Results 191 to 200 of about 560,147 (362)

Erythrocyte: Programmed Cell Death [PDF]

, 2012
Alcira Nesse, Daiana Vota, Daniela Vittori   +2 more
core   +2 more sources

Demonstration of apoptosis (programmed cell death) in rat hepatoma tissue transplanted in the muscle.

, 1992
Kazunori Fukuda, Masamichi Kojiro
openalex   +2 more sources

Is programmed cell death required for neural tube closure? [PDF]

, 1997
Miguel Weil, Michael D. Jacobson, Martin Raff   +2 more
openalex   +1 more source

Analysis of human brain RNA-seq data reveals combined effects of 4 types of RNA modifications and 18 types of programmed cell death on Alzheimer’s disease

Journal of Translational Medicine
Background RNA modification plays a critical role in Alzheimer’s disease (AD) by modulating the expression and function of AD-related genes, thereby affecting AD occurrence and progression.
Ke Ye, Xinyu Han, Mengjie Tian, Lulu Liu, Xu Gao, Qing Xia, Dayong Wang   +6 more
doaj   +1 more source

Programmed cell death in bovine mammary tissue during lactation and involution [PDF]

, 1997
CJ Wilde, CV Addey, Peter Li, David G. Fernig   +3 more
openalex   +1 more source

Changes in the Structure and Function of the Multicatalytic Proteinase (Proteasome) during Programmed Cell Death in the Intersegmental Muscles of the Hawkmoth, Manduca sexta

, 1995
Margaret E. E. Jones, Marcy F. Haire, Peter‐M. Kloetzel, Donald L. Mykles, Lawrence M. Schwartz   +4 more
openalex   +1 more source

Apparent caspase independence of programmed cell death in Dictyostelium [PDF]

, 1998
Robert A. Olie, Françoise Durrieu, Sophie Cornillon, Gary Loughran, Julian D. Gross, William C. Earnshaw, Pierre Golstein   +6 more
openalex   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

Programmed Cell Death in Normal Epidermis and Loricrin Keratoderma. Multiple Functions of Profilaggrin in Keratinization

, 1999
Akemi Ishida‐Yamamoto, Hikaru Tanaka, Hiroshi Nakane, Hidetoshi Takahashi, Yoshio Hashimoto, Hajime Iizuka   +5 more
openalex   +1 more source

KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study explored the impact of KIF5A rs113247976 (p.Pro986Leu), a risk allele for amyotrophic lateral sclerosis (ALS), on phenotypic variability in two Italian ALS cohorts (discovery, n = 865; replication, n = 1174). The minor allele (T) frequency was 0.015.
Arianna Manini, Rosario Vasta, Alberto Brusati, Francesco Scheveger, Silvia Peverelli, Alessio Maranzano, Alberto Doretti, Francesco Gentile, Eleonora Colombo, Maura Brunetti, Cristina Moglia, Antonio Canosa, Umberto Manera, Maurizio Grassano, Davide Gentilini, Stefano Messina, Federico Verde, Claudia Morelli, John E. Landers, Bryan J. Traynor, Adriano Chiò, Vincenzo Silani, Andrea Calvo, Antonia Ratti, Nicola Ticozzi   +24 more
wiley   +1 more source