Results 101 to 110 of about 2,410 (172)

SLC5A1 Gene [PDF]

, 2020
openaire   +1 more source

SLC5A1 wt Allele [PDF]

, 2020
openaire   +1 more source

Expression of differentiated MM markers in E15.5 embryonic kidneys and E12.5 aggregates after 7 days in culture.

, 2015
qRT-PCR results show that, as compared to E12.5 embryonic kidneys, E15.5 embryonic kidneys had a significant decrease in the expression of NPC marker genes (Six2, Eya1 and Gdnf) and a significant increase in the expression of differentiated MM cell ...
Naomi Yanagawa (754863), Shunsuke Yuri (754861), Oak D. Jo (754864), Masaki Nishikawa (754862), Norimoto Yanagawa (754865)   +4 more
core   +1 more source

POLYBROM0-1 MUTATIONS IN CLEAR CELL RENAL CELL CARCINOMA TUMORS FROM PATIENTS IN EASTERN EUROPE

, 2013
There were approximately 65,000 cases of renal cancer worldwide in 2012, the majority being sporadic clear cell renal cell carcinoma (ccRCC). Nearly all patients who progress to metastatic ccRCC will succumb to the disease.
Wells, David W.
core   +1 more source

Metabolic subtypes and immune landscapes in esophageal squamous cell carcinoma: prognostic implications and potential for personalized therapies

BMC Cancer
Background This study aimed to identify metabolic subtypes in ESCA, explore their relationship with immune landscapes, and establish a metabolic index for accurate prognosis assessment.
Xiao-wan Yu, Pei-wei She, Fang-chuan Chen, Ya-yu Chen, Shuang Zhou, Xi-min Wang, Xiao-rong Lin, Qiao-ling Liu, Zhi-jun Huang, Yu Qiu   +9 more
doaj   +1 more source

Table2_Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose–galactose transporter SLC5A1.docx

IntroductionCongenital glucose–galactose malabsorption (CGGM) is a rare autosomal recessive disorder that primarily causes chronic intractable diarrhea.
Sara Guillén-Lopez (17985895), Lizbeth López-Mejía (17985892), Marcela Vela-Amieva (9292218), Rosalía Santillán-Martínez (17985898), María Dolores González-Herrra (17985904), Juan Gaspar Reyes-Magaña (17985910), Melania Abreu (17985901), Rubicel Díaz-Martínez (17985907)   +7 more
core   +1 more source

Table1_Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose–galactose transporter SLC5A1.xlsx

IntroductionCongenital glucose–galactose malabsorption (CGGM) is a rare autosomal recessive disorder that primarily causes chronic intractable diarrhea.
Sara Guillén-Lopez (17985895), Lizbeth López-Mejía (17985892), Marcela Vela-Amieva (9292218), Rosalía Santillán-Martínez (17985898), María Dolores González-Herrra (17985904), Juan Gaspar Reyes-Magaña (17985910), Melania Abreu (17985901), Rubicel Díaz-Martínez (17985907)   +7 more
core   +1 more source

Mutational Landscape of Primary Hyperoxaluria in Morocco: Update and Implications for Diagnosis. [PDF]

Genes (Basel)
Batta O, Rahmuni Y, Lyahyai J, Rchiad Z, Doubaj Y, Sefiani A, Jaouad IC.   +6 more
europepmc   +1 more source

Combined analysis of metabolomics and transcriptomics reveals new indicators for the diagnosis and prognosis of colorectal cancer. [PDF]

Contemp Oncol (Pozn)
Guo M, Jin B.
europepmc   +1 more source

Causal association between antidiabetic drug targets and risk of Bell's palsy: A 2-sample Mendelian randomization study. [PDF]

Medicine (Baltimore)
Lu K, Ye L, Yi X, He Y.
europepmc   +1 more source