Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
KMT2A: Umbrella Gene for Multiple Diseases
by
Lettieri, Antonella
, Ottaviano, Emerenziana
, Parodi, Chiara
, Ghelma, Filippo
, Grazioli, Paolo
, Massa, Valentina
, Gervasini, Cristina
, Colombo, Elisa
, Vignoli, Aglaia
, Milani, Donatella
, Ancona, Silvia
, Castiglioni, Silvia
, Lesma, Elena
, Di Fede, Elisabetta
, Borghi, Elisa
, Bernardelli, Clara
in
Abnormalities, Multiple - diagnosis
/ Abnormalities, Multiple - genetics
/ Animal cognition
/ Animal models
/ Animals
/ Congenital defects
/ Congenital diseases
/ DNA methylation
/ Embryogenesis
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetics
/ Evolutionary conservation
/ Gene expression
/ genes
/ hematopoiesis
/ Histones
/ Humans
/ Intellectual Disability - genetics
/ Lysine
/ methylation
/ Methyltransferase
/ methyltransferases
/ Microbiota
/ microorganisms
/ Mutation
/ neurodevelopment
/ Patients
/ Phenotype
/ Phenotypes
/ Proteins
/ Review
/ Transcription activation
/ transcriptional activation
/ Tumors
2022
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
KMT2A: Umbrella Gene for Multiple Diseases
by
Lettieri, Antonella
, Ottaviano, Emerenziana
, Parodi, Chiara
, Ghelma, Filippo
, Grazioli, Paolo
, Massa, Valentina
, Gervasini, Cristina
, Colombo, Elisa
, Vignoli, Aglaia
, Milani, Donatella
, Ancona, Silvia
, Castiglioni, Silvia
, Lesma, Elena
, Di Fede, Elisabetta
, Borghi, Elisa
, Bernardelli, Clara
in
Abnormalities, Multiple - diagnosis
/ Abnormalities, Multiple - genetics
/ Animal cognition
/ Animal models
/ Animals
/ Congenital defects
/ Congenital diseases
/ DNA methylation
/ Embryogenesis
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetics
/ Evolutionary conservation
/ Gene expression
/ genes
/ hematopoiesis
/ Histones
/ Humans
/ Intellectual Disability - genetics
/ Lysine
/ methylation
/ Methyltransferase
/ methyltransferases
/ Microbiota
/ microorganisms
/ Mutation
/ neurodevelopment
/ Patients
/ Phenotype
/ Phenotypes
/ Proteins
/ Review
/ Transcription activation
/ transcriptional activation
/ Tumors
2022
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
KMT2A: Umbrella Gene for Multiple Diseases
by
Lettieri, Antonella
, Ottaviano, Emerenziana
, Parodi, Chiara
, Ghelma, Filippo
, Grazioli, Paolo
, Massa, Valentina
, Gervasini, Cristina
, Colombo, Elisa
, Vignoli, Aglaia
, Milani, Donatella
, Ancona, Silvia
, Castiglioni, Silvia
, Lesma, Elena
, Di Fede, Elisabetta
, Borghi, Elisa
, Bernardelli, Clara
in
Abnormalities, Multiple - diagnosis
/ Abnormalities, Multiple - genetics
/ Animal cognition
/ Animal models
/ Animals
/ Congenital defects
/ Congenital diseases
/ DNA methylation
/ Embryogenesis
/ Enzymes
/ Epigenesis, Genetic
/ Epigenetics
/ Evolutionary conservation
/ Gene expression
/ genes
/ hematopoiesis
/ Histones
/ Humans
/ Intellectual Disability - genetics
/ Lysine
/ methylation
/ Methyltransferase
/ methyltransferases
/ Microbiota
/ microorganisms
/ Mutation
/ neurodevelopment
/ Patients
/ Phenotype
/ Phenotypes
/ Proteins
/ Review
/ Transcription activation
/ transcriptional activation
/ Tumors
2022
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
KMT2A: Umbrella Gene for Multiple Diseases
2022
Request Book From Autostore
and Choose the Collection Method
Overview
KMT2A (Lysine methyltransferase 2A) is a member of the epigenetic machinery, encoding a lysine methyltransferase responsible for the transcriptional activation through lysine 4 of histone 3 (H3K4) methylation. KMT2A has a crucial role in gene expression, thus it is associated to pathological conditions when found mutated. KMT2A germinal mutations are associated to Wiedemann–Steiner syndrome and also in patients with initial clinical diagnosis of several other chromatinopathies (i.e., Coffin–Siris syndromes, Kabuki syndrome, Cornelia De Lange syndrome, Rubinstein–Taybi syndrome), sharing an overlapping phenotype. On the other hand, KMT2A somatic mutations have been reported in several tumors, mainly blood malignancies. Due to its evolutionary conservation, the role of KMT2A in embryonic development, hematopoiesis and neurodevelopment has been explored in different animal models, and in recent decades, epigenetic treatments for disorders linked to KMT2A dysfunction have been extensively investigated. To note, pharmaceutical compounds acting on tumors characterized by KMT2A mutations have been formulated, and even nutritional interventions for chromatinopathies have become the object of study due to the role of microbiota in epigenetic regulation.
Publisher
MDPI AG,MDPI
Subject
This website uses cookies to ensure you get the best experience on our website.