Hereditas最新文献

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Trimeric complexes of Antp-TBP with TFIIEβ or Exd modulate transcriptional activity Antp-TBP与TFIIEβ或Exd的三聚体复合物可调节转录活性
IF 2.7 3区 生物学
Hereditas Pub Date : 2022-05-30 DOI: 10.1186/s41065-022-00239-8
Gustavo Jiménez-Mejía, Rubén Montalvo-Méndez, Carolina Hernández-Bautista, Claudia Altamirano-Torres, M. Vázquez, M. Zurita, D. Reséndez-Pérez
{"title":"Trimeric complexes of Antp-TBP with TFIIEβ or Exd modulate transcriptional activity","authors":"Gustavo Jiménez-Mejía, Rubén Montalvo-Méndez, Carolina Hernández-Bautista, Claudia Altamirano-Torres, M. Vázquez, M. Zurita, D. Reséndez-Pérez","doi":"10.1186/s41065-022-00239-8","DOIUrl":"https://doi.org/10.1186/s41065-022-00239-8","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"159 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2022-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65774821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Insights into AIM-InDel diversities in Yunnan Miao and Hani ethnic groups of China for forensic and population genetic purposes. 洞察中国云南苗族和哈尼族的 AIM-InDel 多样性,用于法医和人口遗传学目的。
IF 2.1 3区 生物学
Hereditas Pub Date : 2022-05-20 DOI: 10.1186/s41065-022-00238-9
Wei Cui, Shengjie Nie, Yating Fang, Man Chen, Ming Zhao, Qiong Lan, Chunmei Shen, Bofeng Zhu
{"title":"Insights into AIM-InDel diversities in Yunnan Miao and Hani ethnic groups of China for forensic and population genetic purposes.","authors":"Wei Cui, Shengjie Nie, Yating Fang, Man Chen, Ming Zhao, Qiong Lan, Chunmei Shen, Bofeng Zhu","doi":"10.1186/s41065-022-00238-9","DOIUrl":"10.1186/s41065-022-00238-9","url":null,"abstract":"<p><strong>Background: </strong>Ancestry informative markers are regarded as useful tools for inferring the ancestral information of an individual, which have been widely used in the criminal investigations and population genetic studies. Previously, a multiplex amplification panel containing 39 AIM-InDel loci was constructed. This study aims to investigate the genetic polymorphisms of these 39 AIM-InDel loci in Yunnan Hani and Miao ethnic groups, and to uncover their genetic affinities with reference populations based on the AIM-InDel markers.</p><p><strong>Materials and methods: </strong>In this research, 39 AIM-InDel profiles of 203 unrelated Miao individuals and 203 unrelated Hani individuals in Yunnan province of China were acquired. Additionally, we evaluated the genetic polymorphisms of 39 InDel loci in Yunnan Miao and Hani groups. Moreover, the genetic relationships among Yunnan Miao, Hani and reference populations were also clarified based on Nei's genetic distances, pairwise fixation indexes, principal component analyses, phylogenetic analyses, and STRUCTURE analyses.</p><p><strong>Results: </strong>Genetic diversity analyses demonstrated that these InDel loci showed varying degrees of genetic polymorphisms, and could be utilized in forensic identifications in Yunnan Miao and Hani groups. The results of principal component analyses, phylogenetic analyses and Structure analyses revealed that Yunnan Miao and Hani groups had closer genetic relationships with East Asian populations, especially with the populations from Southern China. This research enriched the genetic data of Chinese ethnic minority, and provided ancestral information of Yunnan Miao and Hani groups from the perspective of population genetics.</p>","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"159 1","pages":"22"},"PeriodicalIF":2.1,"publicationDate":"2022-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65774775","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
SKA3 is a prognostic biomarker and associated with immune infiltration in bladder cancer SKA3是一种预后生物标志物,与膀胱癌免疫浸润相关
IF 2.7 3区 生物学
Hereditas Pub Date : 2022-05-11 DOI: 10.1186/s41065-022-00234-z
Chenyang Wang, Shasha Liu, Xinhong Zhang, Yan Wang, P. Guan, Fanyou Bu, Hao Wang, Dawen Wang, Yisheng Fan, Sichuan Hou, Zhilei Qiu
{"title":"SKA3 is a prognostic biomarker and associated with immune infiltration in bladder cancer","authors":"Chenyang Wang, Shasha Liu, Xinhong Zhang, Yan Wang, P. Guan, Fanyou Bu, Hao Wang, Dawen Wang, Yisheng Fan, Sichuan Hou, Zhilei Qiu","doi":"10.1186/s41065-022-00234-z","DOIUrl":"https://doi.org/10.1186/s41065-022-00234-z","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"159 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2022-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65774718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Prevalence and Significance of Leukopenia Induced by Intravenous Iron Therapy in a Large Cohort of Females with Iron Deficiency Anemia (IDA). 缺铁性贫血 (IDA) 女性大样本中静脉注射铁剂诱发白细胞减少症的发生率及意义。
3区 生物学
Hereditas Pub Date : 2022-05-11 DOI: 10.23750/abm.v93i2.11978
Vincenzo De Sanctis, Ashraf T Soliman, Mohamed A Yassin
{"title":"The Prevalence and Significance of Leukopenia Induced by Intravenous Iron Therapy in a Large Cohort of Females with Iron Deficiency Anemia (IDA).","authors":"Vincenzo De Sanctis, Ashraf T Soliman, Mohamed A Yassin","doi":"10.23750/abm.v93i2.11978","DOIUrl":"10.23750/abm.v93i2.11978","url":null,"abstract":"<p><strong>Introduction: </strong>Iron deficiency anemia (IDA) is the most common cause of anemia in both developed and developing countries. Leukopenia is an infrequent side effect of iron therapy reported in the literature as sporadic cases.</p><p><strong>Objective: </strong>To assess the prevalence of leukopenia, neutropenia and/or lymphocytopenia and its possible clinical impact if any, after intravenous iron therapy in adult patients with IDA.</p><p><strong>Patients and methods: </strong>This is a retrospective study conducted in Hamad Medical Corporation, Doha (Qatar). The clinical and biochemical data of 1.567 females (mean age: 29.5 years) with IDA who attended the Hematology Clinic and were treated with intravenous (i.v.) iron therapy were collected and analysed. Complete and differential blood counts and iron profile were studied before and after i.v. iron therapy. In addition, cases who developed infections during the time of leukopenia were noted and checked for possible complications.</p><p><strong>Results: </strong>30 cases (1.91%) developed leukopenia,15 cases (0.95%) developed neutropenia and 12 cases (0.76%) developed lymphocytopenia. All had normal white blood cell counts before treatment. Two patients (6.66%) had infection. One had upper respiratory tract infection and the other had urinary tract infection, the latter was treated with antibiotics. There was no reported other infection during or after i.v. iron therapy.</p><p><strong>Conclusions: </strong>Leukopenia in form of neutropenia or lymphocytopenia may occur as a side effect of i.v. iron therapy, however, its clinical significance appears to be limited.</p>","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"129 1","pages":"e2022183"},"PeriodicalIF":0.0,"publicationDate":"2022-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171860/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85508548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
N6-methyladenosine-related lncRNAs is a potential marker for predicting prognosis and immunotherapy in ovarian cancer n6 -甲基腺苷相关lncrna是预测卵巢癌预后和免疫治疗的潜在标志物
IF 2.7 3区 生物学
Hereditas Pub Date : 2022-03-18 DOI: 10.1186/s41065-022-00222-3
Xin Nie, Jichun Tan
{"title":"N6-methyladenosine-related lncRNAs is a potential marker for predicting prognosis and immunotherapy in ovarian cancer","authors":"Xin Nie, Jichun Tan","doi":"10.1186/s41065-022-00222-3","DOIUrl":"https://doi.org/10.1186/s41065-022-00222-3","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"159 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2022-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65774573","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
LPAR2 correlated with different prognosis and immune cell infiltration in head and neck squamous cell carcinoma and kidney renal clear cell carcinoma LPAR2与头颈部鳞状细胞癌和肾透明细胞癌的不同预后及免疫细胞浸润相关
IF 2.7 3区 生物学
Hereditas Pub Date : 2022-03-04 DOI: 10.1186/s41065-022-00229-w
K. Sun, Riyu Chen, Jing-zhang Li, Zhanxiong Luo
{"title":"LPAR2 correlated with different prognosis and immune cell infiltration in head and neck squamous cell carcinoma and kidney renal clear cell carcinoma","authors":"K. Sun, Riyu Chen, Jing-zhang Li, Zhanxiong Luo","doi":"10.1186/s41065-022-00229-w","DOIUrl":"https://doi.org/10.1186/s41065-022-00229-w","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"159 1","pages":""},"PeriodicalIF":2.7,"publicationDate":"2022-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65774629","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bringing the Second Event to Light (on a Light Box): Cerebral Vasospasm After Aneurysmal Rupture. 让第二事件(在灯箱上)发光:动脉瘤破裂后的脑血管痉挛。
IF 3.5 3区 生物学
Hereditas Pub Date : 2022-03-04 DOI: 10.1007/s12028-022-01456-9
Eelco F M Wijdicks
{"title":"Bringing the Second Event to Light (on a Light Box): Cerebral Vasospasm After Aneurysmal Rupture.","authors":"Eelco F M Wijdicks","doi":"10.1007/s12028-022-01456-9","DOIUrl":"10.1007/s12028-022-01456-9","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"100 1","pages":""},"PeriodicalIF":3.5,"publicationDate":"2022-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85472563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adaptation of the Oxygen Sensing System during Lung Development. 肺发育过程中氧传感系统的适应性
3区 生物学
Hereditas Pub Date : 2022-02-18 eCollection Date: 2022-01-01 DOI: 10.1155/2022/9714669
Karin M Kirschner, Simon Kelterborn, Herrmann Stehr, Johanna L T Penzlin, Charlotte L J Jacobi, Stefanie Endesfelder, Miriam Sieg, Jochen Kruppa, Christof Dame, Lina K Sciesielski
{"title":"Adaptation of the Oxygen Sensing System during Lung Development.","authors":"Karin M Kirschner, Simon Kelterborn, Herrmann Stehr, Johanna L T Penzlin, Charlotte L J Jacobi, Stefanie Endesfelder, Miriam Sieg, Jochen Kruppa, Christof Dame, Lina K Sciesielski","doi":"10.1155/2022/9714669","DOIUrl":"10.1155/2022/9714669","url":null,"abstract":"<p><p>During gestation, the most drastic change in oxygen supply occurs with the onset of ventilation after birth. As the too early exposure of premature infants to high arterial oxygen pressure leads to characteristic diseases, we studied the adaptation of the oxygen sensing system and its targets, the hypoxia-inducible factor- (HIF-) regulated genes (HRGs) in the developing lung. We draw a detailed picture of the oxygen sensing system by integrating information from qPCR, immunoblotting, <i>in situ</i> hybridization, and single-cell RNA sequencing data in <i>ex vivo</i> and <i>in vivo</i> models. HIF1<i>α</i> protein was completely destabilized with the onset of pulmonary ventilation, but did not coincide with expression changes in <i>bona fide</i> HRGs. We observed a modified composition of the HIF-PHD system from intrauterine to neonatal phases: <i>Phd3</i> was significantly decreased, while <i>Hif2a</i> showed a strong increase and the <i>Hif3a</i> isoform <i>Ipas</i> exclusively peaked at P0. Colocalization studies point to the <i>Hif1a-Phd1</i> axis as the main regulator of the HIF-PHD system in mouse lung development, complemented by the <i>Hif3a-Phd3</i> axis during gestation. <i>Hif3a</i> isoform expression showed a stepwise adaptation during the periods of saccular and alveolar differentiation. With a strong hypoxic stimulus, lung <i>ex vivo</i> organ cultures displayed a functioning HIF system at every developmental stage. Approaches with systemic hypoxia or roxadustat treatment revealed only a limited <i>in vivo</i> response of HRGs. Understanding the interplay of the oxygen sensing system components during the transition from saccular to alveolar phases of lung development might help to counteract prematurity-associated diseases like bronchopulmonary dysplasia.</p>","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"105 1","pages":"9714669"},"PeriodicalIF":0.0,"publicationDate":"2022-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886745/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85482317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Risk of Stillbirth for Fetuses With Specific Birth Defects. 有特定出生缺陷的胎儿死产的风险。
3区 生物学
Hereditas Pub Date : 2020-01-01 DOI: 10.1097/AOG.0000000000003614
Dominique Heinke, Eirini Nestoridi, Sonia Hernandez-Diaz, Paige L Williams, Janet W Rich-Edwards, Angela E Lin, Carla M Van Bennekom, Allen A Mitchell, Wendy N Nembhard, Ruth C Fretts, Drucilla J Roberts, C Wes Duke, Suzan L Carmichael, Mahsa M Yazdy
{"title":"Risk of Stillbirth for Fetuses With Specific Birth Defects.","authors":"Dominique Heinke, Eirini Nestoridi, Sonia Hernandez-Diaz, Paige L Williams, Janet W Rich-Edwards, Angela E Lin, Carla M Van Bennekom, Allen A Mitchell, Wendy N Nembhard, Ruth C Fretts, Drucilla J Roberts, C Wes Duke, Suzan L Carmichael, Mahsa M Yazdy","doi":"10.1097/AOG.0000000000003614","DOIUrl":"10.1097/AOG.0000000000003614","url":null,"abstract":"<p><strong>Objective: </strong>To estimate the risk of stillbirth (fetal death at 20 weeks of gestation or more) associated with specific birth defects.</p><p><strong>Methods: </strong>We identified a population-based retrospective cohort of neonates and fetuses with selected major birth defects and without known or strongly suspected chromosomal or single-gene disorders from active birth defects surveillance programs in nine states. Abstracted medical records were reviewed by clinical geneticists to confirm and classify all birth defects and birth defect patterns. We estimated risks of stillbirth specific to birth defects among pregnancies overall and among those with isolated birth defects; potential bias owing to elective termination was quantified.</p><p><strong>Results: </strong>Of 19,170 eligible neonates and fetuses with birth defects, 17,224 were liveborn, 852 stillborn, and 672 electively terminated. Overall, stillbirth risks ranged from 11 per 1,000 fetuses with bladder exstrophy (95% CI 0-57) to 490 per 1,000 fetuses with limb-body-wall complex (95% CI 368-623). Among those with isolated birth defects not affecting major vital organs, elevated risks (per 1,000 fetuses) were observed for cleft lip with cleft palate (10; 95% CI 7-15), transverse limb deficiencies (26; 95% CI 16-39), longitudinal limb deficiencies (11; 95% CI 3-28), and limb defects due to amniotic bands (110; 95% CI 68-171). Quantified bias analysis suggests that failure to account for terminations may lead to up to fourfold underestimation of the observed risks of stillbirth for sacral agenesis (13/1,000; 95% CI 2-47), isolated spina bifida (24/1,000; 95% CI 17-34), and holoprosencephaly (30/1,000; 95% CI 10-68).</p><p><strong>Conclusion: </strong>Birth defect-specific stillbirth risk was high compared with the U.S. stillbirth risk (6/1,000 fetuses), even for isolated cases of oral clefts and limb defects; elective termination may appreciably bias some estimates. These data can inform clinical care and counseling after prenatal diagnosis.</p>","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":"27 1","pages":"133-140"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033649/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85400067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Identification of key microRNAs in the carotid arteries of ApoE−/− mice exposed to disturbed flow 暴露于血流紊乱的ApoE−/-小鼠颈动脉中关键微小RNA的鉴定
IF 2.7 3区 生物学
Hereditas Pub Date : 2019-11-05 DOI: 10.1186/s41065-019-0112-x
Xinzhou Wang, Shuibo Gao, Liping Dai, Zhentao Wang, Hong Wu
{"title":"Identification of key microRNAs in the carotid arteries of ApoE−/− mice exposed to disturbed flow","authors":"Xinzhou Wang, Shuibo Gao, Liping Dai, Zhentao Wang, Hong Wu","doi":"10.1186/s41065-019-0112-x","DOIUrl":"https://doi.org/10.1186/s41065-019-0112-x","url":null,"abstract":"","PeriodicalId":55057,"journal":{"name":"Hereditas","volume":" ","pages":""},"PeriodicalIF":2.7,"publicationDate":"2019-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s41065-019-0112-x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46426076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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