-
Clinical male infertility. II. Critical evaluation of the prospects for therapy.
Reprod Fertil Dev. 1994;6(1):9-12
PMID: 8066228
-
The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs.
Am J Hum Genet. 1999 Jan;64(1):232-49
PMID: 9915963
-
Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm.
Biol Reprod. 1995 Apr;52(4):729-36
PMID: 7779994
-
Nitric oxide inhibition of human sperm motility.
Fertil Steril. 1995 Aug;64(2):408-13
PMID: 7615122
-
Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease.
N Engl J Med. 1995 Sep 7;333(10):638-44
PMID: 7637726
-
1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.
Am J Hum Genet. 1995 Aug;57(2):201-23
PMID: 7668244
-
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene.
Nat Genet. 1995 Aug;10(4):383-93
PMID: 7670487
-
Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome.
Lancet. 1996 May 11;347(9011):1290-3
PMID: 8622504
-
Paleolithic and neolithic lineages in the European mitochondrial gene pool.
Am J Hum Genet. 1996 Jul;59(1):185-203
PMID: 8659525
-
Mitochondrial disorders.
Mol Hum Reprod. 1997 Feb;3(2):133-48
PMID: 9239718
-
Asthenozoospermia and the human sperm mid-piece.
Hum Reprod. 1995 Jan;10(1):116-9
PMID: 7745038
-
Increased frequency of mutations in DNA from infertile men with meiotic arrest.
Hum Reprod. 2000 Jun;15(6):1289-94
PMID: 10831557
-
Human mtDNA haplogroups associated with high or reduced spermatozoa motility.
Am J Hum Genet. 2000 Sep;67(3):682-96
PMID: 10936107
-
The absence of a pyrimidine dimer repair mechanism in mammalian mitochondria.
Proc Natl Acad Sci U S A. 1974 Jul;71(7):2777-81
PMID: 4212385
-
Fate during cell growth of yeast mitochondrial and nuclear DNA after photolytic attachment of the monoazide analog of ethidium.
Biochem Biophys Res Commun. 1979 Sep 27;90(2):582-6
PMID: 389242
-
The role of oxidative phosphorylation in the generation of ATP in human spermatozoa.
J Reprod Fertil. 1981 Sep;63(1):271-8
PMID: 7277330
-
Interdependence of mitochondrial ATP production and extramitochondrial ATP utilization in intact spermatozoa.
Biochim Biophys Acta. 1985 Jul 17;808(2):316-22
PMID: 3848331
-
Normal oxidative damage to mitochondrial and nuclear DNA is extensive.
Proc Natl Acad Sci U S A. 1988 Sep;85(17):6465-7
PMID: 3413108
-
Physiology and pathophysiology of the human spermatozoon: the role of electron microscopy.
J Electron Microsc Tech. 1991 Apr;17(4):412-36
PMID: 1865240
-
Metabolic regulation in mammalian sperm: mitochondrial volume determines sperm length and flagellar beat frequency.
Cell Motil Cytoskeleton. 1991;19(3):180-8
PMID: 1878988
-
A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis.
Cell. 1993 Dec 31;75(7):1287-95
PMID: 8269511
-
Mitochondrial disease and reduced sperm motility.
Hum Reprod. 1993 Nov;8(11):1863-8
PMID: 8288752
-
Mitochondria and male disease.
Nature. 1996 Sep 19;383(6597):224
PMID: 8805695
-
Short-term inhibition of the energy metabolism affects motility but not surface properties of sperm cells.
Biosci Rep. 1996 Feb;16(1):35-40
PMID: 8861538
-
Classification of European mtDNAs from an analysis of three European populations.
Genetics. 1996 Dec;144(4):1835-50
PMID: 8978068
-
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
Am J Hum Genet. 1997 Feb;60(2):381-7
PMID: 9012411
-
Microdeletions in the Y chromosome of infertile men.
N Engl J Med. 1997 Feb 20;336(8):534-9
PMID: 9023089
-
Mitochondrial mutations and male infertility.
Nat Med. 1997 Feb;3(2):124-5
PMID: 9018221
-
Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Genomics. 1997 Jan 1;39(1):8-18
PMID: 9027481
-
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.
Am J Hum Genet. 1997 May;60(5):1107-21
PMID: 9150158
-
The molecular genetics of male infertility.
Bioessays. 1997 Sep;19(9):801-9
PMID: 9297971
-
Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease.
Hum Mol Genet. 1997 Oct;6(11):1835-46
PMID: 9302261
-
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene.
Hum Mol Genet. 1998 Jan;7(1):97-107
PMID: 9384609
-
Correlation of sperm motility with mitochondrial enzymatic activities.
Clin Chem. 1998 Aug;44(8 Pt 1):1616-20
PMID: 9702947