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20 results for author:"Reichwald K."Drop in Literature Citations

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High tandem repeat content in the genome of the short-lived annual fish Nothobranchius furzeri: a new vertebrate model for aging research.

Reichwald K., Lauber C., Nanda I., Kirschner J., Hartmann N., Schories S., Gausmann U., Taudien S., Schilhabel M.B., Szafranski K. et al.

Genome Biol. 10:R16-R16(2009) · UniProtKB (3)

Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.

Muller T.D., Reichwald K., Bronner G., Kirschner J., Nguyen T.T., Scherag A., Herzog W., Herpertz-Dahlmann B., Lichtner P., Meitinger T. et al.

Child Adolesc Psychiatry Ment Health 2:33-33(2008) · Mapped (13)

Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans.

Wermter A.K., Scherag A., Meyre D., Reichwald K., Durand E., Nguyen T.T., Koberwitz K., Lichtner P., Meitinger T., Schafer H. et al.

Eur. J. Hum. Genet. 16:1126-1134(2008) · Mapped (8)

Functional characterization of two novel 5' untranslated exons reveals a complex regulation of NOD2 protein expression.

Rosenstiel P., Huse K., Franke A., Hampe J., Reichwald K., Platzer C., Roberts R.G., Mathew C.G., Platzer M., Schreiber S.

BMC Genomics 8:472-472(2007) · Mapped (7)

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

Friedel S., Reichwald K., Scherag A., Brumm H., Wermter A.K., Fries H.R., Koberwitz K., Wabitsch M., Meitinger T., Platzer M. et al.

BMC Genet. 8:17-17(2007) · Mapped (1)

No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.

Muller T.D., Reichwald K., Wermter A.K., Bronner G., Nguyen T.T., Friedel S., Koberwitz K., Engeli S., Lichtner P., Meitinger T. et al.

Mol. Genet. Metab. 90:429-434(2007) · Mapped (3)

Chicken ovalbumin upstream promoter transcription factor II regulates uncoupling protein 3 gene transcription in Phodopus sungorus.

Fromme T., Reichwald K., Platzer M., Li X.S., Klingenspor M.

BMC Mol. Biol. 8:1-1(2007) · UniProtKB (4)

DNA sequence and analysis of human chromosome 8.

Nusbaum C., Mikkelsen T.S., Zody M.C., Asakawa S., Taudien S., Garber M., Kodira C.D., Schueler M.G., Shimizu A., Whittaker C.A. et al.

Nature 439:331-335(2006) · UniProtKB (470) · Mapped (2)

Mutation analysis of the MCHR1 gene in human obesity.

Wermter A.-K., Reichwald K., Buech T., Geller F., Platzer C., Huse K., Hess C., Remschmidt H., Gudermann T., Preibisch G. et al.

Eur. J. Endocrinol. 152:851-862(2005) · UniProtKB (1) · Mapped (3)

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity.

Schauble N., Reichwald K., Grassl W., Bechstein H., Muller H.C., Scherag A., Geller F., Utting M., Siegfried W., Goldschmidt H. et al.

J. Nutr. 135:1387-1392(2005) · Mapped (3)

The DNA sequence of the human X chromosome.

Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al.

Nature 434:325-337(2005) · UniProtKB (1,199)

Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.

Friedel S., Horro F.F., Wermter A.K., Geller F., Dempfle A., Reichwald K., Smidt J., Bronner G., Konrad K., Herpertz-Dahlmann B. et al.

Am. J. Med. Genet. B Neuropsychiatr. Genet. 132B:96-99(2005) · Mapped (6)

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity.

Geller F., Reichwald K., Dempfle A., Illig T., Vollmert C., Herpertz S., Siffert W., Platzer M., Hess C., Gudermann T. et al.

Am. J. Hum. Genet. 74:572-581(2004) · Mapped (1)

Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759.

Appel S., Filter M., Reis A., Hennies H.C., Bergheim A., Ogilvie E., Arndt S., Simmons A., Lovett M., Hide W. et al.

Eur. J. Hum. Genet. 10:17-25(2002) · UniProtKB (1)

Identification and localization of a new human myotubularin-related protein gene, MTMR8, on 8p22-p23.

Appel S., Reichwald K., Zimmermann W., Reis A., Rosenthal A., Hennies H.C.

Genomics 75:6-8(2001) · UniProtKB (1)

The DNA sequence of human chromosome 21.

Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al.

Nature 405:311-319(2000) · UniProtKB (510)

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions.

Reichwald K., Thiesen J., Wiehe T., Weitzel J., Poustka W.A., Rosenthal A., Platzer M., Stratling W.H., Kioschis P.

Mamm. Genome 11:182-190(2000) · UniProtKB (4) · Mapped (5)

Human renin binding protein: complete genomic sequence and association of an intronic T/C polymorphism with the prorenin level in males.

Knoll A., Schunkert H., Reichwald K., Danser A.H., Bauer D., Platzer M., Stein G., Rosenthal A.

Hum. Mol. Genet. 6:1527-1534(1997) · Mapped (2)

The genomic organization of a human creatine transporter (CRTR) gene located in Xq28.

Sandoval N., Bauer D., Brenner V., Coy J.F., Drescher B., Kioschis P., Korn B., Nyakatura G., Poustka A., Reichwald K. et al.

Genomics 35:383-385(1996) · UniProtKB (1)

Expression of the allatostatin gene in endocrine cells of the cockroach midgut.

Reichwald K., Unnithan G.C., Davis N.T., Agricola H., Feyereisen R.

Proc. Natl. Acad. Sci. U.S.A. 91:11894-11898(1994) · UniProtKB (1)

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