Results 41 to 50 of about 1,092,052 (189)

The styrene-maleic acid copolymer:: a versatile tool in membrane research [PDF]

, 2016
A new and promising tool in membrane research is the detergent-free solubilization of membrane proteins by styrene-maleic acid copolymers (SMAs). These amphipathic molecules are able to solubilize lipid bilayers in the form of nanodiscs that are bounded ...
Sub Membrane Biochemistry & Biophysics, Scheidelaar, Stefan, Dominguez Pardo, Juan, Killian, J Antoinette, Membrane Biochemistry and Biophysics, Dörr, Jonas M, Schäfer, Marre, Koorengevel, Martijn C, van Walree, Cornelis A   +8 more
core   +2 more sources

Early Skin Biopsy in Conradi-Hünermann-Happle Syndrome (X-Linked Dominant Chondrodysplasia Punctata). [PDF]

J Cutan Pathol
Journal of Cutaneous Pathology, Volume 52, Issue 10, Page 597-600, October 2025.
O'Connor C, Bussmann N, Mhaolcatha SN, Heffron C, O'Shea S.   +4 more
europepmc   +2 more sources

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

Collodion Baby

, 2022
Collodion baby (CB) is a rare dermatological condition worldwide of 1: 300.000 birth. A Collodion baby is a newborn whose entire body is covered with an adherent, supple, parchment-like membrane.
Dewi, I. A. (Ida), Savitri, A. A. (A)
core  

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

Mosaic Collodion Membranes as Analogues of the Plasma Membrane [PDF]

Journal of Experimental Biology, 1935
ABSTRACT This paper deals with an attempt to demonstrate selective accumulation of ions by the use of a cell bounded by two dense collodion membranes, one of which was impermeable to anions and the other impermeable to cations. Such a cell would, if successful, constitute a system analogous to many living cells (Brooks, 1929).
openaire   +1 more source

Constrictions and shear stress are key determinants of amyloidogenic light chain (AL) amyloidosis

The FEBS Journal, EarlyView.
In this study, we investigate how flow constrictions and shear stress trigger cardiac antibody light chain (AL) fibril formation and deposition. We mimic the mechanical forces exerted by the heart and the microvasculature network using a mini‐peristaltic pump setup and a grid‐type microchannel network, respectively.
Yuji Goto, Keiichi Yamaguchi, Kichitaro Nakajima, Ikuko Yumen, Ruiming He, Hirokazu Matsuda, Tetsuichi Wazawa, Takeharu Nagai, Nobuhiro Tsukada, Suguru Yamamoto, Johannes Buchner, Hirotsugu Ogi   +11 more
wiley   +1 more source

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

A Novel Homozygous Variant Associated With Distinct Clinical Phenotypes of SDR9C7 Nonsyndromic Epidermal Differentiation Disorder in Two Affected Patients From a Consanguineous Saudi Family

Molecular Genetics &Genomic Medicine, Volume 14, Issue 10, October 2026.
Whole exome sequencing identified a novel homozygous SDR9C7 variant in two affected patients from a consanguineous Saudi family presenting distinct lamellar ichthyosis phenotypes. ABSTRACT Background Nonsyndromic Epidermal Differentiation Disorders (nEDD) are a group of heterogeneous disorders characterized by scaling and erythema.
Faisal Almalki, Zaker Khoj, Essa Alharbi, Osama Alsharif   +3 more
wiley   +1 more source