Artykuły w czasopismach na temat „Collagen variants”
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Richards, Allan J., i Martin P. Snead. "Molecular Basis of Pathogenic Variants in the Fibrillar Collagens". Genes 13, nr 7 (4.07.2022): 1199. http://dx.doi.org/10.3390/genes13071199.
Pełny tekst źródłaKoch, M., B. Bohrmann, M. Matthison, C. Hagios, B. Trueb i M. Chiquet. "Large and small splice variants of collagen XII: differential expression and ligand binding." Journal of Cell Biology 130, nr 4 (15.08.1995): 1005–14. http://dx.doi.org/10.1083/jcb.130.4.1005.
Pełny tekst źródłaNishi, Akari, Hikaru Matsui, Azumi Hirata, Atsushi Mukaiyama, Shun-ichi Tanaka, Takuya Yoshizawa, Hiroyoshi Matsumura, Ryota Nomura, Kazuhiko Nakano i Kazufumi Takano. "Structure, Stability and Binding Properties of Collagen-Binding Domains from Streptococcus mutans". Chemistry 5, nr 3 (1.09.2023): 1911–20. http://dx.doi.org/10.3390/chemistry5030130.
Pełny tekst źródłaFlood, Veronica H., Abraham C. Schlauderaff, Paula M. Jacobi, Tricia L. Slobodianuk, Robert R. Montgomery, Sandra L. Haberichter i The Zimmerman Program Investigators. "VWF Interaction With Type IV Collagen Is Mediated Through Critical VWF A1 Domain Residues". Blood 122, nr 21 (15.11.2013): 29. http://dx.doi.org/10.1182/blood.v122.21.29.29.
Pełny tekst źródłaMikhail, Kristen A., Elizabeth VanSickle i Linda Z. Rossetti. "Milder presentation of osteogenesis imperfecta type VIII due to compound heterozygosity for a predicted loss-of-function variant and novel missense variant inP3H1—further expansion of the phenotypic spectrum". Molecular Case Studies 9, nr 1 (luty 2023): a006260. http://dx.doi.org/10.1101/mcs.a006260.
Pełny tekst źródłaMicale, Lucia, Silvia Morlino, Annalisa Schirizzi, Emanuele Agolini, Grazia Nardella, Carmela Fusco, Stefano Castellana i in. "Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia". Genes 11, nr 12 (17.12.2020): 1513. http://dx.doi.org/10.3390/genes11121513.
Pełny tekst źródłaShida, Yasuaki, Christine Brown, Jeff Mewburn, Kate Sponagle, Ozge Danisment, Barbara Vidal, Carol A. Heagadorn i David Lillicrap. "Comprehensive In Vitro and In Vivo Characterization of Loss and Gain-of-Function Von Willebrand Factor Collagen Binding Variants Using a Mouse Model System",. Blood 118, nr 21 (18.11.2011): 3266. http://dx.doi.org/10.1182/blood.v118.21.3266.3266.
Pełny tekst źródłaLópez-Márquez, Arístides, Matías Morín, Sergio Fernández-Peñalver, Carmen Badosa, Alejandro Hernández-Delgado, Daniel Natera-de Benito, Carlos Ortez i in. "CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant COL6A1 Pathogenic Variant Improves Collagen VI Network in Patient Fibroblasts". International Journal of Molecular Sciences 23, nr 8 (16.04.2022): 4410. http://dx.doi.org/10.3390/ijms23084410.
Pełny tekst źródłaZhytnik, Lidiia, Binh Ho Duy, Marelise Eekhoff, Lisanne Wisse, Gerard Pals, Ene Reimann, Sulev Kõks i in. "Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive P3H1 Pathogenic Variant". Genes 13, nr 3 (24.02.2022): 407. http://dx.doi.org/10.3390/genes13030407.
Pełny tekst źródłaJäälinoja, Juha, Joni Ylöstalo, William Beckett, David J. S. Hulmes i Leena Ala-Kokko. "Trimerization of collagen IX α-chains does not require the presence of the COL1 and NC1 domains". Biochemical Journal 409, nr 2 (21.12.2007): 545–54. http://dx.doi.org/10.1042/bj20070984.
Pełny tekst źródłaNixon, Thomas R. W., Allan J. Richards, Howard Martin, Philip Alexander i Martin P. Snead. "Autosomal Recessive Stickler Syndrome". Genes 13, nr 7 (24.06.2022): 1135. http://dx.doi.org/10.3390/genes13071135.
Pełny tekst źródłaHayashi, Kaichi, Takeaki Ikeuchi, Ryo Morishita, Jun Qian, Kenji Kojima, Teisuke Takita, Keisuke Tanaka, Shunji Hattori i Kiyoshi Yasukawa. "The roles of histidine and tyrosine residues in the active site of collagenase in Grimontia hollisae". Journal of Biochemistry 168, nr 4 (9.05.2020): 385–92. http://dx.doi.org/10.1093/jb/mvaa055.
Pełny tekst źródłaCastroflorio, Enrico, Ana Joaquina Pérez Berná, Arístides López-Márquez, Carmen Badosa, Pablo Loza-Alvarez, Mónica Roldán i Cecilia Jiménez-Mallebrera. "The Capillary Morphogenesis Gene 2 Triggers the Intracellular Hallmarks of Collagen VI-Related Muscular Dystrophy". International Journal of Molecular Sciences 23, nr 14 (11.07.2022): 7651. http://dx.doi.org/10.3390/ijms23147651.
Pełny tekst źródłaPadmanabha, Hansashree, Gautham Arunachal, Pratik Kishore, P. Praveen Sharma, Pooja Mailankody, Rohan R. Mahale, Saraswati Nashi, PS Mathuranath i Sadanandavalli R. Chandra. "Collagen XII-Related Myopathy: An Emerging Spectrum of Extracellular Matrix-Related Myopathy". Neurology India 71, nr 6 (2023): 1257–59. http://dx.doi.org/10.4103/0028-3886.391402.
Pełny tekst źródłaBauer, Anina, John F. Bateman, Shireen R. Lamandé, Eric Hanssen, Shannon G. M. Kirejczyk, Mark Yee, Ali Ramiche i in. "Identification of Two Independent COL5A1 Variants in Dogs with Ehlers–Danlos Syndrome". Genes 10, nr 10 (21.09.2019): 731. http://dx.doi.org/10.3390/genes10100731.
Pełny tekst źródłaTohar, Ran, Tamar Ansbacher, Inbal Sher, Livnat Afriat-Jurnou, Evgeny Weinberg i Maayan Gal. "Screening Collagenase Activity in Bacterial Lysate for Directed Enzyme Applications". International Journal of Molecular Sciences 22, nr 16 (9.08.2021): 8552. http://dx.doi.org/10.3390/ijms22168552.
Pełny tekst źródłaHaberichter, Sandra L., David A. Jakab i Paula M. Jacobi. "Upstream Mechanisms Causing Type 1C Von Willebrand Disease (VWD): Contribution Of Defective Von Willebrand Factor (VWF) Multimerization, Regulated Storage, and Secretion". Blood 122, nr 21 (15.11.2013): 3571. http://dx.doi.org/10.1182/blood.v122.21.3571.3571.
Pełny tekst źródłaZekavat, Seyedeh Maryam, Elizabeth L. Chou, Melica Zekavat, Akhil Pampana, Kaavya Paruchuri, Christian Lacks Lino Cardenas, Satoshi Koyama i in. "Fibrillar Collagen Variants in Spontaneous Coronary Artery Dissection". JAMA Cardiology 7, nr 4 (1.04.2022): 396. http://dx.doi.org/10.1001/jamacardio.2022.0001.
Pełny tekst źródłaMarinella, Gemma, Guja Astrea, Bianca Buchignani, Denise Cassandrini, Stefano Doccini, Massimiliano Filosto, Daniele Galatolo i in. "A Schematic Approach to Defining the Prevalence of COL VI Variants in Five Years of Next-Generation Sequencing". International Journal of Molecular Sciences 23, nr 23 (23.11.2022): 14567. http://dx.doi.org/10.3390/ijms232314567.
Pełny tekst źródłaKiener, Sarah, Heather Troyer, Daniel Ruvolo, Paula Grest, Sara Soto, Anna Letko, Vidhya Jagannathan i in. "Independent COL17A1 Variants in Cats with Junctional Epidermolysis Bullosa". Genes 14, nr 10 (22.09.2023): 1835. http://dx.doi.org/10.3390/genes14101835.
Pełny tekst źródłaSelvam, Pavalan, Shekhar Singh, Angita Jain, Herjot Atwal i Paldeep S. Atwal. "Novel COL11A2 Pathogenic Variants in a Child with Autosomal Recessive Otospondylomegaepiphyseal Dysplasia: A Review of the Literature". Journal of Pediatric Genetics 09, nr 02 (16.10.2019): 117–20. http://dx.doi.org/10.1055/s-0039-1698446.
Pełny tekst źródłaKiener, Sarah, Neoklis Apostolopoulos, Jennifer Schissler, Pascal-Kolja Hass, Fabienne Leuthard, Vidhya Jagannathan, Carole Schuppisser i in. "Independent COL5A1 Variants in Cats with Ehlers-Danlos Syndrome". Genes 13, nr 5 (29.04.2022): 797. http://dx.doi.org/10.3390/genes13050797.
Pełny tekst źródłaO'Connell, Kevin, Michael Posthumus i Malcolm Collins. "Collagen gene interactions and endurance running performance". South African Journal of Sports Medicine 26, nr 1 (20.03.2014): 9. http://dx.doi.org/10.17159/2413-3108/2014/v26i1a404.
Pełny tekst źródłaBrown, J. C., K. Mann, H. Wiedemann i R. Timpl. "Structure and binding properties of collagen type XIV isolated from human placenta." Journal of Cell Biology 120, nr 2 (15.01.1993): 557–67. http://dx.doi.org/10.1083/jcb.120.2.557.
Pełny tekst źródłaBruni, Valentina, Cristina Barbara Spoleti, Andrea La Barbera, Vincenzo Dattilo, Emma Colao, Carmela Votino, Emanuele Bellacchio, Nicola Perrotti, Sabrina Giglio i Rodolfo Iuliano. "A Novel Splicing Variant of COL2A1 in a Fetus with Achondrogenesis Type II: Interpretation of Pathogenicity of In-Frame Deletions". Genes 12, nr 9 (10.09.2021): 1395. http://dx.doi.org/10.3390/genes12091395.
Pełny tekst źródłaShulman, Cole, Emerald Liang, Misato Kamura, Khalil Udwan, Tony Yao, Daniel Cattran, Heather Reich i in. "Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic Variants". Kidney Medicine 3, nr 2 (marzec 2021): 257–66. http://dx.doi.org/10.1016/j.xkme.2020.12.007.
Pełny tekst źródłaPowell, Janet T., Jane Adamson, Shane T. R. MacSweeney, Roger M. Greenhalgh, Steven E. Humphries i Adriano Henney. "Genetic variants of collagen III and abdominal aortic aneurysm". European Journal of Vascular Surgery 5, nr 2 (kwiecień 1991): 145–48. http://dx.doi.org/10.1016/s0950-821x(05)80679-6.
Pełny tekst źródłaSykes, B., D. Ogilvie, P. Wordsworth i R. Smith. "Polymorphic variants of the human type II collagen gene". Bone 7, nr 2 (styczeń 1986): 150. http://dx.doi.org/10.1016/8756-3282(86)90705-2.
Pełny tekst źródłaDada, Suhail, Marilize C. Burger, Franka Massij, Hanli de Wet i Malcolm Collins. "Carpal tunnel syndrome: The role of collagen gene variants". Gene 587, nr 1 (sierpień 2016): 53–58. http://dx.doi.org/10.1016/j.gene.2016.04.030.
Pełny tekst źródłaLanktree, Matthew B., Amirreza Haghighi, Saima Khowaja, Ioan-Andrei Iliuta, Andrew Paterson i York P. Pei. "Type IV Collagen Variants in Patients With Polycystic Kidneys". Journal of the American Society of Nephrology 33, nr 11S (listopad 2022): 152. http://dx.doi.org/10.1681/asn.20223311s1152a.
Pełny tekst źródłaShulman, Cole, Emerald Liang, Misato Kamura, Khalil Udwan, Tony Yao, Daniel C. Cattran, Heather N. Reich i in. "In Silico Prediction Performance for Type IV Collagen Variants". Journal of the American Society of Nephrology 31, nr 10S (październik 2020): 526–27. http://dx.doi.org/10.1681/asn.20203110s1526d.
Pełny tekst źródłaGraves, Lara E., Christie-Lee Wall, Julie N. Briody, Bruce Bennetts, Karen Wong, Ella Onikul, Andrew Biggin i Craig F. Munns. "High Bone Mineral Density Osteogenesis Imperfecta in a Family with a Novel Pathogenic Variant in COL1A2". Hormone Research in Paediatrics 93, nr 4 (2020): 263–71. http://dx.doi.org/10.1159/000510463.
Pełny tekst źródłaTang, Man-Hung Eric, Joseph P. M. Blair, Cecilie Liv Bager, Anne-Christine Bay-Jensen, Kim Henriksen, Claus Christiansen i Morten Asser Karsdal. "Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia". Neurology Genetics 6, nr 5 (10.09.2020): e508. http://dx.doi.org/10.1212/nxg.0000000000000508.
Pełny tekst źródłaRitelli, Marco, Valeria Cinquina, Marina Venturini, Letizia Pezzaioli, Anna Formenti, Nicola Chiarelli i Marina Colombi. "Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome". Genes 10, nr 2 (12.02.2019): 135. http://dx.doi.org/10.3390/genes10020135.
Pełny tekst źródłaSivapalaratnam, Suthesh, Hayman Melissa, Claire Lentaigne, Melissa Chan, Marilena Crescente, Harriet Allan, Katherine Wedderburn i in. "Congenital Aspirin-like Defect As a Result of Autosomal Recessive Variants in PTGS1". Blood 132, Supplement 1 (29.11.2018): 1156. http://dx.doi.org/10.1182/blood-2018-99-118958.
Pełny tekst źródłaAbdulla, Farah, Heather Peck, Ashley Feneran, Ashley Jenkins i Katherine Mullersman. "Distinguishing a Rare Variant of Lipidized Dermatofibroma from Nonlipidized Dermatofibromas in a Patient with Hypothyroidism and Alopecia Areata". Serbian Journal of Dermatology and Venereology 9, nr 2 (27.06.2017): 53–56. http://dx.doi.org/10.1515/sjdv-2017-0008.
Pełny tekst źródłaSavige, Judy, Helen Storey, Elizabeth Watson, Jens Michael Hertz, Constantinos Deltas, Alessandra Renieri, Francesca Mari i in. "Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria". European Journal of Human Genetics 29, nr 8 (15.04.2021): 1186–97. http://dx.doi.org/10.1038/s41431-021-00858-1.
Pełny tekst źródłaBarbeau, Susie, Fannie Semprez, Alexandre Dobbertin, Laurine Merriadec, Florine Roussange, Bruno Eymard, Damien Sternberg i in. "Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ". International Journal of Molecular Sciences 24, nr 22 (11.11.2023): 16217. http://dx.doi.org/10.3390/ijms242216217.
Pełny tekst źródłaChiarelli, Ritelli, Zoppi i Colombi. "Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes". Genes 10, nr 8 (12.08.2019): 609. http://dx.doi.org/10.3390/genes10080609.
Pełny tekst źródłaHoyer, M., N. Drechsel, M. Meyer, C. Meier, C. Hinüber, A. Breier, J. Hahner i in. "Embroidered polymer–collagen hybrid scaffold variants for ligament tissue engineering". Materials Science and Engineering: C 43 (październik 2014): 290–99. http://dx.doi.org/10.1016/j.msec.2014.07.010.
Pełny tekst źródłaVillar-Quiles, Rocío N., Sandra Donkervoort, Alix de Becdelièvre, Corine Gartioux, Valérie Jobic, A. Reghan Foley, Riley M. McCarty i in. "Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related Myopathies". Journal of Neuromuscular Diseases 8, nr 4 (30.07.2021): 633–45. http://dx.doi.org/10.3233/jnd-200577.
Pełny tekst źródłaAksenova, M. E., P. E. Povilaitite, N. E. Konkova i V. V. Dlin. "Diagnostic Value of Type IV Collagen Expression in Renal Glomeruli at Alport’s Syndrome". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 65, nr 6 (22.01.2021): 42–49. http://dx.doi.org/10.21508/1027-4065-2020-65-6-42-49.
Pełny tekst źródłaNowak, Agata A., Kevin Canis, Anne Riddell, Michael A. Laffan i Thomas A. J. McKinnon. "O-linked glycosylation of von Willebrand factor modulates the interaction with platelet receptor glycoprotein Ib under static and shear stress conditions". Blood 120, nr 1 (5.07.2012): 214–22. http://dx.doi.org/10.1182/blood-2012-02-410050.
Pełny tekst źródłaAngwin, Chloe, Angela F. Brady, Marina Colombi, David J. P. Ferguson, Rebecca Pollitt, F. Michael Pope, Marco Ritelli, Sofie Symoens, Neeti Ghali i Fleur S. van Dijk. "Absence of Collagen Flowers on Electron Microscopy and Identification of (Likely) Pathogenic COL5A1 Variants in Two Patients". Genes 10, nr 10 (27.09.2019): 762. http://dx.doi.org/10.3390/genes10100762.
Pełny tekst źródłaDeltas, Constantinos, Gregory Papagregoriou, Stavroula F. Louka, Apostolos Malatras, Frances Flinter, Daniel P. Gale, Susie Gear i in. "Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice". Genes 14, nr 9 (25.08.2023): 1686. http://dx.doi.org/10.3390/genes14091686.
Pełny tekst źródłaTešanović Perković, Deša, Zrinka Bukvić Mokos i Branka Marinović. "Epidermolysis Bullosa Acquisita—Current and Emerging Treatments". Journal of Clinical Medicine 12, nr 3 (1.02.2023): 1139. http://dx.doi.org/10.3390/jcm12031139.
Pełny tekst źródłaMiyamoto-Mikami, Eri, Hiroshi Kumagai, Naoki Kikuchi, Nobuhiro Kamiya, Naokazu Miyamoto i Noriyuki Fuku. "eQTL variants in COL22A1 are associated with muscle injury in athletes". Physiological Genomics 52, nr 12 (1.12.2020): 588–89. http://dx.doi.org/10.1152/physiolgenomics.00115.2020.
Pełny tekst źródłaKantaputra, Piranit Nik, Salita Angkurawaranon, Worrachet Intachai, Chumpol Ngamphiw, Bjorn Olsen, Sissades Tongsima, Timothy C. Cox i James R. Ketudat Cairns. "A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII". Genes 14, nr 2 (26.01.2023): 322. http://dx.doi.org/10.3390/genes14020322.
Pełny tekst źródłaZhytnik, Lidiia, Katre Maasalu, Binh Ho Duy, Andrey Pashenko, Sergey Khmyzov, Ene Reimann, Ele Prans, Sulev Kõks i Aare Märtson. "De novo and inherited pathogenic variants in collagen‐related osteogenesis imperfecta". Molecular Genetics & Genomic Medicine 7, nr 3 (24.01.2019): e559. http://dx.doi.org/10.1002/mgg3.559.
Pełny tekst źródłaChoi, Soon-Il, Se-Joon Woo, Baek-Lok Oh, Jinu Han, Hyun-Taek Lim, Byung-Joo Lee, Kwangsic Joo i in. "Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1". Genes 12, nr 10 (5.10.2021): 1578. http://dx.doi.org/10.3390/genes12101578.
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