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RAB40AL gene
Known as:
RAR2
, RAS-ASSOCIATED PROTEIN RAB40A-LIKE
, Ras like GTPase
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National Institutes of Health
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Related topics
Related topics
1 relation
ras Oncogene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Fiberboards based on filled lignin resin and petiole fibers
M. Ammar
,
Nabawia Mechi
,
Abdelmoumen Hidouri
,
Elimame Elaloui
Journal of the Indian Academy of Wood Science
2018
Corpus ID: 256072751
Fiberboards were manufactured from filled phenolic resins (lignin-formaldehyde or glyoxal) and petiole date palm fibers. Lignin…
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2015
2015
A novel 47.2 Mb duplication on chromosomal bands Xq21.1-25 associated with mental retardation.
Zhijuan Jin
,
L. Yu
,
Juan Geng
,
Jian Wang
,
Xing-ming Jin
,
Hong Huang
Gene
2015
Corpus ID: 30406273
2015
2015
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results.
A. Bianco
,
F. Faletra
,
+5 authors
A. Marcuzzi
Molecular Medicine Reports
2015
Corpus ID: 9393300
Next-generation sequencing (NGS) has generated a large amount of sequence data with the requirement of frequent critical…
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2014
2014
A note of caution on the diagnosis of Martin-Probst syndrome by the detection of the p.D59G mutation in the RAB40AL gene
M. Ołdak
,
Ewelina Ruszkowska
,
+5 authors
R. Płoski
European Journal of Pediatrics
2014
Corpus ID: 3154791
AbstractMartin-Probst syndrome (MPS) is an X-linked multisystem neurodevelopmental disorder, reported to be caused by the p.D59G…
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2012
2012
Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
J. Bedoyan
,
Valerie M. Schaibley
,
+15 authors
Donna M. Martin
Journal of Medical Genetics
2012
Corpus ID: 11617826
Background and aim Martin–Probst syndrome (MPS) is a rare X-linked disorder characterised by deafness, cognitive impairment…
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2007
2007
RLGP: An Efficient Method to Avoid Code Bloating on Genetic Programming
Liangxu Liu
,
Haibin Cai
,
Mingyou Ying
,
Jiajin Le
International Symposium on Mechatronics and its…
2007
Corpus ID: 14545733
Code bloating presents a serious problem in scaling GP to larger and more difficult problems. The studies involving code bloating…
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2002
2002
The Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.
F. Saito-Ohara
,
Y. Fukuda
,
+7 authors
J. Inazawa
American Journal of Human Genetics
2002
Corpus ID: 37673086
A male patient with profound mental retardation, athetosis, nystagmus, and severe congenital hypotonia (Duchenne muscular…
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