Hansmann, Ingo : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (52)
Les plus populaires
Liste
- Liste
- Tableau

1

Molecular Structure and Chromosomal Mapping of the Human Homolog of the Agouti Gene

Heajoon Y. Kwon, Scott J. Bultman, Christiane Löffler, Wen-Ji Chen, Paul J. Furdon, John G. Powell, Anton-Lewis Usala, William Wilkison, Ingo Hansmann and Richard P. Woychik

Journal:

Proceedings of the National Academy of Sciences

Année:

1994

Langue:

english

Fichier:

PDF, 1.69 MB

english, 1994

2

Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7

Hehr, Ute, D�rr, Sylvia, Hagemann, Monika, Hansmann, Ingo, Preiss, Uwe, Br�mme, Sabine

Journal:

American Journal of Medical Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 179 KB

english, 2000

3

Chromosomal mosaicism of trisomy 7 restricted to chorionic villi

Iris Bartels, Rüdiger Rauskolb, Ingo Hansmann, Giovanni Neri

Journal:

American Journal of Medical Genetics Part A

Année:

1986

Langue:

english

Fichier:

PDF, 127 KB

english, 1986

4

The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS)

Ulrich Langenbeck, Isabell Varga, Ingo Hansmann

Journal:

American Journal of Medical Genetics Part A

Année:

1988

Langue:

english

Fichier:

PDF, 381 KB

english, 1988

5

Down syndrome at birth not detected by first-trimester chorionic villus sampling

Iris Bartels, Ingo Hansmann, Ute Holland, Barbara Zoll, Rüdiger Rauskolb

Journal:

American Journal of Medical Genetics Part A

Année:

1989

Langue:

english

Fichier:

PDF, 178 KB

english, 1989

6

Excess of females in chromosomally normal spontaneous abortuses

Dr. Iris Bartels, Ingo Hansmann, Bernd Eiben

Journal:

American Journal of Medical Genetics Part A

Année:

1990

Langue:

english

Fichier:

PDF, 143 KB

english, 1990

7

Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVS

Jürgen Bernert, Iris Bartels, Gudrun Gatz, Ingo Hansmann, Martina Heyat, Paul D. Niedmann, Helga Rehder, Claus Waldenmaier, Barbara Zoll

Journal:

American Journal of Medical Genetics Part A

Année:

1992

Langue:

english

Fichier:

PDF, 395 KB

english, 1992

8

Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression

Paweł Stankiewicz, Hannelore Thiele, Ioannis Giannakudis, Mike Schlicker, Christiane Baldermann, Antje Krüger, Sylvia Dörr, Heike Starke, Ingo Hansmann

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 351 KB

english, 2001

9

Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus

Paweł Stankiewicz, Hannelore Thiele, Christiane Baldermann, Antje Krüger, Ioannis Giannakudis, Sylvia Dörr, Nadeshda Werner, Jürgen Kunz, Gudrun A. Rappold, Ingo Hansmann

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 249 KB

english, 2001

10

Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 gene

Paweł Stankiewicz, Jolanta Rujner, Christiane Löffler, Antje Krüger, Manjunath Nimmakayalu, Bożena Piłacik, Małgorzata Krajewska-Walasek, Anna Gutkowska, Ingo Hansmann, Ioannis Giannakudis

Journal:

American Journal of Medical Genetics Part A

Année:

2001

Langue:

english

Fichier:

PDF, 330 KB

english, 2001

11

Duplication of Xq26.2–q27.1, including SOX3, in a mother and daughter with short stature and dyslalia

Paweł Stankiewicz, Hannelore Thiele, Mike Schlicker, Andrea Cseke-Friedrich, Sylva Bartel-Friedrich, Svetlana A. Yatsenko, James R. Lupski, Ingo Hansmann

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 202 KB

english, 2005

12

Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome

Albrecht Röpke, Annegret Kujat, Mechthild Gräber, Joannis Giannakudis, Ingo Hansmann

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 37 KB

english, 2003

13

Twelve novel JAG1 gene mutations in polish Alagille syndrome patients

Dorota Jurkiewicz, Ewa Popowska, Christiane Gläser, Ingo Hansmann, Małgorzata Krajewska-Walasek

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 119 KB

english, 2005

14

A sterile male with 45,X0 and a Y;22 translocation

Joachim Arnemann, Susanne Schnittger, Georg K. Hinkel, Erika Tolkendorf, Jörg Schmidtke, Ingo Hansmann

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 826 KB

english, 1991

15

Mapping of the ribophorin II (RPN II) gene to human chromosome 20q12–q13.1 by in-situ hybridization

Christiane Löffler, V. V. N. Gopal Rao, Ingo Hansmann

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 187 KB

english, 1991

16

The gene for bone morphogenetic protein 2A (BMP2A) is localized to human chromosome 20pl2 by radioactive and nonradioactive in situ hybridization

V. V. N. Gopal Rao, Christiane Löffler, John M. Wozney, Ingo Hansmann

Journal:

Année:

1992

Langue:

english

Fichier:

PDF, 510 KB

english, 1992

17

A cytogenetic study directly from chorionic villi of 140 spontaneous abortions

Bernd Eiben, Sabine Borgmann, Ingrid Schübbe, Ingo Hansmann

Journal:

Année:

1987

Langue:

english

Fichier:

PDF, 482 KB

english, 1987

18

Meiotic nondisjunction in oocytes from aged Djungarian hamsters correlates with an alteration in meiosis rate but not in univalent formation

Edith Hummler, Franz Theuring, Ingo Hansmann

Journal:

Année:

1987

Langue:

english

Fichier:

PDF, 1.15 MB

english, 1987

19

The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions

Carmen Minguillon, Bernd Eiben, Susan Bähr-Porsch, Martin Vogel, Ingo Hansmann

Journal:

Année:

1989

Langue:

english

Fichier:

PDF, 416 KB

english, 1989

20

Maternal modulation of the inheritable meiosis I error Dipl I in mouse oocytes is associated with the type of mitochondrial DNA

Friedrich Beermann, Edith Hummler, Ulrich Franke, Ingo Hansmann

Journal:

Année:

1988

Langue:

english

Fichier:

PDF, 273 KB

english, 1988

21

A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13

Susanne Schnittger, Friedrich Beermann, Ingo Hansmann

Journal:

Année:

1989

Langue:

english

Fichier:

PDF, 138 KB

english, 1989

22

Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)

Susanne Schnittger, Christiane Höfers, Peter Heidemann, Friedrich Beermann, Ingo Hansmann

Journal:

Année:

1989

Langue:

english

Fichier:

PDF, 875 KB

english, 1989

23

Pattern and frequency of nondisjunction in oocytes from the Djungarian hamster are determined by the stage of first meiotic spindle inhibition

Edith Hummler, Ingo Hansmann

Journal:

Année:

1988

Langue:

english

Fichier:

PDF, 1.51 MB

english, 1988

24

Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age

Friedrich Beermann, Iris Bartels, Ulrich Franke, Ingo Hansmann

Journal:

Année:

1987

Langue:

english

Fichier:

PDF, 1.17 MB

english, 1987

25

Phenotypic variability inHey2 −/−mice and absence ofHEY2mutations in patients with congenital heart defects or Alagille syndrome

Andreas Fischer, Barbara Klamt, Nina Schumacher, Christiane Glaeser, Ingo Hansmann, Hartmut Fenge, Manfred Gessler

Journal:

Mammalian Genome

Année:

2004

Langue:

english

Fichier:

PDF, 230 KB

english, 2004

26

Genomic structure of karyopherin α2 (KPNA2) within a low-copy repeat on chromosome 17q23-q24 and mutation analysis in patients with Russell-Silver syndrome

Sylvia Dörr, Mike Schlicker, Ingo Hansmann

Journal:

Année:

2001

Langue:

english

Fichier:

PDF, 156 KB

english, 2001

27

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

Giannakudis, Joannis, Röpke, Albrecht, Kujat, Annegret, Krajewska-Walasek, Malgorzata, Hughes, Helen, Fryns, Jean-Pierre, Bankier, Agnes, Amor, David, Schlicker, Mike, Hansmann, Ingo

Journal:

European Journal of Human Genetics

Année:

2001

Langue:

english

Fichier:

PDF, 179 KB

english, 2001

28

Parental mosaicism of JAG1 mutations in families with Alagille syndrome

Giannakudis, Joannis, Röpke, Albrecht, Kujat, Annegret, Krajewska-Walasek, Malgorzata, Hughes, Helen, Fryns, Jean-Pierre, Bankier, Agnes, Amor, David, Schlicker, Mike, Hansmann, Ingo

Journal:

European Journal of Human Genetics

Année:

2001

Fichier:

PDF, 37 KB

2001

29

Prenatal diagnosis of genetic disease by chorionic villi sampling

Iris Bartels, Ingo Hansmann

Journal:

Indian Journal of Pediatrics

Année:

1986

Langue:

english

Fichier:

PDF, 650 KB

english, 1986

30

The induction of non-disjunction by irradiation in mammalian oogenesis and spermatogenesis

Ingo Hansmann, Hans-Dieter Probeck

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Année:

1979

Langue:

english

Fichier:

PDF, 497 KB

english, 1979

31

Fanconi's Anaemia Developing Erythroleukaemia

Gregor Prindull, Eberhard Jentsch, Ingo Hansmann

Journal:

European Journal of Haematology

Année:

1979

Langue:

english

Fichier:

PDF, 626 KB

english, 1979

32

Trisomy 4 due to nondisjunction during maternal meiosis II

Iris Bartels, Ingo Hansmann

Journal:

Clinical Genetics

Année:

1986

Langue:

english

Fichier:

PDF, 74 KB

english, 1986

33

Partial deletion of 4p in fetal cells not present in chorionic villi

Bernd Eiben, Michael Leipoldt, Ingrid Schübbe, Rainer Ulbrich, Ingo Hansmann

Journal:

Clinical Genetics

Année:

1988

Langue:

english

Fichier:

PDF, 316 KB

english, 1988

34

Cystatin C (CST3), the Candidate Gene for Hereditary Cystatin C Amyloid Angiopathy (HCCAA), and Other Members of the Cystatin Gene Family Are Clustered on Chromosome 20p11.2

Susanne Schnittger, V.V.N.Gopal Rao, Magnus Abrahamson, Ingo Hansmann

Journal:

Année:

1993

Fichier:

PDF, 513 KB

1993

35

The Gene for the Amyloid Precursor-like Protein APLP2 Is Assigned to Human Chromosome 11q23-q25

Heinz von der Kammer, Christiane Löffler, Jozef Hanes, Jaroslav Klaudiny, Karl Heinz Scheit, Ingo Hansmann

Journal:

Année:

1994

Fichier:

PDF, 410 KB

1994

36

Construction of a Detailed Physical and Transcript Map of the Candidate Region for Russell–Silver Syndrome on Chromosome 17q23–q24

Sylvia Dörr, Alina T. Midro, Claudia Färber, Joannis Giannakudis, Ingo Hansmann

Journal:

Année:

2001

Langue:

english

Fichier:

PDF, 146 KB

english, 2001

37

Paramutation-Like Effects at the Mouse scapinin (Phactr3) Locus

Sebastian Worch, Ingo Hansmann, Dietmar Schlote

Journal:

Journal of Molecular Biology

Année:

2008

Langue:

english

Fichier:

PDF, 624 KB

english, 2008

38

Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library

Stolz, Frank-Michael, Pfau, Hans-Peter, Reipen, Gernot, Schnittger, Susanne, Grzeschik, Karl-Heinz, Hansmann, Ingo

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 1.52 MB

english, 1991

39

The gene for the novel vasoactive peptide endothelin 3 (EDN3) is localized to human chromosome 20q13.2-qter

Gopal Rao, V.V.N., Löffler, Christiane, Hansmann, Ingo

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 200 KB

english, 1991

40

PAX1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in Situ hybridization (ISH and FISH)

Schnittger, Susanne, Gopal Rao, V.V.N., Deutsch, Urban, Gruss, Peter, Balling, Rudi, Hansmann, Ingo

Journal:

Année:

1992

Langue:

english

Fichier:

PDF, 1.37 MB

english, 1992

41

The gene for receptor-linked protein-tyrosine-phosphatase (PTPA) is assigned to human chromosome 20p12-pter by in situ hybridization (ISH and FISH)

Rao, V.V.N. Gopal, Lo¨ffler, Christiane, Sap, Jan, Schlessinger, Joseph, Hansmann, Ingo

Journal:

Année:

1992

Langue:

english

Fichier:

PDF, 280 KB

english, 1992

42

G protein Gsα (GNAS1), the probable candidate gene for albright hereditary osteodystrophy, is assigned to human chromosome 20q12–q13.2

Gopal Rao, V.V.N., Schnittger, Susanne, Hansmann, Ingo

Journal:

Année:

1991

Langue:

english

Fichier:

PDF, 544 KB

english, 1991

43

Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature

Dutta, Usha R., Hansmann, Ingo, Schlote, Dietmar

Journal:

European Journal of Medical Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 915 KB

english, 2015

44

An Mspl and Pstl RFLP detected by probe pFMS22-1.4 [D20S22]

Stolz, Frank-Michael, Hansmann, Ingo

Journal:

Nucleic Acids Research

Année:

1990

Fichier:

PDF, 73 KB

1990

45

Inheritance of a meiosis I error expressed in mouse oocytes and modulated by a maternal factor

Beermann, Friedrich, Jenderny, Jutta, Hummler, Edith, Hansmann, Ingo

Journal:

Genetics Research

Année:

1987

Langue:

english

Fichier:

PDF, 469 KB

english, 1987

46

Impact of prenatal urinomas in patients with posterior urethral valves and postnatal renal function

Kleppe, Stefanie, Schmitt, Joachim, Geipel, Annegret, Gembruch, Ullrich, Hansmann, Manfred, Bartmann, Peter, Franke, Ingo, Heep, Axel

Journal:

Journal of Perinatal Medicine

Année:

2006

Langue:

english

Fichier:

PDF, 82 KB

english, 2006

47

Mathematical Modeling of Oncogenesis Control in Mature T-Cell Populations

Gerdes, Sebastian, Newrzela, Sebastian, Glauche, Ingmar, von Laer, Dorothee, Hansmann, Martin-Leo, Roeder, Ingo

Journal:

Frontiers in Immunology

Année:

2013

Langue:

english

Fichier:

PDF, 711 KB

english, 2013

48

Concepts in mature T-cell lymphomas – highlights from an international joint symposium on T-cell immunology and oncology *

Herling, Marco, Rengstl, Benjamin, Scholtysik, René, Hartmann, Sylvia, Küppers, Ralf, Hansmann, Martin-Leo, Diebner, Hans H., Roeder, Ingo, Abken, Hinrich, Newrzela, Sebastian, Kirberg, Jörg

Journal:

Leukemia and Lymphoma

Année:

2016

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2016

49

2. A Multilocus DNA Fingerprint with Built-in Security Devices

Krawczak, Michael, Schmidtke, Jörg, Epplen, Jörg T, Hansmann, Ingo, Thies, Ulrike

Journal:

Medicine Science and the Law

Année:

1994

Langue:

english

Fichier:

PDF, 876 KB

english, 1994

50

Transcriptomic Meta-Analysis of Multiple Sclerosis and Its Experimental Models

Raddatz, Barbara B. R., Hansmann, Florian, Spitzbarth, Ingo, Kalkuhl, Arno, Deschl, Ulrich, Baumgärtner, Wolfgang, Ulrich, Reiner, Stangel, Martin

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 2.07 MB

english, 2014