Pages that link to "Q36551577"
Jump to navigation
Jump to search
The following pages link to Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations (Q36551577):
Displaying 40 items.
- Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans (Q26862475) (← links)
- Lower urinary tract development and disease (Q27000375) (← links)
- Evidence for inheritance of medullary sponge kidney (Q28284592) (← links)
- Targeted exome sequencing integrated with clinicopathological information reveals novel and rare mutations in atypical, suspected and unknown cases of Alport syndrome or proteinuria (Q28534316) (← links)
- The prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia. (Q33858105) (← links)
- Genetic Drivers of Kidney Defects in the DiGeorge Syndrome (Q34680591) (← links)
- Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations. (Q36320552) (← links)
- Genetics of Vesicoureteral Reflux (Q36658504) (← links)
- Re-Punching Tissue Microarrays Is Possible: Why Can This Be Useful and How to Do It. (Q37200813) (← links)
- A patient with MEN1 typical features and MEN2-like features (Q37226787) (← links)
- To bud or not to bud: the RET perspective in CAKUT. (Q37634304) (← links)
- Medullary sponge kidney: state of the art. (Q38066430) (← links)
- Renin-angiotensin system in ureteric bud branching morphogenesis: implications for kidney disease (Q38141834) (← links)
- RET revisited: expanding the oncogenic portfolio (Q38190360) (← links)
- Genetic, environmental, and epigenetic factors involved in CAKUT. (Q38568437) (← links)
- Routine use of clinical exome-based next-generation sequencing for evaluation of patients with thrombotic microangiopathies (Q38655720) (← links)
- Prorenin receptor controls renal branching morphogenesis via Wnt/β-catenin signaling (Q38723947) (← links)
- Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play. (Q38731983) (← links)
- Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract (Q38822350) (← links)
- Hippo signaling in the kidney: the good and the bad. (Q38838116) (← links)
- Renal development in the fetus and premature infant (Q39119810) (← links)
- Genetic Syndromes Affecting Kidney Development (Q39242469) (← links)
- Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract. (Q39371197) (← links)
- Identification of 8 Novel Mutations in Nephrogenesis-Related Genes in Chinese Han Patients with Unilateral Renal Agenesis (Q39375974) (← links)
- Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism. (Q47155566) (← links)
- Targeting RET-driven cancers: lessons from evolving preclinical and clinical landscapes (Q47601932) (← links)
- Reciprocal Spatiotemporally Controlled Apoptosis Regulates Wolffian Duct Cloaca Fusion. (Q50078193) (← links)
- Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux (Q50482421) (← links)
- Pathogenic Germline Variants in 10,389 Adult Cancers. (Q52602399) (← links)
- Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract. (Q52882939) (← links)
- Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT. (Q53473853) (← links)
- High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT (Q62937752) (← links)
- Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms? (Q64044603) (← links)
- Development of the urogenital system is regulated via the 3'UTR of GDNF (Q64109223) (← links)
- Molecular Mechanisms of Syndromic Cryptorchidism: Data Synthesis of 50 Studies and Visualization of Gene-Disease Network. (Q64994553) (← links)
- SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes (Q90038226) (← links)
- Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease (Q90290929) (← links)
- Medullary Sponge Kidney: Current Perspectives (Q90427529) (← links)
- DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract (Q91529832) (← links)
- Renal developmental genes are differentially regulated after unilateral ureteral obstruction in neonatal and adult mice (Q101476238) (← links)