Results 81 to 90 of about 103,180 (213)
Disuse‐induced muscle atrophy is driven by a non‐metabolic, nuclear function of the enzyme PFKFB3. Acting as a scaffold, PFKFB3 facilitates Nedd4‐mediated ubiquitination and degradation of the anti‐atrophy transcription factor JunB. Inhibiting this novel PFKFB3–Nedd4–JunB signaling axis stabilizes JunB and alleviates muscle wasting, revealing a highly ...
Mengjun Ma +12 more
wiley +1 more source
Osteoarthritis, with different risk factors and classifications is a heterogenous disease. Symptoms poorly correlate with structural damage as seen on plain radiographs.
Nurdan Kotevoğlu +2 more
doaj
Background Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a rare presumed inflammatory chorioretinopathy characterized by creamy, yellow-white placoid lesions at the level of the retinal pigment epithelium (RPE).
Emanuel Mordechaev +2 more
doaj +1 more source
Case of Unilateral Linear Lichen Planus with Bilateral Mucosal Involvement
A form of lichen planus (LP) which follows the Blaschkos line pattern known as linear LP, presents with lichenoid eruptions and violaceous papules in a linear distribution. It is a rare form of LP affecting
Adarshlata Singh +4 more
doaj +1 more source
Neuronal activation leads to astrocytic transient volume changes, activating transient receptor potential ankyrin 1 (TRPA1) channels, leading to Ca2+ influx. Activation of TRPA1 causes the release of D‐serine through BEST1. Finally, the augmented extracellular levels of D‐serine boost neuronal activity by binding GluN1‐containing NMDARs, leading to CBV
Kayoung Han +11 more
wiley +1 more source
Beyond the Marrow: Unilateral Breast Involvement in Acute Lymphoblastic Leukemia
Hematological malignancies involving the breast are exceedingly rare, accounting for less than 1% of all breast tumors. Breast infiltration by acute lymphoblastic leukemia (ALL) is particularly uncommon, with fewer than 25 cases reported in the ...
Ahmet Tuğrul Akkuş +2 more
doaj +1 more source
AI‐enabled de novo design of a TREM1 binder, integrated into a BBB‐crossing and macrophage‐targeted nanoplatform, enables TREM1 degradation and attenuates neuroinflammation, thereby promoting neuroprotection and tissue repair after traumatic brain injury. ABSTRACT Secondary neuroinflammation drives progressive damage after traumatic brain injury (TBI),
Yimin Huang +19 more
wiley +1 more source
Microglial PBRM1 deficiency drives excessive hippocampal neurogenesis by enhancing CCL5–CCR1/5 signaling, leading to autism‐like behaviors. A pro‐inflammatory IL1α+/TNFα+ microglial subset is identified as a key cellular contributor to this process. PBRM1 represses Ccl5 expression at the transcriptional level.
Yang‐Yang Duan +12 more
wiley +1 more source
Lenz microphthalmic syndrome in an Indian patient
A case of Lenz microphthalmia syndrome in a seven-month-old male child having features of unilateral anophthalmia, microcephaly, external ear and finger abnormalities, hydrocele and hypospadias is being reported.
Gupta Arvind +3 more
doaj
Unilateral retinitis pigmentosa in Von Recklinghausen disease: A rare occurrence
Retinitis pigmentosa (RP) is hereditary progressive retinal dystrophy causing symmetrical affliction of both eyes. Neurofibromatosis 1 (NF1)/Von Recklinghausen disease is a hereditary neurocutaneous disorder with ocular involvement.
Kavin Bhogar +3 more
doaj +1 more source

