Results 191 to 200 of about 111,824 (315)
Newborn Bilirubin Screening for Biliary Atresia.
S. Harpavat +2 more
semanticscholar +1 more source
ABSTRACT Liver fibrosis is a shared pathological phenotype of chronic liver diseases of diverse etiologies, including viral hepatitis, alcohol‐associated liver disease and metabolic dysfunction–associated steatohepatitis (MASH), as well as cholestatic liver diseases such as primary biliary cholangitis and primary sclerosing cholangitis, and may ...
Kiminori Kimura, Michinori Kohara
wiley +1 more source
Anesthetic management of a gross type C tracheoesophageal fistula by balloon catheter via tracheostoma in an infant with trisomy 18: A Case Report. [PDF]
Ryo M +4 more
europepmc +1 more source
Aging‐associated upregulation of NPY1R drives p‐CREB activation, triggering inflammation, mitochondrial dysfunction, and extracellular matrix imbalance to promote ovarian senescence. Pharmacological inhibition of NPY1R with BIBO 3304 restores ovarian homeostasis, highlighting a therapeutic strategy for reproductive aging. ABSTRACT Ovarian senescence is
Junnan Fang +15 more
wiley +1 more source
Gonadal Histology and Spawning Season of Otolithoides pama in the Thanlwin River Estuary
ABSTRACT The spawning season of Otolithoides pama in the Thanlwin estuary was estimated through gonadosomatic index (GSI) and histological analyses of gonadal development. A total of 290 specimens (240 females and 50 males) were collected monthly from 5 sites—Ahlat, Kyauk Tan, Daye, Nyaung Pin Seik and Tarana—between January and December 2024.
Thet Htwe Aung
wiley +1 more source
Middle Fossa Dura Implantation of the Bonebridge in Children With Craniofacial Malformations: A Case Report. [PDF]
Sousa Menezes A +5 more
europepmc +1 more source
ABSTRACT FOXA2 (hepatocyte nuclear factor‐3β, HNF‐3β) encodes a transcriptional activator involved in early embryogenesis, particularly in the patterning and differentiation of midline structures such as the neural tube, foregut, and pituitary gland. Its role in human pathogenesis was first suspected when patients with deletion of chromosome 20p11.2 ...
Christopher Connolly +3 more
wiley +1 more source

