Results 41 to 50 of about 5,153 (210)

Displasia folicular dos pelos pretos em cães: revisão

open access: yesPubvet, 2020
As doenças de peles são causas frequentes de atendimento na clínica de pequenos animais. A displasia folicular dos pêlos pretos é uma doença de origem hereditária cuja etiologia ainda não foi totalmente elucidada.
Adriana Leão de Carvalho Lima Gondim   +1 more
doaj   +1 more source

CTNND1‐Related Disorder: New Insight on Prenatal Phenotype

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 3, March 2025.
ABSTRACT CTNND1 is a gene located in 11q12.1, encoding for p120 catenin, a protein involved in maintaining adherent junctions, regulating the epithelial–mesenchymal transition, and transcriptional signaling of different cellular pathways. Pathogenic variants in CTNND1 are classically associated with isolated cleft palate and Blefaro‐cheilo‐dontic ...
B. Conti   +12 more
wiley   +1 more source

Mouse Models in Prostate Cancer Translational Research: From Xenograft to PDX

open access: yesBioMed Research International, Volume 2016, Issue 1, 2016., 2016
Despite the advancement of clinical and preclinical research on PCa, which resulted in the last five years in a decrement of disease incidence by 3‐4%, it remains the most frequent cancer in men and the second for mortality rate. Based on this evidence we present a brief dissertation on numerous preclinical models, comparing their advantages and ...
Domenica Rea   +10 more
wiley   +1 more source

Thymopoietin‐α, ‐β, and ‐γ Isoforms Increased Expression in Cervical Cancer Cells

open access: yesCanadian Journal of Infectious Diseases and Medical Microbiology, Volume 2025, Issue 1, 2025.
Cervical cancer (CC) is a public health concern related to the human papillomavirus (HPV) persistent infection. Minichromosome maintenance 2 (MCM2) has been postulated as a surrogate marker for HPV infection. Thymopoietin (TMPO) is a nuclear protein regulated by E2F such as MCM2 or p16. TMPO can give rise to six different isoforms.
Víctor Huerta-Padilla   +15 more
wiley   +1 more source

Helicobacter pylori y cáncer gástrico

open access: yesRevista Cubana de Medicina Militar, 2020
Introducción: El Helicobacter pylori se ha relacionado con el desarrollo de gastritis crónica atrófica, metaplasia intestinal y displasia, lesiones que pueden evolucionar a carcinoma gástrico. Existen investigaciones que demuestran que la erradicación de
Ludmila Martínez Leyva   +5 more
doaj   +2 more sources

Lesiones gástricas preneoplásicas en pacientes con Helicobacter pylori

open access: yesRevista Cubana de Medicina Militar, 2023
Introducción: Helicobacter pylori es el principal factor de riesgo para el desarrollo de gastritis crónica atrófica y cáncer gástrico de tipo intestinal.
Ludmila Martínez Leyva   +5 more
doaj  

Fetal lower urinary tract obstruction: international Delphi consensus on management and core outcome set

open access: yesUltrasound in Obstetrics &Gynecology, Volume 64, Issue 5, Page 635-650, November 2024.
ABSTRACT Objectives To reach an international expert consensus on the diagnosis, prognosis and management of fetal lower urinary tract obstruction (LUTO) by means of a Delphi procedure, and to use this to define a core outcome set (COS). Methods A three‐round Delphi procedure was conducted among an international panel of experts in fetal LUTO.
H. J. Mustafa   +90 more
wiley   +1 more source

Screening and prevention of HPV‐related anogenital cancers in women living with HIV in Europe: Results from a systematic review

open access: yesHIV Medicine, Volume 25, Issue 7, Page 769-793, July 2024.
Abstract Background Women living with HIV (WLWH) are at increased risk of human papillomavirus (HPV)‐related cancers. Throughout Europe, there is great heterogeneity among guidelines for screening programmes, access to HPV testing and HPV vaccination. The aim of this systematic review is to summarize available data on screening and prevention measures ...
Dagny Krankowska   +7 more
wiley   +1 more source

Mutations in alpha‐B‐crystallin cause autosomal dominant axonal Charcot–Marie–Tooth disease with congenital cataracts

open access: yesEuropean Journal of Neurology, Volume 31, Issue 1, January 2024.
Abstract Background and purpose Mutations in the alpha‐B‐crystallin (CRYAB) gene have initially been associated with myofibrillar myopathy, dilated cardiomyopathy and cataracts. For the first time, peripheral neuropathy is reported here as a novel phenotype associated with CRYAB.
Andrea Cortese   +16 more
wiley   +1 more source

Poliposis adenomatosa familiar

open access: yesOncología, 2022
Presentamos el caso de una mujer de 42 años, con antecedentes de Colectomia con anastomosis Ileo-rectal a los 26 años de edad por Poliposis Adenomatosa Familiar (PAF). Antecedentes de la misma patología en varios parientes.
P. J. Jaramillo   +5 more
doaj  

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