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121por Lodh, Sukanya“…Two congenital disorders, Bardet-Biedl syndrome (BBS) and Alström syndrome (ALMS), can serve as useful models to understand how β-cells are normally produced and regenerated. …”
Publicado 2019
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122“…RESULTS: Leiomyosarcomas showed reduced PR expression. All LMs as well as ALMs and STUMP were stained intensely for PR. Conversely, LMS was strongly stained with p53, while the three non-sarcomatous groups (STUMP, ALM, LM) were either entirely negative or weakly stained for p53. …”
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123por Sheen, Yi-Shuan, Liao, Yi-Hua, Lin, Ming-Hsien, Chiu, Hsien-Ching, Jee, Shiou-Hwa, Liau, Jau-Yu, Chang, Yih-Leong, Chu, Chia-Yu“…However, the expression of IMP-3 has not been investigated in acral lentiginous melanoma (ALM). This study sought to elucidate its prognostic value in ALMs. …”
Publicado 2016
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124“…The majority of the students (>90%) did welcome the introduction of ALM and strongly recommended the use of such methods in teaching many more topics in future. 100% faculty members were of the opinion that many more topics shall be taken up using ALMs. …”
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125por Yang, Cui-Ping, Li, Xiaoyan, Wu, Yong, Shen, Qiushuo, Zeng, Yong, Xiong, Qiuxia, Wei, Mengping, Chen, Chunhui, Liu, Jiewei, Huo, Yongxia, Li, Kaiqin, Xue, Gui, Yao, Yong-Gang, Zhang, Chen, Li, Ming, Chen, Yongbin, Luo, Xiong-Jian“…These convergent lines of evidence suggest that the ALMS1, CSNK2B, and GLT8D1 genes may be involved in pathophysiology of schizophrenia.…”
Publicado 2018
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126“…Updated genetic testing showed pathogenic variants in ALMS1 in the first individual and TUBB4B in the second and third. …”
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127por Zeid, Mohamed, Sayedin, Hani, Nabi, Nauman, Abdelrahman, Mamoun, Jacob, Prem Thomas, Alhadi, Bassem, Giri, Subhasis“…We concluded that active surveillance is the first line of management in all small asymptomatic ALMs. ALMs less than 2 cm do not require active surveillance. …”
Publicado 2022
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128por Sönmez Flitman, Reyhan, Khalili, Bita, Kutalik, Zoltan, Rueedi, Rico, Brümmer, Anneke, Bergmann, Sven“…Using metabomatching, we identified the metabolites corresponding to metabolome features associated with the genes, namely, N-acetylated compounds with ALMS1 and trimethylamine (TMA) with HPS1. Finally, Mendelian randomization analysis supported a potential causal link between the expression of genes in both the ALMS1- and HPS1-loci and their associated metabolite concentrations. …”
Publicado 2021
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129por Szymczak, Barbara“…The aLM isolates possessed 3–7 of the 12 virulence genes: prfA and hly in all aLMs, while iap was not present. …”
Publicado 2023
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130por Kim, Min Kyeong, Kwak, Soo Heon, Kang, Shinae, Jung, Hye Seung, Cho, Young Min, Kim, Seong Yeon, Park, Kyong Soo“…Alström syndrome is caused by a mutation in the ALMS1 gene, and Bardet-Biedl syndrome is caused by mutations in BBS1-16 genes. …”
Publicado 2015
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131por Astuti, Dewi, Sabir, Ataf, Fulton, Piers, Zatyka, Malgorzata, Williams, Denise, Hardy, Carol, Milan, Gabriella, Favaretto, Francesca, Yu‐Wai‐Man, Patrick, Rohayem, Julia, López de Heredia, Miguel, Hershey, Tamara, Tranebjaerg, Lisbeth, Chen, Jian‐Hua, Chaussenot, Annabel, Nunes, Virginia, Marshall, Bess, McAfferty, Susan, Tillmann, Vallo, Maffei, Pietro, Paquis‐Flucklinger, Veronique, Geberhiwot, Tarekign, Mlynarski, Wojciech, Parkinson, Kay, Picard, Virginie, Bueno, Gema Esteban, Dias, Renuka, Arnold, Amy, Richens, Caitlin, Paisey, Richard, Urano, Fumihiko, Semple, Robert, Sinnott, Richard, Barrett, Timothy G.“…We populated it with 628 published disease‐associated variants (December 2016) for: WFS1 (n = 309), CISD2 (n = 3), ALMS1 (n = 268), and SLC19A2 (n = 48) for Wolfram type 1, Wolfram type 2, Alström, and Thiamine‐responsive megaloblastic anemia syndromes, respectively; and included 23 previously unpublished novel germline variants in WFS1 and 17 variants in ALMS1. …”
Publicado 2017
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132por Marozio, Luca, Dassie, Francesca, Bertschy, Gianluca, Canuto, Emilie M., Milan, Gabriella, Cosma, Stefano, Maffei, Pietro, Benedetto, Chiara“…Conclusion: The present case demonstrates for the first time that conceiving is possible for patients with ALMS. Particular attention should be given to the management of AS systemic comorbidities through the course of pregnancy.…”
Publicado 2022
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133“…Interest in and use of article-level metrics (ALMs) has grown rapidly amongst the research community, by researchers, publishers, funders, and research institutions. …”
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134por Fenner, Martin“…Article-level metrics (ALMs) provide a wide range of metrics about the uptake of an individual journal article by the scientific community after publication. …”
Publicado 2013
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135por Vieira, Warren A., Raymond, Michael, Kelley, Kristina, Cherubino, Matthew A., Sahin, Hande, McCusker, Catherine D.“…Grafts of posterior skin from the distal limb regions into posterior ALMs at the base of the limb induce ectopic limb structures. …”
Publicado 2023
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136por Sykes, Ingrid“…Musical voices had been used by members to collect alms and to project the particular spiritual principle of their institution since its foundation in the thirteenth century. …”
Publicado 2011
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137“…Interview data from 11 Amish adults in Lancaster County depict how this aid program supplements traditional congregational alms coverage of medical expenses. The interview data delineate the structure of the program, its operation, and how it encourages cost containment and community interdependence. …”
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138por Zhang, Kai, Xie, Xiaolin, Wang, Chao, Wang, Ha, Xu, Fang, Wang, He, Zhang, Xin, Guan, Haijun, Qu, Hemeng, Zhang, Jizhen“…Contrasting with conventional lightweight mirrors (CLM), the performances of ALM are drastically improved. This paper took the Voronoi mirrors as an ALM case study and introduced a design flow. …”
Publicado 2022
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139“…In practice, the dimensions of charity (alms and infaq) strengthen mechanical solidarity, i.e., collective consciousness and cooperation spirit, to influence social cohesion. …”
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140por Lopour, Madeline Q.R., Schimmenti, Lisa A., Boczek, Nicole J., Kearney, Hutton M., Drack, Arlene V., Brodsky, Michael C.“…OBSERVATIONS: A 13-month-old boy with poor vision and nystagmus was diagnosed with Alström syndrome based on genetic testing that identified a homozygous pathogenic variant, ALMS1 c.2141_2141del (p.Ser714Tyrfs*6), that was only found in his mother and not his father. …”
Publicado 2022
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