Related references
Note: Only part of the references are listed.Dental and Maxillofacial Characteristics of Six Japanese Individuals With Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
Erika Okamura et al.
CLEFT PALATE-CRANIOFACIAL JOURNAL (2013)
Genomic Profiling of a Human Organotypic Model of AEC Syndrome Reveals ZNF750 as an Essential Downstream Target of Mutant TP63
Brian J. Zarnegar et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias
Simone Gana et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2012)
Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome
Rita M. Cabral et al.
GENOMICS (2012)
被撤回的出版物: Stress-induced NQO1 controls stability of C/EBPα against 20S proteasomal degradation to regulate p63 expression with implications in protection against chemical-induced skin cancer (Retracted article. See vol. 36, pg. 2920, 2017)
B. A. Patrick et al.
ONCOGENE (2012)
Wtip and Vangl2 are required for mitotic spindle orientation and cloaca morphogenesis
Ekaterina Bubenshchikova et al.
BIOLOGY OPEN (2012)
Complex SUMO-1 Regulation of Cardiac Transcription Factor Nkx2-5
Mauro W. Costa et al.
PLOS ONE (2011)
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome
Angela L. Duker et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Teashirt 3 Regulates Development of Neurons Involved in Both Respiratory Rhythm and Airflow Control
Xavier Caubit et al.
JOURNAL OF NEUROSCIENCE (2010)
ZNF274 Recruits the Histone Methyltransferase SETDB1 to the 3′ Ends of ZNF Genes
Seth Frietze et al.
PLOS ONE (2010)
Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 Kb
J. H. M. Schuurs-Hoeijmakers et al.
JOURNAL OF MEDICAL GENETICS (2009)
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation
V. Malan et al.
JOURNAL OF MEDICAL GENETICS (2009)
ZNF536, a Novel Zinc Finger Protein Specifically Expressed in the Brain, Negatively Regulates Neuron Differentiation by Repressing Retinoic Acid-Induced Gene Transcription
Zhen Qin et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report
Ryan N. Traylor et al.
MOLECULAR CYTOGENETICS (2009)
Adaptive Evolution in Zinc Finger Transcription Factors
Ryan O. Emerson et al.
PLOS GENETICS (2009)
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2
B. C. Ballif et al.
CLINICAL GENETICS (2008)
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4
Xavier Caubit et al.
DEVELOPMENT (2008)
The proximal Gata4 promoter directs reporter gene expression to Sertoli cells during mouse gonadal development
Severine Mazaud Guittot et al.
BIOLOGY OF REPRODUCTION (2007)
KRAB-containing zinc-finger repressor proteins
R Urrutia
GENOME BIOLOGY (2003)
A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome
D Tentler et al.
JOURNAL OF MEDICAL GENETICS (2000)
Share Paper
