Keywords: ARPKD, autosomal recessive polycystic kidney disease; ADPKD, Autosomal Dominant Polycystic Kidney Disease; nsSNPs, non-synonymous SNPs; SIFT, Sorting Intolerant From Tolerant; PolyPhen2, Polymorphism Phenotyping; NGS, Next generation sequencing; ISP, Ion
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
A novel mutation identified in PKHD1 by targeted exome sequencing: Guiding prenatal diagnosis for an ARPKD family
Keywords: ARPKD, autosomal recessive polycystic kidney disease; ADPKD, autosomal dominant polycystic kidney disease; PKD1, polycystic kidney disease 1; PKD2, polycystic kidney disease 2; PKHD1, polycystic kidney and hepatic disease; CT, computed tomography; SPECT,
Biliary differentiation and bile duct morphogenesis in development and disease
Keywords: ADPKD, Autosomal Dominant Polycystic Kidney Disease; ADPLD, Autosomal Dominant Polycystic Liver Disease; ANIT, alpha-naphthylisothiocyanate; ARPKD, Autosomal Recessive Polycystic Kidney Disease; BMP, Bone Morphogenetic Protein; C/EBP, CCAAT/Enhancer Bindi
Epidermal growth factor-mediated proliferation and sodium transport in normal and PKD epithelial cells
Keywords: ADAM, a disintegrin and metalloprotease; Ang II, angiotensin II; ADPKD, autosomal dominant polycystic kidney disease; ARPKD, autosomal recessive polycystic kidney disease; CCD, cortical collecting duct; CD, collecting duct; DCT, distal convoluted tubule;
Twenty-five Years of Infant Dialysis: A Single Center Experience
Keywords: ARPKD, Autosomal recessive polycystic kidney disease; CCPD, Continuous cycling peritoneal dialysis; CKD, Chronic kidney disease; DD, Deceased donor; ESKD, End-stage kidney disease; G -Tube, Gastrostomy tube; HD, Hemodialysis; iPTH, Intact parathyroid horm
Octreotide Inhibits Hepatic Cystogenesis in a Rodent Model of Polycystic Liver Disease by Reducing Cholangiocyte Adenosine 3′,5′-Cyclic Monophosphate
Keywords: ADPKD, autosomal dominant polycystic kidney disease; ARPKD, autosomal recessive polycystic kidney disease; PCK, polycystic kidney; PCLD, polycystic liver disease; PCNA, proliferating cell nuclear antigen; SSTR, somatostatin receptor; 3-D, 3-dimensional