المؤلفون: Shuye Lin, Hanli Xu, Lin Qin, Mengdi Pang, Ziyu Wang, Meng Gu, Lishu Zhang, Cong Zhao, Xuefeng Hao, Zhiyun Zhang, Weimin Ding, Jianke Ren, Jiaqiang Huang

المصدر: Acta Pharmaceutica Sinica B, Vol 13, Iss 5, Pp 2086-2106 (2023)

مصطلحات موضوعية: Lung cancer, Intratumor heterogeneity, Splice variants, Intragenic CpG methylation, Protease serine 3, Myeloid zinc finger 1, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211383523000576; https://doaj.org/toc/2211-3835

URL الوصول: https://doaj.org/article/5faaba36d4ed4623a59063daac58d8c6

المؤلفون: Lin, Bonan, Zhou, Xiaomeng, Lin, Shuye, Wang, Xiaoyue, Zhang, Meiying, Cao, Baoping, Dong, Yan, Yang, Shuai, Wang, Ji Ming, Guo, Mingzhou, Huang, Jiaqiang

المصدر: Journal of Molecular Medicine. :1-13

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المؤلفون: Miano, Maria Giuseppina, Filippini, Francesco, Trujillo, Mariajos, Conte, Ivan, Lanzara, Carmela, Milln, Jos Maria, De Bernardo, Carmelilia, Grammatico, Barbara, Mangino, Massimo, Torrente, Isabella, Carrozzo, Romeo, Rinaldi, Ernesto, Ventruto, Valerio, Durso, Michele, Ayuso, Carmen, Ciccodicola, Alfredo, TESTA, Francesco, SIMONELLI, Francesca

المساهمون: Miano, Maria Giuseppina, Testa, Francesco, Filippini, Francesco, Trujillo, Mariajo, Conte, Ivan, Lanzara, Carmela, Milln, Jos Maria, De Bernardo, Carmelilia, Grammatico, Barbara, Mangino, Massimo, Torrente, Isabella, Carrozzo, Romeo, Simonelli, Francesca, Rinaldi, Ernesto, Ventruto, Valerio, Durso, Michele, Ayuso, Carmen, Ciccodicola, Alfredo

المصدر: Human Mutation, Vol. 18, No 2 (2001) pp. 101-108

مصطلحات موضوعية: Comparative protein modeling, Male, Models, Molecular, DFNB10, Chromosomes, Human, Pair 21, Genetic Linkage, medicine.medical_treatment, DNA Mutational Analysis, Conserved sequence, Protease, serine, Consanguinity, Genes, Recessive/genetics, Serine Endopeptidases/chemistry/ genetics, Missense mutation, Membrane Protein, Genetics (clinical), Conserved Sequence, ddc:616, Genetics, biology, Linkage, Mutation analysi, Serine Endopeptidases, Chromosomes, Human, Pair 21/genetics, Chromosome Mapping, Neoplasm Proteins, Pedigree, Serine protease, Serine Endopeptidase, Mutation (genetic algorithm), Female, Conserved Sequence/genetics, Human, Tunisia, Genotype, Mutation, Missense/ genetics, Hearing Loss, Sensorineural, Molecular Sequence Data, Hearing Loss, Sensorineural/congenital/ genetics, Mutation, Missense, Locus (genetics), Genes, Recessive, DNA Mutational Analysi, Neoplasm Protein, Genetic, Audiometry, Genetic linkage, DFNB8, Linkage (Genetics)/genetics, medicine, Humans, Amino Acid Sequence, Deafne, Gene, TMPRSS3, Protease, Binding Sites, Base Sequence, Binding Site, Membrane Proteins, Molecular biology, Protein Structure, Tertiary, biology.protein, Transmembrane protease, serine, 3, Non syndromic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffb81ccd60a8b7d8cbd9d5e065c00f7
https://pubmed.ncbi.nlm.nih.gov/11462234

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المؤلفون: Lee J; Department of Biology, College of Natural Sciences, Kyungpook National University, Daegu, South Korea., Baek JI, Choi JY, Kim UK, Lee SH, Lee KY

المصدر: Gene [Gene] 2013 Dec 15; Vol. 532 (2), pp. 276-80. Date of Electronic Publication: 2013 Aug 17.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE

مواضيع طبية MeSH: Genes, Recessive* , Polymorphism, Genetic*, Membrane Proteins/*genetics , Neoplasm Proteins/*genetics , Serine Endopeptidases/*genetics, Adolescent ; Adult ; Amino Acid Sequence ; Base Sequence ; Case-Control Studies ; Child ; Child, Preschool ; Connexin 26 ; Connexins ; DNA Mutational Analysis ; Deafness/diagnostic imaging ; Deafness/genetics ; Deafness/pathology ; Female ; Genetic Association Studies ; Humans ; Infant ; Male ; Middle Aged ; Molecular Sequence Data ; Mutation, Missense ; Pedigree ; Radiography ; Republic of Korea ; Sequence Analysis, DNA ; Vestibule, Labyrinth/diagnostic imaging ; Vestibule, Labyrinth/pathology ; Young Adult

SCR Disease Name: Nonsyndromic Deafness