Search for other papers by Lei Lei in
Google Scholar
PubMed
Search for other papers by Yi-Hua Bai in
Google Scholar
PubMed
Search for other papers by Hong-Ying Jiang in
Google Scholar
PubMed
Search for other papers by Ting He in
Google Scholar
PubMed
Search for other papers by Meng Li in
Google Scholar
PubMed
Search for other papers by Jia-Ping Wang in
Google Scholar
PubMed
mMDEGs are shown in Fig. 3C and D . For the KEGG pathway analysis, it was found that mMDEGs were significantly associated with the ‘T2D’ signaling pathway ( Fig. 3E ). The mMDEGs participating in this pathway were INS , MAFA , and HK2 . Thus, in
Search for other papers by Wenrui Wang in
Google Scholar
PubMed
Search for other papers by Chuan Zhang in
Google Scholar
PubMed
release, accompanied by Pdx1 nuclear translocation and suppression of insulin and GLUT2 gene expression. (D) The p38 MAPK pathway mediates the degradation of endogenous MafA during hyperglycemia. The dotted and solid boxes represent signaling pathway
Search for other papers by Xuhua Mao in
Google Scholar
PubMed
Search for other papers by Hucheng Chen in
Google Scholar
PubMed
Search for other papers by Junmin Tang in
Google Scholar
PubMed
Search for other papers by Liangliang Wang in
Google Scholar
PubMed
Search for other papers by Tingting Shu in
Google Scholar
PubMed
three β-cell-specific transcription factors: Pdx-1, neurogenic differentiation 1 (NeuroD1) and V-maf musculoaponeurotic fibrosarcoma oncogene homologue A (MafA). RT-PCR analysis of the effects of gluco-toxicity showed significantly decreased expression
Department of Anatomy, Shanxi Medical University, Taiyuan, China
Search for other papers by Zhandong Lei in
Google Scholar
PubMed
Search for other papers by Yunfei Chen in
Google Scholar
PubMed
Search for other papers by Jin Wang in
Google Scholar
PubMed
Search for other papers by Yan Zhang in
Google Scholar
PubMed
Search for other papers by Wenjuan Shi in
Google Scholar
PubMed
Search for other papers by Xuejiao Wang in
Google Scholar
PubMed
Search for other papers by Dehai Xing in
Google Scholar
PubMed
Search for other papers by Dongxue Li in
Google Scholar
PubMed
Search for other papers by Xiangying Jiao in
Google Scholar
PubMed
transcription factors, including Pdx1 , Mafa and Foxo1 , play vital roles in β-cell proliferation, development, differentiation, maturation and functional maintenance ( 8 , 17 , 18 , 19 ). Insulin, glucose, growth factors, hormones and nutrients stimulate
Search for other papers by Monia Cito in
Google Scholar
PubMed
Search for other papers by Silvia Pellegrini in
Google Scholar
PubMed
Vita-Salute San Raffaele University, Milan, Italy
Search for other papers by Lorenzo Piemonti in
Google Scholar
PubMed
Search for other papers by Valeria Sordi in
Google Scholar
PubMed
generated a state of uncertainty regarding GABA transdifferentiation effects. Very recently, the transcription factors PDX1 and MAF-A were delivered in vivo with adeno-associated virus to the mouse pancreas through the pancreatic duct to reprogram α
Search for other papers by Hélène Singeisen in
Google Scholar
PubMed
Search for other papers by Mariko Melanie Renzulli in
Google Scholar
PubMed
Search for other papers by Vojtech Pavlicek in
Google Scholar
PubMed
Search for other papers by Pascal Probst in
Google Scholar
PubMed
Search for other papers by Fabian Hauswirth in
Google Scholar
PubMed
Search for other papers by Markus K Muller in
Google Scholar
PubMed
Search for other papers by Magdalene Adamczyk in
Google Scholar
PubMed
Search for other papers by Achim Weber in
Google Scholar
PubMed
Search for other papers by Reto Martin Kaderli in
Google Scholar
PubMed
Search for other papers by Pietro Renzulli in
Google Scholar
PubMed
MEN4, MEN5, and MAFA-related insulinomatosis. MEN syndromes now include five entities, MEN1–5. Clinical definition of MEN Patients with tumors of two or more endocrine organs fulfill the diagnostic criteria of MEN. Furthermore, a familial MEN is