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Results: 1-19 |
Results: 19
X-LINKED DYSKERATOSIS-CONGENITA IS CAUSED BY MUTATIONS IN A HIGHLY CONSERVED GENE WITH PUTATIVE NUCLEOLAR FUNCTIONS
Authors: HEISS NS KNIGHT SW VULLIAMY TJ KLAUCK SM WIEMANN S MASON PJ POUSTKA A DOKAL I
Citation: Ns. Heiss et al., X-LINKED DYSKERATOSIS-CONGENITA IS CAUSED BY MUTATIONS IN A HIGHLY CONSERVED GENE WITH PUTATIVE NUCLEOLAR FUNCTIONS, Nature genetics, 19(1), 1998, pp. 32-38
SEARCHING FOR SUSCEPTIBILITY GENES FOR INFANTILE-AUTISM
Authors: KLAUCK SM POUSTKA F BENNER A SPIELER A POUSTKA A
Citation: Sm. Klauck et al., SEARCHING FOR SUSCEPTIBILITY GENES FOR INFANTILE-AUTISM, American journal of medical genetics, 81(6), 1998, pp. 481-482
X-LINKED DYSKERATOSIS-CONGENITA IS CAUSED BY MUTATIONS IN A HIGHLY CONSERVED GENE ENCODING A PROTEIN WITH PUTATIVE NUCLEOLAR FUNCTIONS
Authors: HEISS NS KNIGHT SW VULLIAMY TJ KLAUCK SM WIEMANN S MASON PJ POUSTKA A DOKAL I
Citation: Ns. Heiss et al., X-LINKED DYSKERATOSIS-CONGENITA IS CAUSED BY MUTATIONS IN A HIGHLY CONSERVED GENE ENCODING A PROTEIN WITH PUTATIVE NUCLEOLAR FUNCTIONS, British Journal of Haematology, 102(1), 1998, pp. 270-271
SEROTONIN TRANSPORTER (5-HTT) GENE VARIANTS ASSOCIATED WITH AUTISM
Authors: KLAUCK SM POUSTKA F BENNER A LESCH KP POUSTKA A
Citation: Sm. Klauck et al., SEROTONIN TRANSPORTER (5-HTT) GENE VARIANTS ASSOCIATED WITH AUTISM, Human molecular genetics, 6(13), 1997, pp. 2233-2238
A GENE IN HUMAN-CHROMOSOME BAND XQ28 (GABRE) DEFINES A PUTATIVE NEW SUBUNIT CLASS OF THE GABA(A) NEUROTRANSMITTER RECEPTOR
Authors: WILKE K GAUL R KLAUCK SM POUSTKA A
Citation: K. Wilke et al., A GENE IN HUMAN-CHROMOSOME BAND XQ28 (GABRE) DEFINES A PUTATIVE NEW SUBUNIT CLASS OF THE GABA(A) NEUROTRANSMITTER RECEPTOR, Genomics, 45(1), 1997, pp. 1-10
GENOMIC STRUCTURE OF A NOVEL LIM DOMAIN GENE (ZNF185) IN XQ28 AND COMPARISONS WITH THE ORTHOLOGOUS MURINE TRANSCRIPT
Authors: HEISS NS GLOECKNER G BACHNER D KIOSCHIS P KLAUCK SM HINZMANN B ROSENTHAL A HERMAN GE POUSTKA A
Citation: Ns. Heiss et al., GENOMIC STRUCTURE OF A NOVEL LIM DOMAIN GENE (ZNF185) IN XQ28 AND COMPARISONS WITH THE ORTHOLOGOUS MURINE TRANSCRIPT, Genomics, 43(3), 1997, pp. 329-338
MOLECULAR-GENETIC ANALYSIS OF THE FMR-1 GENE IN A LARGE COLLECTION OFAUTISTIC PATIENTS
Authors: KLAUCK SM MUNSTERMANN E BIEBERMARTIG B RUHL D LISCH S SCHMOTZER G POUSTKA A POUSTKA F
Citation: Sm. Klauck et al., MOLECULAR-GENETIC ANALYSIS OF THE FMR-1 GENE IN A LARGE COLLECTION OFAUTISTIC PATIENTS, Human genetics, 100(2), 1997, pp. 224-229
THE 5-HT TRANSPORTER GENE-LINKED POLYMORPHIC REGION (5-HTTLPR) IN EVOLUTIONARY PERSPECTIVE - ALTERNATIVE BIALLELIC VARIATION IN RHESUS-MONKEYS
Authors: LESCH KP MEYER J GLATZ K FLUGGE G HINNEY A HEBEBRAND J KLAUCK SM POUSTKA A POUSTKA F BENGEL D MOSSNER R RIEDERER P HEILS A
Citation: Kp. Lesch et al., THE 5-HT TRANSPORTER GENE-LINKED POLYMORPHIC REGION (5-HTTLPR) IN EVOLUTIONARY PERSPECTIVE - ALTERNATIVE BIALLELIC VARIATION IN RHESUS-MONKEYS, Journal of neural transmission, 104(11-12), 1997, pp. 1259-1266
ASSOCIATION OF THE SEROTONIN TRANSPORTER (5-HTT) PROMOTER LONG VARIANT WITH AUTISM
Authors: KLAUCK SM POUSTKA F BENNER A SPIELER A LESCH KP POUSTKA A
Citation: Sm. Klauck et al., ASSOCIATION OF THE SEROTONIN TRANSPORTER (5-HTT) PROMOTER LONG VARIANT WITH AUTISM, American journal of medical genetics, 74(6), 1997, pp. 620-620
ASSOCIATION OF THE SEROTONIN TRANSPORTER (5-HTT) PROMOTER LONG VARIANT WITH AUTISM
Authors: KLAUCK SM POUSTKA F BENNER A SPIELER A LESCH KP POUSTKA A
Citation: Sm. Klauck et al., ASSOCIATION OF THE SEROTONIN TRANSPORTER (5-HTT) PROMOTER LONG VARIANT WITH AUTISM, American journal of human genetics, 61(4), 1997, pp. 1635-1635
A GENE MUTATED IN X-LINKED MYOTUBULAR MYOPATHY DEFINES A NEW PUTATIVETYROSINE PHOSPHATASE FAMILY CONSERVED IN YEAST
Authors: LAPORTE J HU LJ KRETZ C MANDEL JL KIOSCHIS P COY JF KLAUCK SM POUSTKA A DAHL N
Citation: J. Laporte et al., A GENE MUTATED IN X-LINKED MYOTUBULAR MYOPATHY DEFINES A NEW PUTATIVETYROSINE PHOSPHATASE FAMILY CONSERVED IN YEAST, Nature genetics, 13(2), 1996, pp. 175-182
A 900-KB COSMID CONTIG AND 10 NEW TRANSCRIPTS WITHIN THE CANDIDATE REGION FOR MYOTUBULAR MYOPATHY (MTM1)
Authors: KIOSCHIS P ROGNER UC PICK E KLAUCK SM HEISS N SIEBENHAAR R KORN B COY JF LAPORTE J LIECHTIGALLATI S POUSTKA A
Citation: P. Kioschis et al., A 900-KB COSMID CONTIG AND 10 NEW TRANSCRIPTS WITHIN THE CANDIDATE REGION FOR MYOTUBULAR MYOPATHY (MTM1), Genomics, 33(3), 1996, pp. 365-373
IDENTIFICATION OF NOVEL MUTATIONS IN 3 FAMILIES WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY
Authors: KLAUCK SM WILGENBUS P YATES JRW MULLER CR POUSTKA A
Citation: Sm. Klauck et al., IDENTIFICATION OF NOVEL MUTATIONS IN 3 FAMILIES WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY, Human molecular genetics, 4(10), 1995, pp. 1853-1857
HSV TYPE-1 GENOME VARIANTS FROM PERSISTENTLY PRODUCTIVE INFECTIONS INRAJI AND BJAB CELL-LINES
Authors: KLAUCK SM HAMPL W KLEINSCHMIDT AK
Citation: Sm. Klauck et al., HSV TYPE-1 GENOME VARIANTS FROM PERSISTENTLY PRODUCTIVE INFECTIONS INRAJI AND BJAB CELL-LINES, Archives of virology, 140(7), 1995, pp. 1195-1213
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D3S666 LOCUS
Authors: KLAUCK SM YAMAKAWA K SEIZINGER BR
Citation: Sm. Klauck et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D3S666 LOCUS, Human molecular genetics, 3(5), 1994, pp. 840-840
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D3S1255 LOCUS
Authors: KLAUCK SM WHISENANT E WOOD M DRABKIN HA SEIZINGER BR
Citation: Sm. Klauck et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D3S1255 LOCUS, Human molecular genetics, 3(5), 1994, pp. 840-840
EVOLUTIONARY CONSERVATION AND GENOMIC ORGANIZATION OF XAP-4, AN XQ28 LOCATED GENE CODING FOR A HUMAN RAB GDP-DISSOCIATION INHIBITOR (GDI)
Authors: SEDLACEK Z KONECKI DS KORN B KLAUCK SM POUSTKA A
Citation: Z. Sedlacek et al., EVOLUTIONARY CONSERVATION AND GENOMIC ORGANIZATION OF XAP-4, AN XQ28 LOCATED GENE CODING FOR A HUMAN RAB GDP-DISSOCIATION INHIBITOR (GDI), Mammalian genome, 5(10), 1994, pp. 633-639
XAP-4, A NOVEL GENE CODING FOR A RAB GDP-DISSOCIATION INHIBITOR, IS CONSERVED IN EVOLUTION AND RESIDES IN A VERY GENE-RICH REGION OF XQ28
Authors: SEDLACEK Z KONECKI DS KOM B KLAUCK SM POUSTKA A
Citation: Z. Sedlacek et al., XAP-4, A NOVEL GENE CODING FOR A RAB GDP-DISSOCIATION INHIBITOR, IS CONSERVED IN EVOLUTION AND RESIDES IN A VERY GENE-RICH REGION OF XQ28, Cytogenetics and cell genetics, 67(4), 1994, pp. 356-356
CYTOGENETIC AND FLUORESCENCE IN-SITU HYBRIDIZATION STUDIES ON SPORADIC AND HEREDITARY TUMORS ASSOCIATED WITH VON HIPPEL-LINDAU SYNDROME (VHL)
Authors: DECKER HJH KLAUCK SM LAWRENCE JB MCNEIL J SMITH D GEMMILL RM SANDBERG AA NEUMANN HHP SIMON B GREEN J SEIZINGER BR
Citation: Hjh. Decker et al., CYTOGENETIC AND FLUORESCENCE IN-SITU HYBRIDIZATION STUDIES ON SPORADIC AND HEREDITARY TUMORS ASSOCIATED WITH VON HIPPEL-LINDAU SYNDROME (VHL), Cancer genetics and cytogenetics, 77(1), 1994, pp. 1-13
Risultati: 1-19 |