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1 apeutic targets for diet-induced obesity and metabolic disorder.
2 robiotics to attenuate high-fat diet-related metabolic disorder.
3 ice an HFD for 16 wk to initiate HFD-induced metabolic disorder.
4 nd adoptive transfer of AT1-ILCs exacerbated metabolic disorder.
5 dities, including cardiovascular disease and metabolic disorder.
6  conditions, and the etiology of this common metabolic disorder.
7 heral nerves as a new therapeutic target for metabolic disorders.
8  the recent rise of allergic, autoimmune and metabolic disorders.
9 ephalopathy (CADASIL), and mitochondrial and metabolic disorders.
10 ributing to accelerated body weight gain and metabolic disorders.
11 tment of acute liver failure and liver-based metabolic disorders.
12 ns for developing personalized therapies for metabolic disorders.
13 in many cancers, cardiovascular disease, and metabolic disorders.
14 ating the link between arsenite exposure and metabolic disorders.
15 aging and pathological conditions, including metabolic disorders.
16 de a means of treating hepatic steatosis and metabolic disorders.
17 n protecting against HFD-induced obesity and metabolic disorders.
18 tential therapeutic target for mTORC1-driven metabolic disorders.
19 as a consideration in the treatment of liver metabolic disorders.
20 the onset and/or progression of major immune/metabolic disorders.
21 who may be at higher risk for cardiovascular/metabolic disorders.
22 on that contributes to bone dysregulation in metabolic disorders.
23 nalog, could be developed as a treatment for metabolic disorders.
24 and represents a possible new drug target in metabolic disorders.
25 arning and are implicated in glucose-related metabolic disorders.
26 r se causes leptin resistance and associated metabolic disorders.
27 cidate the effect of KHK inhibition on these metabolic disorders.
28  that central vascular impairments may cause metabolic disorders.
29 sing CRISPR/Cas9, as a new strategy to model metabolic disorders.
30 se the risk of fatty liver disease and other metabolic disorders.
31 ating obesity, diabetes and their associated metabolic disorders.
32 e promising agents for treating a variety of metabolic disorders.
33 cally relevant for the prevention of glucose metabolic disorders.
34 munity to pathogens/tumors and in autoimmune/metabolic disorders.
35  safety profiles in the treatment of complex metabolic disorders.
36 ptation to ER stress associated with chronic metabolic disorders.
37 in the aetiology of sleep, mental health and metabolic disorders.
38 t been fully investigated in obesity-related metabolic disorders.
39  promising approach for targeting cancer and metabolic disorders.
40 logical iron reduction on the development of metabolic disorders.
41  as a protective factor in obesity and other metabolic disorders.
42 esting potential target for the treatment of metabolic disorders.
43 eurodegenerative diseases are accompanied by metabolic disorders.
44 rimary cause of obesity and other eating and metabolic disorders.
45 n and oxidative stress in an animal model of metabolic disorders.
46  Its dysregulation causes diabetes and other metabolic disorders.
47 ight serve as a therapeutic target in common metabolic disorders.
48 ising target for therapeutic intervention in metabolic disorders.
49 hts into strategies to treat obesity-related metabolic disorders.
50 , non-alcoholic steatohepatitis, and related metabolic disorders.
51 4 in managing obesity and obesity-associated metabolic disorders.
52 e (NNMT), an enzyme implicated in cancer and metabolic disorders.
53 ts a therapeutic avenue for the treatment of metabolic disorders.
54 mproved therapeutic strategies for combating metabolic disorders.
55 ssociated with increased risk for immune and metabolic disorders.
56 ntergenerational inheritance of diet-induced metabolic disorders.
57 iabetes may lead to promising treatments for metabolic disorders.
58 d has the potential to treat obesity-related metabolic disorders.
59 contribute to muscle wasting associated with metabolic disorders.
60 and excessive storage is a feature of common metabolic disorders.
61 le similar to dysbiotic states described for metabolic disorders.
62 rone is associated with all "Western" cardio-metabolic disorders.
63 c and diagnostic targets for obesity-related metabolic disorders.
64 Indians are known to be at elevated risk for metabolic disorders.
65 se energy expenditure in obesity and related metabolic disorders.
66 cluster of cardiovascular (hypertension) and metabolic disorders.
67 -MCA may be a candidate for the treatment of metabolic disorders.
68 ives to combat the rising global epidemic of metabolic disorders.
69 be associated with chronic liver disease and metabolic disorders.
70 reat neuroinflammation, obesity, and related metabolic disorders.
71 rnutrition increases the risk of obesity and metabolic disorders.
72 ce their pathogenic role in inflammatory and metabolic disorders.
73 omic loci contributing to cardiovascular and metabolic disorders.
74 timately cell death that underlie nearly all metabolic disorders.
75 physiological transitions are known to cause metabolic disorders.
76 based treatments for obesity and its related metabolic disorders.
77 ut microbiome are important risk factors for metabolic disorders.
78 strategy against inflammation, dysbiosis and metabolic disorders.
79 e chronic supposedly noncommunicable, immune/metabolic disorders.
80 a, the association of the gut microbiome and metabolic disorders.
81 evented but also reversed obesity-associated metabolic disorders.
82 midotransferase, result in devastating human metabolic disorders.
83 es associated with diseases such as gout and metabolic disorders.
84 ediated by VDR that might trigger downstream metabolic disorders.
85 s an attractive therapeutic strategy against metabolic disorders.
86 nked mutations in the DHTKD1 gene to several metabolic disorders.
87 rs, neurodegeneration, cancer, diabetes, and metabolic disorders.
88 herapeutic possibilities for ACLY-associated metabolic disorders.
89 in the initiation and progression of several metabolic disorders.
90 a range of musculoskeletal complications and metabolic disorders.
91 o-legal and post mortem examination, with no metabolic disorders.
92 c flexibility is a dominant cause of several metabolic disorders.
93 ans in the prevention and early detection of metabolic disorders.
94 al disease, one of the most common inherited metabolic disorders.
95 een associated with increased risk of cardio-metabolic disorders.
96 ful for the treatment of obesity and related metabolic disorders.
97 lsivity is common in various psychiatric and metabolic disorders.
98 opoietic failure, cancer predisposition, and metabolic disorders.
99 ing the implications of arsenite exposure in metabolic disorders.
100 arget for the treatment of obesity and other metabolic disorders.
101 gulator of blood pressure has been linked to metabolic disorders.
102 ansgenerational passage of obesity and other metabolic disorders, 3) DNA methylation is involved in r
103   Maple syrup urine disease (MSUD) is a rare metabolic disorder, affecting the metabolism of branched
104  obesity (MO) programs offspring obesity and metabolic disorders, although the underlying mechanisms
105 ase and type 2 diabetes MELLITUS (T2DM) is a metabolic disorder, an increasing number of genetic epid
106  to increased adult adiposity, inflammation, metabolic disorder and dyslipidemia in offspring fed a s
107 y differences in REE between patients with a metabolic disorder and healthy participants can be expre
108 sis in renal fibroblasts is an intracellular metabolic disorder and is inherently coupled with inflam
109              Insulin resistance is a complex metabolic disorder and is often associated with type 2 d
110 ovide one of the first examples of ERT for a metabolic disorder and suggest that PEGylated CBS should
111 reproduction, regenerative medicine, cancer, metabolic disorders and ageing.
112 edicting the disease status of patients with metabolic disorders and also the tumor stages and progno
113 ulin resistance are among the most prevalent metabolic disorders and are tightly associated with obes
114  with a variety of human diseases, including metabolic disorders and cancer.
115 ory performance, neurodegenerative diseases, metabolic disorders and cancer.
116  processing of IL1beta, contributing to many metabolic disorders and directing adipocytes to a more i
117  of new therapeutic strategies for inherited metabolic disorders and diseases of aging.
118 f human health against general inflammation, metabolic disorders and disturbances of the digestive sy
119 inhibition approaches for treating other PIP metabolic disorders and highlight the importance of modi
120 iagnosis in 15 out of 17 (88%) children with metabolic disorders and in 5 out of 28 (~18%) children w
121 y liver disease is one of the most prevalent metabolic disorders and it tightly associates with obesi
122 s), aging WT mice (20-22 months) had obvious metabolic disorders and loss of locomotor activity.
123 tribution of signaling pathways that lead to metabolic disorders and NE differentiation of prostate c
124 this coupling is associated with a number of metabolic disorders and neurodegenerative diseases inclu
125 romising drug targets for pharmacotherapy of metabolic disorders and obesity.
126  the past few years, the association between metabolic disorders and periodontitis has been widely st
127 ciated with cardiovascular, psychiatric, and metabolic disorders and triglycerides and high-density l
128 l environments predispose aging offspring to metabolic disorders and type 2 diabetes.
129 pertensive disease, circulatory disease, and metabolic disorders) and 9 disease outcomes (gout, gouty
130  immunodeficiencies, haemoglobinopathies and metabolic disorders) and for the generation of chimeric
131 r (AHR) plays crucial roles in inflammation, metabolic disorder, and cancer.
132 hat is implicated in cardiovascular disease, metabolic disorder, and cancer.
133 uation of oxidative stress, ER stress, lipid metabolic disorder, and cell death signaling.
134 of MGL's role in diet-induced obesity, lipid metabolic disorder, and regulation of appetite.
135 sociated with increased incidence of cancer, metabolic disorders, and affective problems in humans.
136 ion, autoimmune diseases, cardiovascular and metabolic disorders, and cancer reported in shift worker
137 diseases including inflammation, infections, metabolic disorders, and cancer.
138 ogies, including neurodegenerative diseases, metabolic disorders, and cancer.
139 ase, focusing on neurodegenerative diseases, metabolic disorders, and cancer.
140 shown effects in mouse models of obesity and metabolic disorders, and how these might be translated t
141           Diabetes is one of the most common metabolic disorders, and is characterized by the inabili
142 we postulated that AIF1L might contribute to metabolic disorders, and studied it using mouse models.
143   Hepatitis C virus (HCV) infection promotes metabolic disorders, and the severity of lipogenic disea
144 and liver; autoimmune, neurodegenerative and metabolic disorders; and cancer initiation.
145                 The finding that obesity and metabolic disorder are accompanied by chronic low-grade
146                                        These metabolic disorders are associated with perturbations to
147                                              Metabolic disorders are common complications after ortho
148                               DNA damage and metabolic disorders are intimately linked with premature
149                                  Obesity and metabolic disorders are of great societal concern and ge
150                                    Inherited metabolic disorders are often characterized by the lack
151                       Obesity and associated metabolic disorders are related to impairments of the in
152 y is central to the development of these two metabolic disorders, as adipose tissue plays a pivotal r
153 l polycystic ovary syndrome (PCOS), a common metabolic disorder associated with excess circulating an
154 ch reduced with this technology, diminishing metabolic disorders associated with cooling and minimizi
155 ide a potential therapeutic means to control metabolic disorders associated with its dysregulated sec
156 mation) is characteristic of obesity-related metabolic disorders, associated with increased risk of d
157  This suggests the presence of an underlying metabolic disorder beyond fatty liver that may be causat
158  effects and mechanisms of PM2.5 exposure in metabolic disorders, but also revealed the pleotrophic a
159    Consumption of dietary fat contributes to metabolic disorders, but EEC adaptations to high fat fee
160 ith an increased risk of obesity and related metabolic disorders, but the role of sleep in long-term
161 ty and type 2 diabetes are the most frequent metabolic disorders, but their causes remain largely unc
162  of CB1 ameliorates Diet-Induced Obesity and metabolic disorder by modulating macrophage inflammatory
163 nd shows that susceptibility of offspring to metabolic disorder can likely be attributed to epigeneti
164 remendous opportunities for the treatment of metabolic disorders, cancer, autoimmune diseases and etc
165    The available treatment options for these metabolic disorders cannot reverse the disease in most i
166 s an ultra-rare, life-threatening, inherited metabolic disorder caused by deficiency of the mitochond
167 es showed that pseudoxanthoma elasticum is a metabolic disorder caused by reduced circulating levels
168                                  Multisystem metabolic disorders caused by defects in oxidative phosp
169 report five unrelated neonates with a lethal metabolic disorder characterized by cardiomyopathy, corn
170 irment in patients with diabetes mellitus, a metabolic disorder characterized by chronic hyperglycaem
171  Niemann-Pick Type C disease (NPC) is a rare metabolic disorder characterized by disruption of normal
172 cause hereditary tyrosinemia type I (HT1), a metabolic disorder characterized by elevated blood level
173                       Diabetes mellitus is a metabolic disorder characterized by hyperglycemia, which
174                  Pompe disease is a systemic metabolic disorder characterized by lack of acid-alpha g
175                                We describe a metabolic disorder characterized by lipodystrophy, hepat
176 iderable value to the treatment algorithm of metabolic disorders characterized by dysregulated fatty
177 Ds) represent a group of monogenic inherited metabolic disorders characterized by the progressive acc
178 ion is observed in many neurodegenerative or metabolic disorders, congenital malformations are rare.
179 ia (MMA) is one of the most common inherited metabolic disorders, due to deficiency of the mitochondr
180 itive association between obesity-associated metabolic disorders (e.g., hyperlipidemia and diabetes)
181 male mice is vulnerable to a slowly emerging metabolic disorder following EHS that may harbinger long
182       Using the subnetwork of depression and metabolic disorders for functional analysis, the interac
183 at restore physiological feedback control in metabolic disorders foster advanced gene- and cell-based
184  implicated in the development of a range of metabolic disorders from insulin resistance (IR) to hepa
185 neutrophil dysfunction in the rare inherited metabolic disorder GSD-Ib without causing symptomatic hy
186         The percentage of patients killed by metabolic disorder has been estimated to be 30% of the a
187 ion of acylcarnitines (ACs), often caused by metabolic disorders, has been associated with obesity, a
188 h the heterogeneous pathophysiology of human metabolic disorders, has limited the sustainability and
189 ding cancer, neurodegenerative diseases, and metabolic disorders, have been shown to be associated wi
190 rtant role in the development of obesity and metabolic disorders; however, it has not been fully unde
191 sing, metabolic switch implicated in various metabolic disorders; however, its role in inflammation i
192 ical molecular link between inflammation and metabolic disorders; however, the role of adipocyte IKKb
193 y treatment of HCV genotype-associated lipid metabolic disorders.IMPORTANCE Hepatic steatosis is a fr
194 sis may reduce HCV genotype-associated lipid metabolic disorder in liver disease.
195 olic fatty liver disease (NAFLD) is a common metabolic disorder in obese individuals.
196 g maternal HFD during lactation to persisted metabolic disorder in the offspring.
197 velopmental programming, potentially causing metabolic disorders in adults.
198 n but also promotes adiposity and associated metabolic disorders in fat-fed and aged mice.
199 may contribute to drug-induced steatosis and metabolic disorders in humans.
200 s a major risk factor for the development of metabolic disorders in humans.
201 oversupply of glucose-induced severe glucose metabolic disorders in MGs of lactating goats, shifting
202 to prevent gut dysbiosis and obesity-related metabolic disorders in obese individuals.
203           Increasing evidence indicates that metabolic disorders in offspring can result from the fat
204                      The association between metabolic disorders in offspring of obese mothers with d
205 from HFD males into normal zygotes generated metabolic disorders in the F1 offspring and altered gene
206 emale mice has the capacity to cause delayed metabolic disorders in the heart that could influence lo
207                               Examination of metabolic disorders in treatment-refractory depression i
208 de important insights into hormone-dependent metabolic disorders in women.
209 s of selected amino acids (related to inborn metabolic disorders) in the unknown DBS was compared wit
210 in to control obesity and obesity-associated metabolic disorders including insulin resistance, fatty
211  signalling is a pathogenic manifestation of metabolic disorders including obesity and diabetes.
212  adipokine cross-linking innate immunity and metabolic disorders including obesity.
213  risk in pregnancies complicated by maternal metabolic disorders, including diabetes and obesity.
214 stress, whereas superfluous lipolysis causes metabolic disorders, including dyslipidemia and hepatic
215 omeostasis and its alterations contribute to metabolic disorders, including fatty liver and diabetes.
216 n obese mice and reversed the progression of metabolic disorders, including hepatic steatosis, glucos
217 stemic inflammatory disease, associated with metabolic disorders, including high level of low-density
218 s largely unknown despite important roles in metabolic disorders, including obesity and nonalcoholic
219 pathogenic factor that characterizes various metabolic disorders, including obesity and type 2 diabet
220 sue compartments is tightly linked to severe metabolic disorders, including obesity, metabolic syndro
221 nication between the brain and gut underlies metabolic disorders, including obesity.
222 p duration has been associated with risk for metabolic disorders, including weight gain, diabetes, ob
223 eficiency diseases or obesity and associated metabolic disorders, increased risk of cardiovascular di
224 chanism by which hypercholesterolemia or any metabolic disorder increases cancer risk remains unknown
225 training reduced the severity of most of the metabolic disorders induced by a fructose-rich diet and
226  aerobic, strength, and combined training on metabolic disorders induced by a fructose-rich diet.
227 se tissue endocannabinoid levels and prevent metabolic disorders induced by a later high-fat diet (HF
228 results suggest a novel mechanism by which a metabolic disorder induces epigenetic changes to reduce
229  the treatment of conditions associated with metabolic disorders, inhibit KSHV lytic replication.
230  pharmacological target for the treatment of metabolic disorders involving glucose metabolism.
231 as a potential therapeutic strategy to treat metabolic disorders is highly sought after by the pharma
232         The prevalence of chronic immune and metabolic disorders is increasing rapidly.
233 ension and related cardiovascular, renal and metabolic disorders is likely to become even more import
234 elevance to the long-term risk of developing metabolic disorders is unknown.
235                               NKH is a neuro-metabolic disorder lacking quantitative predictors of di
236               Diabetes mellitus is a chronic metabolic disorder lasting for the lifetime of a person.
237 ormerly obese individuals are susceptible to metabolic disorders later in life, even after lifestyle
238                Obesity increases the risk of metabolic disorders like diabetes mellitus and dyslipide
239 ascular system and metabolism, especially in metabolic disorders like diabetes.
240 uided stratification of patients with common metabolic disorders, like diabetes and dyslipidemia, is
241 f factors that participate in the genesis of metabolic disorders linked to excess fat mass.
242 ncludes the sections: Hypertension, Imaging, Metabolic Disorders & Lipids, Neurovascular & Neurodegen
243     Part Two includes the sections: Imaging, Metabolic Disorders & Lipids, Rhythm Disorders, Statisti
244     Part Two includes the sections: Imaging, Metabolic Disorders & Lipids, Rhythm Disorders, Statisti
245 role of HCV in inflammation, immune evasion, metabolic disorders, liver pathogeneses, and efforts in
246                                   Congenital metabolic disorders may be an ideal target for this type
247 umption, which has also been associated with metabolic disorders, may also be linked to periodontal d
248 etroviral therapy frequently develop various metabolic disorders, neurocognitive abnormalities, and c
249 on of mTOR signalling has been implicated in metabolic disorders, neurodegeneration, cancer and agein
250 two essential organelles are associated with metabolic disorders, neurodegenerative diseases, and agi
251 s a robust model for studying the effects of metabolic disorders on the central nervous system.
252  novel therapeutic targets for patients with metabolic disorder or T2D who suffer from anxiety and de
253 ue for noninvasive, early-stage diagnosis of metabolic disorders or diseases.
254 ities commonly associated with the inherited metabolic disorder, phenylketonuria.
255 uction of circulating SCFA may contribute to metabolic disorders promoting the progression of insulin
256 of the cGAS-cGAMP-STING signaling pathway in metabolic disorders remain largely elusive.
257  relationship between the bacteria and these metabolic disorders remains a matter of debate.
258  of adipocyte IKKbeta in obesity and related metabolic disorders remains elusive.
259 he association between sleep deprivation and metabolic disorders such as diabetes and obesity require
260 sociation between air pollution exposure and metabolic disorders such as diabetes.
261 represent a candidate therapeutic target for metabolic disorders such as dyslipidemia.
262 zing radiation increases the risk of chronic metabolic disorders such as insulin resistance and type
263    Moreover, we also discuss advances on how metabolic disorders such as metabolic syndrome and diabe
264 ubsequent metabolism have been implicated in metabolic disorders such as nonalcoholic fatty liver dis
265                                              Metabolic disorders such as obesity and diabetes mellitu
266 induces oxidative stress, which is linked to metabolic disorders such as obesity and diabetes.
267 ne with age and is implicated in age-related metabolic disorders such as obesity and type 2 diabetes
268 between intestinal microbial composition and metabolic disorders such as obesity and type 2 diabetes.
269 ute an appealing target for the treatment of metabolic disorders such as obesity, diabetes and hyperl
270 ontribute to neuronal function as well as to metabolic disorders such as type 2 diabetes mellitus, ob
271 vascular disease (CVD) and mortality through metabolic disorders such as type 2 diabetes.
272 cerbate the development and/or prevalence of metabolic disorders, such as obesity, is currently of gr
273 considered promising therapeutics for common metabolic disorders, such as obesity, liver steatosis, a
274 ism and the pathophysiology of lipid-related metabolic disorders, such as obesity.
275 uman adipose tissue (hAT) is a key player in metabolic disorders, such as Type 2 Diabetes Mellitus (T
276  diseases, including a number of cancers and metabolic disorders, suggesting a role for NNMT as a pot
277 HCS cause holocarboxylase deficiency, a rare metabolic disorder that can be life-threatening if left
278 utations in the leptin gene (ob) result in a metabolic disorder that includes severe obesity(1), and
279  liver disease (NAFLD), a widespread hepatic metabolic disorder that is believed to be a risk factor
280        Obesity and type 2 diabetes (T2D) are metabolic disorders that are linked to microbiome altera
281 r, had preventive and therapeutic effects on metabolic disorders that were dependent on intestine HIF
282 ced gene expression patterns associated with metabolic disorders that were identified in blastocysts
283 f globally increasing risk factors including metabolic disorders, the incidence rates of HCC are stil
284 h the rising rates of obesity and associated metabolic disorders, there is a growing need for effecti
285  are linked to diseases spanning genetic and metabolic disorders to cancer and neurodegeneration.
286 ns, spanning from infections to cancer, from metabolic disorders to neurodegeneration and autoimmune
287 een shown to exhibit increased prevalence of metabolic disorders (type-2 diabetes, cardiovascular dis
288 le of LMP7 in the development of obesity and metabolic disorders using LMP7-deficient mice.
289              This tacrolimus-induced glucose metabolic disorder was caused by the gut microbiota, as
290 N-CDs) electrode for the screening of purine metabolic disorder was described in this paper.
291 pe and diabetic mice, with a known redox and metabolic disorder, we found that the cytoprotective nuc
292 ckout model demonstrates multiple immune and metabolic disorders, we investigated the role of each re
293  alkaloid Berberine (BRB), used for treating metabolic disorders, were studied on ex-vivo leukemic ce
294                                        These metabolic disorders, which are often accompanied by oxid
295 sed dysregulated splicing events and hepatic metabolic disorders, which trigger endoplasmic reticulum
296 e that Alzheimer disease (AD) is a pervasive metabolic disorder with dysregulation in multiple bioche
297 s an obesity- and insulin resistance-related metabolic disorder with progressive pathology.
298 iencies (MADDs) are a heterogeneous group of metabolic disorders with combined respiratory-chain defi
299 C using a small-animal model of a congenital metabolic disorder without immunosuppression.
300  of RXR may be a promising strategy to treat metabolic disorders without side effects.

 
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