المؤلفون: Romero Cortadellas, Lídia

المساهمون: University/Department: Universitat Internacional de Catalunya. Departament de Ciències Bàsiques

مرشدي الرسالة: Sanchez-Fernandez, Mayka

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Iron, Anaemia, Rare disease, Mutation, Genetics, Ciències de la Salut

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/689433

المؤلفون: Chen, B., Chen, T., Zeng, X., Zhang, W., Lu, Q., Hou, Z., Zhou, J., Helal, S.

المصدر: IEEE/ACM Transactions on Computational Biology and Bioinformatics IEEE/ACM Trans. Comput. Biol. and Bioinf. Computational Biology and Bioinformatics, IEEE/ACM Transactions on. 21(4):880-889 Aug, 2024

المؤلفون: Liu, Z., Yang, J., Chen, K., Yang, T., Li, X., Lu, B., Fu, D., Zheng, Z., Luo, C.

المصدر: IEEE Internet of Things Journal IEEE Internet Things J. Internet of Things Journal, IEEE. 11(11):20002-20014 Jun, 2024

المؤلفون: Luo, Yiwen, Yuan, Yixuan

المصدر: 2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Bioinformatics and Biomedicine (BIBM), 2023 IEEE International Conference on. :2133-2136 Dec, 2023

Relation: 2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)

المؤلفون: Guo, Ziyuan, Wang, Yiwei, Liang, Anda, Van Devanter, Wyn, Zhang, Peng

المصدر: 2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Bioinformatics and Biomedicine (BIBM), 2023 IEEE International Conference on. :2729-2736 Dec, 2023

Relation: 2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)

المؤلفون: Çelik, Muhammed Hasan, Gagneur, Julien, Lim, Ryan G, Wu, Jie, Thompson, Leslie M, Xie, Xiaohui

المصدر: Human Genetics and Genomics Advances. 5(3)

مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Rare Diseases, Human Genome, Neurodegenerative, ALS, Brain Disorders, Neurosciences, Amyotrophic Lateral Sclerosis, Humans, Chromatin, Promoter Regions, Genetic, Algorithms, Gene Expression Regulation, Chromatin Immunoprecipitation Sequencing, Histones, Aberrant Gene Expression, Chromatin Accessibility, Epigenetics, Motor Neuron Disease, Multiomics, Outlier Detection, Post-transcriptional Regulation, Rare Disease, Transcriptional Regulation

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8sh544xh
https://escholarship.org/content/qt8sh544xh/qt8sh544xh.pdf

المؤلفون: Durán Fernández, Mónica

مرشدي الرسالة: Meseguer Navarro, Anna, Sarró Tauler, Eduard, Ariceta Iraola, Gema

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Ronyó, Riñón, Kidney, Malaltia de Dent, Enfermedad de Dent, Dent disease, Malaltia rara, Enfermedad Rara, Rare disease, Ciències Experimentals

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/670484

المؤلفون: Leadman, Devon, Xu, Yanji, Qu, Sue, Zhu, Qian

المصدر: 2022 IEEE International Conference on Bioinformatics and Biomedicine (BIBM) Bioinformatics and Biomedicine (BIBM), 2022 IEEE International Conference on. :3263-3266 Dec, 2022

Relation: 2022 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)

المؤلفون: Koutsoukos, Stefanos A.^{Aff1, Aff2}, Bilousova, Ganna^{Aff1, Aff2, IDs13555024012394_cor2}

المصدر: Dermatology and Therapy: Research, treatment and aesthetic interventions in dermatology. :1-14

المؤلفون: Shah, Ayesha^{Aff1, Aff2}, Tabibian, James^{Aff6, Aff7}, Buness, Cynthia^{Aff3, Aff4, Aff5}, Holtmann, Gerald J.^{Aff1, Aff2, IDs10620024084974_cor4}

المصدر: Digestive Diseases and Sciences. :1-6