Results 151 to 160 of about 59,449 (235)
The PbrMADS1–PbrMYB169 complex has uniquely emerged to regulate lignification of stone cells in pear
Journal of Integrative Plant Biology, Volume 68, Issue 1, Page 239-256, January 2026.Genome‐wide association study in pear identified a SEP3‐subfamily transcription factor, PbrMADS1, which interacts with PbrMYB169 to regulate stone cell lignification. The methionine at position 63 in PbrMADS1 was essential for this interaction. This amino acid variation may underlie the functional divergence of homologous SEP3 genes among Rosaceae ...
Yongsong Xue +8 more
wiley +1 more source
Comments on paratrooper‐separation modeling with the DSD/SST formulation and FOIST [PDF]
, 2010 Tayfun E. Tezduyar
openalex +1 more source
Self‐Management Therapies for Temporomandibular Disorders—Evidence From Systematic Reviews
Journal of Oral Rehabilitation, Volume 53, Issue 1, Page 265-281, January 2026.This umbrella review synthesized existing evidence on self‐management therapy for temporomandibular disorder. ABSTRACT Objectives Chronic pain in the orofacial region affects 10%–15% of the general population. It is most often related to temporomandibular disorders (TMD): pain in the masticatory muscles and the temporomandibular joints.
Tessa Bijelic +5 more
wiley +1 more source
Participant experiences of two successful habit-based weight-loss interventions in Australia: a qualitative study [PDF]
, 2018 Cleo, Gina, Hersch, Jolyn, Thomas, Rae
core +1 more source
Animal Venoms as Peptide Libraries for the Discovery of Antiglioblastoma Agents
Biochemistry Research International, Volume 2026, Issue 1, 2026.Glioblastoma is one of the most aggressive and widely recognized types of brain tumors, characterized by significant cellular and molecular diversity and an inherently aggressive nature. The treatment remains highly challenging, with limited effectiveness and persistently low survival rates.
Livia Ramos Santiago +6 more
wiley +1 more source
Case Reports in Medicine, Volume 2026, Issue 1, 2026.Introduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Süleyman Cemil Oğlak +10 more
wiley +1 more source
What Term to Choose: Ambiguous Genitalia or Disorders of Sex Development (DSD)? [PDF]
, 2019 Smail Acimi
openalex +1 more source
StAR Protein Deficiency in Clinical Practice: A Case Series From Saudi Arabia
Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Objectives Steroidogenic acute regulatory (StAR) protein deficiency is a rare autosomal recessive disorder that disrupts steroid hormone biosynthesis, resulting in congenital adrenal hyperplasia (CAH) and variations in sexual development. However, limited data is available in Saudi Arabia.
Abeer Alabduljabbar +6 more
wiley +1 more source