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SRCAP gene
SRCAP gene

Facial features of individuals with proximal and distal truncating... | Download Scientific Diagram
Facial features of individuals with proximal and distal truncating... | Download Scientific Diagram

Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome

SRCAP (Snf2 related CREBBP activator protein) | Gene Report | BioGPS
SRCAP (Snf2 related CREBBP activator protein) | Gene Report | BioGPS

SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody

Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome - ScienceDirect
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome - ScienceDirect

A schematic structure of the SRCAP gene and the locations of mutations... | Download Scientific Diagram
A schematic structure of the SRCAP gene and the locations of mutations... | Download Scientific Diagram

SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody

Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome

Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease | Neurology Genetics
Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease | Neurology Genetics

SRCAP siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
SRCAP siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

Addgene: Mouse 5' Srcap AID GFP Puro
Addgene: Mouse 5' Srcap AID GFP Puro

Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease | Neurology Genetics
Ultra-rare mutations in SRCAP segregate in Caribbean Hispanic families with Alzheimer disease | Neurology Genetics

Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome | BMC Medical Genetics | Full Text
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome | BMC Medical Genetics | Full Text

Purification of a Human SRCAP Complex That Remodels Chromatin by Incorporating the Histone Variant H2A.Z into Nucleosomes | Biochemistry
Purification of a Human SRCAP Complex That Remodels Chromatin by Incorporating the Histone Variant H2A.Z into Nucleosomes | Biochemistry

Cryo-EM structure of human SRCAP complex | Cell Research
Cryo-EM structure of human SRCAP complex | Cell Research

The chromatin remodeler SRCAP promotes self‐renewal of intestinal stem cells | The EMBO Journal
The chromatin remodeler SRCAP promotes self‐renewal of intestinal stem cells | The EMBO Journal

Addgene: pX335 Mouse 5' Srcap gRNA A
Addgene: pX335 Mouse 5' Srcap gRNA A

Selective recognition of histone variant H2A.Z gives insight into mechanism of chromatin remodeling----Institute of Biophysics Chinese Academy of Sciences
Selective recognition of histone variant H2A.Z gives insight into mechanism of chromatin remodeling----Institute of Biophysics Chinese Academy of Sciences

ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv
ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv

Frontiers | Rare diseases of epigenetic origin: Challenges and opportunities
Frontiers | Rare diseases of epigenetic origin: Challenges and opportunities

A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene | European Journal of Human Genetics
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene | European Journal of Human Genetics

Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature - ScienceDirect
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature - ScienceDirect

SRCAP siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
SRCAP siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology

Journal of Cellular Physiology | Cell Biology Journal | Wiley Online Library
Journal of Cellular Physiology | Cell Biology Journal | Wiley Online Library

The ATPase SRCAP is associated with the mitotic apparatus, uncovering novel molecular aspects of Floating-Harbor syndrome | BMC Biology | Full Text
The ATPase SRCAP is associated with the mitotic apparatus, uncovering novel molecular aspects of Floating-Harbor syndrome | BMC Biology | Full Text