About: AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice

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About: AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice Goto Sponge NotDistinct Permalink

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description	artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) 1998年學術文章 (zh) vedecký článok (publikovaný 1998/11/10) (sk) 1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в листопаді 1998 (uk) مقالة علمية (نشرت في 10-11-1998) (ar) 1998 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) article publié dans les Proceedings of the National Academy of Sciences of the United States of America (fr) wetenschappelijk artikel (gepubliceerd op 1998/11/10) (nl) scientific journal article (en) im November 1998 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28586197-2CEB485A-C4DA-4FDE-B8B7-6275A0066913
publication date	1998-11-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28586197-4B20E3BA-1429-4EC7-975F-1132F5987D18
language of work or name	English
cites work	wds:Q28586197-01CA108B-7784-4ABD-8F78-E0DF595939A0 wds:Q28586197-06251495-F756-462A-A523-C854C50C7672 wds:Q28586197-0B8BCC85-F230-4C52-8416-1A9C23D99D9E wds:Q28586197-0DB51BB1-5F93-4E2A-A375-7021D5C0E45D wds:Q28586197-0F18434F-C0EC-48FC-B8D8-892974914DB8 wds:Q28586197-11E53476-C23D-4A10-AE90-418A7A6DC8E3 wds:Q28586197-12012191-A4AA-4C3B-97A3-555B861DC62C wds:Q28586197-200D9CC7-08C6-49A5-A08D-FCD7F14B6D86 wds:Q28586197-203BC73C-35AF-451D-8813-3214D430D7A4 wds:Q28586197-2F75B731-8A1F-4C40-9B85-5B870A509AA3 wds:Q28586197-32F1D521-3978-4B2D-BE1D-1E59081AFC52 wds:Q28586197-36C961B7-90F1-4CEF-ADFE-FDF9258EE2B8 wds:Q28586197-3ECAB704-19FF-43AD-945A-09A482D1DABE wds:Q28586197-404F744C-9052-44A5-A31F-8A842D0FFF5E wds:Q28586197-4538582F-48A0-47E1-A461-261C359EBC7A wds:Q28586197-4CDE8C52-B909-4E38-9CCC-E24DA58B3B72 wds:Q28586197-59F85A68-F97C-46B6-8A78-0753EF98753E wds:Q28586197-5E13EC31-09DF-49ED-A561-4A700210B31B wds:Q28586197-67DA31AB-2775-48B4-9A21-D76E9E9FAFC8 wds:Q28586197-8AB24D13-175F-4255-9EF1-5299035AE736 wds:Q28586197-928DEC40-5BB0-4A4E-B1DD-263339FA5E67 wds:Q28586197-92F48A11-2421-4C56-903D-0FF2E112CF9B wds:Q28586197-9D1E750B-FAD4-4B6D-A032-DB59304E006A wds:Q28586197-9D91A4CE-3EAE-42A1-8AEA-A70C85617FDB wds:Q28586197-9DDD13D0-632D-497E-8F01-9BB1FA01D507 wds:Q28586197-A9C53955-18F7-463C-948D-8551ED9BA673 wds:Q28586197-B0B030C4-49C4-40DD-A7DE-5A5ABDC08476 wds:Q28586197-B5070880-2A1F-4648-8ED9-392AABAA3241 wds:Q28586197-B5B74C00-0A53-48D8-AA9D-1DA3EC07EF7E wds:Q28586197-B8717951-EF47-40F4-BFE1-FB8EEC994180 wds:Q28586197-BC5CC849-B6A5-43F2-B1F1-AD354CC53EF5 wds:Q28586197-C3B280F6-6DDE-47A7-BBEC-B95E888DC762 wds:Q28586197-CC465855-2B0B-46E2-8812-9BFABAA02AEC wds:Q28586197-D166CF91-470D-4D9D-ADB2-3FE3599B9C06 wds:Q28586197-DB287CE5-B4F9-4D2B-90BE-41CFBF9DD3E6 wds:Q28586197-DE6030A1-92E1-4B92-88FF-4FCA5DDAD4B0 wds:Q28586197-E3B543B7-6719-41A3-92B8-3E15F6EDB589 wds:Q28586197-FC8D99A2-80D8-445F-B738-0F167141C1E0
cites work	Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region Morphogens, compartments, and pattern: lessons from drosophila? Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical vertebra and defects in the closure of the sternal rudiments The roles of retinoids in vertebrate development Developmental patterning and evolution of the mammalian viscerocranium: genetic insights into comparative morphology The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages Function of the retinoic acid receptors (RARs) during development (I). Craniofacial and skeletal abnormalities in RAR double mutants Cloning and expression of AP-2, a cell-type-specific transcription factor that activates inducible enhancer elements AP2 inhibits cancer cell growth and activates p21WAF1/CIP1 expression What's in a face? Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxb-4 MARCKS deficiency in mice leads to abnormal brain development and perinatal death Transcription factor AP-2 essential for cranial closure and craniofacial development Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2 Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis Patterning of neural crest derivatives in the avian embryo: in vivo and in vitro studies Chicken transcription factor AP-2: cloning, expression and its role in outgrowth of facial prominences and limb buds. AP-2.2, a novel gene related to AP-2, is expressed in the forebrain, limbs and face during mouse embryogenesis Perinatal lethality and multiple craniofacial malformations in MSX2 transgenic mice. The developmentally regulated transcription factor AP-2 is involved in c-erbB-2 overexpression in human mammary carcinoma Mechanisms identified in the transcriptional control of epithelial gene expression. Derivation of embryonic stem cell lines Transcriptional activation by Myc is under negative control by the transcription factor AP-2 Mouse Otx2 functions in the formation and patterning of rostral head. Repression of a matrix metalloprotease gene by E1A correlates with its ability to bind to cell type-specific transcription factor AP-2. Failure of ventral body wall closure in mouse embryos lacking a procollagen C-proteinase encoded by Bmp1, a mammalian gene related to Drosophila tolloid Pathogenesis of craniofacial and body wall malformations induced by ochratoxin A in mice Partial deletion of chromosome 6p: delineation of the syndrome Regulation of transcription factor AP-2 by the morphogen retinoic acid and by second messengers. The human alpha 2 integrin gene promoter. Identification of positive and negative regulatory elements important for cell-type and developmentally restricted gene expression Prenatal craniofacial development: new insights on normal and abnormal mechanisms Genetics and limb development Ectopic expression of Fgf-4 in chimeric mouse embryos induces the expression of early markers of limb development in the lateral ridge. The rabbit gene for 92-kDa matrix metalloproteinase. Role of AP1 and AP2 in cell type-specific transcription. Limb and lower-body duplications induced by retinoic acid in mice Perspectives on eye development Craniofacial development: knockout mice take one on the chin The lidgap-Gates (lgGa) mutation for open eyelids at birth maps to mouse chromosome 13.
author name string	wds:Q28586197-07D17863-C2E0-4E0E-AB93-C9DDCF45E67A wds:Q28586197-772A1EF0-1968-429A-A74C-183C310CC0FD wds:Q28586197-7A5C513F-2A2B-47F9-8DAA-32F21CB47ABA wds:Q28586197-89EA1834-E7C8-4646-BBE7-E0E046E99603
OpenCitations bibliographic resource ID	wds:Q28586197-A18999C9-7749-409F-AEBE-9A03171DB0EB
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/650360
author name string	J. Zhang

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