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The multifaceted role of heme in cancer
Heme, an iron-containing porphyrin, is of vital importance for cells due to its involvement in
several biological processes, including oxygen transport, energy production and drug …
several biological processes, including oxygen transport, energy production and drug …
Heme metabolism in nonerythroid cells
LS Dunaway, SA Loeb, S Petrillo, E Tolosano… - Journal of Biological …, 2024 - jbc.org
Heme is an iron-containing prosthetic group necessary for the function of several proteins
termed" hemoproteins." Erythrocytes contain most of the body's heme in the form of …
termed" hemoproteins." Erythrocytes contain most of the body's heme in the form of …
Heme accumulation in endothelial cells impairs angiogenesis by triggering paraptosis
Heme is required for cell respiration and survival. Nevertheless, its intracellular levels need
to be finely regulated to avoid heme excess, which may catalyze the production of reactive …
to be finely regulated to avoid heme excess, which may catalyze the production of reactive …
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies
A Lischka, K Eggermann, CJ Record, MF Dohrn… - Brain, 2023 - academic.oup.com
Congenital insensitivity to pain (CIP) and hereditary sensory and autonomic neuropathies
(HSAN) are clinically and genetically heterogeneous disorders exclusively or predominantly …
(HSAN) are clinically and genetically heterogeneous disorders exclusively or predominantly …
Unraveling the role of heme in neurodegeneration
Heme (iron-protoporphyrin IX) is an essential co-factor involved in several biological
processes, including neuronal survival and differentiation. Nevertheless, an excess of free …
processes, including neuronal survival and differentiation. Nevertheless, an excess of free …
Findings from a genoty** study of over 1000 people with inherited retinal disorders in Ireland
The Irish national registry for inherited retinal degenerations (Target 5000) is a clinical and
scientific program to identify individuals in Ireland with inherited retinal disorders and to …
scientific program to identify individuals in Ireland with inherited retinal disorders and to …
Unearthing FLVCR1a: tracing the path to a vital cellular transporter
Abstract The Feline Leukemia Virus Subgroup C Receptor 1a (FLVCR1a) is a member of the
SLC49 Major Facilitator Superfamily of transporters. Initially recognized as the receptor for …
SLC49 Major Facilitator Superfamily of transporters. Initially recognized as the receptor for …
Mitochondrial targeting in neurodegeneration: a heme perspective
Mitochondrial dysfunction has achieved an increasing interest in the field of
neurodegeneration as a pathological hallmark for different disorders. The impact of …
neurodegeneration as a pathological hallmark for different disorders. The impact of …
Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa
Z Li, Y Li, X Chu, K Du, Y Tang, Z **e, M Yu… - …, 2024 - Wiley Online Library
The mutations of the feline leukemia virus subgroup C receptor‐related protein 1 (FLVCR1)
cause ataxia with retinitis pigmentosa. Recent studies indicated a large variation in the …
cause ataxia with retinitis pigmentosa. Recent studies indicated a large variation in the …
Coexistence of Retinitis Pigmentosa and Ataxia in Patients with PHARC, PCARP, and Oliver–McFarlane Syndromes
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of
photoreceptors and retinal pigment epithelial atrophy, leading to severe visual impairment or …
photoreceptors and retinal pigment epithelial atrophy, leading to severe visual impairment or …