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RABL2B gene

Known as: RAB, member of RAS oncogene family-like 2B, RAB-LIKE 2B, RABL2B 
National Institutes of Health

Related topics

Related topics

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RAB13 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Splicing-related single nucleotide polymorphism of RAB, member of RAS oncogene family like 2B (RABL2B) jeopardises semen quality in Chinese Holstein bulls.
RAB, member of RAS oncogene family like 2B (RABL2B) is a member of a poorly characterised clade of the RAS GTPase superfamily… 
Review
2017
Review
2017
Objective Measures of Electrophysiological Responses of Children with Idiopathic Autism Spectrum Disorder and Phelan-McDermid Syndrome to a Contrast-Reversing Checkerboard
The heterogeneity of autism presents many challenges in understanding the disorder. About one thousand genes are implicated in… 
2017
2017
Revisión sistemática y meta-análisis de la región cromosómica 22q13 y la implicación de los genes ARSA, SHANK3, ACR y RABL2B en el Síndrome Phelan-McDermid, el Trastorno del Espectro Autista y la…
2016
2016
Phelan-McDermid syndrome presenting with developmental delays and facial dysmorphisms
Phelan-McDermid syndrome is a rare genetic disorder caused by the terminal or interstitial deletion of the chromosome 22q13.3… 
2014
2014
[Global gene expression responses to Iodine-125 radiation in three human gastric cancer cell lines].
OBJECTIVE To study genome-wide gene expression changes in gastric cancer cells after iodine-125 ¹²⁵(I) particle irradiation… 
2013
2013
RABL-regulated pathways: a new tale in sperm function.
Mammalian sperm have a specialized motile flagellum to provide the unidirectional propulsion required to achieve fertilisation of… 
2011
2011
Constant Splice-Isoform Ratios in Human Lymphoblastoid Cells Support the Concept of a Splico-Stat
Splicing generates mature transcripts from genes in pieces in eukaryotic cells. Overwhelming evidence has accumulated that… 
2010
2010
Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome
We report on a 4‐year‐old girl with severe developmental delay, absent speech, and chromosome 22q13.3 deletion (Phelan–McDermid… 
2010
2010
Analysis of relative gene dosage and expression differences of the paralogs RABL2A and RABL2B by Pyrosequencing.
1999
1999
Two novel human RAB genes with near identical sequence each map to a telomere-associated region: the subtelomeric region of 22q13.3 and the ancestral telomere band 2q13.
Two closely related genes have been identified at 2q13 and 22q13.3. These genes show similarity to members of the RAB family of… 
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