Related references
Note: Only part of the references are listed.miRNA regulation of Sdf1 chemokine signaling provides genetic robustness to germ cell migration
Alison A. Staton et al.
NATURE GENETICS (2011)
Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling
Jing Tian et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Identification of a Submicroscopic 3.2 Mb Chromosomal 16q12.2-13 Deletion in a Child With Short Stature, Mild Developmental Delay, and Craniofacial Anomalies, by High-Density Oligonucleotide Array-a Recognizable Syndrome
Ching-Fen Chang et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
SeqWare Query Engine: storing and searching sequence data in the cloud
Brian D. O'Connor et al.
BMC BIOINFORMATICS (2010)
Collective Chemotaxis Requires Contact-Dependent Cell Polarity
Eric Theveneau et al.
DEVELOPMENTAL CELL (2010)
Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2
Irina V. Grigorieva et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Analysis of SDF-1/CXCR4 signaling in primordial germ cell migration and survival or differentiation in Xenopus laevis
Tomoyo Takeuchi et al.
MECHANISMS OF DEVELOPMENT (2010)
Acquired variation outweighs inherited variation in whole genome analysis of methotrexate polyglutamate accumulation in leukemia
Deborah French et al.
BLOOD (2009)
Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing
Hane Lee et al.
BMC GENOMICS (2009)
Interaction between transcription factors Iroquois proteins 4 and 5 controls cardiac potassium channel Kv4.2 gene transcription
Wenjie He et al.
CARDIOVASCULAR RESEARCH (2009)
The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx
Elisa Rodriguez-Seguel et al.
DEVELOPMENTAL BIOLOGY (2009)
ALX4 dysfunction disrupts craniofacial and epidermal development
Hulya Kayserili et al.
HUMAN MOLECULAR GENETICS (2009)
Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade et al.
NATURE GENETICS (2009)
The neural crest and neural crest cells: discovery and significance for theories of embryonic organization
Brian K. Hall
JOURNAL OF BIOSCIENCES (2008)
Role of the neural crest in face and brain development
Nicole M. Le Douarin et al.
BRAIN RESEARCH REVIEWS (2007)
Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: New syndrome
Hanan A. Hamamy et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Celsius: a community resource for Affymetrix microarray data
Allen Day et al.
GENOME BIOLOGY (2007)
Mutations in different components of FGF signaling in LADD syndrome
E Rohmann et al.
NATURE GENETICS (2006)
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development
CW Cheng et al.
DEVELOPMENTAL BIOLOGY (2005)
The homeodomain transcription factor lrx5 establishes the mouse cardiac ventricular repolarization gradient
DL Costantini et al.
CELL (2005)
Homeodomain revisited: a lesson from disease-causing mutations
YI Chi
HUMAN GENETICS (2005)
Functional characterization of SDF-1 proximal promoter
C García-Moruja et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Genetics of craniofacial development and malformation
AOM Wilkie et al.
NATURE REVIEWS GENETICS (2001)
Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1
TH Malik et al.
EMBO JOURNAL (2001)
GATA3 haplo-insufficiency causes human HDR syndrome
H Van Esch et al.
NATURE (2000)
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I
P Momeni et al.
NATURE GENETICS (2000)