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A Review of Planned, Ongoing Clinical Studies and Recent Development of BNCT in Mainland of China.

• Authors : Zhang, Zizhu; Chong, Yizheng; Liu, Yuanhao

Subjects: IN vitro studies; CANCER cell culture; NEUTRONSCHINA

• Source: Cancers; Aug2023, Vol. 15 Issue 16, p4060, 14p

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Education Full Text (H.W. Wilson)

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Behavioral Comparisons in Autistic Individuals from Multiplex and Singleton Families.

• Authors : Cuccaro, Michael L.; Shao, Yujun; Bass, Meredyth P.

Subjects: Autism; Behavior Patterns; Behavior Problems

• Source: Journal of Autism and Developmental Disorders. Feb 2003 33(1):87-91.5

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Expression Profiling of Substantia Nigra in Parkinson Disease, Progressive Supranuclear Palsy, and Frontotemporal Dementia With Parkinsonism.

• Authors : Hauser, Michael A.; Li, Yi-Ju; Xu, Hong

Subjects: SUBSTANTIA nigra; PARKINSON'S disease; PROGRESSIVE supranuclear palsy

• Source: Archives of Neurology; Jun2005, Vol. 62 Issue 6, p917-921, 5p

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Life After the Screen: Making Sense of Many P-Values.

• Authors : Schmidt, Silke; Shao, Yujun; Hauser, Elizabeth R.

• Source: Genetic Epidemiology; 2001 Supplement S1, Vol. 21, pS546-S551, 6p

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Association Analysis of Chromosome 15 GABAA Receptor Subunit Genes in Autistic Disorder.

• Authors : Menold, Marisa M.; Shao, Yujun; Wolpert, Chantelle M.

• Source: Journal of Neurogenetics; 2001, Vol. 15 Issue 3/4, p245-259, 15p

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Phenotypic Homogeneity Provides Increased Support for Linkage on Chromosome 2 in Autistic Disorder.

• Authors : Shao, Yujun; Raiford, Kimberly L.; Wolpert, Chantelle M.

Subjects: *AUTISM in children; *CHROMOSOMES; *SPEECH

• Source: American Journal of Human Genetics. Apr2002, Vol. 70 Issue 4, p1058. 4p. 2 Charts, 2 Graphs.

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Adjusting for covariates on a slippery slope: linkage analysis of change over time.

• Authors : Rampersaud E; Section of Medical Genetics, Department of Medicine, Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, USA. ; Allen A

Subjects: Time*; Genetic Linkage/Genetic Linkage/Genetic Linkage/*genetics; Blood Pressure/Blood Pressure/Blood Pressure/genetics

• Source: BMC genetics [BMC Genet] 2003 Dec 31; Vol. 4 Suppl 1, pp. S50. Date of Electronic Publication: 2003 Dec 31.Publisher: BioMed Central Country of Publication: England NLM ID: 100966978 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2156

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Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.

• Authors : Shao Y; Duke University Medical Center, Durham, NC 27710, USA.; Cuccaro ML

Subjects: Chromosomes, Human, Pair 15*; Autistic Disorder/Autistic Disorder/Autistic Disorder/*genetics; Autistic Disorder/Autistic Disorder/Autistic Disorder/classification

• Source: American journal of human genetics [Am J Hum Genet] 2003 Mar; Vol. 72 (3), pp. 539-48. Date of Electronic Publication: 2003 Feb 03.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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No association between the WNT2 gene and autistic disorder.

• Authors : McCoy PA; Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.; Shao Y

Subjects: Autistic Disorder/Autistic Disorder/Autistic Disorder/*genetics ; Proto-Oncogene Proteins/Proto-Oncogene Proteins/Proto-Oncogene Proteins/*genetics; Adolescent

• Source: American journal of medical genetics [Am J Med Genet] 2002 Jan 08; Vol. 114 (1), pp. 106-9.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print)

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