Hans-Henrik M. DAHL: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Atomic force microscopy imaging of DNA–cationic liposome complexes optimised for gene transfection into neuronal cells

Louise A. Wangerek, Hans-Henrik M. Dahl, Tim J. Senden, John B. Carlin, David A. Jans, Dave E. Dunstan, Panayiotis A. Ioannou, Robert Williamson, Susan M. Forrest

Journal:

The Journal of Gene Medicine

Year:

2001

Language:

english

File:

PDF, 398 KB

english, 2001

2

A novel splice site mutation in EYA4 causes DFNA10 hearing loss

Michael S. Hildebrand, David Coman, Tao Yang, R.J. McKinlay Gardner, Elizabeth Rose, Richard J.H. Smith, Melanie Bahlo, Hans-Henrik M. Dahl

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 167 KB

english, 2007

3

The pros and cons of mitochondrial manipulation in the human germ line

David R Thorburn, Hans-Henrik M Dahl, Keshav K Singh

Journal:

Year:

2001

Language:

english

File:

PDF, 78 KB

english, 2001

4

Chemical cleavage method for the detection of RNA base changes: Experience in the application to collagen mutations in osteogenesis imperfecta

John F. Bateman, Shireen R. Lamande, Marnie Hannagan, Ingrid Moeller, Hans-Henrik M. Dahl, William G. Cole

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 869 KB

english, 1993

5

Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options

David R. Thorburn, Hans-Henrik M. Dahl

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 291 KB

english, 2001

6

Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2–Xq28

David J. Amor, Hans-Henrik M. Dahl, Melanie Bahlo, Agnes Bankier

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 182 KB

english, 2007

7

Pyruvate dehydrogenase deficiency: Molecular basis for intrafamilial heterogeneity

Tatsuya Fujii, Rudy N. Van Coster, Susan E. Old, Rosella Medori, Susan Winter, Ruth M. Gubits, Paul M. Matthews, Ruth M. Brown, Garry K. Brown, Hans-Henrik M. Dahl, Dr. Darryl C. De Vivo

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 656 KB

english, 1994

8

A novel mutation (P316L) in a female with pyruvate dehydrogenase E1α deficiency

Fumie Takakubo, David R. Thorburn, Ruth M. Brown, Garry K. Brown, Hans-Henrik M. Dahl

Journal:

Year:

1995

Language:

english

File:

PDF, 140 KB

english, 1995

9

Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner ear

Shehnaaz S.M. Manji, Brita S. Sørensen, Tuomas Klockars, Timothy Lam, Wendy Hutchison, Hans-Henrik M. Dahl

Journal:

Journal of Neuroscience Research

Year:

2006

Language:

english

File:

PDF, 1.18 MB

english, 2006

10

Polymorphisms in the human X-linked pyruvate dehydrogenase E1α gene

Hans-Henrik M. Dahl, Wendy M. Hutchison, Zheng Guo, Sue M. Forrest, Lise Lotte Hansen

Journal:

Year:

1991

Language:

english

File:

PDF, 632 KB

english, 1991

11

Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patients

Hiroyuki Ikeda, Y. Matsubara, Hitoshi Mikami, Shigeo Kure, Misao Owada, Tamara Gough, Peter M. Smooker, Marion Dobbs, Hans-Henrik M. Dahl, Richard G. H. Cotton, Kuniaki Narisawa

Journal:

Year:

1997

Language:

english

File:

PDF, 85 KB

english, 1997

12

In Silico Analyses of Mouse Inner-Ear Transcripts

Tuomas Klockars, Teemu Perheentupa, Hans-Henrik M. Dahl

Journal:

Journal of the Association for Research in Otolaryngology

Year:

2003

Language:

english

File:

PDF, 182 KB

english, 2003

13

Survival of Partially Differentiated Mouse Embryonic Stem Cells in the Scala Media of the Guinea Pig Cochlea

Michael S. Hildebrand, Hans-Henrik M. Dahl, Jennifer Hardman, Bryony Coleman, Robert K. Shepherd, Michelle G. de Silva

Journal:

Journal of the Association for Research in Otolaryngology

Year:

2005

Language:

english

File:

PDF, 470 KB

english, 2005

14

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes

Cree, Lynsey M, Samuels, David C, de Sousa Lopes, Susana Chuva, Rajasimha, Harsha Karur, Wonnapinij, Passorn, Mann, Jeffrey R, Dahl, Hans-Henrik M, Chinnery, Patrick F

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 366 KB

english, 2008

15

Cochlear Implants for DFNA17 Deafness

Michael S. Hildebrand, Michelle G. de Silva, R. J. McKinlay Gardner, Elizabeth Rose, Carolyn A. de Graaf, Melanie Bahlo, Hans-Henrik M. Dahl

Journal:

The Laryngoscope

Year:

2006

Language:

english

File:

PDF, 427 KB

english, 2006

16

Isolation and characterisation of the mouse pyruvate dehydrogenase E1α genes

James Fitzgerald, Wendy M. Hutchison, Hans-Henrik M. Dahl

Journal:

Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression

Year:

1992

Language:

english

File:

PDF, 752 KB

english, 1992

17

Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

Canny Sugiana, David J. Pagliarini, Matthew McKenzie, Denise M. Kirby, Renato Salemi, Khaled K. Abu-Amero, Hans-Henrik M. Dahl, Wendy M. Hutchison, Katherine A. Vascotto, Stacey M. Smith, Robert F. Ne

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 1.13 MB

english, 2008

18

Cloning, mapping and expression analysis of the sheep Wilson disease gene homologue

Paul J. Lockhart, Stephen A. Wilcox, Hans-Henrik M. Dahl, Julian F.B. Mercer

Journal:

Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression

Year:

2000

Language:

english

File:

PDF, 629 KB

english, 2000

19

A High-Molecular-Weight Protein Component Required for Natural Messenger Translation in Ascites Tumor Cells

William A. STRYCHARZ, Marjut RANKI, Hans-Henrik M. DAHL

Journal:

Year:

1974

Language:

english

File:

PDF, 618 KB

english, 1974

20

The Purification and Properties of Two Low-Molecular-Weight Proteins Required for the Initiation of Translation in Ascites Tumour Cells

Hans-Henrik M. DAHL, Ebbe TRUELSEN, G. Eric BLAIR

Journal:

Year:

1977

Language:

english

File:

PDF, 683 KB

english, 1977

21

Expression of Recombinant Growth Hormone in Escherichia coli: Effect of the Region between the Shine-Dalgarno Sequence and the ATG Initiation Codon

DALBØGE, HENRIK, CARLSEN, SØREN, JENSEN, EINER BECH, CHRISTENSEN, THORKILD, DAHL, HANS-HENRIK M.

Journal:

Year:

1988

Language:

english

File:

PDF, 239 KB

english, 1988

22

The expression pattern of the pyruvate dehydrogenase E1α subunit genes during spermatogenesis in adult mouse

Fumie Takakubo, Hans-Henrik M. Dahl

Journal:

Experimental Cell Research

Year:

1992

Language:

english

File:

PDF, 17.65 MB

english, 1992

23

An ENU-Induced Mutation of Cdh23 Causes Congenital Hearing Loss, but No Vestibular Dysfunction, in Mice

Shehnaaz S.M. Manji, Kerry A. Miller, Louise H. Williams, Lotte Andreasen, Maria Siboe, Elizabeth Rose, Melanie Bahlo, Michael Kuiper, Hans-Henrik M. Dahl

Journal:

The American Journal of Pathology

Year:

2011

Language:

english

File:

PDF, 4.79 MB

english, 2011

24

Identification of Three Novel Hearing Loss Mouse Strains with Mutations in the Tmc1 Gene

Shehnaaz S.M. Manji, Kerry A. Miller, Louise H. Williams, Hans-Henrik M. Dahl

Journal:

The American Journal of Pathology

Year:

2012

Language:

english

File:

PDF, 3.69 MB

english, 2012

25

Expression of the carrier protein apolipoprotein D in the mouse inner ear

Michael S. Hildebrand, Michelle G. de Silva, Tuomas Klockars, C. Arturo Solares, Keiko Hirose, Jonathan D. Smith, Shutish C. Patel, Hans-Henrik M. Dahl

Journal:

Hearing Research

Year:

2005

Language:

english

File:

PDF, 762 KB

english, 2005

26

Gene expression profiling analysis of the inner ear

Michael S. Hildebrand, Michelle G. de Silva, Tuomas Klockars, Colleen A. Campbell, Richard J.H. Smith, Hans-Henrik M. Dahl

Journal:

Hearing Research

Year:

2007

Language:

english

File:

PDF, 394 KB

english, 2007

27

Mitochondrial myopathy with tRNA Leu(UUR) mutation and complex I deficiency responsive to riboflavin

Robert F. Ogle, John Christodoulou, Elizabeth Fagan, Rozanne B. Blok, Denise M. Kirby, Kaye L. Seller, Hans-Henrik M. Dahl, David R. Thorburn

Journal:

The Journal of Pediatrics

Year:

1997

Language:

english

File:

PDF, 1.82 MB

english, 1997

28

Characterisation of DRASIC in the mouse inner ear

Michael S. Hildebrand, Michelle G. de Silva, Tuomas Klockars, Elizabeth Rose, Margaret Price, Richard J.H. Smith, Wyman T. McGuirt, Helen Christopoulos, Christine Petit, Hans-Henrik M. Dahl

Journal:

Hearing Research

Year:

2004

Language:

english

File:

PDF, 1.15 MB

english, 2004

29

A eutherian X-linked gene, PDHA1, is autosomal in marsupials:A model for the evolution of a second, testis-specific variant in eutherian mammals

Jamie Fitzgerald, Stephen A. Wilcox, Jennifer A. Marshall Graves, Hans-Henrik M. Dahl

Journal:

Year:

1993

Language:

english

File:

PDF, 1.04 MB

english, 1993

30

Getting to the Nucleus of Mitochondrial Disorders: Identification of Respiratory Chain–Enzyme Genes Causing Leigh Syndrome

Hans-Henrik M. Dahl

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 302 KB

english, 1998

31

Genetic Counseling and Prenatal Diagnosis for the Mitochondrial DNA Mutations at Nucleotide 8993

Sarah L. White, Veronica R. Collins, Rory Wolfe, Maureen A. Cleary, Sara Shanske, Salvatore DiMauro, Hans-Henrik M. Dahl, David R. Thorburn

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 371 KB

english, 1999

32

Skewed Segregation of the mtDNA nt 8993 (TrG) Mutation in Human Oocytes

Rozanne B. Blok, Debra A. Gook, David R. Thorburn, Hans-Henrik M. Dahl

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 516 KB

english, 1997

33

Detection of Mutations in Genes Associated with Hearing Loss Using a Microarray-Based Approach

Kirby Siemering, Shehnaaz S.M. Manji, Wendy M. Hutchison, Desiree Du Sart, Dean Phelan, Hans-Henrik M. Dahl

Journal:

The Journal of Molecular Diagnostics

Year:

2006

Language:

english

File:

PDF, 1.65 MB

english, 2006

34

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Arsov, Todor, Mullen, Saul A., Damiano, John A., Lawrence, Kate M., Huh, Linda L., Nolan, Melinda, Young, Helen, Thouin, Anaïs, Dahl, Hans-Henrik M., Berkovic, Samuel F., Crompton, Douglas E., Sadleir

Journal:

Year:

2012

Language:

english

File:

PDF, 64 KB

english, 2012

35

Analysis of pyruvate dehydrogenase expression in embryonic mouse brain: localization and developmental regulation

Fumie Takakubo, Hans-Henrik M. Dahl

Journal:

Developmental Brain Research

Year:

1994

Language:

english

File:

PDF, 2.09 MB

english, 1994

36

Clinical and molecular features of adPEO due to mutations in the Twinkle gene

Sharon Lewis, Wendy Hutchison, Dominic Thyagarajan, Hans-Henrik M Dahl

Journal:

Journal of the Neurological Sciences

Year:

2002

Language:

english

File:

PDF, 202 KB

english, 2002

37

Isolation of β-globin-related genes from a human cosmid library

Grosveld, Frank G., Dahl, Hans-Henrik M., de Boer, Ernie, Flavell, Richard A.

Journal:

Year:

1981

Language:

english

File:

PDF, 1.02 MB

english, 1981

38

ROYAL COLLEGE OF SURGEONS OF ENGLAND: MUSEUM DEMONSTRATIONS.

Dahl, Hans-Henrik M.

Journal:

Year:

1914

Language:

english

File:

PDF, 175 KB

english, 1914

39

Constructing the optimal promotor

Dahl, Hans-Henrik M.

Journal:

Trends in Biochemical Sciences

Year:

1983

Language:

english

File:

PDF, 86 KB

english, 1983

40

Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction

Williams, Louise H., Miller, Kerry A., Dahl, Hans-Henrik M., Manji, Shehnaaz S.M.

Journal:

Hearing Research

Year:

2013

Language:

english

File:

PDF, 2.78 MB

english, 2013

41

X-Chromosome localization of the functional gene for the E1α subunit of the human pyruvate dehydrogenase complex

Brown, Ruth M., Dahl, Hans-Henrik M., Brown, Garry K.

Journal:

Year:

1989

Language:

english

File:

PDF, 2.26 MB

english, 1989

42

A Novel Enzymatic Method for Production of Authentic hGH from an Escherichia Coli produced hGH–Precursor

Dalbøge, Henrik, Dahl, Hans-Henrik M., Pedersen, John, Hansen, Jørli W., Christensen, Thorkild

Journal:

Year:

1987

File:

PDF, 910 KB

1987

43

Glucose metabolism transporters and epilepsy: Only GLUT1 has an established role

Hildebrand, Michael S., Damiano, John A., Mullen, Saul A., Bellows, Susannah T., Oliver, Karen L., Dahl, Hans-Henrik M., Scheffer, Ingrid E., Berkovic, Samuel F.

Journal:

Year:

2014

Language:

english

File:

PDF, 134 KB

english, 2014

44

Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy

Hitomi, Yuki, Heinzen, Erin L., Donatello, Simona, Dahl, Hans-Henrik, Damiano, John A., McMahon, Jacinta M., Berkovic, Samuel F., Scheffer, Ingrid E., Legros, Benjamin, Rai, Myriam, Weckhuysen, Sarah,

Journal:

Annals of Neurology

Year:

2013

Language:

english

File:

PDF, 283 KB

english, 2013

45

Identification of SLC26A4 Mutations in Patients with Hearing Loss and Enlarged Vestibular Aqueduct Using High-Resolution Melting Curve Analysis

Mercer, Stephen, Mutton, Patricia, Dahl, Hans-Henrik M.

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2011

Language:

english

File:

PDF, 210 KB

english, 2011

46

Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia

Damiano, John A., Afawi, Zaid, Bahlo, Melanie, Mauermann, Monika, Misk, Adel, Arsov, Todor, Oliver, Karen L., Dahl, Hans-Henrik M., Shearer, A. Eliot, Smith, Richard J.H., Hall, Nathan E., Mahmood, Kh

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 1.01 MB

english, 2015

47

Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1α subunit

Hansen, Lise Lotte, Horn, Nina, Dahl, Hans-Henrik M., Kruse, Torben A.

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.62 MB

english, 1994

48

Language and Speech Perception Outcomes in Hearing-Impaired Children with and without Connexin 26 Mutations

Dahl, Hans-Henrik M., Wake, Melissa, Sarant, Julia, Poulakis, Zeffie, Siemering, Kirby, Blamey, Peter

Journal:

Audiology & Neuro-Otology

Year:

2003

Language:

english

File:

PDF, 95 KB

english, 2003

49

Gene expression changes during step-wise differentiation of embryonic stem cells along the inner ear hair cell pathway

De Silva, Michelle G., Hildebrand, Michael S., Christopoulos, Helen, Newman, Michelle R., Bell, Katrina, Ritchie, Matthew, Smyth, Gordon K., Dahl, Hans-Henrik M.

Journal:

Acta Oto-Laryngologica

Year:

2006

Language:

english

File:

PDF, 188 KB

english, 2006

50

NcoI and HinfI RFLPs detected with a dihydropteridine reductase cDNA probe

Wake, Samantha, Hutchison, Wendy, Dahl, Hans-Henrik M.

Journal:

Nucleic Acids Research

Year:

1988

Language:

english

File:

PDF, 643 KB

english, 1988