-
1مؤتمر
المؤلفون: Maria, Naomi I, Papoin, Julien, Raparia, Chirag, Sun, Zeguo, Josselsohn, Rachel, Lu, Ailing, Katerji, Hani, Syeda, Mahrukh M, Polsky, David, Paulson, Robert, Kalfa, Theodosia, Barnes, Betsy J, Zhang, Weijia, Blanc, Lionel, Davidson, Anne
المصدر: Cutaneous Lupus & Photosensitivity
-
2دورية أكاديمية
المؤلفون: Tu, Zhaowei, Fan, Cuiqing, Davis, Ashely K, Hu, Mengwen, Wang, Chen, Dandamudi, Akhila, Seu, Katie G, Kalfa, Theodosia A, Lu, Q Richard, Zheng, Yi
المصدر: Cell Reports. 40(2)
مصطلحات موضوعية: Biochemistry and Cell Biology, Biological Sciences, Hematology, Brain Disorders, Regenerative Medicine, Mental Health, Stem Cell Research - Nonembryonic - Non-Human, Stem Cell Research, Autism, Genetics, Intellectual and Developmental Disabilities (IDD), 1.1 Normal biological development and functioning, Underpinning research, Animals, Autistic Disorder, Chromatin, Cytokinesis, DNA-Binding Proteins, Erythroblasts, Mice, Tumor Suppressor Protein p53, rho GTP-Binding Proteins, CHD8, CP: Immunology, P53, Rho GTPases signaling, cytokinesis, erythroid differentiation, Medical Physiology, Biological sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/09x0w7gvTest
-
3دورية أكاديمية
المؤلفون: Sadaf, Alina, Dong, Min, Pfeiffer, Amanda, Korpik, Jennifer, Kalfa, Theodosia A., Latham, Teresa, Vinks, Alexander A., Ware, Russell E., Quinn, Charles T.
المصدر: British Journal of Haematology ; ISSN 0007-1048 1365-2141
-
4دورية أكاديميةMutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III
المؤلفون: Hernández, Gonzalo, Romero-Cortadellas, Lídia, Ferrer-Cortès, Xènia, Venturi, Veronica, Dessy-Rodriguez, Mercedes, Olivella, Mireia, Husami, Ammar, Pérez De Soto, Concepción, Morales-Camacho, Rosario M., Villegas, Ana, González-Fernández, Fernando-Ataulfo, Morado, Marta, Kalfa, Theodosia A., Quintana-Bustamante, Oscar, Pérez-Montero, Santiago, Tornador, Cristian, Segovia, Jose-Carlos, Sánchez, Mayka
الوقت: 61
العلاقة: Haematologica; 108;2; Hernández, Gonzalo; Romero-Cortadellas, Lídia; Ferrer-Cortès, Xènia [et al.]. Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III. Haematologica, 2023, 108(2), p. 581-587. Disponible en: . Fecha de acceso: 23 ene. 204. DOI:10.3324/haematol.2022.281277; http://hdl.handle.net/20.500.12328/3943Test; https://dx.doi.org/10.3324/haematol.2022.281277Test
الإتاحة: https://doi.org/20.500.12328/3943Test
https://doi.org/10.3324/haematol.2022.281277Test
https://hdl.handle.net/20.500.12328/3943Test -
5دورية أكاديمية
المؤلفون: Sekyonda, Zoe, An, Ran, Goreke, Utku, Man, Yuncheng, Monchamp, Karamoja, Bode, Allison, Zhang, Qiaochu, El-Gammal, Yasmin, Kityo, Cissy, Kalfa, Theodosia A., Akkus, Ozan, Gurkan, Umut A.
المساهمون: National Institute of Diabetes and Digestive and Kidney Diseases, American Society of Hematology, National Heart, Lung, and Blood Institute, National Institute of Biomedical Imaging and Bioengineering
المصدر: The Analyst ; volume 149, issue 9, page 2561-2572 ; ISSN 0003-2654 1364-5528
الإتاحة: https://doi.org/10.1039/d3an02071aTest
http://pubs.rsc.org/en/content/articlepdf/2024/AN/D3AN02071ATest -
6دورية أكاديمية
المؤلفون: Coppola, Tiziana, Hughes, Hannah, Finch, Paul T., Hess, Joshua A., Wu, Steve, Prada, Carlos E., Miethke, Alexander G., Zhang, Wenying, Kalfa, Theodosia A.
المصدر: Frontiers in Hematology ; volume 3 ; ISSN 2813-3935
-
7دورية أكاديميةInhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease.
المؤلفون: Noomuna, Panae, Risinger, Mary, Zhou, Sitong, Seu, Katie, Man, Yuncheng, An, Ran, Sheik, Daniel A, Wan, Jiandi, Little, Jane A, Gurkan, Umut A, Turrini, Francesco M, Kalfa, Theodosia, Low, Philip S
المصدر: British journal of haematology. 190(4)
مصطلحات موضوعية: Endothelium, Vascular, Erythrocyte Membrane, Erythrocytes, Abnormal, Plasma, Humans, Anemia, Sickle Cell, Sickle Cell Trait, beta-Thalassemia, Oxygen, Phosphotyrosine, Anion Exchange Protein 1, Erythrocyte, Hemoglobin, Sickle, Protein Kinase Inhibitors, Drug Evaluation, Preclinical, Cell Adhesion, Protein Processing, Post-Translational, Oxidative Stress, Phosphorylation, Erythrocyte Deformability, Cell-Derived Microparticles, Imatinib Mesylate, anion exchanger 1, erythrocyte membrane, haemoglobinopathy, sickle cell disease, tyrosine phosphorylation, Sickle Cell Disease, Rare Diseases, Pain Research, Hematology, Clinical Research, Cardiorespiratory Medicine and Haematology, Immunology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/4zm2120bTest
-
8دورية
المؤلفون: Harms, Frederike L., Rexach, Jessica Erin, Efthymiou, Stephanie, Aynekin, Busra, Per, Hüseyin, Güleç, Ayten, Nampoothiri, Sheela, Sampaio, Hugo, Sachdev, Rani, Stoeva, Radka, Myers, Kasiani, Pena, Loren D. M., Kalfa, Theodosia A., Chard, Marisa, Klassen, Megan, Pries, Megan, Kutsche, Kerstin
المصدر: European Journal of Human Genetics: EJHG; May 2024, Vol. 32 Issue: 5 p558-566, 9p
-
9دورية أكاديمية
المؤلفون: Al-Samkari, Hanny, Shehata, Nadine, Lang-Robertson, Kelly, Bianchi, Paola, Glenthøj, Andreas, Sheth, Sujit, Neufeld, Ellis J, Rees, David C, Chonat, Satheesh, Kuo, Kevin H M, Rothman, Jennifer A, Barcellini, Wilma, van Beers, Eduard J, Pospíšilová, Dagmar, Shah, Ami J, van Wijk, Richard, Glader, Bertil, Mañú Pereira, Maria Del Mar, Andres, Oliver, Kalfa, Theodosia A, Eber, Stefan W, Gallagher, Patrick G, Kwiatkowski, Janet L, Galacteros, Frédéric, Lander, Carl, Watson, Alejandra, Elbard, Riyad, Peereboom, Dore, Grace, Rachael F
المساهمون: Agios Pharmaceuticals
المصدر: The Lancet Haematology ; volume 11, issue 3, page e228-e239 ; ISSN 2352-3026
مصطلحات موضوعية: Hematology
الإتاحة: https://doi.org/10.1016/s2352-3026Test(23)00377-0
https://api.elsevier.com/content/article/PII:S2352302623003770?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2352302623003770?httpAccept=text/plainTest -
10دورية أكاديمية
المؤلفون: Kocoshis, Theodore S., Kalfa, Theodosia A., Miethke, Alexander G., Balistreri, William F., Seu, Katie G., Slaughter, Crystal G., Singh, Ruchi, Mullen, Mary, Kocoshis, Samuel A.
المصدر: Pediatric Research; Mar2024, Vol. 95 Issue 4, p1035-1040, 6p