Results 91 to 100 of about 751 (109)

Cross-Study Meta-Analysis of Blood Transcriptomes in Type 2 Diabetes. [PDF]

Int J Mol Sci
Tkachenko AA, Tonyan ZN, Nasykhova YA, Barbitoff YA, Renev IN, Danilova MM, Basipova AA, Glavnova OB, Polev DE, Chepanov SV, Selkov SA, Golovkin NV, Vlasova ME, Glotov AS.   +13 more
europepmc   +1 more source

An ultrasmall core-shell silica nanoparticle improves antitumour immunity and survival by remodelling suppressive melanoma microenvironments. [PDF]

Nat Nanotechnol
De Leon G, Zhang L, Siddiqui NA, Naguib N, Chen F, Padmanabhan R, Zhang T, Monette S, Socciarelli F, Lee R, Pourbaghi M, Quinn TP, Overholtzer M, Merghoub T, Wiesner U, Wolchok JD, Bradbury MS.   +16 more
europepmc   +1 more source

Gene expression regulation by Ca²⁺ signaling: an updated systematic review. [PDF]

Cell Mol Biol Lett
Zou M, Wang H, Zeng X, Zhang X.
europepmc   +1 more source

Influência do gene TPCN2 no fenótipo da pigmentação da pele e cabelos em amostra do Rio Grande do Sul.

, 2012
Santos, Franciele Lausch dos
core  

Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease [PDF]

International Journal of Molecular Sciences
Albinism is characterized by a variable degree of hypopigmentation affecting the skin and the hair, and causing ophthalmologic abnormalities. Its oculocutaneous, ocular and syndromic forms follow an autosomal or X-linked recessive mode of inheritance ...
Nikoletta Nagy, Judit Danis, Marta Medvecz   +2 more
exaly   +4 more sources

Funktionelle Charakterisierung des Ionenkanals TPCN2 [PDF]

, 2011
Schieder, Michael
core   +3 more sources

Identification of a Novel Gene for Diabetic Traits in Rats, Mice, and Humans [PDF]

Genetics, 2014
The genetic basis of type 2 diabetes remains incompletely defined despite the use of multiple genetic strategies. Multiparental populations such as heterogeneous stocks (HS) facilitate gene discovery by allowing fine mapping to only a few megabases ...
John Parrington, Martin Hessner
exaly   +2 more sources

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The correlation of skin colour, skin reflectance, freckling, MC1R, TYR, IRF-4 and TPCN2 genotypes with naevus pattern within a case-control study of melanoma

2018
Background: In Australia, melanoma remains one of the most deadly cancers, where the estimated risk of being diagnosed by the age of 85 is one in 18. Melanoma risk phenotypes, such as red hair and fair skin, have been well established. This study correlated phenotypic data, such as skin reflectance, freckling, naevus patterns, and genotypic information
openaire   +3 more sources