SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue (English)
- New search for: Jay, Philippe
- New search for: Sahly, Iman
- New search for: Gozé, Catherine
- New search for: Taviaux, Sylvie
- New search for: Poulat, Francis
- New search for: Couly, Gérard
- New search for: Abitbol, Marc
- New search for: Berta, Philippe
- New search for: Jay, Philippe
- New search for: Sahly, Iman
- New search for: Gozé, Catherine
- New search for: Taviaux, Sylvie
- New search for: Poulat, Francis
- New search for: Couly, Gérard
- New search for: Abitbol, Marc
- New search for: Berta, Philippe
In:
Human molecular genetics
;
6
, 7
;
1069-
;
1997
- Article (Journal) / Electronic Resource
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Title:SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue
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Contributors:Jay, Philippe ( author ) / Sahly, Iman ( author ) / Gozé, Catherine ( author ) / Taviaux, Sylvie ( author ) / Poulat, Francis ( author ) / Couly, Gérard ( author ) / Abitbol, Marc ( author ) / Berta, Philippe ( author )
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Published in:Human molecular genetics ; 6, 7 ; 1069-
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Publisher:
- New search for: Oxford University Press
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Publication date:1997-07-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 6, Issue 7
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 971
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Transition from Premutation to Full Mutation in Fragile X Syndrome is Likely to be PrezygoticMoutou, Céline / Vincent, Marie-Claire / Biancalana, Valérie / Mandel, Jean-Louis et al. | 1997
- 981
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Visual Pigment Gene Structure and Expression in Human RetinaeYamaguchi, Tomohiko / Motulsky, Arno G. / Deeb, Samir S. et al. | 1997
- 991
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Interchromosomal Duplications of the Adrenoleukodystrophy Locus: A Phenomenon of Pericentromeric PlasticityEichler, Evan E. / Budarf, Marcia L. / Rocchi, Mariano / Deaven, Larry L. / Doggett, Norman A. / Baldini, Antonio / Nelson, David L. / Mohrenweiser, Harvey W. et al. | 1997
- 1003
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Evidence by Allelic Association-Dependent Methods for a Type 1 Diabetes Polygene (IDDM6) on Chromosome 18q21Merriman, Tony / Twells, Rebecca / Merriman, Marilyn / Eaves, Iain / Cox, Roger / Cucca, Francesco / McKinney, Patricia / Shield, Julian / Baum, David / Bosi, Emanuele et al. | 1997
- 1011
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Evidence for a Type 1 Diabetes Susceptibility Locus (IDDM10) on Human Chromosome 10p11-q11Reed, Peter / Cucca, Francesco / Jenkins, Suzanne / Merriman, Marilyn / Wilson, Amanda / McKinney, Patricia / Bosi, Emanuele / Joner, Geir / Rønningen, Kjersti / Thorsby, Erik et al. | 1997
- 1017
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The Molecular Basis of the Kidd Blood Group Polymorphism and Its Lack of Association With Type 1 Diabetes SusceptibilityOlivès, Bernadette / Merriman, Marilyn / Bailly, Pascal / Bain, Stephen / Barnett, Anthony / Todd, John / Cartron, Jean-Pierre / Merriman, Tony et al. | 1997
- 1021
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Elastin Point Mutations Cause an Obstructive Vascular Disease, Supravalvular Aortic StenosisLi, Dean Y. / Toland, Amanda E. / Boak, Beth B. / Atkinson, Donald L. / Ensing, Gregory J. / Morris, Colleen A. / Keating, Mark T. et al. | 1997
- 1029
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Elastin: Genomic Structure and Point Mutations in Patients with Supravalvular Aortic StenosisTassabehji, Mayada / Metcalfe, Kay / Donnai, Dian / Hurst, Jane / Reardon, William / Burch, Michael / Read, Andrew P. et al. | 1997
- 1037
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Molecular Basis of the Brindled Mouse Mutant (Mobr): A Murine Model of Menkes DiseaseGrimes, Andrew / Hearn, Catherine J. / Lockhart, Paul / Newgreen, Don F. / Mercer, Julian F. B. et al. | 1997
- 1043
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Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transportersKuo, YM / Gitschier, J / Packman, S et al. | 1997
- 1051
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Genetic Predisposition to Phaeochromocytoma: Analysis of Candidate Genes GDNF, RET and VHLWoodward, Emma R. / Eng, Charis / McMahon, Rob / Voutilainen, Raimo / Affara, Nabeel A. / Ponder, Bruce A. J. / Maher, Eamonn R. et al. | 1997
- 1057
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Isolation and Characterisation of the NBR2 Gene Which Lies Head to Head with the Human BRCA1 GeneXu, Chun-Fang / Brown, Melissa A. / Nicolai, Hans / Chambers, Julie A. / Griffiths, Beatrice L. / Solomon, Ellen et al. | 1997
- 1063
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Single Sperm Analysis of the CAG Repeats in the Gene for Machado-Joseph Disease (MJD1): Evidence for Non-Mendelian Transmission of the MJD1 Gene and for the Effect of the Intragenic CGG/GGG Polymorphism on the Intergenerational InstabilityTakiyama, Y. / Sakoe, K. / Soutome, M. / Namekawa, M. / Ogawa, T. / Nakano, I. / Igarashi, S. / Oyake, M. / Tanaka, H. / Tsuji, S. et al. | 1997
- 1069
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SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous TissueJay, Philippe / Sahly, Iman / Gozé, Catherine / Taviaux, Sylvie / Poulat, Francis / Couly, Gérard / Abitbol, Marc / Berta, Philippe et al. | 1997
- 1079
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Translocation Breakpoint Maps 5 kb 3' from TWIST in a Patient Affected with Saethre-Chotzen SyndromeKrebs, Inge / Weis, Isabel / Hudler, Melanie / Rommens, Johanna M. / Roth, Helmut / Scherer, Steven W. / Tsui, Lap-Chee / Füchtbauer, Ernst-Martin / Grzeschik, Karl-Heinz / Tsuji, Kazushiro et al. | 1997
- 1087
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Mutations in the Chediak-Higashi Syndrome Gene (CHS1) Indicate Requirement for the Complete 3801 Amino Acid CHS ProteinKarim, Mohammad A. / Nagle, Deborah L. / Kandil, Hesham H. / Burger, Joachim / Moore, Karen J. / Spritz, Richard A. et al. | 1997
- 1091
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Identification of Mutations in Two Major mRNA Isoforms of the Chediak-Higashi Syndrome Gene in Human and MouseBarbosa, Maria D. F. S. / Barrat, Franck J. / Tchernev, Velizar T. / Nguyen, Quan A. / Mishra, Vishnu S. / Colman, Steven D. / Pastural, Elodie / Dufourcq-Lagelouse, Rémi / Fischer, Alain / Holcombe, Randall F. et al. | 1997
- 1099
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Polymorphisms in the Apolipoprotein(a) Gene and Their Relationship to Allele Size and Plasma Lipoprotein(a) ConcentrationPuckey, Loretto H. / Lawn, Richard M. / Knight, Brian L. et al. | 1997
- 1109
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Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase subunit (PHKB)Burwinkel, B. / Maichele, A. J. / Aagenaes, O. / Bakker, H. D. / Lerner, A. / Shin, Y. S. / Strachan, J. A. / Kilimann, M. W. et al. | 1997
- 1109
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Autosomal Glycogenosis of Liver and Muscle Due to Phosphorylase Kinase Deficiency is Caused by Mutations in the Phosphorylase Kinase {beta} Subunit (PHKB)Burwinkel, Barbara / Maichele, Andrea J. / Aagenaes, Øystein / Bakker, Henk D. / Lerner, Aaron / Shin, Yoon S. / Strachan, Judith A. / Kilimann, Manfred W. et al. | 1997
- 1117
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Human MSH2 Binds to Trinucleotide Repeat DNA Structures Associated with Neurodegenerative DiseasesPearson, Christopher E. / Ewel, Amy / Acharya, Samir / Fishel, Richard A. / Sinden, Richard R. et al. | 1997
- 1125
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Modulation of Disease Severity of Dystrophic Epidermolysis Bullosa By a Splice Site Mutation in Combination with a Missense Mutation in the COL7A1 GeneWinberg, Jan-Olof / Hammami-Hauasli, Nadja / Nilssen, Øivind / Anton-Lamprecht, Ingrun / Naylor, Susan L. / Kerbacher, Karen / Zimmermann, Mirjam / Krajci, Peter / Gedde-Dahl, Tobias / Bruckner-Tuderman, Leena et al. | 1997
- 1137
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A Novel Human Serine-Threonine Phosphatase Related to the Drosophila Retinal Degeneration C (rdgC) Gene is Selectively Expressed in Sensory Neurons of Neural Crest OriginMontini, E. / Rugarli, E. I. / Van de Vosse, E. / Andolfi, G. / Mariani, M. / Puca, A. A. / Consalez, G. G. / den Dunnen, J. T. / Ballabio, A. / Franco, B. et al. | 1997
- 1147
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Missense Mutations in the Human Glutathione Synthetase Gene Result in Severe Metabolic Acidosis, 5-Oxoprolinuria, Hemolytic Anemia and Neurological DysfunctionDahl, Niklas / Pigg, Maritta / Ristoff, Ellinor / Gali, Rayappa / Carlsson, Birgit / Mannervik, Bengt / Larsson, Agne / Board, Philip et al. | 1997
- 1153
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Incomplete Rescue of Cystic Fibrosis Transmembrane Conductance Regulator Deficient Mice by the Human CFTR cDNARozmahel, Richard / Gyömörey, Katalin / Plyte, Sue / Nguyen, Van / Wilschanski, Michael / Durie, Peter / Bear, Christine E. / Tsui, Lap-Chee et al. | 1997
- 1163
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The Oral-Facial-Digital Syndrome Type 1 (OFD1), a Cause of Polycystic Kidney Disease and Associated Malformations, Maps to Xp22.2-Xp22.3Feather, Sally A. / Woolf, Adrian S. / Donnai, Dian / Malcolm, Sue / Winter, Robin M. et al. | 1997
- 1169
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Germline Mutations of the MEN1 Gene in Familial Multiple Endocrine Neoplasia Type 1 and Related StatesAgarwal, Sunita K. / Beth Kester, Mary / Debelenko, Larisa V. / Heppner, Christina / Emmert-Buck, Michael R. / Skarulis, Monica C. / Doppman, John L. / Kim, Young S. / Lubensky, Irina A. / Zhuang, Zhengping et al. | 1997
- 1177
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Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) GeneLemmens, Irma / Van de Ven, Wim J. M. / Kas, Koen / Zhang, Chang X. / Giraud, Sophie / Wautot, Virginie / Buisson, Nathalie / De Witte, Ko / Salandre, Janine / Lenoir, Gilbert et al. | 1997
- 1185
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Dystrobrevin Deficiency at the Sarcolemma of Patients with Muscular DystrophyMetzinger, Laurent / Blake, Derek J. / Squier, Marian V. / Anderson, Louise V. B. / Deconinck, Anne E. / Nawrotzki, Ralph / Hilton-Jones, David / Davies, Kay E. et al. | 1997