Dervla M Connaughton Selected Research

1-amino-3-ethyladamantane (D175)

1/2022

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.

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Dervla M Connaughton Research Topics

Disease

7	Cakut 01/2022 - 01/2018
1	Tuberous Sclerosis (Bourneville's Disease) 06/2021
1	Nephrotic Syndrome (Syndrome, Nephrotic) 12/2020
1	Small Cell Carcinoma 01/2020
1	Neoplasms (Cancer) 01/2020
1	Interstitial Nephritis (Tubulointerstitial Nephritis) 01/2020
1	Chronic Renal Insufficiency 01/2020
1	Autonomic Nervous System Diseases (Dysautonomia) 12/2019
1	Kidney Diseases (Kidney Disease) 01/2018
1	Renal Insufficiency (Renal Failure) 01/2018

Drug/Important Bio-Agent (IBA)

3	Proteins (Proteins, Gene)FDA Link 01/2022 - 01/2018
1	1-amino-3-ethyladamantane (D175)IBA 01/2022
1	Nuclear Receptor Interacting Protein 1IBA 01/2022
1	Tretinoin (Retinoic Acid)FDA LinkGeneric 01/2022
1	Forkhead Transcription Factors (Forkhead Box Proteins)IBA 01/2022
1	trans-sodium crocetinate (crocetin)IBA 06/2021
1	ForminsIBA 12/2020
1	Transcription Factors (Transcription Factor)IBA 10/2020
1	Acetylcholine (Acetylcholine Chloride)FDA Link 12/2019
1	Cholinergic ReceptorsIBA 12/2019
1	Nicotinic Receptors (Nicotinic Acetylcholine Receptor)IBA 12/2019
1	Glycine (Aminoacetic Acid)FDA LinkGeneric 10/2019
1	Mucin-1 (CA 15-3 Antigen)IBA 01/2018

Therapy/Procedure

1	Precision Medicine 01/2020
1	Transplantation 01/2020