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1 nal carcinoma, two chromophobe type, and one lipoma).
2 mour cell types, including fat-cell tumours (lipomas).
3 r (p = 0.044) of a histologically non-benign lipoma.
4 confidence rating of 4 or 5 as positive for lipoma.
5 nign tumors of mesenchymal origin, including lipomas.
6 HMGI-C truncation in the generation of human lipomas.
7 ng multiple angiofibromas, collagenomas, and lipomas.
8 sible role in development and progression of lipomas.
9 well differentiated liposarcomas or atypical lipomas.
10 l segment rearranged in a subset of ordinary lipomas.
11 mosomal segment often rearranged in ordinary lipomas.
12 gn ocular tumors, and central nervous system lipomas.
13 e and efficacious treatment of large colonic lipomas.
14 ce imaging (MRI) findings of rare pancreatic lipomas.
15 , macroscopic fat (<-30 HU) was present in 9 lipomas.
16 bile duct, stomach, oral cavity tumors, and lipomas.
17 low accuracy in the diagnosis of soft-tissue lipomas.
18 ental ages, a cerebellar tumor, and multiple lipomas.
19 on, and have an abnormally high incidence of lipomas.
20 ntial role for HMG I-C in the development of lipomas.
21 nt to perturb adipogenesis and predispose to lipomas.
23 tients had myelodysplastic lesions (19 filar lipoma, 14 syringomyelia, 10 intradural lipoma, eight de
24 astomas, 18 (6%) with fibromas, 12 (4%) with lipomas, 28 (9%) with other benign primary cardiac tumor
25 expression was detected in 7 of 11 ordinary lipomas (63.6%) with alterations at 12q14-15 and in one
27 ding frontonasal dysplasia, interhemispheric lipoma, agenesis of the corpus callosum, tibial hemimeli
32 39 well differentiated adipose neoplasms (19 lipomas and 20 ALTs) of known karyotype using polyclonal
33 ith histologically verified fatty tumors (35 lipomas and 25 well-differentiated liposarcomas) were re
34 motor dysfunction, subcutaneous and visceral lipomas and hemangiomas, and intestinal juvenile polypos
35 pertrophy of the interatrial septum, cardiac lipomas and liposarcomas) conditions, with or without ex
38 nal juvenile polyposis, developmental delay, lipomas, and pigmentation spots of the male genitalia.
40 er syndromes characterized by overgrowth and lipomas are part of the PTEN syndrome spectrum, we ascer
44 that demonstrated imaging characteristics of lipoma, benign peripheral nerve sheath tumor, and vascul
45 that demonstrated imaging characteristics of lipoma, benign peripheral nerve sheath tumor, and vascul
46 , progressive skeletal deformities, invasive lipomas, benign and malignant tumors, and deep venous th
47 ertained six individuals with overgrowth and lipomas but who did not meet the diagnostic criteria for
53 s tumors, epithelioid sarcomas, spindle cell lipomas, dermatofibrosarcoma protuberans, and myofibrobl
54 methemoglobin), 3.lipid-containing lesions (lipoma, dermoid cyst, implanted fatty materials, laminar
56 ilar lipoma, 14 syringomyelia, 10 intradural lipoma, eight dermal sinus, five diastematomyelia, five
59 n particular, increased abundance of fat and lipomas, features strikingly similar to those observed i
60 differentiated mesenchymal tumors, including lipomas, fibroadenomas of the breast, salivary gland ade
63 sion of other mesenchymal tumors (leiomyoma, lipoma, gastrointestinal stromal tumor, leiomyosarcoma,
64 feration of mesenchymal cells in leiomyomas, lipomas, hamartomas,and other diseases has been linked t
65 sferase 3) with stroke, and the LHFPL2 gene (lipoma high mobility group protein I-C fusion partner-li
67 localisation from P9 onwards coincides with lipoma HMGIC fusion partner-like 5 (LHFPL5), a protein t
68 MET components Protocadherin 15a (Pcdh15a), Lipoma HMGIC fusion partner-like 5 (Lhfpl5), and Transme
70 f hair cell stereocilia (TMHS, also known as lipoma HMGIC fusion partner-like 5, LHFPL5), both though
71 ex, including protocadherin 15, cadherin 23, lipoma HMGIC fusion partner-like 5, transmembrane inner
72 nding genes, nucleolar protein 4 (NOL4), and lipoma HMGIC fusion partner-like protein 4 (LHFPL4), whi
73 In conclusion, whole exome sequencing in lipomas identified mutations in genes with a possible ro
76 study examined the prevalence of pancreatic lipomas in a sample of patients undergoing abdominal com
77 dministered, are implicated in the growth of lipomas in different anatomic locations including the ep
79 ontaining preferred translocation partner in lipoma), induced by constitutive activation of STAT5, bu
81 ic the mesenchymal submucosal tumors such as lipoma, leiomyoma, and gastrointestinal stromal tumors.
83 69%), including those with either classic or lipoma-like histology, had rearrangements of the 8q12 PL
90 This is the first case of intramedullary lipoma of the spinal cord that may be related to steroid
91 during continuous culture, whereas APCs from lipomas of patients with PHTS retain their adipogenic po
94 tivity was demonstrated in only two ordinary lipomas: one with 6p21 rearrangement and one with normal
97 , depth, growth noticed by patient, previous lipoma, patient felt pain), Ultrasonographic (size, dept
98 ing to define the mutational spectrum in ten lipoma patients along with their matching control sample
99 a family of proteins that also includes the lipoma preferred partner (LPP) and thyroid receptor-inte
103 Here, we found that CAFs upregulated the lipoma-preferred partner (LPP) gene in microvascular end
105 d receptor-interacting protein 6 (TRIP6) and lipoma-preferred partner (LPP), but not to zyxin itself.
106 a being the most frequent and others such as lipoma) present as endoluminal growth, with defined bord
108 rare, karyotypically distinct group of human lipomas, rearrangements of 6p21-23 produce internal dele
109 ed with development of human tumors, such as lipomas, relatively few examples exist of germline mutat
110 igations of primary cardiac tumors (myxomas, lipomas, rhabdomyomas, and fibromas) have provided insig
113 pillary fibroelastomas (SMR 3.17, P=0.0003), lipomas (SMR 5.0, P=0.0003), other benign tumors (SMR 4.
116 k features of BRR: macrocephaly and multiple lipomas, the latter of which occur in a minority of indi
117 nted genomic insight into the development of lipomas, the most common benign tumor of soft tissue.
118 ons consisted of six adenomatoid tumors, two lipomas, two epidermoid inclusion cysts, two cases of sa
119 differentiated mesenchymal tumors including lipomas, uterine leiomyomas, and pulmonary chondroid ham
122 he tendon sheath, epidermal inclusion cysts, lipomas, vascular lesions, peripheral-nerve tumours, ski
123 eases within the CPA, including meningiomas, lipomas, vascular malformations, hemangiomas, epidermoid
125 peritoneal hernia repair, the anatomy of the lipomas was studied both at the time of surgery and agai
133 88, average: 65.6 years), with 13 pancreatic lipomas, whose cases constituted the basis for 10 contra