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Protein-coding gene in humans
Transcriptional regulator ATRX also known as ATP-dependent helicase ATRX, X-linked helicase II, or X-linked nuclear protein (XNP) is a protein that in
ATRX
Medical condition
Alpha-thalassemia mental retardation syndrome (ATRX), also called alpha-thalassemia X-linked intellectual disability syndrome, nondeletion type or ATR-X
ATR-X_syndrome
Class of enzymes that unpack genetic material
a P-loop, or Walker motif-containing family. The ATRX gene encodes the ATP-dependent helicase, ATRX (also known as XH2 and XNP) of the SNF2 subgroup family
Helicase
Tumors of the nervous or endocrine system within the pancreas
synaptophysin. Genetic testing thereof typically shows altered MEN1 and DAXX/ATRX. The new 2019 WHO classification and grading criteria for neuroendocrine
Pancreatic neuroendocrine tumor
Pancreatic_neuroendocrine_tumor
Type of endocrine gland cancer
PanNet. Other genes that are frequently mutated include DAXX, mTOR, and ATRX. Medical imaging techniques, such as computed tomography (CT scan) and endoscopic
Pancreatic_cancer
Aggressive type of brain cancer
grade glioma, with a non-midline tumor location and with retained nuclear ATRX expression, immunohistochemical negativity for IDH1 R132H suffices for the
Glioblastoma
Tumor of the glial cells of the brain or spine
immunohistochemistry for the presence of R132H-mutant IDH1 and loss of nuclear ATRX. In patients aged >55 years with a histologically typical glioblastoma, without
Glioma
Region of sexual chromosomes exhibiting an autosomal inheritance pattern
Fernandes AD, Tremblay DC, Seah C, Bérubé NG (2008). "The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in
Pseudoautosomal_region
Rare genetic disease
However, mutations have also been found in FMR1, FLNA, UPF3B, CASK, MECP2 and ATRX genes. Mutations on these different genes lead to the different types of
FG_syndrome
Neoplasm in the brain
1p and 19q indicates the tumor is an oligodendroglioma Loss of TP53 and ATRX characterizes astrocytomas Genes EGFR, TERT, and PTEN, are commonly altered
Brain_tumor
Form of dynamic modification
(PRMT). ATRX-syndrome (α-thalassemia X-linked mental retardation) and α-thalassemia myelodysplasia syndrome are caused by mutations in ATRX, a SNF2-related
Chromatin_remodeling
protein UBF, which binds to NOR DNA. In addition to UBF, NORs also bind to ATRX protein, treacle, sirtuin-7 and other proteins. UBF has been identified as
Nucleolus_organizer_region
Type of brain tumor
Diagnosis of diffuse glioma, with astrocytomas mainly being diagnosed under IDH mutant and nuclear ATRX lost.
Astrocytoma
American oncologist (born 1949)
play important roles in cancer, such as PIK3CA, IDH1, IDH2, ARID1A, ARID2, ATRX, DAXX, MLL2, MLL3, CIC, and RNF43. Vogelstein pioneered the idea that somatic
Bert_Vogelstein
Protein-coding gene in the species Homo sapiens
consists of three major protein domains: the Pro-Trp-Trp-Pro (PWWP) domain, the ATRX-DNMT3-DNMT3L (ADD) domain and the catalytic methyltransferase domain. The
DNA (cytosine-5)-methyltransferase 3A
DNA_(cytosine-5)-methyltransferase_3A
the regulation of the human alpha-globin gene cluster and the role of the ATRX protein in genetic disease" 2015 Irwin McLean "for his major contribution
Buchanan_Medal
American researcher
Wickramasinghe J, Zheng H, Kossenkov AV, Lieberman PM (August 2022). "DAXX-ATRX regulation of p53 chromatin binding and DNA damage response". Nature Communications
Paul_Lieberman
Medical condition
proliferation and cell death); 3) mutations in the ATRX gene that encodes transcriptional regulator ATRX protein which contributes to regulating the expression
Undifferentiated pleomorphic sarcoma
Undifferentiated_pleomorphic_sarcoma
the regulation of the human alpha-globin gene cluster and the role of the ATRX protein in genetic disease." 2023 The Genetics Society Medal. Gibbons, Richard
Douglas_Higgs
Medical condition
founded to have a mutation of the gene in the ATRX on the X chromosome, also known as the Xq13 location. ATRX is a gene disease that is associated with other
Smith–Fineman–Myers_syndrome
Project to catalogue genetic mutations responsible for cancer
targets and aneuploidy links thymoma to myasthenia gravis. Sarcoma 206 TP53, ATRX, and RB1 among the few genes recurrently mutated across sarcoma types; copy
The_Cancer_Genome_Atlas
HGNC:33499; Q8WXE1 1316 ATRN HGNC:885; O75882 1317 ATRNL1 HGNC:29063; Q5VV63 1318 ATRX HGNC:886; P46100 1319 ATXN1 HGNC:10548; P54253 1320 ATXN1L HGNC:33279; P0C7T5
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
Iranian-Canadian physician
Xiao-Yang Liu; Noha Gerges; Andrey Korshunov; et al. (12 August 2012). "Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying
Gelareh_Zadeh
myelodysplasia syndrome, somatic; 300448; ATRX Alpha-thalassemia mental retardation syndrome; 301040; ATRX Alport syndrome; 301050; COL4A5 Alport syndrome
List_of_OMIM_disorder_codes
Combination drug
Laboratories". Bloomberg.com. Retrieved 2023-08-24. "Atrix Laboratories, Inc. (ATRX) Receives FDA Approval For Erythromycin/Benzoyl Peroxide", Biospace.com,
Erythromycin/benzoyl_peroxide
American biomedical company
VIPER-assessed activity of only four proteins (IRF3, ARL2BP, ZBTB17, and ATRX). The DarwinOncoMarker achieved a predictability measure (AUC = 0.862) in
DarwinHealth
Epigenetic modification of HSV genetic code
associated with antiviral pathways such as PML, SP100, Daxx, and ATRX. In particular, Daxx and ATRX assemble viral DNA around histone 3, forming heterochromatin
HSV_epigenetics
Protein found in humans
PML-NB disrupted cells were treated and Daxx relocalized with the PML-NB. ATRX, a centromeric heterochromatin component co-localizes with Daxx. This partnership
Death-associated_protein_6
has been used to detect germline mutations in human genes. For example, ATRX for X-linked intellectual disability, and the HBB gene linked to β-thalassemia
Surveyor_nuclease_assay
Human gene
X-linked mental retardation. The third gene located upstream of CXorf26 is ATRX, which encodes for an ATPase/helicase domain, and when mutated causes an
PBDC1
Long non-coding RNA transcribed from telomeres
been shown to be cell cycle regulated via the chromatin-remodeling protein ATRX, with the highest expression of TERRA being present at the G1 phase following
Telomeric repeat–containing RNA
Telomeric_repeat–containing_RNA
conception. The C4orf17 protein interacts with numerous other proteins, such as ATRX, CHD3, KAT2B, KDM1A, PRMT1, and SUV39H1. These specific interactions suggest
C4orf17
ATRX
ATRX
ATRX
ATRX
Boy/Male
Unknown
Origin unknown.
Boy/Male
Hindu, Indian
Light
Boy/Male
Indian
Queen of Sea
Boy/Male
Hindu, Indian
Rankar
Boy/Male
Arabic, Muslim
Confidant
Girl/Female
African, American, Arabic, Australian, British, Christian, English, German, Hindu, Indian, Marwadi, Modern, Tamil
Full of Mystery; Derived from Alicia; Sweet; Honest; Truth; Happy; Darkness Before Midnight; Felicia
Male
Egyptian
, a mystical title of Amen Ra.
Boy/Male
Tamil
Shining
Girl/Female
Australian, British, English
A Stone
Surname or Lastname
English
English : variant spelling of Rountree.
ATRX
ATRX
ATRX
ATRX
ATRX