Results 211 to 220 of about 1,516,986 (362)

The Exchange of Material between Nucleus and Cytoplasm in Peperomia sintenisii [PDF]

, 1910
William H. Brown
openalex   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco, Mònica Roldán, Yalda Jamshidi, Ioannis Georvasilis, Rocío Jadraque Rodríguez, Reza Boostani, Ali Shoeibi, Lluís Armengol, Anna Codina, Ehsan Ghayoor Karimiani, Cristina Hernando‐Davalillo, Loreto Martorell, María Luisa Ramírez Almaraz, Jordi Muchart, Carlos Ortez, Andrés Nascimento, Roser Urreizti, Daniel Natera‐de Benito, Mercedes Serrano   +18 more
wiley   +1 more source

Identification of BoRR gene family in cauliflower: roles in curd development and salt tolerance. [PDF]

BMC Genomics
Song M, Shen Y, Wang J, Yu H, Sheng X, Qiao S, Gu H.   +6 more
europepmc   +1 more source

A CASE OF LITHOTOMY WHERE THE NUCLEUS OF A LARGE PHOSPHATIC CALCULUS WAS THE WHALEBONE MOUTH-PIECE OF A TOBACCO-PIPE. WITH REMARKS. [PDF]

, 1885
Reginald Harrison
openalex   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann, Michelle M. Sonsalla, Cora Luzinski, Fernando Zacahua, David A. Harris, Dudley W. Lamming, Albee Messing   +6 more
wiley   +1 more source

A Combined Neuroanatomy, Ex Vivo Imaging, and Immunohistochemistry Defined MRI Mask for the Human Paraventricular Nucleus of the Thalamus. [PDF]

Hum Brain Mapp
Tetzlaff MR, Leonard BT, Yassa MA, Baram TZ, Rasmussen JM.   +4 more
europepmc   +1 more source

NEUROSECRETION. X. A RELATIONSHIP BETWEEN THE PARAPHYSIS AND THE PARAVENTRICULAR NUCLEUS IN THE GARTER SNAKE (THAMNOPHIS SP.)

, 1951
E. Scharrer
openalex   +2 more sources

THE DEVELOPMENT OF THE VERTEBRATE NERVE-CELL: A CYTOLOGICAL STUDY OF THE NEUROBLAST-NUCLEUS [PDF]

, 1906
John Cameron
openalex   +1 more source

Cumulative protons in hadron-nucleus and nucleus-nucleus interactions [PDF]

Proceedings of XXII International Baldin Seminar on High Energy Physics Problems — PoS(Baldin ISHEPP XXII), 2015
openaire   +2 more sources

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source