 40 consecutive female patients who were scheduled for partial mastectomies were enrolled.[ncbi.nlm.nih.gov] RESULTS: A total of 70 eyes of cataract surgery patients, 33 males and 37 females, with a mean age of 58.5 11.24 years, were included in the study.[ncbi.nlm.nih.gov]

    Missing: cohesion
  • Cornelia De Lange Syndrome

    This gene encodes a key regulator of the Cohesin complex, which controls sister chromatid segregation during both mitosis and meiosis.[ncbi.nlm.nih.gov] Mutations in the sister chromatid cohesion factor genes NIPBL, SMC1A (also called SMC1L1) and SMC3 have been suggested as probable cause of this syndrome.[ncbi.nlm.nih.gov] Relatively few CdLS patients with mutations in SMC1A are known; female carriers have minor facial dysmorphism and cognitive deficiency without major structural abnormalities[ncbi.nlm.nih.gov] LD2F Syndromes with multiple structural anomalies, without predominant body system involvement H00631 Cornelia de Lange syndrome Pathway hsa04110 Cell cycle hsa04114 Oocyte meiosis[genome.jp] Approximately half of all classical cases of CdLS have heterozygous loss of-function mutations in the gene encoding NIPBL, a component of the cohesion-loading apparatus (Dorsett[ncbi.nlm.nih.gov]