المؤلفون: Wanyi Dang, Dali Gao, Guangqi Lyu, David M. Irwin, Songyang Shang, Junnan Chen, Junpeng Zhang, Shuyi Zhang, Zhe Wang

المصدر: Genes, Vol 15, Iss 6, p 739 (2024)

مصطلحات موضوعية: Lhx3, SNP, body size, dog, transgenic mouse, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2073-4425/15/6/739Test; https://doaj.org/toc/2073-4425Test

الوصول الحر: https://doaj.org/article/fdb85619481f415e81d8e5394737d5a0Test

المؤلفون: Shunsaku Homma, Takako Shimada, Ikuo Wada, Katsuji Kumaki, Noboru Sato, Hiroyuki Yaginuma

المصدر: Frontiers in Neuroscience, Vol 16 (2023)

مصطلحات موضوعية: primaxial/abaxial, epaxial/hypaxial, motor neuron, Lhx3, FoxP1, mesoderm, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fnins.2022.1009542/fullTest; https://doaj.org/toc/1662-453XTest

الوصول الحر: https://doaj.org/article/406bba7d0960435186d20dcda012dda6Test

المؤلفون: Dang, Wanyi, Gao, Dali, Lyu, Guangqi, Irwin, David M, Shang, Songyang, Chen, Junnan, Zhang, Junpeng, Zhang, Shuyi, Wang, Zhe

المصدر: Genes (Basel) ; ISSN:2073-4425 ; Volume:15 ; Issue:6

مصطلحات موضوعية: Lhx3, SNP, body size, dog, transgenic mouse

العلاقة: https://doi.org/10.3390/genes15060739Test; https://pubmed.ncbi.nlm.nih.gov/38927675Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11202965Test/

الإتاحة: https://doi.org/10.3390/genes15060739Test
https://pubmed.ncbi.nlm.nih.gov/38927675Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11202965Test/

المؤلفون: Jullien, Nicolas, Saveanu, Alexandru, Vergier, Julia, Marquant, Emeline, Quentien, Marie Helene, Castinetti, Frederic, Galon‐faure, Noémie, Brauner, Raja, Marrakchi Turki, Zinet, Tauber, Maité, El Kholy, Mohamed, Linglart, Agnès, Rodien, Patrice, Fedala, Nora Soumeya, Bergada, Ignacio, Cortet‐rudelli, Christine, Polak, Michel, Nicolino, Marc, Stuckens, Chantal, Barlier, Anne, A., Brue, Thierry, Reynaud, Rachel

المساهمون: Institut de neurophysiopathologie (INP), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital de la Timone CHU - APHM (TIMONE), Service d'endocrinologie, diabète, maladies métaboliques Hôpital de la Conception - APHM, Aix Marseille Université (AMU), Centre Hospitalier d'Aix en Provence Aix-en-Provence (CHIAP ), Fondation Ophtalmologique Adolphe de Rothschild Paris, National Institute of Nutrition, National Institut of Nutrition, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Ain Shams University (ASU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM), CHU de Bab El Oued, Ricardo Gutierrez Children's Hospital, Partenaires INRAE, Centre Hospitalier Régional Universitaire CHU Lille (CHRU Lille), Hôpital Necker - Enfants Malades AP-HP, Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Institut Cochin (IC UM3 (UMR 8104 / U1016)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Hospices Civils de Lyon (HCL), Laboratoire de Biochimie et de Biologie Moléculaire Hôpital de la Conception - APHM, Hôpital de la Conception CHU - APHM (LA CONCEPTION)

المصدر: ISSN: 0300-0664.

مصطلحات موضوعية: ACTH deficiency, candidate gene approach, central hypothyroidism, congenital hypopituitarism, genetic screening, growth hormone deficiency, HESX1, LHX3, LHX4, PROP1, POU1F1, TBX19, OTX2, PROKR2, hypogonadotroph, hypogonadism, Next‐Generation Sequencing, ocular defect, panhypopituitarism, pituitary development, pituitary stalk interruption, transcription factor, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: hal-03225618; https://amu.hal.science/hal-03225618Test; https://amu.hal.science/hal-03225618/documentTest; https://amu.hal.science/hal-03225618/file/Jullien%202020.pdfTest

الإتاحة: https://doi.org/10.1111/cen.14355Test
https://amu.hal.science/hal-03225618Test
https://amu.hal.science/hal-03225618/documentTest
https://amu.hal.science/hal-03225618/file/Jullien%202020.pdfTest

المؤلفون: Kaiser, Christiane

مصطلحات موضوعية: Idiopathic male infertility - Follicle Stimulation Hormone - Beta subunit of FSH - FSHBeta promotor activity - enhancing transcription factor LHX3 - LHX3 bindig sites - SNP (rs10835638) - Sequencing - Binding affinity - Deletion of nucleotides - in vitro mutagenisis - Chinese Hamster Ovarie cells - immortalized mouse gonadotrope pituitary cells (LBetaT2) - Transfection - Reportergene Assay, Idiopathische männliche Unfruchtbarkeit - Follikelstimulationshormon - Beta-Untereinheit von FSH - FSHBeta-Promotoraktivität - Verstärkender Transkriptionsfaktor LHX3 - LHX3-Bindungsstellen - SNP (rs10835638) - Sequenzierung - Bindungsaffinität - Deletion von Nukleotiden - in vitro Mutagenese - Chinesische Hamster-Ovarie-Zellen - immortalisierte gonadotrope Hypophysenzellen der Maus (LBetaT2) - Transfektion - Reportergen-Assay

وصف الملف: kein Volltext verfügbar

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_____10650::ebcf7f9406b76a45b7a70b205965e03cTest

المؤلفون: Giuseppe Crisafulli, Tommaso Aversa, Giuseppina Zirilli, Filippo De Luca, Romina Gallizzi, Malgorzata Wasniewska

المصدر: Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-4 (2018)

مصطلحات موضوعية: Causative gene mutations, Combined pituitary hormone deficiency, HESX1 gene, LHX3 and LHX4 genes, Multiple pituitary hormone deficiency, POU1F1 gene, Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13052-018-0484-yTest; https://doaj.org/toc/1824-7288Test

الوصول الحر: https://doaj.org/article/17493d9bd814427091be4093f2875848Test

المؤلفون: Yoanne M. Clovis, So Yeon Seo, Ji-sun Kwon, Jennifer C. Rhee, Sujeong Yeo, Jae W. Lee, Seunghee Lee, Soo-Kyung Lee

المصدر: Cell Reports, Vol 16, Iss 6, Pp 1642-1652 (2016)

مصطلحات موضوعية: Chx10, Vsx2, Lhx3, Sox14, V2a interneurons, motor neurons, transcription factor, spinal cord, development, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: http://www.sciencedirect.com/science/article/pii/S2211124716308695Test; https://doaj.org/toc/2211-1247Test

الوصول الحر: https://doaj.org/article/e99ca0113299409385c38e3eba844f82Test

المؤلفون: Heejin Nam, Shin Jeon, Hyejin An, Jaeyoung Yoo, Hyo-Jong Lee, Soo-Kyung Lee, Seunghee Lee

المصدر: eLife, Vol 8 (2019)

مصطلحات موضوعية: ARHGAP36, motor neuron, spinal cord, sonic hedgehog, Isl1, Lhx3, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://elifesciences.org/articles/46683Test; https://doaj.org/toc/2050-084XTest

الوصول الحر: https://doaj.org/article/93ac12953b6f47b1834634b8e708fcebTest

المؤلفون: Shunsaku Homma, Takako Shimada, Ikuo Wada, Katsuji Kumaki, Noboru Sato, Hiroyuki Yaginuma

مصطلحات موضوعية: Neuroscience, Biological Engineering, Developmental Biology, Stem Cells, Artificial Intelligence and Image Processing, Endocrinology, Radiology and Organ Imaging, Autonomic Nervous System, Cellular Nervous System, Central Nervous System, Sensory Systems, Clinical Nursing: Tertiary (Rehabilitative), Decision Making, Rehabilitation Engineering, Biomedical Engineering not elsewhere classified, Signal Processing, Neurogenetics, Image Processing, primaxial/abaxial, epaxial/hypaxial, motor neuron, Lhx3, FoxP1, mesoderm, connective tissue

العلاقة: https://figshare.com/articles/dataset/Data_Sheet_1_A_three-component_model_of_the_spinal_nerve_ramification_Bringing_together_the_human_gross_anatomy_and_modern_Embryology_pdf/21902658Test

الإتاحة: https://doi.org/10.3389/fnins.2022.1009542.s001Test
https://figshare.com/articles/dataset/Data_Sheet_1_A_three-component_model_of_the_spinal_nerve_ramification_Bringing_together_the_human_gross_anatomy_and_modern_Embryology_pdf/21902658Test

المؤلفون: D. V. Singh, Deepak Modi, Neha Singh

المصدر: Sexual Development. 16:147-161

مصطلحات موضوعية: Male, Embryology, 46, XX Disorders of Sex Development, Somatic cell, Endocrinology, Diabetes and Metabolism, LIM-Homeodomain Proteins, Biology, Mice, Pregnancy, medicine, Animals, Reproductive system, Disorders of sex development, Gonads, Mullerian Ducts, Gene, Transcription factor, Homeodomain Proteins, LIM Domain Proteins, medicine.disease, Cell biology, DNA-Binding Proteins, Homeobox, Female, Oocyte differentiation, LHX3, Transcription Factors, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b679ef62f338734e5761094861ae97cTest
https://doi.org/10.1159/000518323Test