Results 41 to 50 of about 4,952 (186)

Investigating the Heat Stability and Inactivation Conditions of Decapod Iridescent Virus 1 (DIV1)

Animal Research and One Health, EarlyView.
Heat treatment effectively inactivates decapod iridescent virus 1 (DIV1) under milder conditions than current WOAH recommendations. DIV1 infectivity was eliminated at 56°C for 30 min, 60°C for 15 min, or 70°C for 1 min, providing optimized heat treatment strategies for aquaculture biosecurity and seafood safety.
Yonghui Feng, Xiaomeng Guo, Jingyi Xing, Liang Qiu, Jie Huang   +4 more
wiley   +1 more source

Lamellar icthyosis with bilateral cicatricial ectropion: Case report with review of the literature

Medical Journal of Dr. D.Y. Patil University, 2015
Lamellar ichthyosis (LI), is a rare genodermatoses, that appears at birth and continues throughout a person's life with an autosomal recessive mode of inheritance.
Sonia P Jain
doaj   +1 more source

Osmotic Experiments with Collodion Membranes [PDF]

The Journal of Physical Chemistry, 1910
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openaire   +2 more sources

UNUSUAL PRESENTATION OF ICHTHYOSIS: A CASE REPORT OF COLLODION BABY

, 2023
A newborn with a unique condition, known as “collodion baby,” is born with a rare translucent skin sheet that resembles parchment. This condition is extremely uncommon, occurring in approximately 1 out of 3,00,000 live births.
KEYUR SABNIS; RAJIV GANDHI MEDICAL COLLEGE, THANE, JAYESH PANOT; RAJIV GANDHI MEDICAL COLLEGE, THANE, VANDANA KUMAVAT; RAJIV GANDHI MEDICAL COLLEGE, THANE, MOHIT VIJAY ROJEKAR; RAJIV GANDHI MEDICAL COLLEGE, THANE   +3 more
core  

Bébé pas comme les autres

The Pan African Medical Journal, 2014
Le bébé collodion est un aspect clinique grave caractérisé par une peau luisante, tendue et vernissée; une membrane rigide responsable d'un syndrome dysmorphique.
Nada El Moussaoui, Fatima Jabouirik
doaj   +1 more source

Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation

Molecular Genetics & Genomic Medicine, 2020
Backgroundd Sjogren–Larsson syndrome (SLS) is a rare autosomal recessive disorder, characterized by a triad of spastic tetraplegia or diplegia, congenital ichthyosis, and intellectual disability.
Kamel T. Abidi, Naglaa M. Kamal, Ayman A. Bakkar A., Maram Alotaibi, Haifa Asseri, Kawthar A. Bokari   +5 more
doaj   +1 more source

Endothelial Integrin‐Linked Kinase (ILK) Deficiency Promotes Endothelial Activation and Cardiovascular Dysfunction via Receptor Interacting Protein Kinase‐1 (RIPK1) Enriched‐Extracellular Vesicle Signalling

Journal of Extracellular Vesicles, Volume 15, Issue 6, June 2026.
Endothelial ILK loss drives RIPK1‐enriched EVs that propagate systemic endothelial activation and cardiovascular remodelling. EV cargo remodelling induces early endothelial injury, microvascular dysfunction and chronic cardiac alterations through a RIPK1 dependent pathway.
Alberto Cook‐Calvete, María Delgado‐Marín, Sara Jorquera Ortega, Silvia Moreta, Mercedes Castro‐Pinto, José López‐Menendez, Blanca Rodríguez‐Fernandez, Julia García‐García, Carlos Zaragoza, Marta Saura   +9 more
wiley   +1 more source

Successful outcome of lamellar ichthyosis with oral retinoid therapy: A series of six cases

Indian Journal of Paediatric Dermatology, 2016
Lamellar ichthyosis (LI) is a rare skin disorder inherited as an autosomal recessive trait. Affected babies are born in a collodion membrane that sheds gradually revealing extensive scaling of the skin.
K Pratyusha, P Divya Sree, BSN Reddy
doaj   +1 more source

Targeted regions sequencing identified four novel PNPLA1 mutations in two Chinese families with autosomal recessive congenital ichthyosis

Molecular Genetics & Genomic Medicine, 2020
Background Autosomal recessive congenital ichthyosis (ARCI) is a rare genetically heterogeneous cutaneous disease predominantly characterized by erythroderma, generalized abnormal scaling of the whole body and a collodion membrane at birth.
Liangshan Li, Wenmiao Liu, Yinglei Xu, Miaomiao Li, Qian Tang, Bo Yu, Renmei Cai, Shiguo Liu   +7 more
doaj   +1 more source

Compensatory Interplay Between Clarin‐1 and Clarin‐2 Deafness‐Associated Proteins Governs Phenotypic Variability in Hearing

Advanced Science, Volume 13, Issue 20, 9 April 2026.
Functional compensation between clarin‐1 and clarin‐2 in cochlear hair cells. Hearing loss associated with CLRN1 mutations shows striking phenotypic variability; however, the underlying mechanisms remain poorly understood. This study reveals that clarin‐1 and clarin‐2 function cooperatively in cochlear hair cells to sustain mechanoelectrical ...
Maureen Wentling, Aïda Yakhlef Sanchez, Nicolas Thelen, Müge Senarisoy, Maria Hogg, Steven Condamine, Andrea Lelli, Emilia Wysocka, Pranav Patni, Sandrine Vitry, Kerem Yasin Yildizhan, Sébastien Le Gal, Sylvie Nouaille, Michael R. Bowl, Marc Thiry, Didier Dulon, Sedigheh Delmaghani, Aziz El‐Amraoui   +17 more
wiley   +1 more source