Results 181 to 190 of about 8,343 (220)

Adipose Tissue and Renal Carcinoma: A Protumor Metabolic and Endocrine Alliance. [PDF]

Int J Mol Sci
Ferrando M, Moya Morales DL, Romeo LR, Carrillo MA, Cano RY, Gómez SE, López-Fontana CM, Carón RW, Bruna FA, Pistone-Creydt V.   +9 more
europepmc   +1 more source

Single-cell morphometrics reveals T-box gene-dependent patterns of epithelial tension in the Second Heart field. [PDF]

Nat Commun
Guijarro C, Song S, Aigouy B, Clément R, Villoutreix P, Kelly RG.   +5 more
europepmc   +1 more source

Generation of parathyroid glands from pluripotent stem cells. [PDF]

Endocr J
Kano M.
europepmc   +1 more source

Characterization and lineage tracing of a mouse adipose depot reveal properties conserved with human supraclavicular brown adipose tissue. [PDF]

Stem Cell Reports
Li L, Feldman BJ.
europepmc   +1 more source

Advances in prenatal ultrasound diagnosis of fetal tympanic ring anomalies. [PDF]

Front Med (Lausanne)
Zhang H, Liao R, Li Y, Huang F, Li L, Lyu G.   +5 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Role of TBX1 in human del22q11.2 syndrome

Lancet, The, 2003
Del22q11.2 syndrome is the most frequent known chromosomal microdeletion syndrome, with an incidence of 1 in 4000-5000 livebirths. It is characterised by a 3-Mb deletion on chromosome 22q11.2, cardiac abnormalities, T-cell deficits, cleft palate facial anomalies, and hypocalcaemia. At least 30 genes have been mapped to the deleted region.
Hisato Yagi, Yoshiyuki Furutani, Takashi Sasaki   +2 more
exaly   +3 more sources

Tbx1

Current topics in developmental biology, 2017
Recent data have paved the way to mechanistic studies into the role of Tbx1 during development. Tbx1 is haploinsufficient and is involved in an important genetic disorder. The gene encodes a T-box transcription factor that is expressed from approximately E7.5 in mouse embryos and continues to be expressed in a highly dynamic manner.
A. Baldini, F.G. Fulcoli, E. Illingworth
openaire   +4 more sources

Cloning and characterization of zebrafish tbx1

Gene Expression Patterns, 2003
Tbx1 is one of the genes within the DiGeorge Critical Region (DGCR) and has been recently identified as the critical gene for the cardiovascular anomalies in the DiGeorge mouse models. We have cloned, sequenced and analyzed the zebrafish (Danio rerio) tbx1 cDNA.
Lazaros K, Kochilas, Vijaya, Potluri, Aaron, Gitler, Krithika, Balasubramanian, Alvin J, Chin   +4 more
openaire   +2 more sources

Absence of the vagus nerve in the stomach of Tbx1−/− mutant mice

Neurogastroenterology and Motility, 2011
Tbx1 is a member of the Tbox family of binding domain transcription factors. TBX1 maps within the region of chromosome 22q11 deleted in humans with DiGeorge syndrome (DGS), a common genetic disorder characterized by numerous physical manifestations including craniofacial and cardiac anomalies.
Amélie Calmont, N Thapar, Peter J Scambler   +2 more
exaly   +3 more sources