Results 231 to 240 of about 3,144,487 (302)

Patient with two rare diseases-Renal coloboma syndrome and craniopharyngioma. [PDF]

Radiol Case Rep
Bancevica L, Apine I, Valeina S, Taurina G, Yaacoub WB, Franckevica I, Zaharova J, Malniece I, Baklasova A, Smite Laguna A, Kovalova Z.   +10 more
europepmc   +1 more source

CXCL3 Antagonism Reverses Systemic Antitumor Immune Memory Impairment Associated With High Tumor Burden and Sensitizes Anti‐PD‐1 Therapy

Advanced Science, EarlyView.
This study reveals that large tumors secrete more chemokine CXCL3, which recruits immunosuppressive neutrophils to the periphery, thereby impairing the activation and memory of systemic tumor‑reactive CD8+ T cells. CXCL3 antagonism restores systemic immune memory and enhances the antitumor efficacy of anti‑PD‑1 therapy, offering a potential strategy to
Ji Wang, Xinyu Tang, Zeju Li, Qi Qi, Chang Sun, Wen Sun, Weiya Zhang, Yue Yin, Ya Deng, Peiwen Ling, Yifan Xu, Guangshun Sun, Yi Ren, Hong Pan, Shui Wang, Wenbin Zhou   +15 more
wiley   +1 more source

Ocular Clues to Liver Disease: A Strategic Diagnostic Lens. [PDF]

Diseases
Dahshan M, Dahshan H, Basoglu A, Kadikoy H.   +3 more
europepmc   +1 more source

Hereditary neurodegenerative disorders with spastic-ataxic manifestations: genetic and clinical insights into previously reported variants. [PDF]

Neurogenetics
Ahmad R, Ayaz K, Khan MN, Naeem M, Houlden H.   +4 more
europepmc   +1 more source

The First 40 Years of Molecular Ophthalmology Part Two: Diseases of the Primary Cilium and Heritable Glaucoma: The 2026 Friedenwald Lecture. [PDF]

Invest Ophthalmol Vis Sci
Sheffield VC.
europepmc   +1 more source

Whole-exome sequencing for the genetic diagnosis of early-onset high myopia and associated hereditary eye disorders. [PDF]

BMC Med Genomics
Han C, Wu S, Yang Y, Yang X, Li H.
europepmc   +1 more source

Unilateral Idiopathic Retinal Venous Beading. [PDF]

Turk J Ophthalmol
Karslıoğlu E, Sarıgül Sezenöz A, Yılmaz G.   +2 more
europepmc   +1 more source

Nasal-Predominant Ganglion Cell-Inner Plexiform Layer Thinning Distinguishes Early-Stage Leber Hereditary Optic Neuropathy From Acute Optic Neuritis. [PDF]

Clin Exp Ophthalmol
Takai Y, Yamagami A, Inoue K, Ishikawa H, Takahashi T, Tanaka K.   +5 more
europepmc   +1 more source

Investigations of some hereditary eye diseases causing blindness.

Chinese medical journal, 1984
openaire   +1 more source