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Expression Analyses of C-Terminal-Binding Protein 1 (CtBP1) during Mouse Brain Development.
- Published in:
- Developmental Neuroscience, 2024, v. 46, n. 4, p. 262, doi. 10.1159/000534886
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- Publication type:
- Article
Interdigitating cell sarcoma: A morphologic and immunologic study of lymph node lesions in four cases.
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- Pathology International, 1994, v. 44, n. 5, p. 374, doi. 10.1111/j.1440-1827.1994.tb02938.x
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- Publication type:
- Article
Clinicopathologic study of primary mediastinal non-lymphoblastic non-Hodgkin's lymphomas among the Japanese.
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- Pathology International, 1993, v. 43, n. 1/2, p. 44, doi. 10.1111/j.1440-1827.1993.tb02913.x
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- Publication type:
- Article
Undifferentiated Carcinoma of the Parotid Gland in a 10-Month-old Child.
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- Pathology International, 1990, v. 40, n. 2, p. 149, doi. 10.1111/j.1440-1827.1990.tb01554.x
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- Publication type:
- Article
A CASE OF OVARIAN GRANULOSA CELL TUMOR WITH INVASIVE ADENOCARCINOMA OF THE ENDOMETRIUM. A Case Report and Review of the Japanese Literature.
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- Pathology International, 1988, v. 38, n. 7, p. 947, doi. 10.1111/j.1440-1827.1988.tb02366.x
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- Publication type:
- Article
Knockdown of Son, a mouse homologue of the ZTTK syndrome gene, causes neuronal migration defects and dendritic spine abnormalities.
- Published in:
- Molecular Brain, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13041-020-00622-4
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- Publication type:
- Article
Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient.
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- Mutagenesis, 2016, v. 31, n. 1, p. 61, doi. 10.1093/mutage/gev057
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- Publication type:
- Article
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 8, p. 844, doi. 10.1038/ejhg.2011.47
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- Publication type:
- Article
Interdigitating cell sarcoma. A morphologic, immunohistologic, and enzyme-histochemical study.
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- 1988
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- Publication type:
- journal article
Kit<sup>+</sup> Melanocytes Seem to Contribute to Melanocyte Proliferation After UV Exposure as Precursor Cells.
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- Journal of Investigative Dermatology, 2001, v. 116, n. 6, p. 920, doi. 10.1046/j.0022-202X.2001.01370.x
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- Publication type:
- Article
Age-related changes in BDNF protein levels in human serum: differences between autism cases and normal controls
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- International Journal of Developmental Neuroscience, 2007, v. 25, n. 6, p. 367, doi. 10.1016/j.ijdevneu.2007.07.002
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- Publication type:
- Article
Phenotypes associated with replacement of His<sub>723</sub> by Arg in the Pendred syndrome gene.
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- European Journal of Endocrinology, 2001, v. 145, n. 6, p. 697
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- Publication type:
- Article
Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia.
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- Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00230-3
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- Publication type:
- Article
Distribution of nestin and other stem cell-related molecules in developing and diseased human spinal cord.
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- Pathology International, 2007, v. 57, n. 6, p. 358, doi. 10.1111/j.1440-1827.2007.02108.x
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- Publication type:
- Article
A case of natural killer/T cell lymphoma of the subcutis resembling subcutaneous panniculitis-like T cell lymphoma.
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- Pathology International, 1999, v. 49, n. 3, p. 241, doi. 10.1046/j.1440-1827.1999.00854.x
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- Publication type:
- Article
Monoclonal antibodies against mouse splenic stromal cells.
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- Pathology International, 1997, v. 47, n. 5, p. 275, doi. 10.1111/j.1440-1827.1997.tb04493.x
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- Publication type:
- Article
Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0102944
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- Publication type:
- Article
Loss of Deacetylation Activity of Hdac6 Affects Emotional Behavior in Mice.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030924
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- Publication type:
- Article
Long-term follow-up in patients with Pendred syndrome: vestibular, auditory and other phenotypes.
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- European Archives of Oto-Rhino-Laryngology, 2005, v. 262, n. 9, p. 737, doi. 10.1007/s00405-004-0884-z
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- Publication type:
- Article
Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome.
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- Biomolecules (2218-273X), 2023, v. 13, n. 5, p. 763, doi. 10.3390/biom13050763
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- Publication type:
- Article
STK25 and MST3 Have Overlapping Roles to Regulate Rho GTPases during Cortical Development.
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- Journal of Neuroscience, 2021, v. 41, n. 43, p. 8887, doi. 10.1523/JNEUROSCI.0523-21.2021
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- Publication type:
- Article
A novel LRP6 variant in a Japanese family with oligodontia.
- Published in:
- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00162-w
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- Publication type:
- Article
Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia.
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- Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00161-x
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- Publication type:
- Article
Identification of nuclear localization signals in the human homeoprotein MSX1.
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- Biochemistry & Cell Biology, 2018, v. 96, n. 4, p. 483, doi. 10.1139/bcb-2017-0263
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- Publication type:
- Article
Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region.
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- Human Mutation, 2006, v. 27, n. 1, p. 88, doi. 10.1002/humu.20266
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- Publication type:
- Article
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/ MH4.
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- European Journal of Oral Sciences, 2014, v. 122, n. 1, p. 15, doi. 10.1111/eos.12105
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- Publication type:
- Article
The distribution of neuroligin4, an autism-related postsynaptic molecule, in the human brain.
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- Molecular Brain, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13041-023-00999-y
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- Publication type:
- Article
Long-term stimulation of the subthalamic nucleus in hemiparkinsonian rats: neuroprotection of dopaminergic neurons.
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- Journal of Neurosurgery, 2004, v. 100, n. 4, p. 679, doi. 10.3171/jns.2004.100.4.0679
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- Article
Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.
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- Medical Molecular Morphology, 2023, v. 56, n. 4, p. 266, doi. 10.1007/s00795-023-00364-x
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- Article
Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-09142-5
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- Publication type:
- Article
Expression analysis of type I ARF small GTPases ARF1-3 during mouse brain development.
- Published in:
- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-09142-5
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- Publication type:
- Article
A Novel Constitutively Active c.98G>C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization.
- Published in:
- Human Mutation, 2023, p. 1, doi. 10.1155/2023/8126544
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- Publication type:
- Article
Expression of the CD15 antigen in hepatocellular carcinoma.
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- 1993
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- Publication type:
- journal article
Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.698
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- Publication type:
- Article
Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 4, p. 703, doi. 10.1093/hmg/7.4.703
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- Article
Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14. 1-p12.3.
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- Human Molecular Genetics, 1994, v. 3, n. 4, p. 553
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- Publication type:
- Article
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cells.
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- Epigenetics & Chromatin, 2013, v. 6, n. 1, p. 3, doi. 10.1186/1756-8935-6-38
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- Publication type:
- Article
An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128227
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- Publication type:
- Article
Hodgkin disease with subsequent transformation to CD30 positive non-Hodgkin lymphoma in six patients.
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- Cancer (0008543X), 1999, v. 85, n. 4, p. 970, doi. 10.1002/(SICI)1097-0142(19990215)85:4<970::AID-CNCR27>3.0.CO;2-L
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- Publication type:
- Article
Reduction in miR‐219 expression underlies cellular pathogenesis of oligodendrocytes in a mouse model of Krabbe disease.
- Published in:
- Brain Pathology, 2021, v. 31, n. 5, p. 1, doi. 10.1111/bpa.12951
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- Publication type:
- Article