نتایج جستجو برای: collagen disorder

تعداد نتایج: 655346  

2003
MICHAEL A. CREMER JAMES A. PITCOCK JOHN M. STUART H. KANG S. TOWNES

Relapsing polychondritis is an inflammatory disease of connective tissue characterized by the destruction of hyaline and elastic cartilages . Although the etiology of this disease is unknown, the demonstration of anti-cartilage antibodies in the sera of patients with this disorder suggests an autoimmune mechanism (1, 2) . Recently, Foidart et al . (3) have reported an association between relaps...

Journal: :Blood 1988
B Kehrel L Balleisen R Kokott R Mesters W Stenzinger K J Clemetson J van de Loo

Platelets from a patient with a severe lifelong bleeding tendency, which later spontaneously disappeared, lacked intact thrombospondin and glycoprotein (GP) Ia. Before disappearance of the bleeding disorder, results of coagulation studies and platelet aggregation in response to adenosine diphosphate (ADP), arachidonic acid, thrombin, A23187, epinephrine, and ristocetin were normal. In contrast,...

2018
Qi Yang Hong Xu Jinsi Luo Qinle Zhang Bobo Xie Sheng Yi Xiuliang Rong Jin Wang Zailong Qin Tingting Jiang Li Lin Yangjin Zuo Xin Fan

Osteogenesis imperfecta (OI) is a rare congenital disorder characterized by bone fragility and fractures, and associated with bone deformity, short stature, dentin, ligament and blue‑gray eye sclera. OI is caused by a heterozygous mutation in collagen α‑1(I) chain (COL1A1) or collagen α‑2(I) chain (COL1A2) genes that encode α chains of type I collagen. Collagen α chain peptide contains an N‑pro...

2011
Brian P Kelley Fransiska Malfait Luisa Bonafe Dustin Baldridge Erica Homan Sofie Symoens Andy Willaert Nursel Elcioglu Lionel Van Maldergem Christine Verellen-Dumoulin Yves Gillerot Dobrawa Napierala Deborah Krakow Peter Beighton Andrea Superti-Furga Anne De Paepe Brendan Lee

Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue characterized by bone fragility and alteration in synthesis and posttranslational modification of type I collagen. Autosomal dominant OI is caused by mutations in the genes (COL1A1 or COL1A2) encoding the chains of type I collagen. Bruck syndrome is a recessive disorder featuring congenital contractures in addition to bone ...

عباسعلی پورکبیرره , رقیه ,

For the extraction of type IV collagen, the normal placenaes at term were placed under pepsin digestion (once). To purify the extracted collagen, Saltingout and changing the PH were performed (each step twice). All steps of the extraction and purification were controlled by the SDS-PAGE electrophoresis and finally purified collagen with molecular weight 170 and 185 KD chains were obtain...

Journal: :journal of agricultural science and technology 2013
j. h. choi sh. behanm s. m. kim

collagen, which is widely distributed in pluricellular animals, is one of the most fundamental constituents of the extracellular matrix, and plays mechanically or physiologically important roles in their bodies. in this study, the biochemical and physical characteristics of pepsin-solubilized collagen from the mantle of yesso scallop (ympc), a by-product of processing, was determined. electroph...

Journal: :iranian journal of basic medical sciences 0
armita kakavand hamidi department of biology, faculty of sciences, guilan university, rasht, iran mohammad moghaddam hematology research center, shiraz university of medical sciences, shiraz, iran nasim hatamnejadian skin research center, shahid beheshti university of medical sciences, tehran, iran ahmad ebrahimi cellular-molecular research center (cmerc), research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, iran

objective(s): epidermolysis bullosa is one of the most important series of mechano-bullous heritable skin disorders which is categorized into four major types according to the layer that bullae forms within basement membrane zone. in dystrophic form of the disease, blisters are made in the sublamina densa zone, at the level of type vii collagen protein which produce anchoring fibrils. type vii ...

Journal: :avicenna journal of medical biotechnology 0

background: micropatterning is becoming a powerful tool for studying cells in vitro. this method not only uses very small amount of material but also mimic the microenvironment structure present in living tissues better than flask culturing techniques. in previous studies using micropatterning of extracellular matrix proteins on glass surfaces, the rate of protein detachment from the surface wa...

Journal: :journal of food biosciences and technology 0
n. shokraneh ph. d. student of the department of food science and technology, ayatollah amoli branch, islamic azad university, mazandaran, iran. p. ariaii assistant professor of department of food science and technology, ayatollah amoli branch, islamic azad university, mazandaran, iran. f. rasouli ghahrodi ph.d. student of the department of food science and technology, college of food science and technology, tehran science and research branch, islamic azad university, tehran, iran. f. hasannia ph. d. student of the department of food science and technology, ayatollah amoli branch, islamic azad university, mazandaran, iran. s. sabbaghpour ph. d. student of the department of food science and technology, ayatollah amoli branch, islamic azad university, mazandaran, iran.

oxidative and microbiological degradations are the main factors that determine the quality of food and the shelf life. color and moisture stability are important quality attributes that contribute to meat shelf life, salability and consumer acceptability. there is currently considerable interest in edible films coatings and natural antioxidants because of their potential to improve the quality ...

Journal: :Annals of the rheumatic diseases 1987
A D Croock M Bashar Kahaleh J M Powers

A 57 year old man with nail-patella syndrome (NPS) and associated renal disease is described who developed an inflammatory polyarthropathy and polyarteritis-like vasculitis. Vasculitis and serum complement abnormalities have not previously been reported in NPS. NPS is a rare autosomal dominant connective tissue disorder affecting both mesenchymal and ectodermal tissue. The condition is reviewed...

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