المؤلفون: Vincentz, Joshua W, Firulli, Beth A, Toolan, Kevin P, Osterwalder, Marco, Pennacchio, Len A, Firulli, Anthony B

مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Clinical Sciences, Congenital Heart Disease, Pediatric, Genetics, Cardiovascular, Rare Diseases, Congenital Structural Anomalies, Heart Disease, 1.1 Normal biological development and functioning, Animals, Aorta, Basic Helix-Loop-Helix Transcription Factors, Cardiac Output, Cell Movement, Gene Expression Regulation, Developmental, Heart, Heart Defects, Congenital, Homeodomain Proteins, Mice, Mice, Knockout, Myocardium, Myocytes, Cardiac, Neural Crest, Phenotype, Signal Transduction, Transcription Factors, Cardiac neural crest, Second heart field, Transcription, HAND1, HAND2, bHLH transcription factors, Cardiac outflow track, Congenital heart defects, Biological Sciences, Medical and Health Sciences, Developmental Biology, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3hh2453n
https://escholarship.org/content/qt3hh2453n/qt3hh2453n.pdf

المؤلفون: Toolan, Kevin P¹ (AUTHOR), McGrath, Brian T² (AUTHOR), Brinkmeier, Michelle L¹ (AUTHOR), Camper, Sally A^1,2 (AUTHOR), Bielas, Stephanie L^1,2,3 (AUTHOR)

المصدر: Brain: A Journal of Neurology. Jan2025, Vol. 148 Issue 1, p55-68. 14p.

مصطلحات موضوعية: *GENETIC regulation, *RNA sequencing, *HISTONE methyltransferases, *AUTISM, *GENE expression

المؤلفون: Bando, Hironori, Gergics, Peter, Bohnsack, Brenda L, Toolan, Kevin P, Richter, Catherine E, Shavit, Jordan A, Camper, Sally A

المساهمون: National Eye Institute, Japan Society, National Institutes of Health

المصدر: Human Molecular Genetics ; volume 29, issue 10, page 1648-1657 ; ISSN 0964-6906 1460-2083

الاتاحة: http://dx.doi.org/10.1093/hmg/ddaa064
http://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddaa064/33314214/ddaa064.pdf
http://academic.oup.com/hmg/article-pdf/29/10/1648/33438068/ddaa064.pdf

المؤلفون: Vincentz, Joshua W., Firulli, Beth A., Toolan, Kevin P., Arking, Dan E., Sotoodehnia, Nona, Wan, Juyi, Chen, Peng-Sheng, de Gier-de Vries, Corrie, Christoffels, Vincent M., Rubart-von der Lohe, Michael, Firulli, Anthony B.

المصدر: Circulation Research ; volume 125, issue 6, page 575-589 ; ISSN 0009-7330 1524-4571

الاتاحة: http://dx.doi.org/10.1161/circresaha.119.315313
https://www.ahajournals.org/doi/full/10.1161/CIRCRESAHA.119.315313

المؤلفون: Firulli, Beth A., Milliar, Hannah, Toolan, Kevin P., Harkin, Jade, Fuchs, Robyn K., Robling, Alex G., Firulli, Anthony B.

المساهمون: Anatomy and Cell Biology, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Dimerization, Hand1, Limb development, Mouse, Transcription, bHLH

وصف الملف: application/pdf

Relation: Development (Cambridge, England); Firulli, B. A., Milliar, H., Toolan, K. P., Harkin, J., Fuchs, R. K., Robling, A. G., & Firulli, A. B. (2017). Defective Hand1 phosphoregulation uncovers essential roles for Hand1 in limb morphogenesis. Development (Cambridge, England), 144(13), 2480–2489. https://doi.org/10.1242/dev.149963; https://hdl.handle.net/1805/15295

الاتاحة: https://hdl.handle.net/1805/15295

المؤلفون: Vincentz, Joshua W., Toolan, Kevin P., Zhang, Wenjun, Firulli, Anthony B.

المساهمون: Moon, Anne M., National Heart, Lung, and Blood Institute, National Institute of Arthritis and Musculoskeletal and Skin Diseases, American Heart Association

المصدر: PLOS Genetics ; volume 13, issue 7, page e1006922 ; ISSN 1553-7404

الاتاحة: http://dx.doi.org/10.1371/journal.pgen.1006922
http://dx.plos.org/10.1371/journal.pgen.1006922

المؤلفون: Firulli, Beth A, Toolan, Kevin P, Harkin, Jade, Millar, Hannah, Pineda, Santiago, Firulli, Anthony B

المساهمون: National Institutes of Health

المصدر: Cardiovascular Research ; volume 113, issue 14, page 1732-1742 ; ISSN 0008-6363 1755-3245

الاتاحة: https://doi.org/10.1093/cvr/cvx166
http://academic.oup.com/cardiovascres/article-pdf/113/14/1732/24254480/cvx166.pdf

المؤلفون: Vincentz, Joshua W., Firulli, Beth A., Toolan, Kevin P., Osterwalder, Marco, Pennacchio, Len A., Firulli, Anthony B.

المساهمون: Pediatrics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Cardiac neural crest, Cardiac outflow track, Congenital heart defects, HAND1, HAND2, Second heart field, Transcription, bHLH transcription factors

وصف الملف: application/pdf

Relation: Developmental Biology; Vincentz JW, Firulli BA, Toolan KP, Osterwalder M, Pennacchio LA, Firulli AB. HAND transcription factors cooperatively specify the aorta and pulmonary trunk. Dev Biol. 2021;476:1-10. doi:10.1016/j.ydbio.2021.03.011; https://hdl.handle.net/1805/34755

الاتاحة: https://hdl.handle.net/1805/34755

المؤلفون: Firulli, Beth A., George, Rajani M., Harkin, Jade, Toolan, Kevin P., Gao, Hongyu, Liu, Yunlong, Zhang, Wenjun, Field, Loren J., Liu, Ying, Shou, Weinian, Payne, Ronald Mark, Rubart-von der Lohe, Michael, Firulli, Anthony B.

المساهمون: Pediatrics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Mitral arcade, Heart failure with preserved ejection fraction, Right bundle branch block, Transcription, Cardiac development

وصف الملف: application/pdf

Relation: Cardiovascular Research; Firulli BA, George RM, Harkin J, et al. HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure. Cardiovasc Res. 2020;116(3):605-618. doi:10.1093/cvr/cvz182; https://hdl.handle.net/1805/29443

الاتاحة: https://hdl.handle.net/1805/29443

المؤلفون: Firulli, Beth A, George, Rajani M, Harkin, Jade, Toolan, Kevin P, Gao, Hongyu, Liu, Yunlong, Zhang, Wenjun, Field, Loren J, Liu, Ying, Shou, Weinian, Payne, Ronald Mark, Rubart-von der Lohe, Michael, Firulli, Anthony B

المساهمون: Herman B Wells Center for Pediatric Research, Riley Children’s Foundation, Division of Pediatric Cardiology, Carrolton Buehl McCulloch Chair of Pediatrics, National Institutes of Health

المصدر: Cardiovascular Research ; volume 116, issue 3, page 605-618 ; ISSN 0008-6363 1755-3245

الاتاحة: https://doi.org/10.1093/cvr/cvz182
http://academic.oup.com/cardiovascres/advance-article-pdf/doi/10.1093/cvr/cvz182/28918894/cvz182.pdf
http://academic.oup.com/cardiovascres/article-pdf/116/3/605/33315342/cvz182.pdf

المؤلفون: Vincentz, Joshua W, Firulli, Beth A, Toolan, Kevin P, Arking, Dan E, Sotoodehnia, Nona, Wan, Juyi, Chen, Peng-Sheng, de Gier-de Vries, Corrie, Christoffels, Vincent M, Rubart-von der Lohe, Michael, Firulli, Anthony B

المصدر: Circulation ; volume 138, issue Suppl_1 ; ISSN 0009-7322 1524-4539

الاتاحة: http://dx.doi.org/10.1161/circ.138.suppl_1.17134

المؤلفون: Firulli, Beth A, George, Rajani M, Harkin, Jade, Toolan, Kevin P, Gao, Hongyu, Liu, Yunlong, Zhang, Wenjun, Field, Loren J, Liu, Ying, Shou, Weinian, Payne, Ronald Mark, Lohe, Michael Rubart-von der, Firulli, Anthony B

المصدر: Cardiovascular Research; Mar2020, Vol. 116 Issue 3, p605-618, 14p

مصطلحات موضوعية: CONGENITAL heart disease, HEART failure, HEART abnormalities, HEART conduction system, MYOCARDIUM

المؤلفون: Firulli, Beth A., Toolan, Kevin P., Harkin, Jade, Millar, Hannah, Pineda, Santiago, Firulli, Anthony B.

المساهمون: Pediatrics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Cardiac development, Hand1, Hypoplastic left heart syndrome, Transcription, bHLH

وصف الملف: application/pdf

Relation: Cardiovascular Research; Firulli, B. A., Toolan, K. P., Harkin, J., Millar, H., Pineda, S., & Firulli, A. B. (2017). The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice. Cardiovascular research, 113(14), 1732–1742. doi:10.1093/cvr/cvx166; https://hdl.handle.net/1805/19490

الاتاحة: https://hdl.handle.net/1805/19490