Works matching Friezes

Results: 148

Infinite friezes and triangulations of annuli.

Published in:

Journal of Algebra & Its Applications, 2024, v. 23, n. 12, p. 1, doi. 10.1142/S0219498824502074

By:

Baur, Karin;
Çanakçı, İlke;
Jacobsen, Karin M.;
Kulkarni, Maitreyee C.;
Todorov, Gordana

Publication type:

Article

Ovidius Painted and Printed. The Influence of Metamorphoses Illustrations on Two Friezes in Marca di Ancona.

Published in:

Il Capitale Culturale: Studies on the Value of Cultural Heritage, 2023, p. 327, doi. 10.13138/2039-2362/3307

By:

Casamassima, Francesca

Publication type:

Article

CLASSICAL SCULPTURE FROM THE ATHENIAN AGORA, PART 2: THE FRIEZES OF THE TEMPLE OF ARES (TEMPLE OF ATHENA PALLENIS).

Published in:

Hesperia, 2019, v. 88, n. 4, p. 625, doi. 10.2972/hesperia.88.4.0625

By:

Stewart, Andrew;
Driscoll, Eric;
Estrin, Seth;
Gleason, Natalie J.;
Lawrence, Erin;
Levitan, Rebecca;
Lloyd-Knauf, Samantha;
Turbeville, Kelsey

Publication type:

Article

A Unique Art Form: The Friezes of Pirgí.

Published in:

Leonardo, 2004, v. 37, n. 3, p. 234, doi. 10.1162/0024094041139409

By:

James, Alice V.;
James, David A.;
Kalisperis, Loukas N.

Publication type:

Article

Tropical friezes and the index in higher homological algebra.

Published in:

Mathematical Proceedings of the Cambridge Philosophical Society, 2021, v. 171, n. 1, p. 23, doi. 10.1017/S0305004120000031

By:

JØRGENSEN, PETER

Publication type:

Article

Heronian Friezes.

Published in:

IMRN: International Mathematics Research Notices, 2021, v. 2021, n. 1, p. 648, doi. 10.1093/imrn/rnaa057

By:

Fomin, Sergey;
Setiabrata, Linus

Publication type:

Article

On Tropical Friezes Associated with Dynkin Diagrams.

Published in:

IMRN: International Mathematics Research Notices, 2013, v. 2013, n. 18, p. 4243, doi. 10.1093/imrn/rns176

By:

Guo, L.

Publication type:

Article

Die Caracallathermen in Rom, das Hafengymnasium in Ephesos -- und die Friese des „Partherdenkmals“.

Published in:

Römische Historische Mitteilungen, 2022, v. 64, p. 89, doi. 10.1553/rhm64s89

By:

THÜR, HILKE

Publication type:

Article

BEHIND THE WALL OF SILENCE: THE JOURNEY OF EMPOWERMENT OF THE OTHER VOICE FROM THE INTRICATE FRIEZES OF THE VICTORIAN FEMALE NARRATIVE TO THE LOFTY PILLARS OF THE LAW.

Published in:

BAS - British & American Studies, 2019, v. 25, p. 33

By:

AVARVAREI, SIMONA CATRINEL;
DOMINTE, NICOLETA RODICA

Publication type:

Article

Assessment of Architectural Terracotta Friezes in Bologna.

Published in:

Journal of Architectural Conservation, 2012, v. 18, n. 2, p. 41, doi. 10.1080/13556207.2012.10785110

By:

Galli, Claudio;
Conserva, Francesco

Publication type:

Article

Friezing and tyred—tyre tread patterns as friezes.

Published in:

International Journal of Mathematical Education in Science & Technology, 2001, v. 32, n. 4, p. 602, doi. 10.1080/002073901750334745

By:

Lynch, Mark A. M.

Publication type:

Article

A bridge between Conway–Coxeter friezes and rational tangles through the Kauffman bracket polynomials.

Published in:

Journal of Knot Theory & Its Ramifications, 2019, v. 28, n. 14, p. N.PAG, doi. 10.1142/S0218216519500834

By:

Kogiso, Takeyoshi;
Wakui, Michihisa

Publication type:

Article

REPRODUCTION OF HISTORIC DECORATIVE CEILINGS AND WALL FRIEZES IN TEXAS.

Published in:

Journal of Interior Design, 1978, v. 4, n. 1, p. 34, doi. 10.1111/j.1939-1668.1978.tb00485.x

By:

Harwood, Buie;
McKee, Betty

Publication type:

Article

Woven rope friezes.

Published in:

Mathematics Magazine, 1999, v. 72, n. 1, p. 32, doi. 10.1080/0025570X.1999.11996695

By:

Farris, Frank A.;
Rossing, Nils Kristian

Publication type:

Article

Coxeter Friezes and Triangulations of Polygons.

Published in:

American Mathematical Monthly, 2013, v. 120, n. 6, p. 553, doi. 10.4169/amer.math.monthly.120.06.553

By:

Henry, Claire-Soizic

Publication type:

Article

Quantum Numbers and q-Deformed Conway–Coxeter Friezes.

Published in:

Mathematical Intelligencer, 2021, v. 43, n. 2, p. 61, doi. 10.1007/s00283-021-10061-1

By:

Morier-Genoud, Sophie;
Ovsienko, Valentin

Publication type:

Article

FRIEZES, STRINGS AND CLUSTER VARIABLES.

Published in:

Glasgow Mathematical Journal, 2012, v. 54, n. 1, p. 27, doi. 10.1017/S0017089511000322

By:

ASSEM, IBRAHIM;
DUPONT, GRÉGOIRE;
SCHIFFLER, RALF;
SMITH, DAVID

Publication type:

Article

Relief in the round: terracotta classicism and the Homeric friezes of Ickworth House.

Published in:

Sculpture Journal, 2024, v. 33, n. 3, p. 355, doi. 10.3828/sj.2024.33.3.03

By:

Marshall, Sebastian

Publication type:

Article

Growth behaviour of periodic tame friezes.

Published in:

Revista Mathematica Iberoamericana, 2019, v. 35, n. 2, p. 575, doi. 10.4171/rmi/1063

By:

Baur, Karin;
Fellner, Klemens;
Parsons, Mark J.;
Tschabold, Manuela

Publication type:

Article

Imperial Homecoming(s) and the Ara Pacis Augustae in 13 BC.

Published in:

Acta Antiqua Academiae Scientiarum Hungaricae, 2024, v. 63, n. 2/3, p. 427, doi. 10.1556/068.2023.00104

By:

Coşkun, Altay

Publication type:

Article

Imperial Homecoming(s) and the Ara Pacis Augustae in 13 BC.

Published in:

Acta Antiqua Academiae Scientiarum Hungaricae, 2023, v. 63, n. 2/3, p. 427, doi. 10.1556/068.2023.00104

By:

Coşkun, Altay

Publication type:

Article

SOME COUNTING FORMULAE FOR $\lambda $ -QUIDDITIES OVER THE RINGS ${\mathbb {Z}}/2^{m}{\mathbb {Z}}$.

Published in:

Bulletin of the Australian Mathematical Society, 2025, v. 111, n. 1, p. 1, doi. 10.1017/S0004972724000340

By:

MABILAT, FLAVIEN

Publication type:

Article

Meanders, knots, labyrinths and mazes.

Published in:

Journal of Knot Theory & Its Ramifications, 2016, v. 25, n. 9, p. -1, doi. 10.1142/S0218216516410091

By:

Kappraff, Jay;
Radović, Ljiljana;
Jablan, Slavik

Publication type:

Article

Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations.

Published in:

2018

By:

Warren, Hannah E.;
Louie, Raymond J.;
Friez, Michael J.;
Frías, Jaime L.;
Leroy, Jules G.;
Spranger, Jürgen W.;
Skinner, Steven A.;
Champaigne, Neena L.

Publication type:

Case Study

Importance of genetic testing in global health during the evaluation of familial microcephaly.

Published in:

Clinical Case Reports, 2016, v. 4, n. 10, p. 968, doi. 10.1002/ccr3.669

By:

Molinero, Isaac;
Broman‐Fulks, Jordan;
Lyons, Michael J.;
Matheus, Maria Gisele;
Chaubey, Alka;
DuPont, Barbara R.;
Friez, Michael J.;
Skinner, Steve A.;
Holden, Kenton R.

Publication type:

Article

X-Linked Creatine Transporter Deficiency Presenting as a Mitochondrial Disorder.

Published in:

Journal of Child Neurology, 2010, v. 25, n. 8, p. 1009, doi. 10.1177/0883073809352109

By:

Hathaway, Samantha C.;
Friez, Michael;
Limbo, Kimberly;
Parker, Colette;
Salomons, Gajja S.;
Vockley, Jerry;
Wood, Tim;
Abdul-Rahman, Omar A.

Publication type:

Article

MECP2 Mutations Found in Patients Initially Referred for Angelman Syndrome Testing.

Published in:

Journal of Genetic Counseling, 2002, v. 11, n. 6, p. 495

By:

Heleski, R.;
Friez, M.;
Best, R.;
Corning, K.

Publication type:

Article

Rehearsal for Deep Song.

Published in:

Journal of Contemporary Painting, 2024, v. 10, n. 1/2, p. 155, doi. 10.1386/jcp_00069_1

By:

Lasurt, Lola

Publication type:

Article

What an artist saw: Tracing a local iconographic tradition for the Temple of Hatshepsut at Deir el-Bahari.

Published in:

Polish Archaeology in the Mediterranean, 2021, v. 30, n. 1, p. 187, doi. 10.31338/uw.2083-537X.pam30.1.09

By:

Stupko-Lubczynska, Anastasiia

Publication type:

Article

Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.

Published in:

Translational Psychiatry, 2013, v. 3, n. 10, p. 1, doi. 10.1038/tp.2013.91

By:

Plummer, J. T.;
Evgrafov, O. V.;
Bergman, M. Y.;
Friez, M.;
Haiman, C. A.;
Levitt, P.;
Aldinger, K. A.

Publication type:

Article

Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c. 109C>T (p. R37X).

Published in:

Clinical Genetics, 2015, v. 87, n. 5, p. 461, doi. 10.1111/cge.12420

By:

Basehore, M.J.;
Michaelson‐Cohen, R.;
Levy‐Lahad, E.;
Sismani, C.;
Bird, L.M.;
Friez, M.J.;
Walsh, T.;
Abidi, F.;
Holloway, L.;
Skinner, C.;
McGee, S.;
Alexandrou, A.;
Syrrou, M.;
Patsalis, P.C.;
Raymond, G.;
Wang, T.;
Schwartz, C.E.;
King, M.‐C.;
Stevenson, R.E.

Publication type:

Article

Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1482, doi. 10.1038/ejhg.2015.29

By:

Bronicki, Lucas M;
Redin, Claire;
Drunat, Severine;
Piton, Amélie;
Lyons, Michael;
Passemard, Sandrine;
Baumann, Clarisse;
Faivre, Laurence;
Thevenon, Julien;
Rivière, Jean-Baptiste;
Isidor, Bertrand;
Gan, Grace;
Francannet, Christine;
Willems, Marjolaine;
Gunel, Murat;
Jones, Julie R;
Gleeson, Joseph G;
Mandel, Jean-Louis;
Stevenson, Roger E;
Friez, Michael J

Publication type:

Article

A novel intermediate mucolipidosis II/IIIαβ caused by GNPTAB mutation in the cytosolic N-terminal domain.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 5, p. 594, doi. 10.1038/ejhg.2013.207

By:

Leroy, Jules G;
Sillence, David;
Wood, Tim;
Barnes, Jarrod;
Lebel, Robert Roger;
Friez, Michael J;
Stevenson, Roger E;
Steet, Richard;
Cathey, Sara S

Publication type:

Article

Novel FGFR3 mutations in exon 7 and implications for expanded screening of achondroplasia and hypochondroplasia: a response to Heuertz et al.

Published in:

2008

By:

Friez, Michael J.;
Wilson, Joseph A. P.

Publication type:

Letter

X‐Linked intellectual disability update 2022.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 1, p. 144, doi. 10.1002/ajmg.a.63008

By:

Schwartz, Charles E.;
Louie, Raymond J.;
Toutain, Annick;
Skinner, Cindy;
Friez, Michael J.;
Stevenson, Roger E.

Publication type:

Article

Mosaicism of common pathogenic MECP2 variants identified in two males with a clinical diagnosis of Rett syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 10, p. 2988, doi. 10.1002/ajmg.a.62913

By:

Cooley Coleman, Jessica A.;
Fee, Timothy;
Bend, Renee;
Louie, Raymond;
Annese, Fran;
Stallworth, Jennifer;
Worthington, Jessica;
Buchanan, Caroline Black;
Everman, David B.;
Skinner, Steven;
Friez, Michael J.;
Jones, Julie R.;
Spellicy, Catherine J.

Publication type:

Article

Schimke XLID syndrome results from a deletion in BCAP31.

Published in:

American Journal of Medical Genetics. Part A, 2020, v. 182, n. 9, p. 2168, doi. 10.1002/ajmg.a.61755

By:

Louie, Raymond J.;
Collins, Debra L.;
Friez, Michael J.;
Skinner, Cindy;
Schwartz, Charles E.;
Stevenson, Roger E.

Publication type:

Article

Clark‐Baraitser syndrome is associated with a nonsense alteration in the autosomal gene TRIP12.

Published in:

American Journal of Medical Genetics. Part A, 2020, v. 182, n. 3, p. 595, doi. 10.1002/ajmg.a.61443

By:

Louie, Raymond J.;
Friez, Michael J.;
Skinner, Cindy;
Baraitser, Michael;
Clark, Robin D.;
Schwartz, Charles E.;
Stevenson, Roger E.

Publication type:

Article

Biallelic deletions of the Waardenburg II syndrome gene, SOX10, cause a recognizable arthrogryposis syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2018, v. 176, n. 9, p. 1968, doi. 10.1002/ajmg.a.40362

By:

Stevenson, Roger E.;
Vincent, Victoria;
Spellicy, Catherine J.;
Friez, Michael J.;
Chaubey, Alka

Publication type:

Article

Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.

Published in:

American Journal of Medical Genetics. Part A, 2017, v. 173, n. 5, p. 1219, doi. 10.1002/ajmg.a.38144

By:

Louie, Raymond J.;
Tan, Queenie K.‐G.;
Gilner, Jennifer B.;
Rogers, R. Curtis;
Younge, Noelle;
Wechsler, Stephanie B.;
McDonald, Marie T.;
Gordon, Barbara;
Saski, Christopher A.;
Jones, Julie R.;
Chapman, Shelley J.;
Stevenson, Roger E.;
Sleasman, John W.;
Friez, Michael J.

Publication type:

Article

A Novel Familial Autosomal Dominant Mutation in ARID1B Causing Neurodevelopmental Delays, Short Stature, and Dysmorphic Features.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3313, doi. 10.1002/ajmg.a.37945

By:

Smith, Joshua A.;
Holden, Kenton R.;
Friez, Michael J.;
Jones, Julie R.;
Lyons, Michael J.

Publication type:

Article

Identification of a novel insertion mutation in FGFR3 that causes thanatophoric dysplasia type 1.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1573, doi. 10.1002/ajmg.a.37609

By:

Lindy, Amanda S.;
Basehore, Monica J.;
Munisha, Mumingjiang;
Williams, Aimee Leanne;
Friez, Michael J.;
Writzl, Karin;
Willems, Patrick;
Dougan, Scott T.

Publication type:

Article

Beyond Ohdo Syndrome: A Familial Missense Mutation Broadens the MED12 Spectrum.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3180, doi. 10.1002/ajmg.a.37354

By:

Langley, Katherine G.;
Brown, Jordan;
Gerber, Richard J.;
Fox, Janelle;
Friez, Michael J.;
Lyons, Michael;
Schrier Vergano, Samantha A.

Publication type:

Article

Truncating mutations in LRP4 lead to a prenatal lethal form of Cenani-Lenz syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2391, doi. 10.1002/ajmg.a.36647

By:

Lindy, Amanda S.;
Bupp, Caleb P.;
McGee, Stephen J.;
Steed, Erin;
Stevenson, Roger E.;
Basehore, Monica J.;
Friez, Michael J.

Publication type:

Article

The intellectual disabilities evaluation and advice system (IDEAS): Outcome of the first 55 cases.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 5, p. 1102, doi. 10.1002/ajmg.a.36456

By:

Hunter, Alasdair G.W.;
Graham, John M.;
Neri, Giovanni;
Rogers, R. Curtis;
Stevenson, Roger E.;
Turner, Gillian;
Friez, Michael J.

Publication type:

Article

MECP2 duplication: Possible cause of severe phenotype in females.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 4, p. 1029, doi. 10.1002/ajmg.a.36380

By:

Scott Schwoerer, Jessica;
Laffin, Jennifer;
Haun, Joanne;
Raca, Gordana;
Friez, Michael J.;
Giampietro, Philip F.

Publication type:

Article

Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphism.

Published in:

American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 5, p. 1109, doi. 10.1002/ajmg.a.33833

By:

Franek, Karl J.;
Butler, Julia;
Johnson, John;
Simensen, Richard;
Friez, Michael J.;
Bartel, Frank;
Moss, Tonya;
DuPont, Barbara;
Berry, Katherine;
Bauman, Margaret;
Skinner, Cindy;
Stevenson, Roger E.;
Schwartz, Charles E.

Publication type:

Article

A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.

Published in:

Brain: A Journal of Neurology, 2010, v. 133, n. 5, p. 1391, doi. 10.1093/brain/awq071

By:

Garbern, James Y.;
Neumann, Manuela;
Trojanowski, John Q.;
Lee, Virginia M.-Y.;
Feldman, Gerald;
Norris, Joy W.;
Friez, Michael J.;
Schwartz, Charles E.;
Stevenson, Roger;
Sima, Anders A. F.

Publication type:

Article

Recommendations by the ClinGen Rett/Angelman‐like expert panel for gene‐specific variant interpretation methods.

Published in:

Human Mutation, 2022, v. 43, n. 8, p. 1097, doi. 10.1002/humu.24302

By:

McKnight, Dianalee;
Bean, Lora;
Karbassi, Izabela;
Beattie, Katelynn;
Bienvenu, Thierry;
Bonin, Hope;
Fang, Ping;
Chrisodoulou, John;
Friez, Michael;
Helgeson, Maria;
Krishnaraj, Rahul;
Meng, Linyan;
Mighion, Lindsey;
Neul, Jeffrey;
Percy, Alan;
Ramsden, Simon;
Zoghbi, Huda;
Das, Soma

Publication type:

Article

Inside Back Cover, Volume 41, Issue 1.

Published in:

Human Mutation, 2020, v. 41, n. 1, p. ii, doi. 10.1002/humu.23967

By:

Hijazi, Hadia;
Coelho, Fernanda S.;
Gonzaga‐Jauregui, Claudia;
Bernardini, Laura;
Mar, Soe S.;
Manning, Melanie A.;
Hanson‐Kahn, Andrea;
Naidu, SakkuBai;
Srivastava, Siddharth;
Lee, Jennifer A.;
Jones, Julie R.;
Friez, Michael J.;
Alberico, Thomas;
Torres, Barbara;
Fang, Ping;
Cheung, Sau Wai;
Song, Xiaofei;
Davis‐Williams, Angelique;
Jornlin, Carly;
Wight, Patricia A.

Publication type:

Article