Results 211 to 220 of about 393,854 (363)
CÁNCER HEREDITARIO DE MAMA HEREDITARY BREAST CÁNCER
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
Mortality from Breast Cancer in Women under 50 Years of Age in Colombia. [PDF]
González Mariño MA.
europepmc +1 more source
Toma de decisión en la prevención del cáncer de mama [PDF]
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
¿La quimioterapia neoadyuvante proporciona algún beneficio para la desescalada quirúrgica en el cáncer de mama HER2 (Ó?) luminal B? [PDF]
Ayşegül Aktaş +4 more
openalex +1 more source
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 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]
Moraes CL +5 more
europepmc +1 more source
Metástasis calcificada de nódulo axilar en un cáncer de mama: reporte de un caso
Jonathan Pérez Restrepo
openalex +1 more source
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

