Results 211 to 220 of about 393,854 (363)

CÁNCER HEREDITARIO DE MAMA HEREDITARY BREAST CÁNCER

open access: yesRevista Chilena de Radiología, 2008
En cáncer de mama, aproximadamente el 10% de los casos corresponde a síndromes hereditarios. Una porción significante de estos, un 30%, se atribuye a la herencia de mutaciones en genes BRCA1 y BRCA2 característico del síndrome de cáncer de mama y/u ...
Sonia Margarit
doaj  

Toma de decisión en la prevención del cáncer de mama [PDF]

open access: yes
Breast cancer is one of the most common cancers among women and the leading cause of death in women between the ages of 45-60 in most developed countries.
Esserman, Laura, Ozanne, Elissa
core   +1 more source

Micro‐Organ Chip Deciphers Tumor‐Derived G‐CSF as Remote Commander of Lung Pre‐Metastatic Niche via VEGFA‐KDR Cascade

open access: yesAdvanced Science, EarlyView.
Breast cancer reprograms the lung into a receptive pre‐metastatic niche via a novel G‐CSF–VEGFA–KDR signaling axis. Using a micro‐organ chip that enables contact‐independent coculture, this study uncovers how tumor‐secreted G‐CSF activates lung capillary KDR to drive angiogenesis and prime the soil for metastasis—without direct tumor contact.
Jingxin Zhang   +12 more
wiley   +1 more source

A Mitochondrial DNA‐Releasing Photosensitizer Potentiates Innate Immunity for Tumor Eradication and Prevention

open access: yesAggregate, EarlyView.
A mitochondria‐targeted photosensitizer, MQ‐PPy, with strong reactive oxygen species generation and mtDNA‐releasing capability, has been developed for photo‐induced antitumor immunoactivation. Upon light irradiation, MQ‐PPy induces mitochondrial oxidative damage and activates the cGAS‐STING pathway, promoting immunogenic cell death and cytotoxic T‐cell
Yanhe An   +7 more
wiley   +1 more source

Prognostic Impact of AGR3 Protein Expression in Breast Cancer: A Systematic Review and Meta-analysis. [PDF]

open access: yesRev Bras Ginecol Obstet, 2023
Moraes CL   +5 more
europepmc   +1 more source

TBX3‐ Related Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous pathogenic variants in TBX3 cause Ulnar‐Mammary syndrome (UMS). The phenotype is classically characterized by upper limb defects, apocrine/mammary gland hypoplasia, hypogonadism, and various midline defects. However, the clinical spectrum is highly variable, and some individuals may present with a mild or atypical presentation ...
Ziv Halperin, Karin Weiss
wiley   +1 more source

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