نتایج جستجو برای: ژن tfap2a

تعداد نتایج: 15895  

2017
James P. De Andrade Allison W. Lorenzen Vincent T. Wu Maria V. Bogachek Jung M. Park Vivian W. Gu Claire M. Sevenich Victoria C. Cassady Anna C. Beck Mikhail V. Kulak Robert A. Robinson Geeta Lal Ronald J. Weigel

Cancer stem cells (CSCs) are expanded in anaplastic thyroid cancer (ATC) and standard treatment approaches have failed to improve survival, suggesting a need to specifically target the CSC population. Recent studies in breast and colorectal cancer demonstrated that inhibition of the SUMO pathway repressed CD44 and cleared the CSC population, mediated through SUMO-unconjugated TFAP2A. We sought ...

Journal: :Journal of Investigative Dermatology 2022

The aryl hydrocarbon receptor (AHR) is an environmental sensor and ligand-activated transcription factor that involved in epithelial homeostasis barrier development of the skin. Through genome-wide transcriptomic epigenomic analyses human primary keratinocytes upon AHR activation using TCDD we identified early late responsive genes. genes were enriched for canonical factors known to promote ker...

2017
Norliyana Zainolabidin Sandhya P. Kamath Ayesha R. Thanawalla Albert I. Chen

GABAergic inhibitory neurons in the cerebellum are subdivided into Purkinje cells and distinct subtypes of interneurons from the same pool of progenitors, but the determinants of this diversification process are not well defined. To explore the transcriptional regulation of the development of cerebellar inhibitory neurons, we examined the role of Tfap2A and Tfap2B in the specification of GABAer...

Journal: :Development 2005
Robert D Knight Yashar Javidan Tailin Zhang Sarah Nelson Thomas F Schilling

AP2 transcription factors regulate many aspects of embryonic development. Studies of AP2a (Tfap2a) function in mice and zebrafish have demonstrated a role in patterning mesenchymal cells of neural crest origin that form the craniofacial skeleton, while the mammalian Tfap2b is required in both the facial skeleton and kidney. Here, we show essential functions for zebrafish tfap2a and tfap2b in de...

Journal: :Reproductive Biology and Endocrinology 2007
Koichi Ushizawa Toru Takahashi Misa Hosoe Hiroko Ishiwata Kanako Kaneyama Keiichiro Kizaki Kazuyoshi Hashizume

BACKGROUND Cell-cell communication is an important factor in feto-maternal units during placentogenesis. The placenta produces pivotal hormones and cytokines for communication between cotyledonary villi and the maternal caruncle. Gene expression in bovine placenta throughout pregnancy was comprehensively screened by a cDNA microarray, and we searched for a common transcription factor in a gene ...

Journal: :American journal of medical genetics. Part A 2011
Jeff M Milunsky Tom M Maher Geping Zhao Zhenyuan Wang John B Mulliken David Chitayat Michele Clemens Heather J Stalker Mislen Bauer Michele Burch Sébastien Chénier Michael L Cunningham Arlene V Drack Sandra Janssens Audrey Karlea Regan Klatt Usha Kini Ophir Klein Augusta M Lachmeijer Andre Megarbane Nancy J Mendelsohn Wendy S Meschino Geert R Mortier Sandhya Parkash C Renai Ray Angharad Roberts Amy Roberts Willie Reardon Rhonda E Schnur Rosemarie Smith Miranda Splitt Kamer Tezcan Margo L Whiteford Derek A Wong Roberto Zori Angela E Lin

Branchio-oculo-facial syndrome (BOFS; OMIM#113620) is a rare autosomal dominant craniofacial disorder with variable expression. Major features include cutaneous and ocular abnormalities, characteristic facies, renal, ectodermal, and temporal bone anomalies. Having determined that mutations involving TFAP2A result in BOFS, we studied a total of 30 families (41 affected individuals); 26/30 (87%) ...

Journal: :Development 2003
Robert D Knight Sreelaja Nair Sarah S Nelson Ali Afshar Yashar Javidan Robert Geisler Gerd-Joerg Rauch Thomas F Schilling

The neural crest is a uniquely vertebrate cell type that gives rise to much of the craniofacial skeleton, pigment cells and peripheral nervous system, yet its specification and diversification during embryogenesis are poorly understood. Zebrafish homozygous for the lockjaw (low) mutation show defects in all of these derivatives and we show that low (allelic with montblanc) encodes a zebrafish t...

ژورنال: :مجله دانشگاه علوم پزشکی مازندران 0
مریم فضائلی maryam fazaeli phd student in general linguistics, faculty of literature and humanities, ferdowsi university of mashhad, mashhad, iranمشهد: میدان آزادی، دانشگاه فردوسی مشهد، گروه زبانشناسی رؤیا مهدیه roya mahdie msc student in speech and language therapy, varastegan institute for medical science, mashhad, iranدانشجوی کارشناسی ارشد گفتاردرمانی، مرکز آموزش عالی علوم پزشکی وارستگان، مشهد، ایران یوسف شفقتی yousef shafaghati professor, department of clinical genetics, cellular- molecular and cells stems research center, university of social welfare and rehabilitation sciences, tehran, iranاستاد، گروه ژنتیک، مرکز تحقیقات سلولی- مولکولی و سلول های بنیادی، دانشگاه علوم بهزیستی و توانبخشی، تهران، ایران

سندرم برانکیو-اکولو- فاسیال اختلال نادر با وراثت اتوزومال غالب است که ناشی از اختلال تکامل قوس های برانکیال می باشد. هدف از این مطالعه گزارشی از وجود این سندرم در پسربچه ای برای نخستین بار در ایران است. بیمار موردی تک­ گیر بود که در زمان مراجعه به گفتاردرمانی 2 سال و 9 ماهه بود. محصول حاملگی اول مادر (زایمان طبیعی) بود. زوجین سالم و خویشاوند درجه 3 (پسرخاله- دخترخاله) بودند. علائم ظاهری بارز وی...

Journal: :Development 2004
Alejandro Barrallo-Gimeno Jochen Holzschuh Wolfgang Driever Ela W Knapik

Neural crest progenitor cells are the main contributors to craniofacial cartilage and connective tissue of the vertebrate head. These progenitor cells also give rise to the pigment, neuronal and glial cell lineages. To study the molecular basis of neural crest differentiation, we have cloned the gene disrupted in the mont blanc (mob(m610)) mutation, which affects all neural crest derivatives. U...

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