نتایج جستجو برای: i receptor

تعداد نتایج: 1572301  

Journal: :Journal of immunotherapy and precision oncology 2023

ABSTRACT Poly (adenosine diphosphate-ribose) polymerase inhibitors (PARP)i are emerging as standard oncology treatments in various tumor types. The indications will expand PARPi being investigated breast cancer subtypes. Currently, except for BRCA1/2 mutation carriers with human epidermal growth factor receptor 2 (HER2)-negative cancer, there is inadequate identification of predictive biomarker...

Journal: :The Journal of clinical investigation 1989
W L Lowe M Adamo H Werner C T Roberts D LeRoith

We have examined, in liver and extrahepatic tissues, the effects of fasting on total insulin-like growth factor I (IGF-I) mRNA levels, on levels of different IGF-I mRNAs generated by alternative splicing of the primary IGF-I transcript, and on IGF-I receptor binding and mRNA levels. A 48-h fast decreased total IGF-I mRNA levels by approximately 80% in lung and liver, approximately 60% in kidney...

Cyclizine (1-benzhydryl-4-methyl-piperazine, CAS 82-92-8, CYC, I), a piperazine derivative, belongs to H1 antihistamine group of drugs that shows such pharmacological properties as anti-inflammatory, anti-allergic and anti-platelet effects, similar to other H1-receptor antagonists. In this study, two new tolyl and cumene derivatives of I (1-ethyl-4-[(p-isopropylphenyl) (p-tolyl) methyl]-piperaz...

Journal: :Arteriosclerosis, Thrombosis, and Vascular Biology 2010

Journal: :Zoological science 1998
J Honda S Takeuchi H Fukamachi S Takahashi

Insulin-like growth factor-I (IGF-I) is produced in the liver and other peripheral tissues in response to growth hormone (GH) stimuli. IGF-I regulates diverse physiological functions in an autocrine and/or paracrine manner. IGF-I and IGF-I receptor (type-I receptor) are expressed in human and rat pituitary glands. However, the cell types of IGF-I-expressing cells and target cells of IGF-I in th...

2006
Masahiko Miura Shiwei Li Renato Baserga

Recent evidence has shown that the insulin-like growth factor I (IGF-I) receptor plays a major role in the establishment and maintenance of transformation. To identify domains in the IGF-I receptor that are nec essary for transformation, the tyrosine at residue 950 of the human IGF-I receptor cDNA was mutated to phenylalanine, and the plasmid expressing the mutant receptor was stably transfecte...

Journal: :iranian journal of allergy, asthma and immunology 0
simin almasi firouzgar hospital, iran university of medical sciences (iums), tehran, iran saeed aslani rheumatology research center, tehran university of medical sceinces, tehran, iran hadi poormoghim firouzgar hospital, iran university of medical sciences (iums), tehran, iran ahmad reza jamshidi rheumatology research center, tehran university of medical sciences, tehran, iran shiva poursani rheumatology research center, tehran university of medical sceinces, tehran, iran mehdi mahmoudi rheumatology research center, tehran university of medical sceinces, tehran, iran

no abstract

Background: Denileukin diftitox (trade name, Ontak) is the first recombinant immunotoxin (IM), in which the binding domain of diphtheria toxin has been replaced by the amino acid sequence of human interleukin-2 (DT389IL-2) using genetic engineering. Purity, stability, and structural property of the protein are critical factors for the scale-up production of this fusion protein. In this IM, loca...

Journal: :The Journal of clinical investigation 1991
S M Rosenthal A Brunetti E J Brown P W Mamula I D Goldfine

Muscle is an important target tissue for insulin-like growth factor (IGF) action. The presence of specific, high affinity IGF receptors, as well as the expression of IGF peptides and binding proteins by muscle suggest that a significant component of IGF action in this tissue is mediated through autocrine and/or paracrine mechanisms. To explore autocrine/paracrine action of IGFs in muscle, we st...

Journal: :iranian journal of pharmaceutical sciences 0
anurekha jaina b.r. nahata college of pharmacy, mandsaur, india sumit ratnawat b.r. nahata college of pharmacy, mandsaur, india s.c. chaturvedi shree aurobindo institute of pharmacy, india

a series of angiotensin ii (a ii) receptor antagonist of some substituted 5-(biphenyl-4-ylmethyl) pyrazole were subjected to qsar analysis using hansch and fujita-ban model, by using combination of thermodynamic, electronic, spatial descriptor and presence or absence of substituent respectively. several qsar model were obtained using stepwise regression analysis. two models from both the method...

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