Results 211 to 220 of about 2,389,640 (367)

II. Adrenal Cortex and Steroid 21-Hydroxylase Autoantibodies in Children with Organ-Specific Autoimmune Diseases: Markers of High Progression to Clinical Addison’s Disease [PDF]

, 1997
Corrado Betterle, M Volpato, Bernard Rees Smith, Jadwiga Furmaniak, Shu Chen, Renato Zanchetta, Nella Augusta Greggio, B. Pedini, Marco Boscaro, Fabio Presotto   +9 more
openalex   +1 more source

Progress in Aptamer Research and Future Applications

ChemistryOpen, EarlyView.
This paper mainly describes the screening method of aptamer, the screening difficulties and improvement methods of small molecule aptamer, and the application and treatment of aptamer. It explores the latest progress and application of aptamers, and summarises them, thus indicating some problems that still exist in this field.
Song Liu, Xiaolu Li, Huyang Gao, Jing Chen, Hongfeng Jiang   +4 more
wiley   +1 more source

Growth characteristics of children with 21-hydroxylase deficiency and the value of steroid hormones in height assessment. [PDF]

BMC Pediatr
Chong H, Pi Y, Zhang Y, Li Y, Xing Y, Zhang H.   +5 more
europepmc   +1 more source

Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [PDF]

, 1996
Lucia Ghizzoni, R Virdis, Alessandra Vottero, Marco Cappa, Maria Elisabeth Street, Maria Zampolli, Lourdes Ibáñez, S Bernasconi   +7 more
openalex   +1 more source

The Omics‐Driven Machine Learning Path to Cost‐Effective Precision Medicine in Chronic Kidney Disease

PROTEOMICS, EarlyView.
ABSTRACT Chronic kidney disease (CKD) poses a significant and growing global health challenge, making early detection and slowing disease progression essential for improving patient outcomes. Traditional diagnostic methods such as glomerular filtration rate and proteinuria are insufficient to capture the complexity of CKD.
Marta B. Lopes, Roberta Coletti, Flore Duranton, Griet Glorieux, Mayra Alejandra Jaimes Campos, Julie Klein, Matthias Ley, Paul Perco, Alexia Sampri, Aviad Tur‐Sinai   +9 more
wiley   +1 more source

Unique Case Report: A Rare Association of 21-Hydroxylase Deficiency with Triple X Karyotype. [PDF]

Genes (Basel)
de Sousa Azulay RS, Facundo AN, Sousa SSE, Nascimento GC, Magalhães M, de Oliveira Neto CP, de Abreu JDMF, Lago DCF, da Silva Pereira Damianse S, de Carvalho VC, Nascimento CA, Rodrigues VP, Coeli-Lacchini FB, de Castro M, Dos Santos Faria M.   +14 more
europepmc   +1 more source

Adrenal Lymphocytic Infiltration and Adrenocortical Tumors in a Patient with 21-Hydroxylase Deficiency [PDF]

, 1999
Deborah P. Merke, Stefan R. Bornstein, Demetrios T. Braddock, George P. Chrousos   +3 more
openalex   +1 more source

Investigation of the Urinary Peptidome to Unravel Collagen Degradation in Health and Kidney Disease

PROTEOMICS, EarlyView.
ABSTRACT Naturally occurring fragments of collagen type I alpha 1 chain (COL1A1) have been previously associated with chronic kidney disease (CKD), with some fragments showing positive and others negative associations. Using urinary peptidome data from healthy individuals (n = 1131) and CKD patients (n = 5585) this aspect was investigated in detail ...
Ioanna K. Mina, Luis F. Iglesias‐Martinez, Matthias Ley, Lucas Fillinger, Paul Perco, Justyna Siwy, Harald Mischak, Vera Jankowski   +7 more
wiley   +1 more source

Rare Types of Congenital Adrenal Hyperplasias Other Than 21-hydroxylase Deficiency [PDF]

J Clin Res Pediatr Endocrinol
İsakoca M, Erdeve Ş, Çetinkaya S.
europepmc   +1 more source

The orphan nuclear receptor NGFI-B regulates expression of the gene encoding steroid 21-hydroxylase.

, 1993
Thomas E. Wilson, A R Mouw, Cheryl A. Weaver, Jeffrey Milbrandt, K L Parker   +4 more
openalex   +1 more source