نتایج جستجو برای: loss of function mice mutants

تعداد نتایج: 21309946  

Journal: :The Journal of clinical investigation 2007
Sanja Sever Mehmet M Altintas Sharif R Nankoe Clemens C Möller David Ko Changli Wei Joel Henderson Elizabetta C del Re Lianne Hsing Ann Erickson Clemens D Cohen Matthias Kretzler Dontscho Kerjaschki Alexander Rudensky Boris Nikolic Jochen Reiser

Kidney podocytes and their foot processes maintain the ultrafiltration barrier and prevent urinary protein loss (proteinuria). Here we show that the GTPase dynamin is essential for podocyte function. During proteinuric kidney disease, induction of cytoplasmic cathepsin L leads to cleavage of dynamin at an evolutionary conserved site, resulting in reorganization of the podocyte actin cytoskeleto...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه ارومیه 1377

the methods which are used to analyze microstrip antennas, are divited into three categories: empirical methods, semi-empirical methods and full-wave analysis. empirical and semi-empirical methods are generally based on some fundamental simplifying assumptions about quality of surface current distribution and substrate thickness. thses simplificatioms cause low accuracy in field evaluation. ful...

Journal: :PLoS ONE 2007
Adrienne Anginot Romain Dacquin Marlène Mazzorana Pierre Jurdic

Bone resorption by osteoclasts is necessary to maintain bone homeostasis. Osteoclast differentiation from hematopoietic progenitors and their activation depend on M-CSF and RANKL, but also requires co-stimulatory signals acting through receptors associated with DAP12 and FcRgamma adaptors. Dap12 mutant mice (KDelta75) are osteopetrotic due to inactive osteoclasts but, surprisingly, these mice a...

Journal: :The Journal of biological chemistry 2004
Gbolahan W Okunade Marian L Miller Gail J Pyne Roy L Sutliff Kyle T O'Connor Jonathan C Neumann Anastasia Andringa Daniel A Miller Vikram Prasad Thomas Doetschman Richard J Paul Gary E Shull

The relative importance of plasma membrane Ca2+-ATPase (PMCA) 1 and PMCA4 was assessed in mice carrying null mutations in their genes (Atp2b1 and Atp2b4). Loss of both copies of the gene encoding PMCA1 caused embryolethality, whereas heterozygous mutants had no overt disease phenotype. Despite widespread and abundant expression of PMCA4, PMCA4 null (Pmca4-/-) mutants exhibited no embryolethalit...

Journal: :Journal of Investigative Dermatology 2022

Androgenetic alopecia is a common form of pattern hair loss, characterized by miniaturized follicles (HFs) at the front and parietal scalp, while hairs on occipital scalp are preserved. Moreover, different sites human body exhibit distinct types patterns HFs. Understanding molecular basis this heterogeneity will help to design targeted treatment strategies. The Wnt signalling pathway its Dickko...

Journal: :Neuro-oncology 2022

Abstract Glioblastoma (GBM) is the most common primary malignant neoplasm with poor survival despite treatment. Developing effective therapies remains challenging due to intratumoral heterogeneity, which drives therapeutic resistance and recurrence. To understand how genetic events alter epigenome enhance clonal fitness, we developed an isogenic human neural progenitor cell (NPC)-based model of...

Journal: :Neuron 2017
Shu-Ling Chiu Graham Hugh Diering Bing Ye Kogo Takamiya Chih-Ming Chen Yuwu Jiang Tejasvi Niranjan Charles E. Schwartz Tao Wang Richard L. Huganir

Learning depends on experience-dependent modification of synaptic efficacy and neuronal connectivity in the brain. We provide direct evidence for physiological roles of the recycling endosome protein GRASP1 in glutamatergic synapse function and animal behavior. Mice lacking GRASP1 showed abnormal excitatory synapse number, synaptic plasticity, and hippocampal-dependent learning and memory due t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Burkhard Jakob Gaga Kochlamazashvili Maria Jäpel Aziz Gauhar Hans H Bock Tanja Maritzen Volker Haucke

Brain development and function depend on the directed and coordinated migration of neurons from proliferative zones to their final position. The secreted glycoprotein Reelin is an important factor directing neuronal migration. Loss of Reelin function results in the severe developmental disorder lissencephaly and is associated with neurological diseases in humans. Reelin signals via the lipoprot...

Journal: :Infection and immunity 2007
Rishi D Pathirana Neil M O'Brien-Simpson Gail C Brammar Nada Slakeski Eric C Reynolds

The contributions of three proteinase genes (rgpA, rgpB, and kgp) to the virulence of Porphyromonas gingivalis W50 were investigated in the murine periodontitis model. Mice were orally inoculated with eight doses (1 x 10(10) cells per dose) of rgpA, rgpB, kgp, rgpA rgpB, or rgpA rgpB kgp isogenic mutants, and the level of alveolar bone loss, immune response induced, and number of bacterial cell...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه یزد 1388

the present research was conducted to accomplish two purposes. firstly, it aimed to explore and describe schematic structure or what halliday and hassan (1989, p.64) have called “generic structure potential” (gsp) of american english, iranian persian and iranian english newspaper editorials within systemic functional linguistics. secondly, a quantitative cross-comparison was made to investigate...

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