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Nanbert Zhong

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Zhan Zhang; Yueshu Zhao; Shihong Cui; Jing Pan; Nanbert Zhong
Preterm births in countries with a very high human development index.
Xinliang Zhao; Ying Chen; Gan Qiu; Mei Xiao; Nanbert Zhong
Reducing preterm births in China.
Li Wang; Wang Peirong; Wu Yang; Xinliang Zhao; W Ted Brown; Edmund C Jenkins; Weina Ju; Nanbert Zhong
A proteomic study of Hutchinson-Gilford progeria syndrome: Application of 2D-chromotography in a premature aging disease.

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All Publications

2013: Zhan Zhang; Yueshu Zhao; Shihong Cui; Jing Pan; Nanbert Zhong
Preterm births in countries with a very high human development index.
Lancet 2013;381(9875):1355.
2012: Xinliang Zhao; Ying Chen; Gan Qiu; Mei Xiao; Nanbert Zhong
Reducing preterm births in China.
Lancet 2012;380(9848):1144-5; author reply 1145.
2012: Li Wang; Wang Peirong; Wu Yang; Xinliang Zhao; W Ted Brown; Edmund C Jenkins; Weina Ju; Nanbert Zhong
A proteomic study of Hutchinson-Gilford progeria syndrome: Application of 2D-chromotography in a premature aging disease.
Biochemical and biophysical research communications 2012;417(4):1119-26.
2011: Chen Shen; Xin-liang Zhao; Weina Ju; Xiao-bing Zou; Li-rong Huo; Wu Yan; Jun-hua Zou; Guo-di Yan; Edmund C Jenkins; W Ted Brown; Nanbert Zhong
A proteomic investigation of B lymphocytes in an autistic family: a pilot study of exposure to natural rubber latex (NRL) may lead to autism.
Journal of molecular neuroscience : MN 2011;43(3):443-52.
2011: Wang Peirong; Weina Ju; Dan Wu; li wang; Ming Yan; Junhua Zou; Bing He; Edmund C Jenkins; W Ted Brown; Nanbert Zhong
A two-dimensional protein fragmentation-proteomic study of neuronal ceroid lipofuscinoses: identification and characterization of differentially expressed proteins.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 2011;879(5-6):304-16.
2010: Guodi Yan; Yayong Liang; Ying Wang; Wei Huang; Xiaobing Zou; Nanbert Zhong
[Copy number variation analysis of a Chinese Han family with autism spectrum disorder].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2010;27(6):654-8.
2010: Li-Rong Huo; Weina Ju; Ming Yan; Jun-Hua Zou; Wu Yan; Bing He; Xin-Liang Zhao; Edmund C Jenkins; W Ted Brown; Nanbert Zhong
Identification of differentially expressed transcripts and translatants targeted by knock-down of endogenous PCBP1.
Biochimica et biophysica acta 2010;1804(10):1954-64.
2009: Bing He; Junyan Li; Gang Wang; Weina Ju; Yadong Lu; Yongyong Shi; Lin He; Nanbert Zhong
Association of genetic polymorphisms in the type II deiodinase gene with bipolar disorder in a subset of Chinese population.
Progress in neuro-psychopharmacology & biological psychiatry 2009;33(6):986-90.
2009: Christopher P Howson; Nanbert Zhong; Carmencita Padilla; Khalid Yunis; Roberto Giugliani
The March of Dimes Global Network for Maternal and Infant Health: Harnessing the power of experts in lower-income countries to improve the health of women, mothers, newborns and babies.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2009;41(4):392-4.
2009: Nanbert Zhong
Translational medicine: Application of research to clinical practice.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2009;41(4):381-2.
2009: Zeng-min Tian; Tao Chen; Nanbert Zhong; Zhi-chao Li; Feng Yin; Shuang Liu
Clinical study of transplantation of neural stem cells in therapy of inherited cerebellar atrophy.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2009;41(4):456-8.
2009: Li-rong Huo; Chen Shen; Wei-na Ju; Jun-hua Zou; Wu Yan; W Ted Brown; Nanbert Zhong
Identification of novel partner proteins of PCBP1.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2009;41(4):402-8.
2009: Wei-na Ju; W Ted Brown; Nanbert Zhong
Association of progerin-interactive partner proteins with lamina proteins: Mel18 is associated with emerin in HGPS.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2009;41(4):397-401.
2009: Y-X Zhang; Y-P Zhang; Y Gu; F-J Guan; S-L Li; J-S Xie; Y Shen; B-L Wu; W Ju; Edmund C. Jenkins; W T Brown; Nanbert Zhong
Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH.
Clinical genetics 2009;75(2):133-40.
2008: Li-Rong Huo; Nanbert Zhong
Identification of transcripts and translatants targeted by overexpressed PCBP1.
Biochimica et biophysica acta 2008;1784(11):1524-33.
2008: Ke Zou; Jian Liu; Ning Zhu; Jianhong Lin; Qi Liang; W Ted Brown; Yan Shen; Nanbert Zhong
Identification of FMRP-associated mRNAs using yeast three-hybrid system.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(6):769-77.
2008: S Song; C Shen; G Song; X Mao; G Yan; xiangfeng wang; Ming Yan; Nanbert Zhong
A novel c.545-546insG mutation in the loricrin gene correlates with a heterogeneous phenotype of loricrin keratoderma.
The British journal of dermatology 2008;159(3):714-9.
2008: X Wang; Zheng Wang; Ming Yan; Shangzhi Huang; Tian-Jian Chen; Nanbert Zhong
Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations.
Behavioral and brain functions : BBF 2008;4():20.
2007: Shu-Juan Song; Shu-Juan Song; Ming Yan; Xiao-Zhu Wang; Yuan-Zhi Zhang; Jun-Hua Zou; Nanbert Zhong
[The same mutation Glu208Lys in the GJB1 gene was detected in 2 families with X-linked Charcot-Marie-Tooth disease].
Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2007;29(7):800-4.
2007: Yun Ren; Xishi Liu; Duan Ma; Youji Feng; Nanbert Zhong
Down-regulation of the progesterone receptor by the methylation of progesterone receptor gene in endometrial cancer cells.
Cancer genetics and cytogenetics 2007;175(2):107-16.
2006: Yuan-Zhi Zhang; Nanbert Zhong
[The emphases and basic procedures of genetic counseling in psychotherapeutic model].
Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2006;28(11):1440-4.
2006: Shujuan Song; Yuanzhi Zhang; Biao Chen; Yuanjin Zhang; Manjie Wang; Yueying Wang; Ming Yan; Junhua Zou; Yu Huang; Nanbert Zhong
Mutation frequency for Charcot-Marie-Tooth disease type 1 in the Chinese population is similar to that in the global ethnic patients.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(8):532-5.
2006: Nanbert Zhong
Peking University Center of Medical Genetics (PUCMG): a comprehensive medical genetics program in China.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):6-7.
2006: Meng Hou; Man-jie Wang; Nanbert Zhong
Principal genetic syndromes and autism: from phenotypes, proteins to genes.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):110-5.
2006: Xiao-zhu Wang; Nanbert Zhong
Clinical and genetic features of DYT1 and DYT5.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):107-9.
2006: Shu-juan Song; Yuan-zhi Zhang; Biao Chen; Man-jie Wang; Yue-ying Wang; Yuan-jin Zhang; Ming Yan; Nanbert Zhong
No mutation was detected in the LMNA gene among sporadic Charcot-Marie-Tooth patients.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):78-9.
2006: Yuan Lu; Xi-shi Liu; Yue-xiang Wang; Hou-Yan Song; Nanbert Zhong
Study of microsatellite instability in epithelial ovarian tumors.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):62-5.
2006: Yan-ping Xia; Ming-wei Zhu; Xiao-tian Li; He-ping Zhou; Jing Wang; Ju-xiang Lv; Nanbert Zhong
Chromosomal abnormalities and adverse pregnancy outcome with maternal serum second trimester triple screening test for fetal Down syndrome in 4,860 Chinese women.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):49-52.
2006: Weina Ju; Anetta Wronska; Dorota Moroziewicz; Rocksheng Zhong; Natalia Wisniewski; Anna Jurkiewicz; Michael Fiory; Krystyna E Wisniewski; Lance Johnston; W Ted Brown; Nanbert Zhong
Genotype-phenotype analyses of classic neuronal ceroid lipofuscinosis (NCLs): genetic predictions from clinical and pathological findings.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):41-8.
2006: Dorota Moroziewicz; Weina Ju; Rocksheng Zhong; Nanbert Zhong
N-terminal segments are the functional domains of CLN3-encoded battenin for protein interactions.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2006;38(1):38-40.
2005: Nanbert Zhong; Gabriel Radu; Weina Ju; W Ted Brown
Novel progerin-interactive partner proteins hnRNP E1, EGF, Mel 18, and UBC9 interact with lamin A/C.
Biochemical and biophysical research communications 2005;338(2):855-61.
2005: Gail Seigel; J Wagner; Anetta Wronska; L Campbell; Weina Ju; Nanbert Zhong
Progression of early postnatal retinal pathology in a mouse model of neuronal ceroid lipofuscinosis.
Eye (London, England) 2005;19(12):1306-12.
2005: Tian-Jian Chen; Nanbert Zhong
Medical genetics is playing an important role in the public health care in China. Conference Report for the International Conference of Medical Genetics 2004, Beijing.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):5-7.
2005: Dan Wu; Bai-yan Wu; Hong-ye Liang; Nanbert Zhong
[The application of RNAi to the medical genetics].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):106-11.
2005: Yuan-zhi Zhang; Nanbert Zhong
[Molecular genetics of Charcot-Marie-Tooth disease].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):100-5.
2005: Shu-juan Song; Yuan-zhi Zhang; Nanbert Zhong
[Laminopathies--one gene, multiple diseases].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):96-9.
2005: Qi Zeng; Hong-ping Zhang; Xi-shi Liu; Nanbert Zhong
[The role of biomarkers CK7, Vim and P53 in the development of subtypes of endometrial carcinoma].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):81-4.
2005: Nanbert Zhong; Weina Ju; Dorota Moroziewicz; Anetta Wronska; Marilyn Li; Krystyna Wisniewski; Susan Sklower Brooks; Edmund C. Jenkins; W Ted Brown
Prenatal diagnostic testing for infantile and late-infantile neuronal ceroid lipofusinoses (NCL) using allele specific primer extension (ASPE).
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):20-5.
2002: Weina Ju; R Zhong; S Moore; Dorota Moroziewicz; Julia R Currie; P Parfrey; W Ted Brown; Nanbert Zhong
Identification of novel CLN2 mutations shows Canadian specific NCL2 alleles.
Journal of medical genetics 2002;39(11):822-5.
2001: Krystyna E Wisniewski; Nanbert Zhong; M Philippart
Pheno/genotypic correlations of neuronal ceroid lipofuscinoses.
Neurology 2001;57(4):576-81.
2001: Nanbert Zhong; Krystyna E Wisniewski
Outlook for future treatment.
Advances in genetics 2001;45():217-24.
2001: Krystyna E Wisniewski; Elizabeth Kida; Adam A Golabek; Wojciech Kaczmarski; F Connell; Nanbert Zhong
Neuronal ceroid lipofuscinoses: classification and diagnosis.
Advances in genetics 2001;45():1-34.
2000: Nanbert Zhong; Dorota Moroziewicz; Weina Ju; Anna Jurkiewicz; L Johnston; Krystyna E Wisniewski; W Ted Brown
Heterogeneity of late-infantile neuronal ceroid lipofuscinosis.
Genetics in medicine : official journal of the American College of Medical Genetics 2000;2(6):312-8.
2000: Nanbert Zhong
Neuronal ceroid lipofuscinoses and possible pathogenic mechanism.
Molecular genetics and metabolism 2000;71(1-2):195-206.
2000: Krystyna E Wisniewski; Elizabeth Kida; F Connell; Nanbert Zhong
Neuronal ceroid lipofuscinoses: research update.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2000;21(3 Suppl):S49-56.
1999: J M Hartikainen; Weina Ju; Krystyna E Wisniewski; Dorota Moroziewicz; AL Kaczmarski; L Mclendon; D Zhong; C T Suarez; W Ted Brown; Nanbert Zhong
Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene.
Molecular genetics and metabolism 1999;67(2):162-8.
1999: Nanbert Zhong; Weina Ju; W Ted Brown; L Ye; Edmund C. Jenkins; Nicole Schupf
Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease.
American journal of medical genetics 1999;84(3):309-10.
1999: Pornprot Limprasert; Nanbert Zhong; Julia R Currie; W Ted Brown
Possible founder effects for FRAXE alleles.
American journal of medical genetics 1999;84(3):286-90.
1999: Nanbert Zhong; Weina Ju; D Nelson; Carl Dobkin; W Ted Brown
Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation.
American journal of medical genetics 1999;84(3):268-71.
1999: Nanbert Zhong; Weina Ju; W Xu; L Ye; Y Shen; G Wu; S H Chen; R Jin; X F Hu; A Yang; X Liu; P Poon; C Pang; Y Zheng; L Song; P Zhao; B Fu; H Gu; W Ted Brown
Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.
American journal of medical genetics 1999;84(3):191-4.
1999: Edmund C. Jenkins; Guang Yeong Wen; K S Kim; Nanbert Zhong; V J Sapienza; H Hong; J Chen; S Y Li; George E Houck; X Ding; Sarah L Nolin; Carl Dobkin; W Ted Brown
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies.
American journal of medical genetics 1999;83(4):342-6.
1999: Carl Dobkin; X Ding; S Li; George E Houck; Sarah L Nolin; Anne Glicksman; Nanbert Zhong; Edmund C. Jenkins; W Ted Brown
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection.
American journal of medical genetics 1999;83(4):338-41.
1999: Nanbert Zhong; L Ye; Weina Ju; W Ted Brown; John A Tsiouris; I Cohen
5-HTTLPR variants not associated with autistic spectrum disorders.
Neurogenetics 1999;2(2):129-31.
1999: Krystyna E Wisniewski; AL Kaczmarski; Elizabeth Kida; F Connell; Wojciech Kaczmarski; MP Michalewski; Dorota Moroziewicz; Nanbert Zhong
Reevaluation of neuronal ceroid lipofuscinoses: atypical juvenile onset may be the result of CLN2 mutations.
Molecular genetics and metabolism 1999;66(4):248-52.
1998: Nanbert Zhong; Krystyna E Wisniewski; J Hartikainen; Weina Ju; Dorota Moroziewicz; L Mclendon; Susan Sklower Brooks; W Ted Brown
Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosis.
Clinical genetics 1998;54(3):234-8.
1998: Krystyna E Wisniewski; Nanbert Zhong; Wojciech Kaczmarski; AL Kaczmarski; Susan Sklower Brooks; W Ted Brown
Studies of atypical JNCL suggest overlapping with other NCL forms.
Pediatric neurology 1998;18(1):36-40.
1998: Nanbert Zhong; Krystyna E Wisniewski; AL Kaczmarski; Weina Ju; W M Xu; W W Xu; L Mclendon; B Liu; Wojciech Kaczmarski; Susan Sklower Brooks; W Ted Brown
Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene.
Human genetics 1998;102(1):57-62.
1998: Krystyna E Wisniewski; Nanbert Zhong; Wojciech Kaczmarski; AL Kaczmarski; Elizabeth Kida; W Ted Brown; K O Schwarz; Alice Lazzarini; A J Rubin; Edward S Stenroos; William G Johnson; Thomas Wisniewski
Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis.
Annals of neurology 1998;43(1):106-10.
1997: Pornprot Limprasert; Nanbert Zhong; Carl Dobkin; W Ted Brown
Polymorphism of FXR1 showing lack of association with autism.
American journal of medical genetics 1997;74(4):453-4.
1997: Wojciech Kaczmarski; Elizabeth Kida; A Lach; R Rubenstein; Nanbert Zhong; Krystyna E Wisniewski
Expression studies of CLN3 protein.
Neuropediatrics 1997;28(1):33-6.
1997: K E Wiśniewski; Nanbert Zhong; Elizabeth Kida; Wojciech Kaczmarski; AL Kaczmarski; F Connell; Susan Sklower Brooks; W Ted Brown
Atypical late infantile and juvenile forms of neuronal ceroid lipofuscinosis and their diagnostic difficulties.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 1997;35(2):73-9.
1996: Sarah L Nolin; F A Lewis; L L Ye; George E Houck; A E Glicksman; Pornprot Limprasert; S Y Li; Nanbert Zhong; A E Ashley; Eleanor Feingold; Stephanie L Sherman; W Ted Brown
Familial transmission of the FMR1 CGG repeat.
American journal of human genetics 1996;59(6):1252-61.
1996: Nanbert Zhong; Weina Ju; D Curley; D Wang; J Pietrofesa; G Wu; Y Shen; C Pang; P Poon; X Liu; S Gou; E Kajanoja; Markku Ryynänen; Carl Dobkin; W Ted Brown
A survey of FRAXE allele sizes in three populations.
American journal of medical genetics 1996;64(2):415-9.
1996: Carl Dobkin; Sarah L Nolin; I Cohen; V Sudhalter; M G Bialer; X H Ding; Edmund C. Jenkins; Nanbert Zhong; W Ted Brown
Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skin.
American journal of medical genetics 1996;64(2):296-301.
1996: W Ted Brown; George E Houck; X Ding; Nanbert Zhong; Sarah L Nolin; Anne Glicksman; Carl Dobkin; Edmund C. Jenkins
Reverse mutations in the fragile X syndrome.
American journal of medical genetics 1996;64(2):287-92.
1996: Nanbert Zhong; Weina Ju; J Pietrofesa; D Wang; Carl Dobkin; W Ted Brown
Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes.
American journal of medical genetics 1996;64(2):261-5.
1996: Nanbert Zhong; E Kajanoja; B Smits; J Pietrofesa; D Curley; D Wang; Weina Ju; Sarah L Nolin; Carl Dobkin; Markku Ryynänen; W Ted Brown
Fragile X founder effects and new mutations in Finland.
American journal of medical genetics 1996;64(1):226-33.
1995: Nanbert Zhong; W Yang; Carl Dobkin; W Ted Brown
Fragile X gene instability: anchoring AGGs and linked microsatellites.
American journal of human genetics 1995;57(2):351-61.
1994: Nanbert Zhong; X Liu; S Gou; George E Houck; S Li; Carl Dobkin; W Ted Brown
Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
American journal of medical genetics 1994;51(4):417-22.
1994: Nanbert Zhong; L Ye; Carl Dobkin; W Ted Brown
Fragile X founder chromosome effects: linkage disequilibrium or microsatellite heterogeneity?
American journal of medical genetics 1994;51(4):405-11.
1993: Nanbert Zhong; Carl Dobkin; W Ted Brown
A complex mutable polymorphism located within the fragile X gene.
Nature genetics 1993;5(3):248-53.
1993: W Ted Brown; George E Houck; A Jeziorowska; F N Levinson; X Ding; Carl Dobkin; Nanbert Zhong; J Henderson; S S Brooks; Edmund C. Jenkins
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.
JAMA : the journal of the American Medical Association 1993;270(13):1569-75.