Search Results - "HENKE, Lotte"

Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications by Ballantyne, Kaye N., Goedbloed, Miriam, Fang, Rixun, Schaap, Onno, Lao, Oscar, Wollstein, Andreas, Choi, Ying, van Duijn, Kate, Vermeulen, Mark, Brauer, Silke, Decorte, Ronny, Poetsch, Micaela, von Wurmb-Schwark, Nicole, de Knijff, Peter, Labuda, Damian, Vézina, Hélène, Knoblauch, Hans, Lessig, Rüdiger, Roewer, Lutz, Ploski, Rafal, Dobosz, Tadeusz, Henke, Lotte, Henke, Jürgen, Furtado, Manohar R., Kayser, Manfred

“…Nonrecombining Y-chromosomal microsatellites (Y-STRs) are widely used to infer population histories, discover genealogical relationships, and identify males…”
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Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit by Goedbloed, Miriam, Vermeulen, Mark, Fang, Rixun N., Lembring, Maria, Wollstein, Andreas, Ballantyne, Kaye, Lao, Oscar, Brauer, Silke, Krüger, Carmen, Roewer, Lutz, Lessig, Rüdiger, Ploski, Rafal, Dobosz, Tadeusz, Henke, Lotte, Henke, Jürgen, Furtado, Manohar R., Kayser, Manfred

“…The Y-chromosomal short tandem repeat (Y-STR) polymorphisms included in the AmpF l STR® Yfiler® polymerase chain reaction amplification kit have become widely…”
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Characteristics and Frequency of Germline Mutations at Microsatellite Loci from the Human Y Chromosome, as Revealed by Direct Observation in Father/Son Pairs by Kayser, Manfred, Roewer, Lutz, Hedman, Minttu, Henke, Lotte, Henke, Jürgen, Brauer, Silke, Krüger, Carmen, Krawczak, Michael, Nagy, Marion, Dobosz, Tadeusz, Szibor, Reinhard, de Knijff, Peter, Stoneking, Mark, Sajantila, Antti

“…A number of applications of analysis of human Y-chromosome microsatellite loci to human evolution and forensic science require reliable estimates of the…”
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OCA2481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations by Yuasa, Isao, Umetsu, Kazuo, Harihara, Shinji, Miyoshi, Aya, Saitou, Naruya, Park, Kyung Sook, Dashnyam, Bumbein, Jin, Feng, Lucotte, Gérard, Chattopadhyay, Prasanta K., Henke, Lotte, Henke, Jürgen

“…Asians as well as Europeans have light skin, for which no genes to date are known to be responsible. A mutation, Ala481Thr (c.G1559A), in the oculocutaneous…”
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A Comprehensive Analysis of Recently Integrated Human Ta L1 Elements by Myers, Jeremy S., Vincent, Bethaney J., Udall, Hunt, Watkins, W. Scott, Morrish, Tammy A., Kilroy, Gail E., Swergold, Gary D., Henke, Jurgen, Henke, Lotte, Moran, John V., Jorde, Lynn B., Batzer, Mark A.

“…The Ta ( transcribed, subset a) subfamily of L1 LINEs ( long interspersed elements) is characterized by a 3-bp ACA sequence in the 3′ untranslated region and…”
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Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific by Yuasa, Isao, Nakagawa, Mayumi, Umetsu, Kazuo, Harihara, Shinji, Matsusue, Aya, Nishimukai, Hiroaki, Fukumori, Yasuo, Saitou, Naruya, Park, Kyung Sook, Jin, Feng, Lucotte, Gérard, Chattopadhyay, Prasanta K, Henke, Lotte, Henke, Jürgen

“…Isoelectric focusing has revealed that human complement factor I (CFI) is controlled by two polymorphic alleles, CFI(*)A and CFI(*)B, and a few rare variant…”
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A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles by Yuasa, Isao, Irizawa, Yoshito, Nishimukai, Hiroaki, Fukumori, Yasuo, Umetsu, Kazuo, Nakayashiki, Nori, Saitou, Naruya, Henke, Lotte, Henke, Jürgen

“…In this study, a short tandem repeat (STR) polymorphism in intron 7 of the human complement factor I (CFI) gene was studied in 637 DNA samples obtained from…”
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A Japanese-specific allele in the GALNT11 gene by Yuasa, Isao, Umetsu, Kazuo, Matsusue, Aya, Nishimukai, Hiroaki, Harihara, Shinji, Fukumori, Yasuo, Saitou, Naruya, Jin, Feng, Chattopadhyay, Prasanta K, Henke, Lotte, Henke, Jürgen

“…Abstract In this study, five single nucleotide polymorphisms (SNPs) in the ABCC4 , FBN1 , CEP152 , ZNF804B , and GALNT11 genes were investigated to assess…”
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HERC1 polymorphisms: population-specific variations in haplotype composition by Yuasa, Isao, Umetsu, Kazuo, Nishimukai, Hiroaki, Fukumori, Yasuo, Harihara, Shinji, Saitou, Naruya, Jin, Feng, Chattopadhyay, Prasanta K., Henke, Lotte, Henke, Jürgen

“…Human HERC1 is one of six HERC proteins and may play an important role in intracellular membrane trafficking. The human HERC1 gene is suggested to have been…”
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Identification and characterization of novel rapidly mutating Y‐chromosomal short tandem repeat markers by Ralf, Arwin, Lubach, Delano, Kousouri, Nefeli, Winkler, Christian, Schulz, Iris, Roewer, Lutz, Purps, Josephine, Lessig, Rüdiger, Krajewski, Pawel, Ploski, Rafal, Dobosz, Tadeusz, Henke, Lotte, Henke, Jürgen, Larmuseau, Maarten H. D., Kayser, Manfred

“…Short tandem repeat polymorphisms on the male‐specific part of the human Y‐chromosome (Y‐STRs) are valuable tools in many areas of human genetics. Although…”
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Characterization of genomic rearrangements of the α1-acid glycoprotein/orosomucoid gene in Ghanaians by Yuasa, I., Nakamura, H., Henke, L., Henke, J., Nakagawa, M., Irizawa, Y., Umetsu, K.

“…In this study, the structure of the α1-acid glycoprotein (AGP), or orosomucoid (ORM), gene was investigated in a Ghanaian mother and her child, who shared an…”
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Long-term results of allogeneic penetrating limbo-keratoplasty in total limbal stem cell deficiency by Reinhard, Thomas, Spelsberg, Helga, Henke, Lotte, Kontopoulos, Theodoros, Enczmann, Jürgen, Wernet, Peter, Berschick, Peter, Sundmacher, Rainer, Böhringer, Daniel

“…To determine the prognosis of allogeneic penetrating limbo-keratoplasty in patients with total limbal stem cell deficiency and to find out if donor limbal stem…”
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Detection of manipulation in doping control urine sample collection: a multidisciplinary approach to determine identical urine samples by Thevis, Mario, Geyer, Hans, Mareck, Ute, Sigmund, Gerd, Henke, Jürgen, Henke, Lotte, Schänzer, Wilhelm

“…Manipulation of urine sampling in sports drug testing is considered a violation of anti-doping rules and is consequently sanctioned by regulatory authorities…”
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Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis by KAYSER, Manfred, LAO, Oscar, HOHOFF, Carsten, ILLING, Anett, JONKISZ, Anna, KUZNIAR, Piotr, LEBIODA, Arleta, LESSIG, Rüdiger, LEWICKI, Slawomir, MACIEJEWSKA, Agnieszka, MONIES, Dorota Marta, PAWLOWSKI, Ryszard, ANSLINGER, Katja, POETSCH, Micaela, SCHMID, Dagmar, SCHMIDT, Ulrike, SCHNEIDER, Peter M, STRADMANN-BELLINGHAUSEN, Beate, SZIBOR, Reinhard, WEGENER, Rudolf, WOZNIAK, Marcin, ZOLEDZIEWSKA, Magdalena, ROEWER, Lutz, AUGUSTIN, Christa, DOBOSZ, Tadeusz, PLOSKI, Rafal, BARGEL, Grazyna, EDELMANN, Jeanett, ELIAS, Sahar, HEINRICH, Marielle, HENKE, Jürgen, HENKE, Lotte

“…To test for human population substructure and to investigate human population history we have analysed Y-chromosome diversity using seven microsatellites…”
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A paternity case with three genetic incompatibilities between father and child due to maternal uniparental disomy 21 and a mutation at the Y chromosome by Mansuet-Lupo, Audrey, Henke, Jurgen, Henke, Lotte, Blank, Cornelia, Ernsting, Anette, Kozlowski, Peter, Rouger, Philippe, Van Huffel, Veronique

“…Abstract A parentage case is described that revealed a potentially erroneous exclusion from paternity in three systems, two on chromosome 21 and one on…”
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Penetrating limbo-keratoplasty for granular and lattice corneal dystrophy: survival of donor limbal stem cells and intermediate-term clinical results by Spelsberg, Helga, Reinhard, Thomas, Henke, Lotte, Berschick, Peter, Sundmacher, Rainer

“…To assess clinical follow-up data, and to identify donor epithelial cells after homologous penetrating central limbo-keratoplasty in patients with granular and…”
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Searching for the origin of Romanies: Slovakian Romani, Jats of Haryana and Jat Sikhs Y-STR data in comparison with different Romani populations by Nagy, Melinda, Henke, Lotte, Henke, Jürgen, Chatthopadhyay, Prasanta K, Völgyi, Antónia, Zalán, Andrea, Peterman, Orsolya, Bernasovská, Jarmila, Pamjav, Horolma

“…Abstract Haplotype frequencies for 11 Y-STR markers (DYS19, DYS389I, DYS389II, DYS390, DYS391, DYS392, DYS393, DYS385, DYS437, DYS438 and DYS439) in a Romani…”
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Supplemented Data on Mutation Rates in 33 Autosomal Short Tandem Repeat Polymorphisms by Henke, Lotte, Henke, Jürgen

“…POPULATION: 106–8598 meioses studied in German Caucasians…”
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Which short tandem repeat polymorphisms are required for identification? Lessons from complicated kinship cases by Henke, Jürgen, Henke, Lotte

“…This paper presents 5 examples of complicated deficient parentage cases, which were sufficiently resolved by extensive DNA typing using short tandem repeat…”
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New alleles and mutational events at 14 STR loci from different German populations by Becker, Dorit, Bender, Klaus, Edelmann, Jeanett, Götz, Frank, Henke, Lotte, Hering, Sandra, Hohoff, Carsten, Hoppe, Karolin, Klintschar, Michael, Muche, Matthias, Rolf, Burkhard, Szibor, Reinhard, Weirich, Volker, Jung, Martin, Brabetz, Werner

“…Abstract The molecular origin of DNA mutations and the mutation rates were analyzed at 14 short tandem repeat (STR) loci with samples from trio cases derived…”
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