Results 151 to 160 of about 119,685 (338)

437 MOLECULAR CLONING OF THE BOVINE 21 HYDROXYLASE GENE [PDF]

, 1985
Bon-Cnu Chung, Karla J. Matteson, Walter L. Miller   +2 more
openalex   +1 more source

Molecular imprinting for neurology: Materials, applications, and limitations

Ibrain, EarlyView.
Molecularly imprinted materials: diagnostic, therapeutic and research applications in neurology. Molecularly imprinted materials offer high specificity and affinity for target molecules in neurological applications. This review highlights their synthesis, characterisation, and use in diagnostics, research and therapeutics.
Xiaohan Ma, Yingqi Ma, Claudia Marino, Alessandro Poma   +3 more
wiley   +1 more source

Infertilité primaire révélant un bloc en 21 hydroxylase : à propos d’un cas

, 2018
Sara Askaoui, G. El Mghari, N. El Ansari
openalex   +1 more source

1 ANALYSIS OF POINT MUTATIONS (PM) OF CYP 21B GENE IN PATIENTS WITH 21-HYDROXYLASE DEFICIENCY (CAH) [PDF]

, 1994
Andrea Dardis, N Saracco, Marco A. Rivarola, Alicia Belgorosky   +3 more
openalex   +1 more source

Clinical Relevance and Diagnostic Utility of Standard Serum Biomarkers in Advanced Chronic Kidney Disease: A Single‐Center Observational Study From Bangladesh

iLABMED, EarlyView.
This study evaluated conventional and emerging biochemical markers for assessing chronic kidney disease (CKD) progression in Bangladeshi patients elevated serum uric acid and parathyroid hormone levels, along with reduced eGFR, vitamin D, and albumin levels, were significantly associated with CKD, highlighting their potential as cost‐effective early ...
Fazlul Haque, Md. Samiul Islam, Nafsoon Rahman, Ayub Zawad, Sadia Afrin, Pulak Kanti Palit, Tanjil Hasan, Md. Isahak Ali, Shafin Ahmed, Akram Hossain, Marina Khatun, Tabassuma Marzia Prome, Md. Shah Alam, Ashekul Islam   +13 more
wiley   +1 more source

Genetic Analysis of Classical 21-Hydroxylase Deficiency Using Polymerase Chain Reaction and Allele-Specific Oligonucleotide Hybridization

, 1993
Eishin Ogawa, Toshihiro Ohura, Yutaka Igarashi, Kuniaki Narisawa, Keiya Tada   +4 more
openalex   +2 more sources

Synergistic Effect of Partially Inactivating Mutations in Steroid 21-Hydroxylase Deficiency¹ [PDF]

, 1997
Andrej Nikoshkov, Svetlana Lajić, Mikael Holst, Anna Wedell, Holger Luthman   +4 more
openalex   +1 more source

Disorders of sex development (DSD): an overview of recent scientific advances [PDF]

, 2014
Developments in biotechnology have radically altered clinical and research themes in the small field of disorders of sex development, as in other rare medical conditions. In the age of genetics, an increasing number of DSDs have been identified. Aided by
Conway, GS
core  

Schisantherin A: Remodeling Gut Microbiota to Activate the Gut–Immune–Neural–Adipose Axis for Thermogenesis

iNew Medicine, EarlyView.
ABSTRACT The global obesity epidemic necessitates safe and effective strategies to enhance energy expenditure. Schisantherin A (Sin A), a lignan derived from Schisandra chinensis, has demonstrated metabolic benefits, yet its systemic mechanism remains unclear.
Ling Yin
wiley   +1 more source

Molecular crosstalk via exosomes in lung cancer progression

Interdisciplinary Medicine, EarlyView.
“Molecular and theranostics roles of exosomes in Lung Cancer.” Abstract Exosomes play a critical role in lung cancer metastasis, facilitating tumor progression through intercellular communication between cancer cells and the tumor microenvironment. These nanosized extracellular vesicles carry bioactive molecules such as proteins, nucleic acids, and ...
Rajib Dhar, Vinoth Kumarasamy, Brian G. Oliver, Vetriselvan Subramaniyan   +3 more
wiley   +1 more source