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Identification of differentially expressed microRNAs across the developing human brain

Molecular psychiatry, 2014-07, Vol.19 (7), p.848-852

2014

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Methylation of an intronic region regulates miR-199a in testicular tumor malignancy

Oncogene, 2011-08, Vol.30 (31), p.3404-3415

2011

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Genome-wide DNA methylation profiling reveals novel epigenetically regulated genes and non-coding RNAs in human testicular cancer

British journal of cancer, 2010-01, Vol.102 (2), p.419-427

2010

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Functional genomics of human brain development and implications for autism spectrum disorders

Translational psychiatry, 2015-10, Vol.5 (10), p.e665-e665

2015

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Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation

Human genetics, 1999-07, Vol.105 (1-2), p.120-126

1999

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Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutations

Journal of inherited metabolic disease, 1997-03, Vol.20 (1), p.67-73

1997

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Testicular seminoma in a patient with a constitutively activating mutation of the luteinizing hormone/chorionic gonadotropin receptor

European journal of endocrinology, 1998-07, Vol.139 (1), p.101

1998

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Severe skeletal complications in Japanese patients with type 1 Gaucher disease

Journal of inherited metabolic disease, 1999-02, Vol.22 (1), p.63-73

1999

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Gitelman's syndrome (familial hypokalemia-hypomagnesemia)

Journal of nephrology, 2001-01, Vol.14 (1), p.43-47

2001

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Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Human genetics, 1995-06, Vol.95 (6), p.717-720

1995

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Development of a human mitochondria-focused cDNA microarray (hMitChip) and validation in skeletal muscle cells: implications for pharmaco- and mitogenomics

The pharmacogenomics journal, 2006-09, Vol.6 (5), p.333-342

2006

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Mutation screening of 17 Japanese patients with neuropathic Gaucher disease

Human genetics, 1996-08, Vol.98 (2), p.167-171

1996

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Kidney abnormalities in Hajdu-Cheney syndrome

Pediatric nephrology (Berlin, West), 1996-12, Vol.10 (6), p.712-715

1996

Volltextzugriff (PDF)

GermlncRNA: a unique catalogue of long non-coding RNAs and associated regulations in male germ cell development

Database : the journal of biological databases and curation, 2015, Vol.2015, p.bav044-bav044

2015

Volltextzugriff (PDF)

Do clocks run clockwise?

Pediatric annals, 1995-11, Vol.24 (11), p.564, 591

Rennert, O M

1995

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Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3)

American journal of medical genetics, 1998-09, Vol.79 (3), p.209-214

1998

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Managed care and the Hippocratic Oath

Pediatric annals, 1996-12, Vol.25 (12), p.657

Rennert, O M

1996

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Characterization of the cDNA encoding human nucleophosmin and studies of its role in normal and abnormal growth

Biochemistry (Easton), 1989-02, Vol.28 (3), p.1033-1039

1989

Volltextzugriff (PDF)

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers

Proceedings of the Association of American Physicians, 1997-09, Vol.109 (5), p.478-482

1997

Volltextzugriff (PDF)

Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease

European journal of pediatrics, 2001, Vol.160 (1), p.21-25

2001

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Tissue Zinc and Copper Levels in Diabetic C57BL/KsJ (db/db) Mice Fed a Zinc-Deficient Diet: Lack of Evidence for Specific Depletion of Tissue Zinc Stores

The Journal of nutrition, 1988-12, Vol.118 (12), p.1502-1508

1988

Volltextzugriff (PDF)

Cloning of a Human Acid Sphingomyelinase cDNA with a New Mutation That Renders the Enzyme Inactive

Journal of biochemistry (Tokyo), 1993-07, Vol.114 (1), p.15-20

1993

Volltextzugriff (PDF)

Zinc deficiency acts as a co-teratogen with alcohol in fetal alcohol syndrome

Pediatric research, 1985-09, Vol.19 (9), p.944-947

1985

Volltextzugriff (PDF)

Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online

Human mutation, 1998, Vol.11 (4), p.333-334

1998

Volltextzugriff (PDF)

Congenital Adrenal Hyperplasia: Molecular Genetics and Alternative Approaches to Treatment

Critical reviews in clinical laboratory sciences, 1999-01, Vol.36 (4), p.329-363

1999

Volltextzugriff (PDF)

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Identification of differentially expressed microRNAs across the developing human brain

Methylation of an intronic region regulates miR-199a in testicular tumor malignancy

Genome-wide DNA methylation profiling reveals novel epigenetically regulated genes and non-coding RNAs in human testicular cancer

Functional genomics of human brain development and implications for autism spectrum disorders

Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation

Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutations

Testicular seminoma in a patient with a constitutively activating mutation of the luteinizing hormone/chorionic gonadotropin receptor

Severe skeletal complications in Japanese patients with type 1 Gaucher disease

Gitelman's syndrome (familial hypokalemia-hypomagnesemia)

Characteristics of gene mutations among 32 unrelated Japanese Gaucher disease patients : absence of the common Jewish 84GG and 1226G mutations

Development of a human mitochondria-focused cDNA microarray (hMitChip) and validation in skeletal muscle cells: implications for pharmaco- and mitogenomics

Mutation screening of 17 Japanese patients with neuropathic Gaucher disease

Kidney abnormalities in Hajdu-Cheney syndrome

GermlncRNA: a unique catalogue of long non-coding RNAs and associated regulations in male germ cell development

Do clocks run clockwise?

Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3)

Managed care and the Hippocratic Oath

Characterization of the cDNA encoding human nucleophosmin and studies of its role in normal and abnormal growth

Segregation of Allgrove (triple-A) syndrome in Puerto Rican kindreds with chromosome 12 (12q13) polymorphic markers

Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher disease

Tissue Zinc and Copper Levels in Diabetic C57BL/KsJ (db/db) Mice Fed a Zinc-Deficient Diet: Lack of Evidence for Specific Depletion of Tissue Zinc Stores

Cloning of a Human Acid Sphingomyelinase cDNA with a New Mutation That Renders the Enzyme Inactive

Zinc deficiency acts as a co-teratogen with alcohol in fetal alcohol syndrome

Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online

Congenital Adrenal Hyperplasia: Molecular Genetics and Alternative Approaches to Treatment

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