المؤلفون: Isabella Silins, Adrian Moreno, Anders Wall, Franklin Aigbirhio, Mark Gurnell, Morris Brown, Sara Roslin, Gunnar Antoni, Per Hellman, Anders Sundin, Mark Lubberink

المصدر: EJNMMI Research, Vol 14, Iss 1, Pp 1-7 (2024)

مصطلحات موضوعية: [18F]CETO, Positron emission tomography, Primary aldosteronism, Adrenal, Tumour, Adenoma, Medical physics. Medical radiology. Nuclear medicine, R895-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2191-219X

URL الوصول: https://doaj.org/article/d628e206005c408e88ea115660ee12aa

المؤلفون: Flaviu Bulat, Friederike Hesse, Bala Attili, Chandra Solanki, Iosif A. Mendichovszky, Franklin Aigbirhio, Finian J. Leeper, Kevin M. Brindle, André A. Neves

المصدر: Cancers, Vol 15, Iss 5, p 1564 (2023)

مصطلحات موضوعية: cell death, apoptosis, tumor, imaging, C2Am, TRAIL-R2, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2072-6694/15/5/1564; https://doaj.org/toc/2072-6694

URL الوصول: https://doaj.org/article/9a036bceb1624dddbb1c7bcf9cd9cd1b

المؤلفون: Flaviu Bulat, Friederike Hesse, De-En Hu, Susana Ros, Connor Willminton-Holmes, Bangwen Xie, Bala Attili, Dmitry Soloviev, Franklin Aigbirhio, Finian. J. Leeper, Kevin M. Brindle, André A. Neves

المصدر: EJNMMI Research, Vol 10, Iss 1, Pp 1-14 (2020)

مصطلحات موضوعية: Cell death, PET, C2Am, Synaptotagmin-I, Tumor, TRAILR2, Medical physics. Medical radiology. Nuclear medicine, R895-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2191-219X

URL الوصول: https://doaj.org/article/e21d4f55168b4903adafd4356cd7f69c

المؤلفون: Katalin Solti, Wei-Li Kuan, Balázs Fórizs, Gergely Kustos, Judith Mihály, Zoltán Varga, Balázs Herberth, Éva Moravcsik, Róbert Kiss, Manuela Kárpáti, Anna Mikes, Yanyan Zhao, Tímea Imre, Jean-Christophe Rochet, Franklin Aigbirhio, Caroline H. Williams-Gray, Roger A. Barker, Gergely Tóth

المصدر: Neurobiology of Disease, Vol 142, Iss , Pp 104971- (2020)

مصطلحات موضوعية: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0969996120302461; https://doaj.org/toc/1095-953X

URL الوصول: https://doaj.org/article/cf8c2877f3424441a63e97e4ed53e2dd

المؤلفون: Katalin Solti, Wei-Li Kuan, Balázs Fórizs, Gergely Kustos, Judith Mihály, Zoltán Varga, Balázs Herberth, Éva Moravcsik, Róbert Kiss, Manuela Kárpáti, Anna Mikes, Yanyan Zhao, Tímea Imre, Jean-Christophe Rochet, Franklin Aigbirhio, Caroline H. Williams-Gray, Roger A. Barker, Gergely Tóth

المصدر: Neurobiology of Disease, Vol 134, Iss , Pp - (2020)

مصطلحات موضوعية: DJ-1, Parkinson's, Alzheimer's, Aggregation, Amyloid, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0969996119303043; https://doaj.org/toc/1095-953X

URL الوصول: https://doaj.org/article/c118d4f98c9b470dac01ee0fb27ed0a7

المؤلفون: Alessandra Cavaliere, Katrin C. Probst, Stephen J. Paisey, Christopher Marshall, Abdul K. H. Dheere, Franklin Aigbirhio, Christopher McGuigan, Andrew D. Westwell

المصدر: Molecules, Vol 25, Iss 3, p 704 (2020)

مصطلحات موضوعية: fluorination, protides, fluorine-18, radiolabelling, pet imaging, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/25/3/704; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/2e11479901e84c4b8e768815c561ddf1

المؤلفون: Probst FJ; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., James RA; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Burrage LC; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Bohan TP; Department of Neurology, Memorial Hermann Texas Medical Center, Houston, TX, USA., Ward Melver CH; Genetic Center, Children's Hospital Medical Center Of Akron, Akron, OH, USA., Magoulas P; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Austin E; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Franklin AI; Department of Developmental Pediatrics, Texas Children's Hospital, Houston, TX, USA., Azamian M; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Xia F; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Patel A; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Bacino C; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Belmont JW; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Ware SM; Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA., Shaw C; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Cheung SW; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA., Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, MS BCM225, Houston, TX, USA. seemal@bcm.tmc.edu.

المصدر: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2015 Jun 14; Vol. 10, pp. 75. Date of Electronic Publication: 2015 Jun 14.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 17/*genetics , Heart Defects, Congenital/*genetics, Child, Preschool ; Chromosome Deletion ; DNA Copy Number Variations/genetics ; Female ; Genetic Predisposition to Disease ; Humans ; Infant ; Infant, Newborn ; Male

المؤلفون: Wiszniewski W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Hunter JV, Hanchard NA, Willer JR, Shaw C, Tian Q, Illner A, Wang X, Cheung SW, Patel A, Campbell IM, Gelowani V, Hixson P, Ester AR, Azamian MS, Potocki L, Zapata G, Hernandez PP, Ramocki MB, Santos-Cortez RL, Wang G, York MK, Justice MJ, Chu ZD, Bader PI, Omo-Griffith L, Madduri NS, Scharer G, Crawford HP, Yanatatsaneejit P, Eifert A, Kerr J, Bacino CA, Franklin AI, Goin-Kochel RP, Simpson G, Immken L, Haque ME, Stosic M, Williams MD, Morgan TM, Pruthi S, Omary R, Boyadjiev SA, Win KK, Thida A, Hurles M, Hibberd ML, Khor CC, Van Vinh Chau N, Gallagher TE, Mutirangura A, Stankiewicz P, Beaudet AL, Maletic-Savatic M, Rosenfeld JA, Shaffer LG, Davis EE, Belmont JW, Dunstan S, Simmons CP, Bonnen PE, Leal SM, Katsanis N, Lupski JR, Lalani SR

المصدر: American journal of human genetics [Am J Hum Genet] 2013 Aug 08; Vol. 93 (2), pp. 197-210. Date of Electronic Publication: 2013 Jun 27.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Base Sequence* , Genetic Predisposition to Disease* , Sequence Deletion*, Aging, Premature/*genetics , Language Development Disorders/*genetics , Leukoencephalopathies/*genetics , Tetraspanins/*genetics, Age of Onset ; Aging, Premature/complications ; Aging, Premature/ethnology ; Aging, Premature/pathology ; Asian People ; Brain/metabolism ; Brain/pathology ; Child ; Child, Preschool ; Chromosomes, Human, Pair 2 ; Exons ; Female ; Humans ; Language Development Disorders/complications ; Language Development Disorders/ethnology ; Language Development Disorders/pathology ; Leukoencephalopathies/complications ; Leukoencephalopathies/ethnology ; Leukoencephalopathies/pathology ; Magnetic Resonance Imaging ; Male ; Molecular Sequence Data ; Pedigree ; Sequence Analysis, DNA

المؤلفون: Franklin AI; Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK S3 7HF., Bensa D, Adams H, Coldham I

المصدر: Organic & biomolecular chemistry [Org Biomol Chem] 2011 Mar 21; Vol. 9 (6), pp. 1901-7. Date of Electronic Publication: 2011 Jan 31.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101154995 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-0539 (Electronic) Linking ISSN: 14770520 NLM ISO Abbreviation: Org Biomol Chem Subsets: MEDLINE

مواضيع طبية MeSH: Alkaloids/*chemical synthesis , Bridged-Ring Compounds/*chemical synthesis, Crystallography, X-Ray ; Cyclization ; Models, Molecular ; Molecular Structure