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

Cyclin H

p36, cyclin H
Top mentioned proteins: PCNA, CAN, HAD, POLYMERASE, ACID
Papers on p36
[Application of chromosome microarray analysis for prenatal diagnosis of a fetus with partial duplication of 1p and uniparental disomy of chromosome 6].
Yang et al., Nanjing, China. In Zhonghua Yi Xue Yi Chuan Xue Za Zhi, Jan 2016
The genetic diagnosis for the fetus was therefore 46,XY, arr 1p36.33 p36.32(849 466-4 090 472)×2-3, (6)×2 hmz.
Identification of genomic aberrations in hemangioblastoma by droplet digital PCR and SNP microarray highlights novel candidate genes and pathways for pathogenesis.
Toren et al., Tel Aviv-Yafo, Israel. In Bmc Genomics, Dec 2015
The most frequently gained regions were on chromosomes 1 (p36.32)
Three-way complex variant translocation involving short arm chromosome (1;9;22)(p36;q34;q11) in a chronic myeloid leukemia patient.
Rasool et al., Quetta, Pakistan. In Oncol Lett, Sep 2015
The present study describes a three-way (1;9;22)(p36;q34;q11) Ph chromosome translocation in a 24-year-old female with CML.
Epithelioid Hemangioendothelioma of the Maxillary Sinus.
Tabaee et al., New York City, United States. In Head Neck Pathol, Jun 2015
Additionally, recent studies have described a recurrent genetic fusion WWTR1-CAMTA1 in EHE, involving t(1;3) (p36;q25).
A rapid and sensitive loop-mediated isothermal amplification procedure (LAMP) for Mycoplasma hyopneumoniae detection based on the p36 gene.
Shao et al., Nanjing, China. In Genet Mol Res, 2014
The aim of this study was to establish a method for sensitive and rapid diagnosis of Mycoplasma hyopneumoniae in clinical specimens.
Chromosome 18q-syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision.
Messina et al., Siena, Italy. In Ital J Pediatr, 2012
and terminal duplication of 1p (1p36.32-p36.33).
Therapy-related acute leukemia with mixed phenotype and t(9;22)(q32;q11.2): a case report and review of the literature.
Lee et al., Seoul, South Korea. In Hum Pathol, 2012
Only 2 cases of therapy-related acute leukemia with mixed phenotype have been reported so far: one with hyperploidy and the other with t(1;21)(p36;q22).
Histologic grading and prognostic biomarkers in salivary gland carcinomas.
Seethala, Pittsburgh, United States. In Adv Anat Pathol, 2011
Comparative genomic hybridization has revealed several chromosomal regions (such as 1p32-p36, 6q23-q27) of prognostic interest in adenoid cystic carcinoma.
Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.
Park et al., Seoul, South Korea. In Cancer Genet Cytogenet, 2010
We present an unusual case study on acute myeloid leukemia associated with t(1;3) and extreme thrombocytosis, along with a thorough review on relevant literature of t(1;3) cases (58 patients).
Rb inactivation in cell cycle and cancer: the puzzle of highly regulated activating phosphorylation of CDK4 versus constitutively active CDK-activating kinase.
Roger et al., Brussels, Belgium. In Cell Cycle, 2010
Its activation requires binding to a D-type cyclin and then T-loop phosphorylation at T172 by the only identified CDK-activating kinase in animal cells, cyclin H-CDK7.
Ménage-à-trois 1 is critical for the transcriptional function of PPARgamma coactivator 1.
Schneider et al., Houston, United States. In Cell Metab, 2007
The Cdk7/cyclin H/ménage-à-trois 1 (MAT1) heterotrimer has proposed functions in transcription as the kinase component of basal transcription factor TFIIH and is activated in adult hearts by Gq-, calcineurin-, and biomechanical stress-dependent pathways for hypertrophic growth.
Xpd/Ercc2 regulates CAK activity and mitotic progression.
Suter et al., New York City, United States. In Nature, 2003
General transcription factor IIH (TFIIH) consists of nine subunits: cyclin-dependent kinase 7 (Cdk7), cyclin H and MAT1 (forming the Cdk-activating-kinase or CAK complex), the two helicases Xpb/Hay and Xpd, and p34, p44, p52 and p62 (refs 1-3).
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas.
Gray et al., San Francisco, United States. In Nat Genet, 2001
Using array CGH, we further narrowed the loci for LOH9 and LOH16 and defined new or previously unappreciated recurrent regions of copy-number decrease on chromosomes 6, 8 and 14 (syntenic with human chromosomes 12p11-p13, 16q24.3 and 13q11-q32, respectively) and regions of copy-number increase on chromosomes 2 and 4 (syntenic to human chromosomes 20q13.2 and 1p32-p36, respectively).
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).
Fontaine et al., Paris, France. In Nat Genet, 2000
We previously localized the SJS1 locus to chromosome 1p34-p36.1 and found no evidence of genetic heterogeneity.
Molecular structure of human TFIIH.
Egly et al., Illkirch-Graffenstaden, France. In Cell, 2000
Immunolabeling experiments localize several subunits: p44, within the ring structure, forms the base of the protruding protein density which includes the cdk7 kinase, cyclin H, and MAT1.
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