scholarly article | Q13442814 |
P50 | author | Daniel Geschwind | Q18631415 |
Christian Windpassinger | Q30089871 | ||
Peter Kroisel | Q89998496 | ||
Axel Schumacher | Q108573003 | ||
P2093 | author name string | John B Vincent | |
Klaus Wagner | |||
Thomas Schwarzbraun | |||
Joao Oliveira | |||
Erwin Petek | |||
Lisa Ofner | |||
Michael K Ledinegg | |||
P2860 | cites work | Activation of the ERK/MAPK pathway by an isoform of rap1GAP associated with G alpha(i) | Q22010516 |
Molecular cloning of a novel mitogen-inducible nuclear protein with a Ran GTPase-activating domain that affects cell cycle progression | Q24336122 | ||
Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). | Q24540157 | ||
Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms | Q24554353 | ||
Basic local alignment search tool | Q25938991 | ||
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences | Q27860580 | ||
The genome sequence of Drosophila melanogaster | Q27860796 | ||
Rheb is a direct target of the tuberous sclerosis tumour suppressor proteins | Q28207283 | ||
Cloning and characterization of GRIPE, a novel interacting partner of the transcription factor E12 in developing mouse forebrain | Q28219308 | ||
Identification and characterization of the tuberous sclerosis gene on chromosome 16 | Q28257738 | ||
Retroposed copies of the HMG genes: a window to genome dynamics | Q31141174 | ||
Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly | Q33679460 | ||
Familial idiopathic brain calcification with autosomal dominant inheritance | Q34419279 | ||
The role of class I HLH genes in neural development--have they been overlooked? | Q35158118 | ||
A role of the tuberous sclerosis gene-2 product during neuronal differentiation | Q41035940 | ||
Microcephaly with extensive calcium deposits and demyelination | Q41939964 | ||
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosis | Q42664041 | ||
Heterogeneous Amino Acids in Ras and Rap1A Specifying Sensitivity to GAP Proteins | Q42825154 | ||
Molecular characterisation of a 3.5 Mb interstitial 14q deletion in a child with several phenotypic anomalies | Q43074232 | ||
A gain-of-function screen for genes controlling motor axon guidance and synaptogenesis in Drosophila | Q46088826 | ||
Defining the breakpoints of proximal chromosome 14q rearrangements in nine patients using flow-sorted chromosomes | Q47618825 | ||
The age of Alu subfamilies | Q48067918 | ||
Rates of conservative and radical nonsynonymous nucleotide substitutions in mammalian nuclear genes | Q73400097 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | brain | Q1073 |
P304 | page(s) | 577-86 | |
P577 | publication date | 2004-09-01 | |
P1433 | published in | Genomics | Q5533503 |
P1476 | title | Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue | |
P478 | volume | 84 |
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