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1.
Indian J Dermatol ; 66(3): 314-317, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34446957

RESUMO

Several biologic agents have been approved for use in dermatology and other disciplines of medicine. However, based on the mechanism of action and a track record of the response, these agents are being increasingly used for off-label purposes to garner control of more remote and difficult disease processes. Herein, we present three difficult to treat patients where innovative uses of biologics beyond their approved indications have yielded good responses. Our first patient was a case of bullous pemphigoid, who showed excellent response to omalizumab. The second case was a patient of lepromatous leprosy with tenosynovitis and erythema nodosum leprosum, who was treated effectively with infliximab. Our third case was a treatment-resistant pyoderma gangrenosum, where infliximab showed a very good response. In the present study, we report the cases to highlight the usefulness of biologics that can expand much beyond the routine FDA approved indications.

2.
J Cosmet Dermatol ; 20(12): 3808-3811, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34213802

RESUMO

Scar formation is a consequence of wound healing that developed from damaged tissue either from physical injury or surgical incision. A hypertrophic scar develops due to an abnormal healing response to trauma. It might lead to serious functional and cosmetic disability. There are numerous methods mentioned in the literature to treat such scars but to date, no single method has been known to cure them. In this review, we focused on differences between various types of nonsurgical management of hypertrophic scar focusing on the indication, mechanism of action, and efficacy of the pulsed dye laser (PDL), fractional carbon dioxide laser (fCO2), Er-YAG laser, and intense pulse light (IPL). The literature research included peer-reviewed articles (clinical trials or scientific reviews) which were identified by searching electronic databases like PubMed till January 2021 and reference lists of respective articles. Only articles published in the English language were included.


Assuntos
Cicatriz Hipertrófica , Lasers de Corante , Lasers de Gás , Lasers de Estado Sólido , Cicatriz/etiologia , Cicatriz/patologia , Cicatriz Hipertrófica/etiologia , Cicatriz Hipertrófica/patologia , Humanos , Lasers de Corante/uso terapêutico , Lasers de Gás/uso terapêutico , Resultado do Tratamento , Cicatrização
3.
Appl Opt ; 60(16): 4544-4556, 2021 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-34143008

RESUMO

These days when integrated circuit (IC) designers are facing an uphill task in limiting energy/heat dissipation, reversible computing is emerging as a potential candidate with vast application in fields like nanotechnology, quantum-dot cellular automata, and low power IC. Optical reversible logics have turned up to offer high speed and low energy computations with almost no loss of input information when a certain (arithmetic or logical) operation is performed. This paper explores an optical implementation of an optimized Fredkin gate that is employed to design an $ N:2^N $ reversible decoder. The optical designs have been carried out using the electro-optic effect of a lithium niobate ($ {{\rm LiNbO}_3}$)-based Mach-Zehnder interferometer under the beam propagation method (BPM) with Optiwave's OptiBPM tool. The mathematical model of output power of these designs is also performed along with its validation in MATLAB.

4.
Indian J Dermatol ; 61(1): 88-90, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26955103

RESUMO

Pilomatricoma is a benign tumor arising from the hair matrical cells. Most pilomatricomas appear in the first two decades of life as a solitary skin to a bluish colored nodule on head-neck area with an occasional sign of inflammation. Here, we present a case of pilomatricoma which appeared at 36 years of age with a history of recurrent inflammation and discharge mimicking ruptured epidermal cyst.

5.
J Mol Biol ; 426(5): 1095-108, 2014 Mar 06.
Artigo em Inglês | MEDLINE | ID: mdl-24075869

RESUMO

HIV-1 (human immunodeficiency virus type 1) uses its trimeric gp160 envelope (Env) protein consisting of non-covalently associated gp120 and gp41 subunits to mediate entry into human T lymphocytes. A facile virus fusion mechanism compensates for the sparse Env copy number observed on viral particles and includes a 22-amino-acid, lentivirus-specific adaptation at the gp41 base (amino acid residues 662-683), termed the membrane proximal external region (MPER). We show by NMR and EPR that the MPER consists of a structurally conserved pair of viral lipid-immersed helices separated by a hinge with tandem joints that can be locked by capping residues between helices. This design fosters efficient HIV-1 fusion via interconverting structures while, at the same time, affording immune escape. Disruption of both joints by double alanine mutations at Env positions 671 and 674 (AA) results in attenuation of Env-mediated cell-cell fusion and hemifusion, as well as viral infectivity mediated by both CD4-dependent and CD4-independent viruses. The potential mechanism of disruption was revealed by structural analysis of MPER conformational changes induced by AA mutation. A deeper acyl chain-buried MPER middle section and the elimination of cross-hinge rigid-body motion almost certainly impede requisite structural rearrangements during the fusion process, explaining the absence of MPER AA variants among all known naturally occurring HIV-1 viral sequences. Furthermore, those broadly neutralization antibodies directed against the HIV-1 MPER exploit the tandem joint architecture involving helix capping, thereby disrupting hinge function.


Assuntos
Proteína gp120 do Envelope de HIV/química , Proteína gp41 do Envelope de HIV/química , Fusão de Membrana/fisiologia , Internalização do Vírus , Sequência de Aminoácidos , Espectroscopia de Ressonância de Spin Eletrônica , Citometria de Fluxo , Proteína gp120 do Envelope de HIV/genética , Proteína gp120 do Envelope de HIV/metabolismo , Proteína gp41 do Envelope de HIV/genética , Proteína gp41 do Envelope de HIV/metabolismo , Infecções por HIV/genética , Infecções por HIV/metabolismo , Infecções por HIV/virologia , HIV-1/fisiologia , Humanos , Espectroscopia de Ressonância Magnética , Dados de Sequência Molecular , Mutação/genética , Fragmentos de Peptídeos/química , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/metabolismo , Homologia de Sequência de Aminoácidos
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