Search Results - "next generation sequencing"

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family by Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

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Genomic characteristics of SARS-CoV-2 in Beijing, China, 2021 by Zhaomin Feng, Shujuan Cui, Bing Lyu, Zhichao Liang, Fu Li, Lingyu Shen, Hui Xu, Peng Yang, Quanyi Wang, Daitao Zhang, Yang Pan

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Based on Immune Microenvironment and Genomic Status, Exploring Immunotherapy in Advanced Hidradenocarcinoma: A Retrospective Analysis by Jing Lin, Li Zhu, Yanping Chen, Qian Li, Zhiheng Ke, Huishan Zhang, Yufang Huang, Jianping Lu, Yu Chen

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A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report by Soheila Zareifar, Hassan Dastsooz, Mahdi Shahriari, Mohammad Ali Faghihi, Golsa Shekarkhar, Mohammadreza Bordbar, Omid Reza Zekavat, Nader Shakibazad

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Diffuse pulmonary meningotheliomatosis with pan-TRK expression by immunohistochemistry: a novel finding and potential pitfall by Cansu Karakas, Michael A. Nead, Moises J. Velez

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Targeted gene panel for genetic testing of south Indian children with steroid resistant nephrotic syndrome by Annes Siji, K. N. Karthik, Varsha Chhotusing Pardeshi, P. S. Hari, Anil Vasudevan

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TMP3-NTRK1 rearranged uterine sarcoma: A case report by William Boyle, Anthony Williams, Sudha Sundar, Jason Yap, Philippe Taniere, Pauline Rehal, Raji Ganesan

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Gene panel for the diagnosis of epidermolysis bullosa: proposal for a viable and efficient approach, by Luiza Monteavaro Mariath, Ana Elisa Kiszewski, Jeanine Aparecida Frantz, Marina Siebert, Ursula Matte, Lavínia Schuler-Faccini

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Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report by Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C. Elalaoui, Maria Mansouri, Lamia Boualla, Alexandre DIonne-Laporte, Dan Spiegelman, Patrick A. Dion, Patrick Cossette, Guy A. Rouleau, Abdelaziz Sefiani

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Circular RNA Expression Profiling and the Potential Role of hsa_circ_0089172 in Hashimoto's Thyroiditis via Sponging miR125a-3p by Si Xiong, Huiyong Peng, Xiangmei Ding, Xuehua Wang, Li Wang, Chenguang Wu, Shengjun Wang, Huaxi Xu, Yingzhao Liu

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Atypical CHARGE associated with a novel frameshift mutation of CHD7 in a Chinese neonatal patient by Yan-ping Xu, Li-ping Shi, Jiajun Zhu

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Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report by Youhong Fang, Weizhong Gu, Youyou Luo, Jie Chen

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Clemastine Ameliorates Perioperative Neurocognitive Disorder in Aged Mice Caused by Anesthesia and Surgery by Wensi Wu, Xiaojun Zhang, Jiaxin Zhou, Hongmei Yang, Junjun Chen, Le Zhao, Junying Zhong, Wei-jye Lin, Wei-jye Lin, Zhi Wang

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Successful early fetal sex determination using cell-free fetal DNA isolated from maternal capillary blood: A pilot study by Nadiya Kazachkova, Julia Gontar, Oleg Verlinsky, Igor Ilyin

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IPEX Syndrome: Improved Knowledge of Immune Pathogenesis Empowers Diagnosis by Federica Barzaghi, Laura Passerini

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SWI/SNF-deficient undifferentiated/rhabdoid carcinoma of the gallbladder carrying a POLE mutation in a 30-year-old woman: a case report by Tiemo S. Gerber, Abbas Agaimy, Arndt Hartmann, Michael Habekost, Wilfried Roth, Albrecht Stenzinger, Peter Schirmacher, Beate K. Straub

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BRCA-mutated gastric adenocarcinomas are associated with chromosomal instability and responsiveness to platinum-based chemotherapy by Ji Hyun Oh, Chang Ohk Sung, Hyung-Don Kim, Sung-Min Chun, Jihun Kim

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Retinoblastoma genetics screening and clinical management by Himika Gupta, Sivasankar Malaichamy, Ashwin Mallipatna, Sakthivel Murugan, Nallathambi Jeyabalan, Vishnu Suresh Babu, Anuprita Ghosh, Arkasubhra Ghosh, Sam Santhosh, Somasekar Seshagiri, Vedam L. Ramprasad, Govindasamy Kumaramanickavel

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Relevance of PD-L1 Non-Coding Polymorphisms on the Prognosis of a Genetically Admixed NSCLC Cohort by Machado-Rugolo J, Gutierrez Prieto T, Fabro AT, Parra Cuentas ER, Sá VK, Baldavira CM, Rainho CA, Castelli EC, Farhat C, Takagaki TY, Nagai MA, Capelozzi VL

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Mutation Breeding and Efficiency Enhancing Technologies for Resistance to Striga in Cereals

Table of Contents: “…Striga as a constraint to cereal production in sub-Saharan Africa and the role of host plant resistance -- Physical mutagenesis in cereal crops -- Screening for resistance to Striga hermonthica in mutagenized sorghum and upland rice in Burkina Faso -- Mutation breeding for resistance to Striga hermonthica in sorghum and rice for sustainable food production in Sudan -- Phenotyping for resistance to Striga asiatica in rice and maize mutant populations in Madagascar -- An agar-based method for determining mechanisms of Striga resistance in sorghum -- Histological analysis of Striga infected plants -- Striga germination stimulant analysis -- Identification of closely related polymorphisms with Striga resistance using next generation sequencing -- Rapid cycling and generation advancement for accelerated mutation breeding in sorghum -- Anther culture of rice for accelerated development of doubled haploid Striga resistant germplasm.…”
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