A Meindl Selected Research

X-Linked 9 Mental Retardation

9/2004

A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9).

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A Meindl Research Topics

Disease

2	Breast Neoplasms (Breast Cancer) 12/2011 - 09/2008
2	Neoplasms (Cancer) 12/2011 - 01/2001
2	congenital stationary Night blindness 11/2000 - 07/2000
1	Lymphatic Metastasis 12/2011
1	Hyper-IgM Immunodeficiency Syndrome (Hyper-IgM Syndrome) 09/2009
1	Inflammation (Inflammations) 01/2007
1	X-Linked Mental Retardation (Mental Retardation, X Linked) 09/2004
1	X-Linked 9 Mental Retardation 09/2004
1	Intellectual Disability (Idiocy) 09/2004
1	Androgen-Insensitivity Syndrome (Testicular Feminization) 04/2002
1	Ocular Albinism 03/2001
1	Renal Cell Carcinoma (Grawitz Tumor) 01/2001
1	Sarcoma (Soft Tissue Sarcoma) 01/2001
1	Alveolar Soft Part Sarcoma 01/2001
1	Myopia 07/2000
1	Strabismus (Squint) 07/2000
1	Lymphoma (Lymphomas) 02/2000

Drug/Important Bio-Agent (IBA)

2	DNA (Deoxyribonucleic Acid)IBA 03/2001 - 01/2001
1	Genetic Markers (Genetic Marker)IBA 12/2011
1	Epidermal Growth Factor (EGF)IBA 12/2011
1	CD40 Ligand (CD40L)IBA 09/2009
1	Codon (Codons)IBA 09/2008
1	Proline (L-Proline)FDA Link 09/2008
1	Antinuclear AntibodiesIBA 01/2007
1	MethyltransferasesIBA 09/2004
1	Proteins (Proteins, Gene)FDA Link 09/2004
1	Testosterone (Sustanon)FDA Link 04/2002
1	Transcription Factors (Transcription Factor)IBA 01/2001
1	Leucine-Rich Repeat ProteinsIBA 11/2000
1	Retinaldehyde (Retinal)IBA 07/2000
1	AntigensIBA 02/2000
1	RNA (Ribonucleic Acid)IBA 02/2000
1	Membrane Proteins (Integral Membrane Proteins)IBA 02/2000