派博傳思國際中心

標題: Titlebook: Mechanism and Genetic Susceptibility of Neurological Disorders; Andleeb Khan,Mashoque Ahmad Rather,Ghulam Md Ashra Book 2024 The Editor(s) [打印本頁]

作者: Limbic-System 時間: 2025-3-21 17:28
書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders影響因子(影響力)

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders影響因子(影響力)學科排名

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders網絡公開度

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders網絡公開度學科排名

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders被引頻次

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders被引頻次學科排名

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders年度引用

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders年度引用學科排名

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders讀者反饋

書目名稱Mechanism and Genetic Susceptibility of Neurological Disorders讀者反饋學科排名

作者: GOAD 時間: 2025-3-21 21:26

作者: 廢墟 時間: 2025-3-22 03:19
Mashoque Ahmad Rather,Andleeb Khan,Hayate Javed,Sadaf Jahan,Rizwana Tabassum,Rubia Begum

作者: yohimbine 時間: 2025-3-22 06:20
Liam Goldman,Mario P. Espinosa,Manish Kumar,Luca H. Debs,Fernando L. Vale,Kumar Vaibhav

作者: Fracture 時間: 2025-3-22 08:58

作者: Systemic 時間: 2025-3-22 16:10

作者: 貴族 時間: 2025-3-22 17:22
Durafshan Sakeena Syed,Mohamad Sultan Khan,Urba Afnan,Mohd Jamaal Dar,Tariq Maqbool

作者: 強有力 時間: 2025-3-23 00:57

作者: 額外的事 時間: 2025-3-23 04:25

作者: REP 時間: 2025-3-23 07:20

作者: 羊欄 時間: 2025-3-23 10:09
Mohd Yasir Khan,Hamda Khan,Farah Maarfi,Afreen Khanam,Ziaul Hasan,Arbab Husain

作者: APO 時間: 2025-3-23 15:24
Book 2024mphasizes the role played by a diverse array of genes in the development and progression of these conditions, highlighting the multifaceted genetic susceptibility that underlies their manifestation.?.?

作者: 提升 時間: 2025-3-23 18:19

作者: FRONT 時間: 2025-3-24 01:42
Gulzar Ahmed Rather,Vishal Mathur,Muzafar Riyaz,Raman Yadav,Anima Nanda,Arif Jamal Siddiqui,Mashoques of man are given considerable attention. Some previous attempts to define such vital goals are analysed and criticized. A new characterization is proposed, in which the vital goals are conceptually linked to the notion of happiness. A person‘s vital goals are such states of affairs as are necessary and toge978-94-015-7768-7

作者: Neutral-Spine 時間: 2025-3-24 06:17
Priyanka Singh,Komal Gupta,Manu Sharma,Shobhit Kumars of man are given considerable attention. Some previous attempts to define such vital goals are analysed and criticized. A new characterization is proposed, in which the vital goals are conceptually linked to the notion of happiness. A person‘s vital goals are such states of affairs as are necessary and toge978-94-015-7768-7

作者: Electrolysis 時間: 2025-3-24 08:14

作者: MEN 時間: 2025-3-24 14:07

作者: 蒙太奇 時間: 2025-3-24 16:54
Head Trauma: Etiology, Pathophysiology, Clinical Manifestation, and Biomarkers,velop treatments, and to enact preventative actions to reduce the global burden of the traumatic injuries to the head. These endeavors have resulted in an overall reduced deaths and TBI-related hospitalizations. In this contemporary chapter, we dissect different etiologies and the pathophysiology of

作者: 巧思 時間: 2025-3-24 20:06
Current Understanding of DNA Methylation in the Pathogenesis of Neuropathic Pain,n channels expressed transcriptionally under the regulation of these proteins in the dorsal root ganglia following nerve injury, which is frequently utilized in neuropathic pain models. A deeper understanding of the epigenetic reprogramming involved in the transition from acute to chronic pain may l

作者: 避開 時間: 2025-3-25 00:46
Decoding Dystrophin Gene Mutations: Unraveling the Mysteries of Muscular Dystrophy,es around the age of 4, but it can extend to involve the heart, gastrointestinal tract, and respiratory muscles later in the disease course, and the weakness intensifies with time. Although the severity and survival time might vary for DMD, BMD, and DCM, dystrophinopathy has no cure except for the r

作者: 裝入膠囊 時間: 2025-3-25 03:25
Etiology of Ataxia: A Mechanistic Insight of Autoimmune, Toxicity, and Genetic Approach,lude pathogenic repeat extensions (CAG, CTG, GAA), DNA repair anomalies, gene-sequence alteration, point mutations, and mode of inheritance transmission. Additionally, the role of degenerative ataxia concerning multiple system atrophy and idiopathic late-onset cerebellar ataxia-related neurological

作者: Orgasm 時間: 2025-3-25 10:26
miRNA Dysregulation in Schizophrenia,hizophrenia, are known to implicate aberrant miRNAs expression and malfunction in their pathogenesis. This study shows that in schizophrenia, the levels of mature miRNA present in the cerebral cortex as well as in peripheral blood mononuclear cells (PBMCs) were altered. In this chapter, we summarize

作者: 小丑 時間: 2025-3-25 14:17
Axonal Degeneration, Impaired Axonal Transport, and Synaptic Dysfunction in Motor Neuron Disorder,(PMA). These diseases reflect symptoms of muscle cramps, dysphagia, spasticity, muscle weakness, atrophy, disturbance of neuropsychiatric behavior, and loss of homeostasis. There is a strong correlation between MNDs and axonal transport impairment, as evidence suggests the defective anterograde and

作者: intimate 時間: 2025-3-25 15:54
Genetic Modulators in Amyotrophic Lateral Sclerosis,iple factors contributing to the development of ALS, including defects in the metabolism of RNA and DNA, disturbance in DNA repair mechanism, protein homeostasis dysfunction, damage in nucleocytoplasmic transport, oxidative stress (OS), excitotoxicity, axonal transport alteration, neuroinflammation,

作者: Communal 時間: 2025-3-25 22:14
Modulators and Poststroke Behavioral Changes,equently experience emotional and behavioral changes, which includes irritability, cognitive impairment, disability, inattention, disorientation, and feelings of anger, anxiety, or depression. Despite a plethora of neuroscientific initiatives and therapeutic efforts, several remedial pages are still

作者: 現實 時間: 2025-3-26 03:24

作者: slipped-disk 時間: 2025-3-26 07:07

作者: 憲法沒有 時間: 2025-3-26 09:18
Gene Editing Tool for Neurodegenerative Diseases,or addressing these challenges. Emerging gene-editing tools (GETs), such as CRISPR-Cas9 and zinc finger nucleases (ZFNs), offer promising potential for correcting defective genes or DNA, leading to the restoration of lost neural function and connectivity. Furthermore, the integration of GETs with st

作者: 血友病 時間: 2025-3-26 13:20
Lumbar Disc Disease: An Overview, the spine, bad posture, weight gain, and inheritance, can be linked to the cause of LDS. Low backache, leg discomfort, sensations of numbness or tingling in the lower extremities or feet, weaknesses, and trouble walking or standing are some of the signs of LDS. Diagnosis of LDS typically involves i

作者: adumbrate 時間: 2025-3-26 19:55

作者: 說笑 時間: 2025-3-26 21:15
Rahul Saxena,Babita,Suyash Saxena,Sudipta Kundu such as those from the less-distant planets, particularly the photons from the Jupiter red-spot. The development of the photoacoustic circular analysers a deca978-90-481-8355-5978-94-015-7644-4Series ISSN 1389-2185

作者: Constitution 時間: 2025-3-27 03:20
978-981-99-9406-9The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapor

作者: 顯而易見 時間: 2025-3-27 06:08
https://doi.org/10.1007/978-981-99-9404-5Neurological diseases; Genetic susceptibility; Modulators in Neurological disorders; Metal Homeostasis;

作者: flammable 時間: 2025-3-27 11:44

作者: 柳樹；枯黃 時間: 2025-3-27 16:13

作者: Coronation 時間: 2025-3-27 21:18

作者: Bumptious 時間: 2025-3-27 23:51

作者: 移植 時間: 2025-3-28 02:29
Current Understanding of DNA Methylation in the Pathogenesis of Neuropathic Pain,fe. Injury to peripheral sensory nerves is well documented to change the expression of genes in the neurons and sensory nerves, which has a significant impact on the spinal cord’s synaptic plasticity and the onset and progression of chronic pain. N-methyl-D-aspartate (NMDA) receptors and α2δ1 are ex

作者: 厚顏無恥 時間: 2025-3-28 09:35
Decoding Dystrophin Gene Mutations: Unraveling the Mysteries of Muscular Dystrophy,ferent types including Duchenne, Becker, congenital, Emery–Dreifuss, oculopharyngeal, facioscapulohumeral, myotonic, and limb-girdle muscular dystrophy. Dystrophin gene mutation causes dystrophinopathy, including Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and DMD-associated

作者: 能夠支付 時間: 2025-3-28 11:19
Etiology of Ataxia: A Mechanistic Insight of Autoimmune, Toxicity, and Genetic Approach,vous system are the cerebellum and the spinal cord. Ataxia etiology is associated with an extensive variation in acquired and genetic factors. Therefore, this chapter provides an overview of the background of ataxia and categorizes it into acquired and genetic based on the underlying causes of this

作者: ANTH 時間: 2025-3-28 14:41

作者: 吹牛者 時間: 2025-3-28 19:31
Muscular Dystrophy: Underlying Cellular and Molecular Mechanisms and Various Nanotherapeutic Approaoth dominant and recessive and can be autosomal or X-linked. These disorders are marked by gradual muscle degeneration and diminished muscle potency of variable severity depending on the stage and onset age of the disease, as well as the distribution of affected muscles. In most cases, patients ulti

作者: CRAMP 時間: 2025-3-28 23:05

作者: 財主 時間: 2025-3-29 06:44
,Alterations in Receptor Genes in Huntington’s Disease,genes in HD are investigated, with a specific focus on the role of these genes in the disease and the receptors that are altered. Receptor genes play a crucial role in HD by encoding proteins involved in cellular signal transduction. Dysfunction in these receptors can disrupt normal cellular activit

作者: 新娘 時間: 2025-3-29 08:12
Genetic Modulators in Amyotrophic Lateral Sclerosis,e loss of motor neurons in the cortical, spinal cord, and brainstem regions. This neuronal death leads to paralysis and, in later stages, respiratory failure, often resulting in death. The incidence of ALS is relatively low, with around 1–2 people approx. per 100,000 annually and life expectancy for

作者: Astigmatism 時間: 2025-3-29 14:59
Modulators and Poststroke Behavioral Changes,l necrosis, a dynamic and complex event. Stroke ranks third in terms of disability-adjusted life years and this condition is the second major cause of mortality. The cerebral vasculature, an important target of oxi-inflammatory stress-driven biomolecular degradation, is interestingly playing a signi

作者: opportune 時間: 2025-3-29 17:05
,Presynaptic Dysfunction in Parkinson’s Disease,These signs are brought on by dopamine neuronal deprivation in the substantia nigra of the brain. The drugs available will lessen the symptoms but the advancement of the disease cannot be ceased. Different studies manifested that synaptic dysfunction and degradation of axons take place earlier than

作者: 動機 時間: 2025-3-29 21:58