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Showing results for bodian he
Search for Boqian He instead (1 results)
Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Rajagopal VM, Watanabe K, Mbatchou J, Ayer A, Quon P, Sharma D, Kessler MD, Praveen K, Gelfman S, Parikshak N, Otto JM, Bao S, Chim SM, Pavlopoulos E, Avbersek A, Kapoor M, Chen E, Jones MB, Leblanc M, Emberson J, Collins R, Torres J, Morales PK, Tapia-Conyer R, Alegre J, Berumen J; GHS-REGN DiscovEHR collaboration; Regeneron Genetics Center; Shuldiner AR, Balasubramanian S, Abecasis GR, Kang HM, Marchini J, Stahl EA, Jorgenson E, Sanchez R, Liedtke W, Anderson M, Cantor M, Lederer D, Baras A, Coppola G. Rajagopal VM, et al. Nat Genet. 2023 Jul;55(7):1138-1148. doi: 10.1038/s41588-023-01417-8. Epub 2023 Jun 12. Nat Genet. 2023. PMID: 37308787 Free PMC article.
Olfactory ensheathing cell tumor with neurofibroma-like features: a case report and review of the literature.
Lin SC, Chen MH, Lin CF, Ho DM. Lin SC, et al. J Neurooncol. 2010 Mar;97(1):117-22. doi: 10.1007/s11060-009-9986-1. Epub 2009 Aug 19. J Neurooncol. 2010. PMID: 19690802 Review.
Most of the tumor cells were immuno-reactive for S-100 protein. Staining for Leu 7 (CD57 or HNK-1) was negative. Bodian method illustrated many axons within the tumor. Ultrastructural study of the tumor cells showed features compatible with those of olfactory ensheathing c …
Most of the tumor cells were immuno-reactive for S-100 protein. Staining for Leu 7 (CD57 or HNK-1) was negative. Bodian method illust …
[Haploidentical stem cell transplantation for acute myeloid leukemia associated with adult-onset Shwachman-Diamond syndrome].
Uemura Y, Hirakawa T, Matsunawa M, Kozuki K, Saiki Y, Takimoto M, Sano F, Watanabe K, Inoue Y, Arai A. Uemura Y, et al. Rinsho Ketsueki. 2022;63(2):94-98. doi: 10.11406/rinketsu.63.94. Rinsho Ketsueki. 2022. PMID: 35264508 Japanese.
A 21-year-old man presented with bone marrow failure, short stature, fatty degeneration of the pancreas on CT images, and Shwachman-Bodian-Diamond syndrome (SBDS) gene abnormalities (exon 2: c.258+2T>C and deletion of exon 3). ...
A 21-year-old man presented with bone marrow failure, short stature, fatty degeneration of the pancreas on CT images, and Shwachman-Bodia …
The Acanthamoeba SBDS, a cytoskeleton-associated gene, is highly expressed during phagocytosis and encystation.
Wang YJ, Lin WC, He MS. Wang YJ, et al. J Microbiol Immunol Infect. 2021 Jun;54(3):482-489. doi: 10.1016/j.jmii.2019.11.003. Epub 2019 Dec 14. J Microbiol Immunol Infect. 2021. PMID: 31882330 Free article.
BACKGROUND/PURPOSE: Shwachman-Bodian-Diamond syndrome (SBDS) protein is widely present in eukaryotes from vertebrates to protozoa. ...
BACKGROUND/PURPOSE: Shwachman-Bodian-Diamond syndrome (SBDS) protein is widely present in eukaryotes from vertebrates to protozoa. .. …
Neuropathological investigation of cerebral white matter lesions caused by closed head injury.
Onaya M. Onaya M. Neuropathology. 2002 Dec;22(4):243-51. doi: 10.1046/j.1440-1789.2002.00456.x. Neuropathology. 2002. PMID: 12564763
Formalin-fixed brains were cut coronally so as to make paraffin-embedded hemispheric sections. Then these sections were stained conventionally (HE, Bodian, Kluver-Barrera and Holzer) and immunohistochemically (GFAP) to assess axonal decrease, myelin pallor and gliosis by t …
Formalin-fixed brains were cut coronally so as to make paraffin-embedded hemispheric sections. Then these sections were stained conventional …
Shwachman-Diamond syndrome: first molecular diagnosis in a Brazilian child.
Alves C, Fernandes JC, Sampaio S, Paiva Rde M, Calado RT. Alves C, et al. Rev Bras Hematol Hemoter. 2013;35(4):290-2. doi: 10.5581/1516-8484.20130058. Rev Bras Hematol Hemoter. 2013. PMID: 24106450 Free PMC article.
A molecular study revealed biallelic mutations in the Shwachman-Bodian-Diamond Syndrome gene (183-184TA-CT K62X in exon 2 and a 258+2T-C transition) confirming the diagnosis of Shwachman-Diamond Syndrome. A non-pathologic, silent nucleotide A to G transition at position 20 …
A molecular study revealed biallelic mutations in the Shwachman-Bodian-Diamond Syndrome gene (183-184TA-CT K62X in exon 2 and a 258+2 …
Novel myopathy in a newborn with Shwachman-Diamond syndrome and review of neonatal presentation.
Topa A, Tulinius M, Oldfors A, Hedberg-Oldfors C. Topa A, et al. Am J Med Genet A. 2016 May;170A(5):1155-64. doi: 10.1002/ajmg.a.37593. Epub 2016 Feb 11. Am J Med Genet A. 2016. PMID: 26866830
Shwachman-Diamond-Bodian syndrome (SDS) is a pleiotropic disorder in which the main features are bone marrow dysfunction and pancreatic insufficiency. ...
Shwachman-Diamond-Bodian syndrome (SDS) is a pleiotropic disorder in which the main features are bone marrow dysfunction and pancreat …
NER rat strain: a new type of genetic model in epilepsy research.
Noda A, Hashizume R, Maihara T, Tomizawa Y, Ito Y, Inoue M, Kobayashi K, Asano Y, Sasa M, Serikawa T. Noda A, et al. Epilepsia. 1998 Jan;39(1):99-107. doi: 10.1111/j.1528-1157.1998.tb01281.x. Epilepsia. 1998. PMID: 9578020 Free article.
Pathologic study included hematoxylin-and-eosin (HE), Kluver-Barrera's, modified Bodian silver, and neo-Timm's staining. RESULTS: After the F9 generation, 94%-98% of NER exhibited spontaneous tonic-clonic convulsions, beginning with neck and forelimb clonus, wild jumping/r …
Pathologic study included hematoxylin-and-eosin (HE), Kluver-Barrera's, modified Bodian silver, and neo-Timm's staining. RESULTS: Aft …
33 results