標題: Titlebook: Clinical Relevance of Genetic Factors in Pulmonary Diseases; Takeshi Kaneko Book 2018 Springer Nature Singapore Pte Ltd. 2018 Smoking.Bron [打印本頁] 作者: 年邁 時間: 2025-3-21 19:06
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases影響因子(影響力)
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases影響因子(影響力)學科排名
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases網(wǎng)絡公開度
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases網(wǎng)絡公開度學科排名
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases被引頻次
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases被引頻次學科排名
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases年度引用
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases年度引用學科排名
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases讀者反饋
書目名稱Clinical Relevance of Genetic Factors in Pulmonary Diseases讀者反饋學科排名
作者: crucial 時間: 2025-3-21 21:29 作者: 攀登 時間: 2025-3-22 03:46
https://doi.org/10.1007/978-3-031-48542-8Recent advances in analytical techniques have yielded enormous quantities of diverse types of individual biological information, including genomic, epigenomic, transcriptomic, proteomic, metabolomic, and microbiomic data. Using this vast array of biometric information, new pulmonary disease phenotyp作者: 背景 時間: 2025-3-22 06:00 作者: 漸強 時間: 2025-3-22 11:00
https://doi.org/10.1007/978-3-319-75671-4pe is likely to be more closely related to a specific pathogenetic mechanism, and focusing on a particular phenotype may increase the power of genetic studies and consequently lead to a better understanding of an endotype defined by a distinct functional or pathobiological mechanism. Genetic predisp作者: prostatitis 時間: 2025-3-22 13:01 作者: prostatitis 時間: 2025-3-22 17:28
Irrigation with Saline Water in Pugliafficiency. PCD is usually inherited in an autosomal recessive manner and is genetically heterogeneous. Of the 30 mutations that are known to cause PCD, those affecting the ., ., ., ., ., ., and . 15–21%, 2–9%, 4–5%, 3%, 2–10%, 2–8%, and 6% of patients, respectively. In terms of the relationship betw作者: Radiation 時間: 2025-3-22 22:32 作者: 聚集 時間: 2025-3-23 02:12 作者: Substitution 時間: 2025-3-23 09:04 作者: 獨裁政府 時間: 2025-3-23 12:44 作者: 拒絕 時間: 2025-3-23 14:05
M. Jamil,M. Ashraf,S. Rehman,E. S. Rhang to efficacy, toxicity, safety, and responsiveness. An understanding of the genetic variants underlying interindividual differences in drug pharmacokinetics and pharmacodynamics could move us toward personalized precision medicine in which cutting-edge pharmacogenomic analyses are used. In additio作者: LARK 時間: 2025-3-23 18:46 作者: IOTA 時間: 2025-3-24 00:57 作者: 阻擋 時間: 2025-3-24 02:28 作者: 搏斗 時間: 2025-3-24 10:05 作者: Catheter 時間: 2025-3-24 14:17 作者: 指數(shù) 時間: 2025-3-24 18:33 作者: 責任 時間: 2025-3-24 20:20 作者: 妨礙 時間: 2025-3-25 02:35 作者: 人類的發(fā)源 時間: 2025-3-25 05:31
Mycobacterial Infection: TB and NTM—What Are the Roles of Genetic Factors in the Pathogenesis of Mycmycobacteria are linked to mycobacterial disease susceptibility. The elucidation of genetic factors underlying mycobacterial disease can reveal the contribution of specific genes to immunological processes essential for the pathogenesis and control of mycobacterial infections in humans.作者: sinoatrial-node 時間: 2025-3-25 11:28
Genetic Factors in Sleep Disorders: What Are the Roles of Genetic Factors in the Pathogenesis of Sleic predispositions with psychiatric disorders and sleep reactivity. Familial fatal insomnia is an autosomal-dominant genetic disorder caused by a mutation in the prion protein (.) gene. Although advances in genetics have resulted in identification of genetic causes of some sleep disorders, further s作者: OTHER 時間: 2025-3-25 14:59
Pharmacokinetics, Pharmacodynamics, and Toxicities: What Should We Know About Genetic Factors that Ang to efficacy, toxicity, safety, and responsiveness. An understanding of the genetic variants underlying interindividual differences in drug pharmacokinetics and pharmacodynamics could move us toward personalized precision medicine in which cutting-edge pharmacogenomic analyses are used. In additio作者: 褪色 時間: 2025-3-25 16:43 作者: 無法治愈 時間: 2025-3-25 23:07 作者: Common-Migraine 時間: 2025-3-26 03:56 作者: Entreaty 時間: 2025-3-26 04:38
https://doi.org/10.1007/978-981-10-8144-6Smoking; Bronchial Athma; COPD; Airway Disease; Heriditary Disease; Non-Heriditary Disease; IPF; Pulmonary 作者: infringe 時間: 2025-3-26 11:32
978-981-13-4074-1Springer Nature Singapore Pte Ltd. 2018作者: EXULT 時間: 2025-3-26 13:09
Takeshi KanekoDescribes the underlying genetic basis of common pulmonary diseases and discusses their pathogenesis and pathophysiology.Provide an essential basis for understanding different subtypes and phonotypes.作者: 無力更進 時間: 2025-3-26 19:35 作者: patella 時間: 2025-3-26 23:34 作者: overshadow 時間: 2025-3-27 01:11
Breeding Efforts and Biotechnologyve revealed the genetic components of common diseases. Genetic mapping is an unbiased method to comprehensively identify genes and biological pathways involved in diseases or traits. Genome-wide association studies (GWASs) have convincingly identified disease-associated loci. Most of the associated 作者: Mystic 時間: 2025-3-27 07:38
https://doi.org/10.1007/978-3-319-75671-4thma and for identifying targets of treatment for the syndrome. As with studies of other common complex diseases, genetic studies of asthma have led to considerable advances in the understanding of this disease. Genome-wide association studies have greatly advanced the identification of the most imp作者: VALID 時間: 2025-3-27 09:40
Amrita Srivastav,Tushar Khare,Vinay Kumar This is because approximately 15% of the smoking population eventually suffer from this disease, while the others sustain normal lungs despite their smoking habit. A well-known causal gene of COPD is the serine protease inhibitor A1 (SERPINA1) gene, which causes hereditary severe α1-antitrypsin (A1作者: Junction 時間: 2025-3-27 16:46 作者: GOAT 時間: 2025-3-27 18:41 作者: 辭職 時間: 2025-3-28 00:50 作者: hauteur 時間: 2025-3-28 05:48
Seville Flowers,Frederick R. Evans. HHT is often found to be the underlying cause of pulmonary arteriovenous malformations (PAVMs). Mutations in ., ., ., ., ., and . have been identified in cases of HPAH. Mutations in ., ., and . have been identified in cases of HHT. The average penetrance of . mutations is only 30% in HPAH. In cont作者: 果仁 時間: 2025-3-28 06:23
Irrigation with Saline Water in Pugliaoped countries and now being more prevalent than tuberculosis. Severe mycobacterial disease is mostly confined to patients who are immunocompromised either by acquired or inherited causes. Genetic aberrations in pathways critical for host defense against mycobacteria—which involve functional interle作者: prosthesis 時間: 2025-3-28 12:59
Bacterial Reduction of Selenium, germline mutations, inherited gene alterations, and single-nucleotide polymorphisms. Germline mutations and inherited gene alterations are related to the development of familial lung cancer, and certain single-nucleotide polymorphisms are associated with an increase in the risk of lung cancer. Othe作者: 考博 時間: 2025-3-28 16:36
Andrew C. Chang,Deborah Brawer Silva last 50?years. Malignant mesothelioma is characterized by a long latency period of 40?years between initial exposure to asbestos and tumor development, indicating that multiple somatic genetic alterations contribute to its carcinogenesis. Molecular genetic studies have identified multiple chromosom作者: 清晰 時間: 2025-3-28 20:41 作者: Meditate 時間: 2025-3-29 02:35 作者: 公共汽車 時間: 2025-3-29 06:35 作者: 同步左右 時間: 2025-3-29 10:44 作者: Femine 時間: 2025-3-29 14:36 作者: 豎琴 時間: 2025-3-29 16:34
Approaches to Understanding the Genetic Basis of Complex Diseases: Overview—What Is the Rationale fove revealed the genetic components of common diseases. Genetic mapping is an unbiased method to comprehensively identify genes and biological pathways involved in diseases or traits. Genome-wide association studies (GWASs) have convincingly identified disease-associated loci. Most of the associated 作者: 最后一個 時間: 2025-3-29 19:59 作者: Outwit 時間: 2025-3-30 00:41
COPD: Hereditary (A1-AT) and Non-hereditary—What Are the Roles of Genetic Factors in the Pathogenesi This is because approximately 15% of the smoking population eventually suffer from this disease, while the others sustain normal lungs despite their smoking habit. A well-known causal gene of COPD is the serine protease inhibitor A1 (SERPINA1) gene, which causes hereditary severe α1-antitrypsin (A1作者: 天賦 時間: 2025-3-30 04:05
Cystic Fibrosis, Primary Ciliary Dyskinesia, and Diffuse Panbronchiolitis: Hereditary and Non-heredining genetic disorder in Caucasians, caused by mutations in a single gene on the long arm of chromosome 7 that encodes the cystic fibrosis transmembrane conductance regulator (CFTR). The predominant CFTR mutation is Phe508del, yet more than 2000 variants in this gene have been identified, which can 作者: 硬化 時間: 2025-3-30 08:13 作者: 話 時間: 2025-3-30 12:57
Other Diffuse Lung Diseases: Diffuse Cystic Lung Diseases (LAM, TSC, BHD), Sarcoidosis, Pulmonary Als. LAM occurs in patients with tuberous sclerosis complex (TSC-LAM) and as a sporadic form in patients who do not have tuberous sclerosis (S-LAM). Patients with TSC-LAM have germline mutations either in TSC1 located on chromosome 9q34 or TSC2 located on chromosome 16p13.3, and the majority have a ge作者: 錯誤 時間: 2025-3-30 19:36
Pulmonary Vascular Diseases: Pulmonary Hypertension and HHT—What Are the Roles of Genetic Factors in. HHT is often found to be the underlying cause of pulmonary arteriovenous malformations (PAVMs). Mutations in ., ., ., ., ., and . have been identified in cases of HPAH. Mutations in ., ., and . have been identified in cases of HHT. The average penetrance of . mutations is only 30% in HPAH. In cont作者: 踉蹌 時間: 2025-3-30 22:13 作者: 整理 時間: 2025-3-31 00:52 作者: Painstaking 時間: 2025-3-31 07:29 作者: Diskectomy 時間: 2025-3-31 12:17
Genetic Factors in Sleep Disorders: What Are the Roles of Genetic Factors in the Pathogenesis of SleOSA) is a common and complex sleep disorder and has heritability. A recent genome-wide association study (GWAS) identified some genetic risks for OSA with genome-wide levels of significance for the first time. Congenital central hypoventilation syndrome has causative mutations in the paired-like hom作者: 聽寫 時間: 2025-3-31 15:08 作者: ostracize 時間: 2025-3-31 21:01
EGFR: How Important Is EGFR Mutation Status in the Management of Lung Cancer?ammed cell death. Along with the molecular biology of the cell, over the last several decades, numerous other important factors that contribute to cell growth, differentiation, and proliferation processes have been found. In contrast to normal cells, cancer cells have the capacity to proliferate wit作者: grieve 時間: 2025-4-1 00:18
ALK and Others: How Important Are ALK and Other Mutations in the Management of Lung Cancer?ular-targeted agents. Over the last decade, treatment strategies for non-small cell lung cancer (NSCLC) patients have rapidly evolved beyond conventional chemotherapy with molecular-targeted agents. Gene aberration in . (.) or . (.) has successfully being targeted, and the corresponding tyrosine kin
