Results 61 to 70 of about 4,277 (205)

Bianchi Type III String Cosmological Models with Time Dependent Bulk Viscosity

, 2007
Bianchi type III string cosmological models with bulk viscous fluid for massive string are investigated. To get the determinate model of the universe, we have assumed that the coefficient of bulk viscosity ($\xi$) is inversely proportional to the ...
Anirudh Pradhan, Bali R, Kibble T W B, Landau L D, Maharaj S D, Raj Bali, Selijak U, Selijak U, Thorne K S, Wang X X, Wang X X, Wang X X, Wang X X, Yadav M K, Yadav M K, Zel'dovich Ya B, Zel'dovich Ya B, Zel'dovich Ya B   +17 more
core   +2 more sources

Deoxysphingolipids as candidate biomarkers for a novel SPTLC1 mutation associated with HSAN-I [PDF]

Neurology Genetics, 2019
Hereditary sensory and autonomic neuropathy type 1 (HSAN-I)—an autosomal dominant, mainly sensory neuropathy—typically affects patients in their second and third decades, presenting with ulcerations and lancinating pain attacks.1 Diagnosis is heavily dependent on genetic analysis, focusing on 6 genes: serine palmitoyltransferase ( SPT ) long chain base
Boso, Federica, Armirotti, Andrea, Taioli, Federica, Ferrarini, Moreno, Nobbio, Lucilla, Cavallaro, Tiziana, Fabrizi, Gian Maria   +6 more
openaire   +2 more sources

Signaling Regulation of FAM134‐Dependent ER‐Phagy in Cells

Journal of Cellular Physiology, Volume 240, Issue 1, January 2025.
ABSTRACT The endoplasmic reticulum (ER) is a pivotal organelle responsible for protein and lipid synthesis, calcium homeostasis, and protein quality control within eukaryotic cells. To maintain cellular health, damaged or excess portions of the ER must be selectively degraded via a process known as selective autophagy, or ER‐phagy.
Alessandro Palma, Alessio Reggio
wiley   +1 more source

Spacelike Ricci Inheritance Vectors in a Model of String Cloud and String Fluid Stress Tensor

, 2005
We study the consequences of the existence of spacelike Ricci inheritance vectors (SpRIVs) parallel to $x^a$ for model of string cloud and string fluid stress tensor in the context of general relativity.
Carot J, Collinson C D, Duggal K L, Greenberg P S, H sn  Baysal, Ihsan Yilmaz, Katzin G H, Kibble T W S, Letelier P S, Zeldovich Ya B   +9 more
core   +1 more source

Human genetic defects of sphingolipid synthesis

Journal of Inherited Metabolic Disease, Volume 48, Issue 1, January 2025.
Abstract Sphingolipids are ubiquitous lipids, present in the membranes of all cell types, the stratum corneum and the circulating lipoproteins. Autosomal recessive as well as dominant diseases due to disturbed sphingolipid biosynthesis have been identified, including defects in the synthesis of ceramides, sphingomyelins and glycosphingolipids.
Patricia Dubot, Frédérique Sabourdy, Thierry Levade   +2 more
wiley   +1 more source

Uncoupling neurotrophic function from nociception of nerve growth factor: what can be learned from a rare human disease?

Neural Regeneration Research, 2019
Nerve growth factor (NGF) is a powerful trophic factor that provides essential support for the survival and differentiation of sympathetic and sensory neurons during development.
Kijung Sung, Wanlin Yang, Chengbiao Wu
doaj   +1 more source

Burmese Buddhist Imagery of the Early Bagan Period (1044-1113) [PDF]

, 2006
Buddhism is an integral part of Burmese culture. While Buddhism has been practiced in Burma for around 1500 years and evidence of the religion is found throughout the country, nothing surpasses the concentration of Buddhist monuments found at Bagan ...
Galloway, Charlotte Kendrick
core   +1 more source

Relationship between proprioception at the knee joint and gait ataxia in HSAN III [PDF]

Movement Disorders, 2013
ABSTRACTBackgroundHereditary sensory and autonomic neuropathy type III features marked ataxic gait that progressively worsens over time. We assessed whether proprioceptive disturbances can explain the ataxia.MethodsProprioception at the knee joint was assessed using passive joint angle matching in 18 patients and 14 age‐matched controls; 5 patients ...
Macefield, Vaughan G. (R11708), Norcliffe-Kaufmann, Lucy, Axelrod, Felicia B., Kaufmann, Horacio   +3 more
openaire   +3 more sources

Congenital Insensitivity to Pain and Anhidrosis With Orthopedic and Self‐Injury Complications in a 5‐Year‐Old Boy: A Case Report

Clinical Case Reports, Volume 12, Issue 12, December 2024.
ABSTRACT Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder because of NTRK1 gene mutations, leading to an inability to perceive pain and temperature and lack of sweating. Its rarity and unique clinical challenges, such as severe injuries from the inability to sense pain, make reporting cases critical.
Zubair Amin, Humza Saeed, Syed Imam Naufil, Sadaf Saba, Abdullah Imtiaz, Syed Hassan Akhlaq, Muhammad Husnain Ahmad, Masab Ali   +7 more
wiley   +1 more source

"Congenital Sensory Neuropathy as a Differential Diagnosis for Phagocytic Immunodeficiency "

Iranian Journal of Allergy, Asthma and Immunology, 2006
There are few reports about congenital indifference to pain or Hereditary and Sensory Autonomic Neuropathy (HSAN). Several investigations for pathophysiology of this syndrome have been performed and different classifications about it.
Mohammad Gharagozlou, Fariborz Zieh, Parviz Tabatabaei, Gholamreza Zamani   +3 more
doaj