نتایج جستجو برای: mutated dtxa chain
تعداد نتایج: 320291 فیلتر نتایج به سال:
diphtheria is a fatal disease caused by exotoxin of corynebacterium diphtheria . this toxin consists of two chains, catalytic chain (a) and binding (b) chain. by binding chain (b), the toxin binds to its receptor on numerous body cells such as myocardial, kidney and peripheral nerve cells. after entering, catalytic chain (a) inhibits protein synthesis and finally can cause cell dea...
Mitochondria contain their own DNA (mtDNA), which codes for 13 proteins (all subunits of the respiratory chain complexes), 22 tRNAs and 2 rRNAs. Several mtDNA point mutations as well as deletions have been shown to be causative in well-defined mitochondrial disorders. A mixture of mutated and wild type mtDNA (heteroplasmy) is found in most of these disorders. Inheritance of mtDNA is maternal, a...
Healthy individuals have soluble (extracellular) DNA in their blood, and increased amounts are present in cancer patients. Here we report the detection of specific sequences of the cystic fibrosis and K-ras genes in plasma DNA from normal donors by amplification with the polymerase chain reaction. In addition, mutated K-ras sequences are identified by polymerase chain reaction utilizing allele-...
مقدمه: دیفتری ناشی از باسیل کورینه باکتریوم، بیماری مهلکی است که بقراط در 5 قرن قبل از میلاد آنرا شرح داده است.عامل این بیماری کشنده، اگزوتوکسین DTx میباشد. دیفتریاتوکسین شامل دو زنجیره کاتالیتیک(A) و اتصال دهنده(B) میباشد. این توکسین با واسطه زنجیره Bبه رسپتور بسیاری از سلولهای اندام های بدن از جمله میوکارد ، اعصاب محیطی وکلیه ها متصل شده و زنجیره A پس از ورود به سلول، باعث مهار سنتز پروتئین...
مقدمه: دیفتری ناشی از باسیل کورینه باکتریوم، بیماری مهلکی است که بقراط در 5 قرن قبل از میلاد آنرا شرح داده است.عامل این بیماری کشنده، اگزوتوکسین dtx می باشد. دیفتریاتوکسین شامل دو زنجیره کاتالیتیک(a) و اتصال دهنده(b) می باشد. این توکسین با واسطه زنجیره bبه رسپتور بسیاری از سلولهای اندام های بدن از جمله میوکارد ، اعصاب محیطی وکلیه ها متصل شده و زنجیره a پس از ورود به سلول، باعث مهار سنتز پروتئین...
Alanine scanning was used to determine the affinity contributions of 10 side chain amino acids (residues at position 50-60 inclusive) of H chain complementarity-determining region 2 (HCDR2) of the somatically mutated high-affinity anti-p-azophenylarsonate Ab, 36-71. Each mutated H chain gene was expressed in the context of mutated (36-71L) and the unmutated (36-65L) L chains to also assess the ...
Immunoglobulin (Ig)M 1 IgD 1 B cells are generally assumed to represent antigen-inexperienced, naive B cells expressing variable (V) region genes without somatic mutations. We report here that human IgM 1 IgD 1 peripheral blood (PB) B cells expressing the CD27 cell surface antigen carry mutated V genes, in contrast to CD27-negative IgM 1 IgD 1 B cells. IgM 1 IgD 1 CD27 1 B cells resemble class-...
Immunoglobulin (Ig)M+IgD+ B cells are generally assumed to represent antigen-inexperienced, naive B cells expressing variable (V) region genes without somatic mutations. We report here that human IgM+IgD+ peripheral blood (PB) B cells expressing the CD27 cell surface antigen carry mutated V genes, in contrast to CD27-negative IgM+IgD+ B cells. IgM+IgD+CD27(+) B cells resemble class-switched and...
Mutations of ventricular essential myosin light chain disturb myosin binding and sarcomeric sorting.
AIMS We tested the hypothesis that mutations in the human ventricular essential myosin light chain (hVLC-1) that are associated with hypertrophic cardiomyopathy (HCM) affect protein structure, binding to the IQ1 motif of cardiac myosin heavy chain (MYH) and sarcomeric sorting in neonatal cardiomyocytes. METHODS AND RESULTS We employed circular dichroism and surface plasmon resonance spectrosc...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید