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Results: 1-12 |
Results: 12
THE ANHIDROTIC ECTODERMAL DYSPLASIA GENE (EDA) UNDERGOES ALTERNATIVE SPLICING AND ENCODES ECTODYSPLASIN-A WITH DELETION MUTATIONS IN COLLAGENOUS REPEATS
Authors: BAYES M HARTUNG AJ EZER S PISPA J THESLEFF I SRIVASTAVA AK KERE J
Citation: M. Bayes et al., THE ANHIDROTIC ECTODERMAL DYSPLASIA GENE (EDA) UNDERGOES ALTERNATIVE SPLICING AND ENCODES ECTODYSPLASIN-A WITH DELETION MUTATIONS IN COLLAGENOUS REPEATS, Human molecular genetics (Print), 7(11), 1998, pp. 1661-1669
EXPRESSION OF THE ANHIDROTIC ECTODERMAL DYSPLASIA GENE IS REDUCED IN SKIN-CANCER COINCIDING WITH REDUCED E-CADHERIN
Authors: MONTONEN O EZER S LAURIKKALA J KARJALAINENLINDSBERG ML THESLEFF I KERE J SAARIALHOKERE U
Citation: O. Montonen et al., EXPRESSION OF THE ANHIDROTIC ECTODERMAL DYSPLASIA GENE IS REDUCED IN SKIN-CANCER COINCIDING WITH REDUCED E-CADHERIN, Experimental dermatology, 7(4), 1998, pp. 168-174
THE GENE DEFECTIVE IN ANHIDROTIC ECTODERMAL DYSPLASIA IS EXPRESSED INTHE DEVELOPING EPITHELIUM, NEUROECTODERM, THYMUS, AND BONE
Authors: MONTONEN O EZER S SAARIALHOKERE UK HERVA R KARJALAINENLINDSBERG ML KAITILA I SCHLESSINGER D SRIVASTAVA AK THESLEFF I KERE J
Citation: O. Montonen et al., THE GENE DEFECTIVE IN ANHIDROTIC ECTODERMAL DYSPLASIA IS EXPRESSED INTHE DEVELOPING EPITHELIUM, NEUROECTODERM, THYMUS, AND BONE, The Journal of histochemistry and cytochemistry, 46(3), 1998, pp. 281-289
ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) PROTEIN EXPRESSED IN MCF-7 CELLS ASSOCIATES WITH CELL-MEMBRANE AND INDUCES ROUNDING
Authors: EZER S SCHLESSINGER D SRIVASTAVA A KERE J
Citation: S. Ezer et al., ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) PROTEIN EXPRESSED IN MCF-7 CELLS ASSOCIATES WITH CELL-MEMBRANE AND INDUCES ROUNDING, Human molecular genetics, 6(9), 1997, pp. 1581-1587
THE TABBY PHENOTYPE IS CAUSED BY MUTATION IN A MOUSE HOMOLOG OF THE EDA GENE THAT REVEALS NOVEL MOUSE AND HUMAN EXONS AND ENCODES A PROTEIN(ECTODYSPLASIN-A) WITH COLLAGENOUS DOMAINS
Authors: SRIVASTAVA AK PISPA J HARTUNG AJ DU YZ EZER S JENKS T SHIMADA T PEKKANEN M MIKKOLA ML KO MSH THESLEFF I KERE J SCHLESSINGER D
Citation: Ak. Srivastava et al., THE TABBY PHENOTYPE IS CAUSED BY MUTATION IN A MOUSE HOMOLOG OF THE EDA GENE THAT REVEALS NOVEL MOUSE AND HUMAN EXONS AND ENCODES A PROTEIN(ECTODYSPLASIN-A) WITH COLLAGENOUS DOMAINS, Proceedings of the National Academy of Sciences of the United Statesof America, 94(24), 1997, pp. 13069-13074
CHANGES IN ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) GENE-EXPRESSION CORRELATE WITH DIMINISHED E-CADHERIN PRODUCTION
Authors: MONTONEN O EZER S KERE J SAARIALHOKERE U
Citation: O. Montonen et al., CHANGES IN ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) GENE-EXPRESSION CORRELATE WITH DIMINISHED E-CADHERIN PRODUCTION, Journal of investigative dermatology, 109(3), 1997, pp. 422-422
THE GENE DEFECTIVE IN ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) IS EXPRESSED IN THE DEVELOPING EPITHELIUM, NEUROECTODERM AND BONE
Authors: MONTONEN O EZER S HERVA R KARJALAINENLINDSBERG ML KAITILA I SCHLESSINGER D SRIVASTAVA A THESLEFF I KERE J SAARIALHOKERE U
Citation: O. Montonen et al., THE GENE DEFECTIVE IN ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) IS EXPRESSED IN THE DEVELOPING EPITHELIUM, NEUROECTODERM AND BONE, Journal of investigative dermatology, 108(4), 1997, pp. 360-360
CLONING AND EXPRESSION OF TABBY
Authors: SRIVASTAVA A PEKKANEN M MONTONEN O EZER S KERE J THESLEFF I
Citation: A. Srivastava et al., CLONING AND EXPRESSION OF TABBY, Developmental biology, 186(2), 1997, pp. 116-116
FUNCTIONAL-ANALYSIS OF ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) GENE-PRODUCT
Authors: KERE J EZER S MONTONEN O SAARIALHOKERE U BAYES M PISPA J LAURIKKALA J SRIVASTAVA AK THESLEFF I SCHLESSINGER D
Citation: J. Kere et al., FUNCTIONAL-ANALYSIS OF ANHIDROTIC ECTODERMAL DYSPLASIA (EDA) GENE-PRODUCT, American journal of human genetics, 61(4), 1997, pp. 223-223
EDA GENE HOMOLOG IS MUTATED TO ACCOUNT FOR DEFICIENT ECTODERMAL DEVELOPMENT IN TABBY (TA) MICE, AND REVEALS A NOVEL ALTERNATIVE 3'-HUMAN EXON
Authors: SRIVASTAVA AK PISPA J DU Y HARTUNG AP EZER S JENKS T SHIMADA T PEKKANEN M KO MSH THESLEFF I KERE J SCHLESSINGER D
Citation: Ak. Srivastava et al., EDA GENE HOMOLOG IS MUTATED TO ACCOUNT FOR DEFICIENT ECTODERMAL DEVELOPMENT IN TABBY (TA) MICE, AND REVEALS A NOVEL ALTERNATIVE 3'-HUMAN EXON, American journal of human genetics, 61(4), 1997, pp. 2036-2036
X-LINKED ANHIDROTIC (HYPOHIDROTIC) ECTODERMAL DYSPLASIA IS CAUSED BY MUTATION IN A NOVEL TRANSMEMBRANE PROTEIN
Authors: KERE J SRIVASTAVA AK MONTONEN O ZONANA J THOMAS N FERGUSON B MUNOZ F MORGAN D CLARKE A BAYBAYAN P CHEN EY EZER S SAARIALHOKERE U DELACHAPELLE A SCHLESSINGER D
Citation: J. Kere et al., X-LINKED ANHIDROTIC (HYPOHIDROTIC) ECTODERMAL DYSPLASIA IS CAUSED BY MUTATION IN A NOVEL TRANSMEMBRANE PROTEIN, Nature genetics, 13(4), 1996, pp. 409-416
UTILIZATION OF A POLYMORPHIC VARIABLE-NUMBER-TANDEM-REPEAT DNA REGIONWITHIN THE RB1 GENE FOR EARLY DIAGNOSIS OF HEREDITARY RETINOBLASTOMA
Authors: HERZOG R ARUSH MWB EZER S ON MG LEV Z
Citation: R. Herzog et al., UTILIZATION OF A POLYMORPHIC VARIABLE-NUMBER-TANDEM-REPEAT DNA REGIONWITHIN THE RB1 GENE FOR EARLY DIAGNOSIS OF HEREDITARY RETINOBLASTOMA, Israel journal of medical sciences, 29(5), 1993, pp. 312-313
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