Jove
Visualize
联系我们

相关概念视频

Nephrotic Syndrome I : Introduction01:24

Nephrotic Syndrome I : Introduction

9
Nephrotic Syndrome is a chronic kidney disorder defined by clinical findings such as severe proteinuria, hypoalbuminemia, hyperlipidemia, and edema. These symptoms result from damage to the glomeruli, the kidney’s filtering units, increasing their permeability to proteins.Definition and Meaning:Proteinuria, defined as the loss of more than 3.5 grams of protein per day in adults, is a crucial feature of nephrotic syndrome. This condition is often accompanied by edema, the accumulation of...
9
Nephrotic Syndrome II : Assessment and Medical Management01:26

Nephrotic Syndrome II : Assessment and Medical Management

8
IntroductionNephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.AssessmentPatient History: Document...
8
Nephrotic Syndrome III : Nursing Management01:24

Nephrotic Syndrome III : Nursing Management

19
Nursing management for nephrotic syndrome adapts as the disease progresses, with strategies evolving to address advancing symptoms and complications.Early-Stage Management In the early stages, nursing interventions for nephrotic syndrome resemble those used in managing acute glomerulonephritis, focusing on symptom monitoring, fluid balance, and managing mild to moderate edema.Vital Signs: Regularly monitor blood pressure, pulse, respiratory rate, and temperature to promptly identify...
19
Nephrons01:10

Nephrons

2.7K
The kidneys are intricate organs with millions of working units known as nephrons. Each nephron features two major structures: the renal corpuscle, which facilitates blood plasma filtration, and the renal tubule, which handles the glomerular filtrate. Blood supply is directly linked to the nephrons. The renal corpuscle consists of the glomerulus, a capillary network, and the Bowman's capsule, a double-walled epithelial structure that encases the glomerulus. The filtering of blood plasma...
2.7K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

10.7K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.7K
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

2.4K
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
2.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Factors Associated with Vaccination Status of Neonates in the Tertiary Referral Department of Neonatology and Neonatal Intensive Care in the North-Eastern Region of Poland.

Vaccines·2025
Same author

Metabolic Interactions in the Tumor Microenvironment of Classical Hodgkin Lymphoma: Implications for Targeted Therapy.

International journal of molecular sciences·2025
Same author

Comparative Evaluation of Urinary Biomarkers in Wilms Tumor Survivors and Children with Chronic Kidney Disease.

International journal of molecular sciences·2025
Same author

Recent Developments in Pediatric Nephrology.

Journal of clinical medicine·2025
Same author

Effects of <i>GBA1</i> Variants and Prenatal Exposition on the Glucosylsphingosine (Lyso-Gb1) Levels in Gaucher Disease Carriers.

International journal of molecular sciences·2024
Same author

Long- and Short-Term Glucosphingosine (lyso-Gb1) Dynamics in Gaucher Patients Undergoing Enzyme Replacement Therapy.

Biomolecules·2024
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关实验视频

Updated: Jul 15, 2025

Induction of Nephrotic Syndrome in Mice by Retrobulbar Injection of Doxorubicin and Prevention of Volume Retention by Sustained Release Aprotinin
07:38

Induction of Nephrotic Syndrome in Mice by Retrobulbar Injection of Doxorubicin and Prevention of Volume Retention by Sustained Release Aprotinin

Published on: May 6, 2018

8.5K

由NUP93致病变体引起的类固醇耐药性脏综合征

Anna Wasilewska1, Agnieszka Rybi-Szuminska1, Pawel Dubiela2,3

  • 1Paediatric Nephrology Department, Medical University of Bialystok, Waszyngtona 17, 15-273 Białystok, Poland.

Journal of clinical medicine
|September 28, 2023
PubMed
概括

类固醇耐药性性综合征 (SRNS) 可能有遗传原因,包括NUP93变种. 这一案例突显了在患有SRNS的儿科患者中特定的NUP93变异的临床相关性.

关键词:
在 NUP93中使用 NUP93.在SRNS中,SRNS是SRNS.新的病原性变体核孔复合蛋白质的核孔复合蛋白质儿科病学 儿科病学类固醇耐药性性综合征

更多相关视频

Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
07:15

Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway

Published on: August 23, 2024

464
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K

相关实验视频

Last Updated: Jul 15, 2025

Induction of Nephrotic Syndrome in Mice by Retrobulbar Injection of Doxorubicin and Prevention of Volume Retention by Sustained Release Aprotinin
07:38

Induction of Nephrotic Syndrome in Mice by Retrobulbar Injection of Doxorubicin and Prevention of Volume Retention by Sustained Release Aprotinin

Published on: May 6, 2018

8.5K
Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
07:15

Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway

Published on: August 23, 2024

464
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K

科学领域:

  • 遗传学 遗传学 是一个
  • 儿科脏病学 儿科脏病学
  • 分子生物学分子生物学

背景情况:

  • 类固醇治疗是性综合征的标准,但15-20%的患者具有抗药性.
  • 遗传因素与超过10%的类固醇耐药性性综合征 (SRNS) 病例有关.
  • 核孔复合体基因变异是儿科SRNS的新兴原因,NUP93变异是显著的.

研究的目的:

  • 报告儿童患者中SRNS的病例,其中已确定NUP93变体.
  • 为NUP93变种提供临床数据,目前的数量有限.
  • 为了研究特定的NUP93变体的临床相关性.

主要方法:

  • 一名患有SRNS的12岁男孩接受了基因组测试,针对50个脏综合征相关基因.
  • 该患者有类固醇和非类固醇免疫抑制治疗的病史.
  • 确定了两个NUP93变种 (c.2326C>T和c.1162C>T).

主要成果:

  • 该患者出现了早期发病的严重SRNS,包括脏范围蛋白尿和低albuminemia.
  • 只有NUP93基因在这个患者身上发现了基因突变.
  • 这是第一例报告的异质合体患者,患有c.2326C>T和c.1162C>T NUP93变异,并有确定的SRNS病史.

结论:

  • NUP93变种是SRNS的罕见但重要的原因.
  • 临床数据对于建立遗传SRNS的护理标准至关重要.
  • c.1162C>T NUP93变种可能在SRNS中具有临床意义.