Results 81 to 90 of about 8,849 (148)
Collecting duct carcinoma of the kidney.
Chinese medical journal, 1998 To describe the clinical, pathologic and immunohistochemical characteristics of collecting duct carcinoma (CDC) of the kidney.Five cases of CDC (3 males and 2 females, aged 41 to 67 years) were identified between January, 1990 and December, 1994. Routine histopathologic study and immunohistochemical examinations of the surgical specimens were performed.
G, Ren, S, Shi, X, Yu
openaire +1 more source
Specialized expression of simple O-glycans along the rat kidney nephron [PDF]
, 2017 Glycosyltransferases can exhibit tissue-specific expression. By histochemistry glycosyltransferases and their products can be localized to specific cell types in organs of complex cellular composition.
Roth, Jürgen +3 more
core
Validation of preoperative variables and stratification of patients to help predict benefit of cytoreductive nephrectomy in the targeted therapy ERA [PDF]
, 2017 Kim, Eric H +4 more
core +2 more sources
Parvalbumin: calcium and magnesium buffering in the distal nephron [PDF]
, 2017 Parvalbumin (PV) is a classical member of the EF-hand protein superfamily that has been described as a Ca2+ buffer and Ca2+ transporter/shuttle protein and may also play an additional role in Mg2+ handling.
Devuyst, Olivier +4 more
core
Comprehensive molecular characterization of collecting duct carcinoma for therapeutic vulnerability
EMBO Molecular MedicineCollecting duct carcinoma (CDC) is an aggressive rare subtype of kidney cancer with unmet clinical needs. Little is known about its underlying molecular alterations and etiology, primarily due to its rarity, and lack of preclinical models.
Peiyong Guan +27 more
doaj +1 more source
CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT) [PDF]
, 2017 Background. Recently, we identified a microduplication in chromosomal band 1q21.1 encompassing the CHD1L/ALC1 gene encoding a chromatin-remodelling enzyme in congenital anomalies of the kidneys and urinary tract (CAKUT) patient. Methods.
Brockschmidt, Antje +14 more
core
Journal of the Korean Society of RadiologySynchronous renal malignancies are seldom encountered or diagnosed post-renal resection. A combination of renal cell carcinoma (RCC) and urothelial carcinoma (UC) is most commonly reported.
Sang Bin Bae +2 more
doaj +1 more source
Clear cell renal cell carcinoma located in sinus renalis confused with renal pelvis mass in image [PDF]
, 2011 Wu, Pengjie +5 more
core +2 more sources