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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.


Rhino, H-R
This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by multiple regulatory ORFs that exist upstream of the primary ORF. Mutations in one of these upstream ORFs, U2HR, cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009] (from NCBI)
Top mentioned proteins: HAD, CAN, AGE, OUT, iMpact
Papers on Rhino
Clinical Characterization of Children Presenting to the Hospital with Enterovirus D68 Infection During the 2014 Outbreak in St. Louis.
Srinivasan et al., Saint Louis, United States. In Pediatr Infect Dis J, Feb 2016
The goal of our study is to characterize the illness severity and clinical presentation of children infected with enterovirus-D68 (EV-D68) in comparison to non-EV-D68-Human Rhino/Enteroviruses (HR/EV).
Evaluation of the coracoid and coracoacromial arch geometry on Thiel-embalmed cadavers using the three-dimensional MicroScribe digitizer.
Soames et al., Dundee, United Kingdom. In J Shoulder Elbow Surg, Jan 2016
METHODS: Thirty pairs of scapulae from 20 female and 10 male deceased donors, average age of 82 years (range, 62-101 years), were scanned and measurements taken using the 3-dimensional (3D) MicroScribe digitizer (Immersion Corp, San Jose CA, USA) and Rhino software (McNeel North America, Seattle, WA, USA).
[Primary Parotid Carcinoma: Influence of a Two-step Procedure on the Oncological Outcome].
Veit et al., Ulm, Germany. In Laryngorhinootologie, Jan 2016
Material and methods: The study includes clinical and histological data of patients with parotid cancer which were treated in the Department of Oto-Rhino-Laryngology and Head and Neck Surgery of the University Medical Center Ulm between 2004 and 2014.
A retrospective analysis of eleven cases of invasive rhino-orbito-cerebral mucormycosis presented with orbital apex syndrome initially.
Xu et al., Qingdao, China. In Bmc Ophthalmol, Dec 2015
BACKGROUND: Rhino-orbito-cerebral mucormycosis(ROCM) is an invasive fungal infection that usually occurs in immunocompromised patients and sometimes presents as orbital apex syndrome(OAS) initially.
Recurrent Rhino-Ocular-Cerebral Mucormycosis in a Leukemic Child: A Case Report and Review of Pediatric Literature.
Santoro et al., Bari, Italy. In Pediatr Rep, Oct 2015
We report a case of acute lymphoblastic leukemia complicated by rhino-oculo-cerebral mucormycosis in a pediatric patient.
The Archiv für Ohrenheilkunde (Archive of Otology): a structural analysis of the first 50 years (1864-1914).
Steger et al., Halle, Germany. In Eur Arch Otorhinolaryngol, Jun 2015
In 1864, Anton von Tröltsch in Würzburg, Hermann Schwartze in Halle/Saale, and Adam Politzer in Vienna founded the Archiv für Ohrenheilkunde (Archive of Otology), the ancestor of the European Archives of Oto-Rhino-Laryngology and Head and Neck.
[Upper airway stimulation in obstructive sleep apnea].
Maurer et al., Mannheim, Germany. In Laryngorhinootologie, Apr 2015
The workgroup "sleep medicine" of the German Society of Oto-Rhino-Laryngology, Head and Neck Surgery supports theses activities with the help of the newly founded task force "Neurostimulation in Sleep Apnea".
Genetic background of supernumerary teeth.
Dundar et al., İzmir, Turkey. In Eur J Dent, 2015
Less common syndromes that are associated with ST are; Fabry Disease, Ellis-van Creveld syndrome, Nance-Horan syndrome, Rubinstein-Taybi Syndrome and Trico-Rhino-Phalangeal syndrome.
[Rhino-orbito-cerebral mucormycosis: two case reports in the light of the literature].
Dereköy et al., Çanakkale, Turkey. In Kulak Burun Bogaz Ihtis Derg, 2014
Rhino-orbito-cerebral mucormycosis is an acute onset and often fatal disease.
The rhino-deadlock-cutoff complex licenses noncanonical transcription of dual-strand piRNA clusters in Drosophila.
Brennecke et al., Vienna, Austria. In Cell, 2014
Here, we show that a complex composed of Rhino, Deadlock, and Cutoff (RDC) defines dual-strand piRNA clusters genome-wide in Drosophila ovaries.
The HP1 homolog rhino anchors a nuclear complex that suppresses piRNA precursor splicing.
Theurkauf et al., Worcester, United States. In Cell, 2014
The Drosophila HP1 homolog Rhino is required for germline piRNA production.
UAP56 couples piRNA clusters to the perinuclear transposon silencing machinery.
Theurkauf et al., Worcester, United States. In Cell, 2012
We show that UAP56 colocalizes with the cluster-associated HP1 variant Rhino, that nuage granules containing Vasa localize directly across the nuclear envelope from cluster foci containing UAP56 and Rhino, and that cluster transcripts immunoprecipitate with both Vasa and UAP56.
Hairless plays a role in formation of inner root sheath via regulation of Dlx3 gene.
Yoon et al., Seoul, South Korea. In J Biol Chem, 2012
regulation of Dlx3 by HR affects the IRS keratin expression, thus modulating the formation of IRS of hair follicle.
Identification of a novel U2HR mutation c.14C>T in a Chinese patient with Marie Unna hereditary hypotrichosis.
Zhang et al., Beijing, China. In Eur J Dermatol, 2012
We have identified a novel heterozygous missense mutation in a Chinese patient with Marie Unna hereditary hypotrichosis.
Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function.
Shen et al., Taiwan. In Biochim Biophys Acta, 2011
deletion mutants of hairless indicate that the JmjC domain contributes to the co-repressor activity
Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families.
Ahmad et al., Islamabad, Pakistan. In J Dermatol, 2011
DNA sequence analysis of the HR gene revealed three novel mutations including two nonsense (p.Cys690X, p.Arg819X) and a missense (p.Pro1157Arg) in four families with congenital atrichia with papular lesions.
Downregulation of Foxe1 by HR suppresses Msx1 expression in the hair follicles of Hr(Hp) mice.
Yoon et al., Seoul, South Korea. In Bmb Rep, 2011
Foxe1 mRNA expression was suppressed in HR-overexpressing skin, as well as in HR-expressing keratinocytes.
A DNA damage response screen identifies RHINO, a 9-1-1 and TopBP1 interacting protein required for ATR signaling.
Elledge et al., Boston, United States. In Science, 2011
Three DDR candidates, the RNA processing protein INTS7, the circadian transcription factor CLOCK, and a previously uncharacterized protein RHINO, were recruited to sites of DNA damage.
Transposon silencing by piRNAs.
Moazed et al., Boston, United States. In Cell, 2009
In this issue, Klattenhoff et al. (2009) report that an HP1 family protein, Rhino, is required for piRNA generation and transposon silencing in Drosophila germline cells.
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