Novel variants in UBE2B gene and idiopathic male infertility.
暂无分享,去创建一个
L. Singh | K. Thangaraj | B. Chakravarty | A. Khattri | D. Rani | N. Gupta | S. Panneerdoss | M. Deenadayal | V. Suryavathi | K. Gopal
[1] L. Singh,et al. Allelic variation in the NPY gene in 14 Indian populations , 2007, Journal of Human Genetics.
[2] L. Singh,et al. Single nucleotide polymorphisms in alcohol dehydrogenase genes among some Indian populations , 2007, American journal of human biology : the official journal of the Human Biology Council.
[3] C. Tyler-Smith,et al. Y-chromosomal insights into the genetic impact of the caste system in India , 2007, Human Genetics.
[4] L. Singh,et al. A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent. , 2006, Fertility and sterility.
[5] L. Singh,et al. Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome , 2006, Acta neurologica Scandinavica.
[6] L. Singh,et al. A novel human sex-determining gene linked to Xp11.21-11.23. , 2006, The Journal of clinical endocrinology and metabolism.
[7] L. Singh,et al. A to G transitions at 260, 386 and 437 in DAZL gene are not associated with spermatogenic failure in Indian population. , 2006, International journal of andrology.
[8] G. Chaubey,et al. Genetic affinities among the lower castes and tribal groups of India: inference from Y chromosome and mitochondrial DNA , 2006, BMC Genetics.
[9] G. Chaubey,et al. In situ origin of deep rooting lineages of mitochondrial Macrohaplogroup 'M' in India , 2006, BMC Genomics.
[10] Gang Chen,et al. Survey of the two polymorphisms in DAZL, an autosomal candidate for the azoospermic factor, in Japanese infertile men and implications for male infertility. , 2005, Molecular human reproduction.
[11] G. Chaubey,et al. Reconstructing the Origin of Andaman Islanders , 2005, Science.
[12] M. Gabut,et al. The SR Protein SC35 Is Responsible for Aberrant Splicing of the E1α Pyruvate Dehydrogenase mRNA in a Case of Mental Retardation with Lactic Acidosis , 2005, Molecular and Cellular Biology.
[13] G. Chaubey,et al. Different population histories of the Mundari- and Mon-Khmer-speaking Austro-Asiatic tribes inferred from the mtDNA 9-bp deletion/insertion polymorphism in Indian populations , 2005, Human Genetics.
[14] M. Stephens,et al. Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-data Imputation , 2022 .
[15] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[16] L. Singh,et al. Y chromosome deletions in azoospermic men in India. , 2003, Journal of andrology.
[17] H. Tempest,et al. The genetic basis of infertility. , 2003, Reproduction.
[18] L. Singh,et al. Sperm mitochondrial mutations as a cause of low sperm motility. , 2003, Journal of Andrology.
[19] J. Hoeijmakers,et al. Loss of HR6B Ubiquitin-Conjugating Activity Results in Damaged Synaptonemal Complex Structure and Increased Crossing-Over Frequency during the Male Meiotic Prophase , 2003, Molecular and Cellular Biology.
[20] J. Llorca. Computer programs for epidemiologists. PEPI v. 4.0 , 2002 .
[21] L. Singh,et al. CAG repeat expansion in the androgen receptor gene is not associated with male infertility in Indian populations. , 2002, Journal of andrology.
[22] Shio‐Jean Lin,et al. Association of a single-nucleotide polymorphism of the deleted-in-azoospermia-like gene with susceptibility to spermatogenic failure. , 2002, The Journal of clinical endocrinology and metabolism.
[23] M. Hochstrasser. SP-RING for SUMO New Functions Bloom for a Ubiquitin-like Protein , 2001, Cell.
[24] P. Patrizio,et al. Larger trinucleotide repeat size in the androgen receptor gene of infertile men with extremely severe oligozoospermia. , 2001, Journal of andrology.
[25] P. Donnelly,et al. A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.
[26] P L Pearson,et al. Towards an understanding of the genetics of human male infertility: lessons from flies. , 2000, Trends in genetics : TIG.
[27] J. Venables,et al. Lessons from knockout and transgenic mice for infertility in men , 2000, Journal of endocrinological investigation.
[28] L. Chasin,et al. Multiple Splicing Defects in an Intronic False Exon , 2000, Molecular and Cellular Biology.
[29] Li Chen,et al. Evidence for an Interaction between Ubiquitin-Conjugating Enzymes and the 26S Proteasome , 2000, Molecular and Cellular Biology.
[30] J. Hoeijmakers,et al. Knockout mouse model and gametogenic failure , 1998, Molecular and Cellular Endocrinology.
[31] A. Ciechanover. Ubiquitin–mediated proteolysis and male sterility , 1996, Nature Medicine.
[32] J. Hoeijmakers,et al. Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification , 1996, Cell.
[33] A. Montagnani. [Clinical aspects of male infertility]. , 1967, Minerva dermatologica.
[34] N. Reynolds,et al. Role of the DAZ genes in male fertility. , 2005, Reproductive biomedicine online.
[35] S. Fleming,et al. The possible biological and reproductive functions of ubiquitin. , 2001, Human reproduction update.