Results 231 to 240 of about 119,685 (338)

Child rate, pregnancy outcome and ovarian function in females with classical 21‐hydroxylase deficiency [PDF]

, 2000
JARMO JÄÄSKELÄINEN, MARITTA HIPPELÄINEN, Olavi Kiekara, Raimo Voutilainen   +3 more
openalex   +1 more source

Heterologous plastoquinone production using a newly identified O2‐dependent cyanobacterial hydroxylase

The FEBS Journal, EarlyView.
In this study, we confirm that PlqH is the hydroxylase operating in plastoquinone biosynthesis in photosynthetic cyanobacteria (Cyanobacteriia). Our phylogenetic analyses demonstrate that cyanobacterial PlqH homologues originated from hydroxylases involved in ubiquinone biosynthesis in bacteria. Plastoquinone production in Escherichia coli was achieved
Morgane Roger‐Margueritat, Margot Beltran, Juliette Schnoebelen, Laura Flandrin, Wafa Rezali, Eline Michel, Sophie S. Abby, Fabien Pierrel   +7 more
wiley   +1 more source

Endothelial dysfunction in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: current knowledge and novel biomarkers. [PDF]

Front Endocrinol (Lausanne)
Hubska J, Roszkowska Z, Bobrowicz M, Iwaniuk S, Rak-Makowska B, Ambroziak U.   +5 more
europepmc   +1 more source

Oxygen‐independent expression of HIF‐1α during the cell cycle in hepatocellular carcinoma cells controls essential metabolic pathways under normoxia

The FEBS Journal, EarlyView.
In Huh7 cells, HIF‐1α is essential as it maintains the expression of proteins involved in glycolysis and steroid/cholesterol biosynthesis both under normoxia and hypoxia. On the other hand, in HeLa cells, these pathways are induced by HIF‐1α only under hypoxia.
Ioanna‐Maria Gkotinakou, Christina Arseni, Kreon Koukoulas, Martina Samiotaki, George Panayotou, George Simos, Ilias Mylonis   +6 more
wiley   +1 more source

Hypoxia regulates Th17/Treg balance by altering chromatin accessibility and gene expression

The FEBS Journal, EarlyView.
T‐cell differentiation into Th17 or iTreg cells is key to inflammation control. Integrated RNA‐seq and ATAC‐seq analyses reveal that hypoxia induces more extensive gene expression changes in iTreg cells. Elevated levels of Hif1a and Stat3, along with increased accessibility to key transcription factor motifs, may predispose these cells toward ...
Mariana Cázares‐Olivera, Shiyang Song, Sofia Ylinen, Talha Qureshi, Bin Li, Zhi Chen   +5 more
wiley   +1 more source

Evaluation of Sleep Health in Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

J Clin Endocrinol Metab
Golob L, Mercado-Munoz Y, Liu W, Singh A, Hodges JS, Siegel L, Morero H, Gao Z, Tipp A, Simon SL, Sarafoglou K.   +10 more
europepmc   +1 more source

Supplemental documents of Impact of growth-promoting therapies on puberty, growth, and final height in classical 21-hydroxylase deficiency

Yavas Abali, Zehra, Yildiz, Melek, Abali, Saygin, Moniri, Ariorad, Bas, Firdevs, Onal, Hasan, Cilsaat, Gizem, Toksoy, Guven, Turan, Serap, Poyrazoglu, Sukran, Uyguner, Zehra Oya, Bundak, Ruveyde, Bereket, Abdullah, Darendeliler, Feyza, guran, tulay   +14 more
openalex   +1 more source

Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening

, 2017
Shih‐Yao Liu, Cheng-Ting Lee, Yi‐Ching Tung, Yin‐Hsiu Chien, Wuh‐Liang Hwu, Wen–Yu Tsai   +5 more
openalex   +1 more source

Regulation of PHOX2B gene expression by the long non‐coding natural antisense RNA PHOX2B‐AS1

The FEBS Journal, EarlyView.
PHOX2B is a transcription factor essential for autonomic nervous system development. We identify and characterize PHOX2B‐AS1, a human long non‐coding antisense transcript at the PHOX2B locus, along with its murine counterpart. Our findings reveal bidirectional transcription and reciprocal regulation: PHOX2B activates PHOX2B‐AS1, whereas PHOX2B‐AS1 ...
Simona Di Lascio, Ana Lucia Cuadros Gamboa, Martina Bertocchi, Filippo Chiesa, Francesca Cargnin, Ettore Mosca, Paride Pelucchi, Viviana Tritto, Stefania Corti, Isabella Ceccherini, Paola Riva, Roberta Benfante, Diego Fornasari   +12 more
wiley   +1 more source

Treatment and Follow-up of Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Childhood and Adolescence [PDF]

J Clin Res Pediatr Endocrinol
Peltek Kendirci HN, Ünal E, Dündar İ, Buluş AD, Odabaşı Güneş S, Şıklar Z.   +5 more
europepmc   +1 more source