Spontaneous Thyrotropin and Cortisol Secretion Interactions in Patients with Nonclassical 21-Hydroxylase Deficiency and Control Children1 [PDF]
Lucia Ghizzoni+7 more
openalex +1 more source
ABSTRACT Background This study investigates the impact of hormone therapy (HT) on the diagnostic performance of 18F‐piflufolastat PET/CT in OSPREY (NCT02981368) cohort B patients with recurrent or metastatic prostate cancer. Methods 18F‐piflufolastat PET/CT was evaluated in OSPREY cohort B patients (n = 117 men) with elevated prostate‐specific antigen (
Lawrence Saperstein+9 more
wiley +1 more source
Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications. [PDF]
Concolino P, Falhammar H.
europepmc +1 more source
STUDY OF THE CYP21 GENE IN AN ARGENTINIAN POPULATION OF PATIENTS (P) WITH 21-HYDROXYLASE ENZYME DEFICIENCY (CAH) [PDF]
Andrea Dardis+3 more
openalex +1 more source
Engineering plant immune circuit: walking to the bright future with a novel toolbox
Generating and developing disease‐resistant plant varieties are required to maintain a sustainable food stockpile and the environment. The ability to engineer immune regulatory components through several approaches, such as genetic transformation, CRISPR/Cas‐mediated gene knockdown/knockout, decoy engineering, pathogen effector‐based strategy, RNAi ...
Uyen Thi Vuong+6 more
wiley +1 more source
Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency [PDF]
Odabaşı Güneş S+5 more
europepmc +1 more source
Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency [PDF]
Deborah P. Merke+7 more
openalex +1 more source
Dissecting Microscopic Colitis Immunopathophysiology: Insights From Basic Research
ABSTRACT Microscopic colitis is an inflammatory bowel disease (IBD) comprising two clinically undiscernible entities: collagenous colitis and lymphocytic colitis. Collagenous colitis associates with HLA genes and displays a Th1/Tc1–Th17/Tc17 profile with pericryptal myofibroblast activity, water malabsorption and secondary fluid loss due to altered ...
Andreas Münch+1 more
wiley +1 more source
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome. [PDF]
Kim JH, Kim GH, Yoo HW, Choi JH.
europepmc +1 more source