Results 191 to 200 of about 8,236 (247)

GPR97 variants and their influence on pathological myopia: implications for glucocorticoid treatment. [PDF]

Res Pharm Sci
Zhao Q, Mu Z, Gu H, Cheng W, Xu Y, Jiang Y, Wu G, Pu L.   +7 more
europepmc   +1 more source

Toward Sustainable Enzyme Production From Agro‐Industrial Residues: Optimizing pH and Soyhull Particle Size in Fungal Fermentation

Journal of Surfactants and Detergents, EarlyView.
Sustainable enzyme production from soyhull fermentation. ABSTRACT Carbohydrase enzymes are critical to sustainable detergent formulations, enabling effective cleaning at lower temperatures and reduced resource use. To improve the economic and environmental viability of enzyme production, this study explored soybean hulls—a low‐value agricultural by ...
Ashwin Sancheti, Lu‐Kwang Ju
wiley   +1 more source

Novel homozygous <i>SYNE1</i> missense variant in late onset autosomal recessive cerebellar ataxia 1: a case report. [PDF]

Ther Adv Neurol Disord
Selmaj I, Himmelreich N, Selmaj K.
europepmc   +1 more source

Integrated characterization of Greek fennel genotypes through morpho‐agronomical characteristics, yield components and phytochemical compounds

JSFA reports, Volume 5, Issue 3, Page 91-103, March 2025.
Abstract Background Fennel (Foeniculum vulgare Mill.) is a widely cultivated vegetable and aromatic‐medicinal plant. In this research, field studies assessed 12 fennel genotypes of diverse origin, comprising 10 Greek accessions and two European commercial varieties, focusing on their morpho‐agronomical traits, phenolic compounds and antioxidant ...
Kalliopi I. Kadoglidou, Christos Maliachovas, Parthenopi Ralli, Maria Irakli, Nektaria Tsivelika, Athanasios G. Mavromatis, Paschalina Chatzopoulou   +6 more
wiley   +1 more source

Identification of a novel ACADSB variant for the presymptomatic diagnosis of 2-Methylbutyryl-CoA dehydrogenase deficiency through newborn screening in Iran. [PDF]

Orphanet J Rare Dis
Nasri M, Mahdieh N, Abbasi F, Mohsenipour R, Abdolahpour S.   +4 more
europepmc   +1 more source

Long QT interval syndrome type 2 caused by a new missense mutation of KCNH2 gene: A case report. [PDF]

Medicine (Baltimore)
Ma Y, Wang L, Wu S, Peng C.
europepmc   +1 more source

Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with <i>SGSH</i> and <i>GALNS</i> Deficiencies. [PDF]

Genes (Basel)
Awan FN, Zulfiqar S, Eiman L, Asif M, Hussain MS, Dahl N, Baig SM, Oda H.   +7 more
europepmc   +1 more source

Diverse and rare candidate MODY gene variants were identified in one-fifth of a Bangladeshi cohort with nonobese, nonautoimmune youth-onset diabetes. [PDF]

Sci Rep
Hasan M, Sultana N, Shil KK, Abdus-Salam SB, Nayem MR, Oliver M, Padinjyarekara A, Golani T, Rabbi MFA, Salimullah M, Akhteruzzaman S, Hasanat MA.   +11 more
europepmc   +1 more source

Evaluating the VOCORDER device for early disease detection through breath analysis: study protocol for a two-phase clinical study. [PDF]

BMJ Open
Kontopidou F, Swift SJ, Kokkotis C, Moustakidis S, Kavouras I, Vidaki AN, Brebou S, Zavvos V, Panagiotou A, Iatrou C, Grosomanidis D, Zacharouli Z, Giannoukos S.   +12 more
europepmc   +1 more source

Linking 3DP manufacturing with SIFT-MS volatiles organic compound analysis

, 2023
openaire   +1 more source