Results 161 to 170 of about 3,348,298 (337)

[Allogeneic hematopoietic stem cell transplantation for Familial platelet disorder with a propensity for acute myeloid malignancies with Runx1 germline mutations: a case report and literature review]. [PDF]

Zhonghua Xue Ye Xue Za Zhi, 2022
Wang LL, Guan J, Cheng P, Zhang T, Cheng H, Zou L.   +5 more
europepmc   +1 more source

Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets

Journal of Thrombosis and Haemostasis, 2014
Ana C Glembotsky, Dominique Bluteau, Dominique Bluteau, Y. R. Espasandin, N. Goette, R. Marta, C. P. M. Oyarzún, L. Korin, P. Lev, R. Laguens, F. Molinas, H. Raslova, P. Heller   +12 more
semanticscholar   +1 more source

The Multitarget Compound ZLY032 Achieves Treatment of Chronic Wounds

Advanced Science, EarlyView.
ZLY032, a dual free fatty acid receptor 1/peroxisome proliferator‐activated receptor δ agonist, accelerates wound healing in normal/diabetic/methicillin‐resistant Staphylococcus aureus‐infected models by promoting angiogenesis, reducing inflammation, and exhibiting antibacterial activity via argininosuccinate lyase targeting, with demonstrated efficacy
Manyu Gong, Zhiyuan Du, Tiantian Gong, Yu Wang, Chenchen Yin, Bosi Sun, Zijia Liu, Lianru Chen, Zibin Liao, Wenxin Wang, Tianjiao Zhao, Yifei Wang, Ying Dong, Kexin Wang, Mengru Ma, Weijun Li, Jiacheng Li, Haodong Li, Congcong Lin, Ying Zhang, Yu Liu, Xin Liu, Tao Ban, Hongxia Bao, Ying Zhang, Yang Zhang, Zheng Li, Lei Jiao   +27 more
wiley   +1 more source

(7) Platelet Abnormality in the Systemic Disorders

, 1983
Atsushi Kuramoto
openalex   +2 more sources

Novel heterozygous missense mutation in the platelet glycoprotein Ibβ gene associated with isolated giant platelet disorder [PDF]

, 2001
Shinji Kunishima, Tomoki Naoe, Tadashi Kamiya, Hidehiko Saito   +3 more
openalex   +1 more source

Bidirectional Interaction Between the Brain and Bone in Traumatic Brain Injury

Advanced Science, EarlyView.
Traumatic brain injury (TBI) disrupts the blood–brain barrier and activates neuroimmune responses, causing metabolic disturbances and long‐term bone mass loss. Concurrent fractures accelerate healing and enhance osteogenesis but disrupt regulatory mechanisms, leading to altered bone dynamics and exacerbating neuroinflammation, complicating recovery ...
Wei Zhang, Jun Zou, Lingli Zhang
wiley   +1 more source

GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant

Stem Cell Research, 2019
Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) is a rare platelet disorder caused by mutations in RUNX1. We generated an iPSC line (GENYOi005-A) from a FPDMM patient with a non-previously reported variant p.Thr196Ala.
Mar Lamolda, Rosa Montes, Iris Simón, Sonia Perales, Gonzalo Martínez-Navajas, Lourdes Lopez-Onieva, Rosa Ríos-Pelegrina, Raimundo García del Moral, Carmen Griñan-Lison, Juan A. Marchal, Maria L. Lozano, Veronica Ramos-Mejia, Jose Rivera, Jose M. Bastida, Pedro J. Real   +14 more
doaj  

An unclassified platelet function disorder associated with bleeding tendency.

, 1987
Yasuyuki Endo, Shigeo Mamiya, H Niitsu, Keiko Iwamoto, Sumiko Hamanaka, Akira Miura   +5 more
openalex   +2 more sources

Pathogenetic analysis of three cases with a bleeding disorder characterized by defective platelet aggregation induced by Ca²⁺ ionophores [PDF]

, 2001
Ichiro Fuse, Wataru Higuchi, Y. Uesugi, Yoshifusa Aizawa   +3 more
openalex   +1 more source

Evaluation of the neutrophil/lymphocyte ratio, platelet/lymphocyte ratio, and mean platelet volume as inflammatory markers in children with attention‐deficit hyperactivity disorder

Psychiatry and Clinical Neurosciences, 2018
S. Avcil
semanticscholar   +1 more source