المؤلفون: Dionne O; Biochemistry and Functional Genomic Department, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Canada. Electronic address: olivier.dionne@usherbrooke.ca., Abolghasemi A; Biochemistry and Functional Genomic Department, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Canada., Corbin F; Biochemistry and Functional Genomic Department, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Canada., Çaku A; Biochemistry and Functional Genomic Department, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Canada.

المصدر: Psychiatry research [Psychiatry Res] 2024 Jul; Vol. 337, pp. 115962. Date of Electronic Publication: 2024 May 16.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Ireland NLM ID: 7911385 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7123 (Electronic) Linking ISSN: 01651781 NLM ISO Abbreviation: Psychiatry Res Subsets: MEDLINE

مواضيع طبية MeSH: Fragile X Syndrome*/metabolism , Fragile X Syndrome*/physiopathology , Endocannabinoids*/metabolism, Humans ; Animals ; Metabolic Networks and Pathways ; Fragile X Mental Retardation Protein/genetics ; Fragile X Mental Retardation Protein/metabolism

المؤلفون: Verpeut JL; Department of Psychology, Arizona State University, Tempe, United States.

المصدر: ELife [Elife] 2024 Jul 16; Vol. 13. Date of Electronic Publication: 2024 Jul 16.

نوع المنشور: Journal Article; Editorial

بيانات الدورية: Publisher: eLife Sciences Publications, Ltd Country of Publication: England NLM ID: 101579614 Publication Model: Electronic Cited Medium: Internet ISSN: 2050-084X (Electronic) Linking ISSN: 2050084X NLM ISO Abbreviation: Elife Subsets: MEDLINE

مواضيع طبية MeSH: Fragile X Syndrome*/physiopathology , Cerebellum*/physiology , Disease Models, Animal* , Learning*, Animals ; Mice ; Fragile X Mental Retardation Protein/genetics ; Fragile X Mental Retardation Protein/metabolism

المؤلفون: Le Poulennec T; Departement of Endocrinology and Reproductive Medicine, centre de référence des maladies endocriniennes rares de la croissance et du développement, centre de référence des pathologies gynécologiques rares, IE3M, hôpital Pitié-Salpêtrière, AP-HP, Paris, France; Sorbonne université médecine, Paris, France; Hôpital Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France. Electronic address: tiphaine.lepoulennec@aphp.fr., Dubreuil S; Departement of Endocrinology and Reproductive Medicine, centre de référence des maladies endocriniennes rares de la croissance et du développement, centre de référence des pathologies gynécologiques rares, IE3M, hôpital Pitié-Salpêtrière, AP-HP, Paris, France; Sorbonne université médecine, Paris, France; Hôpital Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France., Grynberg M; Departement of Reproductive Medicine Clamart, hôpital Béclère, AP-HP, France; Hôpital Béclère, 157, rue de la Porte-de-Trivaux, 92140 Clamart, France., Chabbert-Buffet N; Departement of Obstetrics Gynecology and Reproductive Medicine, hôpital Tenon, AP-HP, Sorbonne université médecine, Paris, France; Hôpital Tenon, 4, rue de la Chine, 75020 Paris, France., Sermondade N; Hôpital Tenon, 4, rue de la Chine, 75020 Paris, France; Departement of Reproductive Biology, hôpital Tenon, AP-HP, Sorbonne université médecine, Paris, France., Fourati S; Sorbonne université médecine, Paris, France; Hôpital Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France; Departement of Endocrine Biochemistry and oncology, hôpital Pitié-Salpêtrière-Charles-Foix, AP-HP, Paris, France., Siffroi JP; Genetics Departement, Inserm UMR_S_933, hôpital Armand-Trousseau, AP-HP, Paris, France; Hôpital Armand-Trousseau, 26, avenue du Dr Arnold-Netter, 75012 Paris, France., Héron D; Genetics Department, hôpital Pitié-Salpêtrière, AP-HP, Paris, France; Hôpital Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France., Bachelot A; Departement of Endocrinology and Reproductive Medicine, centre de référence des maladies endocriniennes rares de la croissance et du développement, centre de référence des pathologies gynécologiques rares, IE3M, hôpital Pitié-Salpêtrière, AP-HP, Paris, France; Sorbonne université médecine, Paris, France; Hôpital Pitié-Salpêtrière, 47-83, boulevard de l'Hôpital, 75013 Paris, France.

المصدر: Annales d'endocrinologie [Ann Endocrinol (Paris)] 2024 Jul; Vol. 85 (4), pp. 269-275. Date of Electronic Publication: 2024 May 01.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: France NLM ID: 0116744 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2213-3941 (Electronic) Linking ISSN: 00034266 NLM ISO Abbreviation: Ann Endocrinol (Paris) Subsets: MEDLINE

مواضيع طبية MeSH: Fragile X Mental Retardation Protein*/genetics , Ovarian Reserve*/physiology , Ovarian Reserve*/genetics , Primary Ovarian Insufficiency*/genetics , Fertility Preservation*/methods, Humans ; Female ; Adult ; Retrospective Studies ; Pregnancy ; Mutation ; Fragile X Syndrome/genetics ; Fragile X Syndrome/epidemiology ; Infertility, Female/genetics ; Infertility, Female/etiology ; Infertility, Female/therapy ; Cohort Studies ; Anti-Mullerian Hormone/blood

المؤلفون: Wang F; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, U.S.A., Mehta P; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, U.S.A., Bach I; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA 01605, U.S.A.

المصدر: Biochemical Society transactions [Biochem Soc Trans] 2024 Jun 26; Vol. 52 (3), pp. 1099-1107.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Portland Press On The Behalf Of The Biochemical Society Country of Publication: England NLM ID: 7506897 Publication Model: Print Cited Medium: Internet ISSN: 1470-8752 (Electronic) Linking ISSN: 03005127 NLM ISO Abbreviation: Biochem Soc Trans Subsets: MEDLINE

مواضيع طبية MeSH: RNA, Long Noncoding*/genetics , RNA, Long Noncoding*/metabolism , Ubiquitin-Protein Ligases*/metabolism , Ubiquitin-Protein Ligases*/genetics , X Chromosome Inactivation*, Animals ; Female ; Mice ; Gene Expression Regulation, Developmental ; X Chromosome/genetics ; X Chromosome/metabolism

المؤلفون: Sandoval SO; Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Department of Neuroscience, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI, 53705, USA., Méndez-Albelo NM; Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Department of Neuroscience, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Molecular Cellular Pharmacology Training Program, University of Wisconsin-Madison, Madison, WI, 53705, USA., Xu Z; Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Department of Neuroscience, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.; Graduate Program in Cell and Molecular Biology, University of Wisconsin-Madison, Madison, WI, 53705, USA., Zhao X; Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA. xinyu.zhao@wisc.edu.; Department of Neuroscience, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA. xinyu.zhao@wisc.edu.

المصدر: Journal of neurodevelopmental disorders [J Neurodev Disord] 2024 Jun 13; Vol. 16 (1), pp. 30. Date of Electronic Publication: 2024 Jun 13.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Internet ISSN: 1866-1955 (Electronic) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: MEDLINE

مواضيع طبية MeSH: Disease Models, Animal* , Fragile X Syndrome*/genetics , Fragile X Syndrome*/physiopathology, Animals ; Humans ; Fragile X Mental Retardation Protein/genetics ; Pluripotent Stem Cells

المؤلفون: Liu S; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Zhang X; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Yao X; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Wang G; Comprehensive Cancer Center, Beckman Research Institute, City of Hope Medical Center, Duarte, CA, USA.; Department of Molecular & Cellular Endocrinology, Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA, USA., Huang S; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Chen P; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Tang M; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Cai J; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China.; Clinical Research Center, the Affiliated Hospital of Guizhou Medical University, Guiyang, China., Wu Z; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Zhang Y; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Xu R; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Liu K; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., He K; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.; University of Chinese Academy of Sciences, Beijing, China., Wang Y; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China., Jiang L; Comprehensive Cancer Center, Beckman Research Institute, City of Hope Medical Center, Duarte, CA, USA.; Department of Molecular & Cellular Endocrinology, Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA, USA., Wang QA; Comprehensive Cancer Center, Beckman Research Institute, City of Hope Medical Center, Duarte, CA, USA.; Department of Molecular & Cellular Endocrinology, Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA, USA., Rui L; Department of Molecular and Integrative Physiology, the University of Michigan Medical School, Ann Arbor, MI, USA., Liu J; Cellular Signaling Laboratory, Key Laboratory of Molecular Biophysics of Ministry of Education, Huazhong University of Science and Technology, Wuhan, China., Liu Y; Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences; TaiKang Center for Life and Medical Sciences; the Institute for Advanced Studies; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China. liuyong31279@whu.edu.cn.

المصدر: Nature cell biology [Nat Cell Biol] 2024 Jun; Vol. 26 (6), pp. 917-931. Date of Electronic Publication: 2024 May 07.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Macmillan Magazines Ltd Country of Publication: England NLM ID: 100890575 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-4679 (Electronic) Linking ISSN: 14657392 NLM ISO Abbreviation: Nat Cell Biol Subsets: MEDLINE

مواضيع طبية MeSH: Protein Serine-Threonine Kinases*/metabolism , Protein Serine-Threonine Kinases*/genetics , Endoribonucleases*/metabolism , Endoribonucleases*/genetics , X-Box Binding Protein 1*/metabolism , X-Box Binding Protein 1*/genetics , Endoplasmic Reticulum Stress*, Humans ; Animals ; RNA Splicing ; DNA-Binding Proteins/metabolism ; DNA-Binding Proteins/genetics ; Endoplasmic Reticulum/metabolism ; Endoplasmic Reticulum/genetics ; Stress Granules/metabolism ; Stress Granules/genetics ; Regulatory Factor X Transcription Factors/metabolism ; Regulatory Factor X Transcription Factors/genetics ; Transcription Factors/metabolism ; Transcription Factors/genetics ; Unfolded Protein Response ; Mice ; HeLa Cells ; Cytoplasmic Granules/metabolism ; Cytoplasmic Granules/genetics ; Signal Transduction

المؤلفون: Knab T; Städtische Gesundheitsdienste, Zurich, Switzerland., Gaisl T; Pneumology Department, University Hospital Zurich, Zurich, Switzerland., Steinack C; Pneumology Department, University Hospital Zurich, Zurich, Switzerland., Kallweit T; Department of Medical Oncology and Hematology, University Hospital Zurich, Zurich, Switzerland., Ulrich S; Pneumology Department, University Hospital Zurich, Zurich, Switzerland., Roeder M; Pneumology Department, University Hospital Zurich, Zurich, Switzerland maurice.roeder@usz.ch.

المصدر: BMJ case reports [BMJ Case Rep] 2024 Jul 22; Vol. 17 (7). Date of Electronic Publication: 2024 Jul 22.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: Tomography, X-Ray Computed*, Humans ; Male ; Diagnosis, Differential ; Aged ; Genetic Diseases, X-Linked/diagnosis ; Genetic Diseases, X-Linked/complications ; Cough/etiology ; Dyspnea/etiology ; Uveitis/diagnosis ; Uveitis/drug therapy ; Fever/etiology ; Lung/diagnostic imaging ; Hereditary Autoinflammatory Diseases/diagnosis ; Hereditary Autoinflammatory Diseases/drug therapy ; Hereditary Autoinflammatory Diseases/complications ; Syndrome ; Dermatitis, Exfoliative/diagnosis ; Dermatitis, Exfoliative/etiology ; Cryptogenic Organizing Pneumonia/diagnosis ; Cryptogenic Organizing Pneumonia/drug therapy

المؤلفون: Ziegler BM; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Abelleyro MM; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Marchione VD; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Lazarte N; Unidad de Bioinformática, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Ledesma MM; Unidad de Bioinformática, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Elhelou L; Hematology, Fundación de la Hemofilia, Buenos Aires, Argentina., Neme D; Hematology, Fundación de la Hemofilia, Buenos Aires, Argentina., Rossetti LC; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Medina-Acosta E; Center for Biosciences and Biotechnology, State University of North Fluminense Darcy Ribeiro, Campos dos Goytacazes, Brazil., Giliberto F; Laboratorio de Distrofinopatías, Facultad de Farmacia y Bioquímica, Cátedra de Genética, Universidad de Buenos Aires, Buenos Aires, Argentina.; Instituto de Inmunología, Genética y Metabolismo (INIGEM), CONICET-UBA, Buenos Aires, Argentina., De Brasi C; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina., Radic CP; Laboratorio de Genética Molecular de la Hemofilia, Instituto de Medicina Experimental, CONICET-Academia Nacional de Medicina, Buenos Aires, Argentina yocpamelita@yahoo.com.ar.

المصدر: Journal of medical genetics [J Med Genet] 2024 Jul 19; Vol. 61 (8), pp. 769-776. Date of Electronic Publication: 2024 Jul 19.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: X Chromosome Inactivation*/genetics , Hemophilia A*/genetics , Pedigree*, Humans ; Female ; Male ; Algorithms ; Exome Sequencing/methods ; Factor VIII/genetics ; Chromosomes, Human, X/genetics ; Genomics/methods ; DNA Copy Number Variations/genetics ; Mutation/genetics ; Adult

المؤلفون: Klusek J; Department of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia., Will E; Department of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia., Christensen T; Department of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia., Caravella K; Department of Psychiatry, Carolina Institute for Developmental Disabilities, The University of North Carolina at Chapel Hill School of Medicine., Hogan A; Department of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia., Sun J; Department of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia., Smith J; Department of Psychology, University of South Carolina, Columbia., Fairchild AJ; Department of Psychology, University of South Carolina, Columbia., Roberts JE; Department of Psychology, University of South Carolina, Columbia.

المصدر: Journal of speech, language, and hearing research : JSLHR [J Speech Lang Hear Res] 2024 Jul 09; Vol. 67 (7), pp. 2316-2332. Date of Electronic Publication: 2024 Jun 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: American Speech-Language-Hearing Association Country of Publication: United States NLM ID: 9705610 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-9102 (Electronic) Linking ISSN: 10924388 NLM ISO Abbreviation: J Speech Lang Hear Res Subsets: MEDLINE

مواضيع طبية MeSH: Fragile X Mental Retardation Protein*/genetics, Humans ; Male ; Female ; Child, Preschool ; Fragile X Syndrome/genetics ; Fragile X Syndrome/psychology ; Mutation ; Language Development Disorders/genetics ; Language Development Disorders/psychology ; Social Communication Disorder/genetics ; Social Communication Disorder/psychology

المؤلفون: Alsafy MAM; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Alexandria University, Abis 10th, Alexandria, PO 21944, Egypt., El-Gendy SAA; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Alexandria University, Abis 10th, Alexandria, PO 21944, Egypt., Atkinson B; Hounsfield Facility, School of Biosciences, University of Nottingham, College Road, Sutton Bonington, Leicestershire LE12 5RD, UK., Sturrock CJ; Hounsfield Facility, School of Biosciences, University of Nottingham, College Road, Sutton Bonington, Leicestershire LE12 5RD, UK., Kamal BM; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, University of Sadat City, Sadat City 6010230, Egypt., Alibhai A; School of Veterinary Medicine and Science, Faculty of Medicine and Health Science, University of Nottingham, College Road, Sutton Bonington, Leicestershire LE12 5RD, UK., Abd-Elhafeez HH; Department of Cell and Tissues, Faculty of Veterinary Medicine, Assiut University, Assiut 71526, Egypt., Soliman S; Department of Histology, Faculty of Veterinary Medicine, South Valley University, Qena 83523, Egypt., Rashwan AM; Department of Anatomy and Embryology, Faculty of Veterinary Medicine, Damanhour University, Al Gomhouria St, Scientic Campus, Damanhour 22511, Egypt., Roshdy K; Department of Histology and Cytology, Faculty of Veterinary Medicine, Alexandria University, Abis 10th, Alexandria, PO 21944, Egypt., Rutland CS; School of Veterinary Medicine and Science, Faculty of Medicine and Health Science, University of Nottingham, College Road, Sutton Bonington, Leicestershire LE12 5RD, UK.

المصدر: Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada [Microsc Microanal] 2024 Jul 04; Vol. 30 (3), pp. 574-593.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 9712707 Publication Model: Print Cited Medium: Internet ISSN: 1435-8115 (Electronic) Linking ISSN: 14319276 NLM ISO Abbreviation: Microsc Microanal Subsets: MEDLINE

مواضيع طبية MeSH: Microscopy, Electron, Scanning* , X-Ray Microtomography*, Animals ; Cattle ; Spectrometry, X-Ray Emission ; Bone and Bones/ultrastructure