نتایج جستجو برای: brody myopathy
تعداد نتایج: 12892 فیلتر نتایج به سال:
the objectives of this study were to identify a suitable mathematical model for describing the growth curve of baluchi sheep based on monthly records of live weight from birth to yearling; and to evaluate the efficacies of nonlinear mixed effect model (nlmm) and the nonlinear fixed effect model (nlm) methodologies. growth models were fitted to a total of 16,650 weight–age data belonging to 2071...
The purpose of this study was to describe growth curve in Baluchi sheep by application of nonlinear growth models. The weight records of 1228 and 676 Baluchi male and female lambs for birth weight, one-month, two-month, three-month, four-month, six-month, nine-month and one year of age were studied. These data had been collected by Baluchi Sheep Breeding Center in Mashhad (Abbas Abad) during 20...
A Brody curve, a.k.a. normal curve, is a holomorphic map f from the complex line C to the complex projective space P such that the family of its translations {z 7→ f(z + a) : a ∈ C} is normal. We prove that Brody curves omitting n hyperplanes in general position have growth order at most one, normal type. This generalizes a result of Clunie and Hayman who proved it for n =
Zahra Jehan Iqbal, MD, Long Cao, MD, Karl Chiang, MD, Sundeep Adusumalli, MD, Farah Khalid, BA, Rajasekhar Nekkanti, MD From the Department of Internal Medicine, Division of Heath Sciences and Brody School of Medicine, East Carolina University, Greenville, North Carolina, Department of Cardiology, Division of Heath Sciences and Brody School of Medicine East Carolina University, Greenville, Nort...
mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (mlasa) syndrome is a rare autosomal recessive disorder of oxidative phosphorylation and iron metabolism. the association between myopathy and sideroblastic anemia was initially reported in 1974. here we report an 8.5 year old boy with normal cognitive function, suffering from chronic progressive weakness in his lower extremities...
Synonyms: MmD, Multi-minicore disease, Minicore myopathy, Multicore myopathy, Multiminicore myopathy, Minicore myopathy with hand involvement, antenatal onset minicore myopathy with arthrogryposis, Minicore myopathy with external ophthalmoplegia, Multicore myopathy with external ophthalmoplegia, Multiminicore disease with external opthalmoplegia, SEPN1-related congenital muscular dystrophy, rig...
hereditary inclusion body myopathy (hibm) is an adult-onset hereditary myopathy, usually with distal onset and quadriceps sparing. this myopathy is autosomal recessive and associated to upd-n-acetylglucosamine-2-epimerase/n-acetylmannosamine kinase (gne) gene mutations. in this study, we report a novel gne homozygous point mutation c.1834t>g that results in amino acid substitution of cysteine 6...
Sarcolipin (SLN) is a low-molecular-weight protein that copurifies with the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase (SERCA1). Genomic DNA and cDNA encoding human sarcolipin (SLN) were isolated and characterized and the SLN gene was mapped to chromosome 11q22-q23. Human, rabbit, and mouse cDNAs encode a protein of 31 amino acids. Homology of SLN with phospholamban (PLN) su...
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